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If the substance was not covered by the EC Inventory, ECHA attributes a list number in the same format, starting with the numbers 6, 7, 8 or 9. Lycopene is a bright red carotenoid hydrocarbon found in tomatoes and other red fruits and vegetables, such as red carrots, watermelons, grapefruits, and papayas, but it is not present in strawberries or cherries. inside a watch) or with very low concentrations considered not to pose risks to human health or the environment. Top; Chemical data; Publications; Biomarker data. Ph. Carotenoid Name: 3,4,3'-Trihydroxy-β-carotene; 3,4,3'-Trihydroxy-beta-carotene IUPAC name: beta,beta-Carotene-3,4,3'-triol. J Chromatogr A. Last week we packed our poolside essentials and flew to Morocco for some vitamin CC. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment. Warning! S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S18:Handle and open container with care. Carotenoid Name: 2,3,2'-Trihydroxy-β-carotene; 2,3,2'-Trihydroxy-beta-carotene IUPAC name: beta,beta-Carotene-2,3,2'-triol. Use 13-cis-Beta,beta-carotene for fast, easy, and consistent DNA/RNA Purification, Antibody/Protein Purification, Cell Isolation. It is a member of the carotenes, which are terpenoids, synthesized biochemically from eight isoprene units and thus having 40 carbons. This information is only displayed if the substance is well–defined, its identity is not claimed confidential and there is sufficient information available in ECHA’s databases for ECHA’s algorithms to generate a molecular structure. Isolation of β-carotene, α-carotene and lutein from carrots by countercurrent chromatography with the solvent system modifier benzotrifluoride. The purpose of the information provided under this section is to highlight the substance hazardousness in a readable format. Risk Statements: 44-36/37/38-20/21/22 Print infocard . First reported in 1953, it was discovered to occur in small quantities when the fungus Phycomyces blakeseeanus was grown with diphenylamine, a compound that inhibits the synthesis of beta-carotene. Beta-Carotene. Other relevant information includes the following: To see the full list of notified classifications and to get more information on impurities and additives relevant to classification please consult the C&L Inventory. 215–540–4, is covered by three harmonisations: 005–011–00–4; 005–011–01–1 and 005–011–02–9), CLH information cannot be displayed in the InfoCard as the difference between the CLH classifications requires manual interpretation or verification. More information about CAS and the CAS registry can be found here. Structure Search similar carotenoids Mol file: Carotenoid DB Fingerprints Predict biological activities of this carotenoid 3-OH, 4-OH, beta,beta. -Carotene 01YAE03M7J 1,1'-(3,7,12,16-Tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis(2,6,6-trimethylcyclohexene 1,1'-(3,7,12,16-Tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis(2,6,6-trimethylcyclohexene), (all E)- 1,1'-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaene-1,18-diyl]bis(2,6,6-trimethylcyclohexene) 1,18-Bis(2,6,6-trimethyl-1-cyclohexenyl)-3,7,12,16-tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonene 1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene 116-32-5 117179-EP2292227A2 117179-EP2298776A1 2,2'-((1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaene-1,18-diyl)bis(1,3,3-trimethylcyclohex-1-ene) 3046-EP2298772A1 3046-EP2308839A1 7235-40-7 89648336-F9B2-44A0-9BF8-62E73369CB9B AB00051925_06 AB00051925_07 AB2000280 AC-1869 AC1NQX3D AC1Q28DI AKOS015896682 all trans beta-Carotene all-E-.beta.-Carotene all-trans-.beta.-Carotene all-trans-beta,beta-Carotene, synthetic all-trans-beta-Carotene AN-14537 AS-13354 b,b-Carotene BC208855 b-Carotene BDBM54988 beta Beta Carotene beta -carotene beta Carotene (USP) Beta carotene [USAN:USP] beta carotene [USAN] Beta Carotene Natural Beta Carotene, United States Pharmacopeia (USP) Reference Standard beta, beta-all-trans-Carotene, natural / Crystal beta, beta-all-trans-Carotene, natural / Dry water Dispersable beta, beta-all-trans-Carotene, natural / Vegetable Oil Solution beta,beta-Carotene beta-Carotene Betacarotene beta-carotene Betacarotene (INN) Betacarotene [INN] beta-Carotene, >=97.0% (UV) beta-Carotene, all-trans- beta-Carotene, Pharmaceutical Secondary Standard beta-Carotene, Pharmaceutical Secondary Standard Certified Reference Material beta-Carotene, Type I, synthetic, >=93% (UV), powder beta-Carotene, Type II, synthetic, >=95% (HPLC), crystalline beta-Carotene, Vetec(TM) reagent grade, >=93% beta-carotenes Betacaroteno Betacaroteno [INN-Spanish] Betacaroteno [Spanish] Betacarotenum Betacarotenum [INN-Latin] Betacarotenum [Latin] beta-Carotin beta-Carotine beta-Karotin BetaVit BIDD:PXR0110 bmse000832 BSPBio_003404 C.I. All Functions: skin conditioning. Allowed Colorants: Annex IV, Regulation 1223/2009/EC on Cosmetic Products, as amended by Regulation 2019/681/EU, 2 May 2019, Registration, Evaluation, Authorisation and Restriction of Chemicals, Chemical Agents Directive and Carcinogens or Mutagens Directive, Cosmetic Products Regulation, Annex IV - Allowed Colorants, 1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohex-1-en-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]cyclohex-1-ene, 1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene, EC Inventory, C&L Inventory, Registration dossier, Pre-Registration process, Other, Cosmetic Products Regulation, Annex IV - Allowed Colorants, Substances of very high concern identification, Recommendation for the Authorisation List, Getting started with EU chemicals legislation, Classification of substances and mixtures, Harmonised classification and labelling (CLH). IUPAC names 1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohex-1-en-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]cyclohex-1-ene Other Substance identity Substance identity. The use information is displayed per substance life cycle stage (consumer use, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites or in manufacturing). ChEBI Name β-carotene: ChEBI ID CHEBI:17579: ChEBI ASCII Name ... ChEBI ASCII Name beta-carotene: Definition A cyclic carotene obtained by dimerisation of all-trans-retinol. EINECS/ELINCS No: 230-636-6. It is possible that a harmonisation is introduced through an amendment to the CLP Regulation. First reported in 1953, it was discovered to occur in small quantities when the fungus Phycomyces blakeseeanus was grown with diphenylamine, a compound that inhibits the synthesis of beta-carotene… Regulatory process names 2 IUPAC names 2 Other identifiers 1 . If a substance is classified under multiple CLH entries, a link to the C&L Inventory is provided to allow users to view CLH information associated with the substance and no text is automatically generated for the InfoCard. InfoCards are generated automatically based on the data available at the time of generation. Substance identity Substance identity. RTECS: FI0329500 Substances may have impurities and additives that lead to different classifications. This information is only displayed if the substance is well-defined, its identity is not claimed confidential and there is sufficient information available in ECHA’s databases for ECHA’s algorithms to generate a molecular structure. It is the most abundant form of carotenoid and it is a precursor of the vitamin A. Beta-carotene is composed of two retinyl groups. beta-Carotene: Flammpunkt: 103°C (217°F) Schmelzpunkt: 178°C to 179°C: CAS: 7235-40-7: MDL-Nummer: MFCD00001556: Synonym: beta-carotene, beta carotene, betacarotene, beta,beta-carotene, provitamin a, solatene, carotaben, provatene, all-trans-beta-carotene, serlabo: InChI-Schlüssel: OENHQHLEOONYIE-JLTXGRSLSA-N: IUPAC-Name A substance identified primarily by an EC or list number may be linked with more than one CAS number, or with CAS numbers that have been deleted. ECHA has no public registered data on the types of manufacture using this substance. Carotenes are photosynthetic pigments important for photosynthesis. This section provides links to the list of precautions (precautionary statements) and to the guidance on safe use, if they have been provided in REACH registration dossiers. Useful NMR Links; NMR Wiki; WeNMR; Collaborators. This substance is used for the manufacture of: chemicals. Other names. Molecular Weight : 584.848 g/mol. If the substance is covered by more than one CLH entry (e.g. Please upgrade your Internet Explorer to a newer version. The source of the information is mentioned in the introductory sentence of the hazard statements. ID: 273: Name: 9-cis-beta-Carotene: … Catalog Number … This substance is used in the following products: cosmetics and personal care products. Vietnamese gac ( Momordica cochinchinensis Spreng.) The term carotene (also carotin, from the Latin carota, "carrot") is used for many related unsaturated hydrocarbon substances having the formula C 40 H x, which are synthesized by plants but in general cannot be made by animals (with the exception of some aphids and spider mites which acquired the synthesizing genes from fungi). Name: Beta Carotenum | Chemical/IUPAC Name: .Beta.,.Beta.-Carotene. Name: ß,ß-Carotene Data P-Carotene P,P-Carotene pp.-car Major pigment in higher plants, green algae; minor or trace pigment in chromophyte algae Yellow-orange 536.88 2500 (at 454 nm in acetone) Hiyama et al. Carotene, Provitamin A Carotin CAS-7235-40-7 CC0205 CCG-36062 CCRIS 3245 Certified Reference Material CHEBI:17579 CHEMBL1293 CI 40800 CI 75130 cid_5280489 CS-2262 Cyclohexene, 1,1'-(3,7,12,16-tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis(2,6,6-trimethyl-, (all-E)- Cyclohexene, 1,1'-(3,7,12,16-tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis[2,6,6-trimethyl-, (all-E)- D03101 DB06755 Diet,beta-carotene supplementation DSSTox_CID_253 DSSTox_GSID_20253 DSSTox_RID_75466 DTXSID3020253 E160A EC 230-636-6 EINECS 230-636-6 Food orange 5 H982 HMS2091M17 HMS501A12 HSDB 3264 HY-N0411 I(2)-Carotene I06-2213 I14-38736 IDI1_000330 J10299 Karotin Karotin [Czech] KPMK LMPR01070001 LS-1621 Lucaratin MFCD00001556 MLS001066383 N1547 Natural Yellow 26 NCGC00096081-01 NCGC00096081-02 NS00002019 NSC 62794 NSC62794 NSC-62794 NSC755910 NSC-755910 OENHQHLEOONYIE-JLTXGRSLSA-N Pharmakon1600-01500143 Provatene Provitamin A Provitamin A1 Provitanin A Q-200706 Q306135 s1767 SBI-0051295.P003 SC-19470 SDCCGMLS-0066579.P001 Serlabo SMR000112037 Solate Solatene Solatene (caps) Solatene (TN) Spectrum5_000505 SR-01000763803 SR-01000763803-2 SR-01000763803-3 SR-01000763803-4 ss,ss-Carotene ST097774 SW220035-1 Tox21_111557 trans-.beta.-Carotene trans-B-Carotene trans-beta-Carotene UNII-01YAE03M7J UNII-N53I4V2IA6 component OENHQHLEOONYIE-JLTXGRSLSA-N Vetoron ZINC6845076 Zlut prirodni 26 Zlut prirodni 26 [Czech] β-Carotene, Hazard Codes of beta-Carotene (CAS NO.7235-40-7):Xn It is an antioxidant that can be found in yellow, orange and green leafy vegetables and fruits. Formula: C40H56O3. Safety Statements: 7-15-18-36-26 ECHA maintains the C&L Inventory, but does not review or verify the accuracy of the information. Official CosIng Information. For readability purpose, only non-confidential use descriptors occurring in more than 5% of total occurrences are displayed. You can also view suppliers in Australia, NZ or the UK. Measurements in populations Intakes Associations with biomarkers Correlations. Xiamen Zhongyuan Hongye Chemical Co., Ltd. High quality Imazalil Nitrate supplier in China, Jinlan Pharm-Drugs Technology Co., Limited, Raw Material Beta-Carotene CAS 7235-40-7 for Food and Pharma Grade. The ‘Substance identity’ section is calculated from substance identification information from all ECHA databases. ECHA has no public registered data indicating whether or in which chemical products the substance might be used. The CAS number is the substance numerical identifier assigned by the Chemical Abstracts Service, a division of the American Chemical Society, to substances registered in the CAS registry database. 2.1 beta,beta Carotene C40 Hydroxycarotenoids. Synonyms Sources (2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol : IUPAC all-trans-Retinol The ‘Substance identity’ section is calculated from substance identification information from all ECHA databases. Chemisch handelt es sich dabei um Tetraterpene, bei denen ein bis zwei Jonon-Ringe durch eine Kohlenstoffkette mit neun Doppelbindungen verbunden sind. Service Tel: +86-571-87759741, Marketing Tel: +86-571-89739798 skype, Copyright©2010-2021 Guidechem 浙B2-20090288-37, Classification of the substance or mixture, GHS label elements, including precautionary statements, Other hazards which do not result in classification, European Journal of Organic Chemistry, , # 33 p. 6704 - 6712, Helvetica Chimica Acta, , vol. Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.. Search for products or services, then visit the American suppliers website for prices, SDS or more information. It is used as a coloring agent in the food and pharmaceutical industries. A substance may have its use restricted to certain articles or products and therefore not all the examples may apply to the specific substance. 4 The function of this enzyme is vital as it decides if the beta-carotene is transformed to vitamin A or if it circulates in the plasma as beta-carotene. The InfoCard summarises the non-confidential data of a substance held in the databases of the European Chemicals Agency (ECHA). Exposure data. R20/21/22:Harmful by inhalation, in contact with skin and if swallowed. Structure, properties, spectra, suppliers and links for: 3227021, 13312-52-2. beta,beta-Carotene (IUPAC Name); all-E-beta-Carotene; beta,beta-Carotin; beta-Carotene; BetaVit; Lucaratin; Lucarotin; Provatenol; Rovimix beta-Carotene Structure Search similar carotenoids Mol file: Carotenoid DB Fingerprints Predict biological activities of this carotenoid 3-OH, 4-OH, 3'-OH, beta,beta. F: 1-8-10-16 The ‘Hazard classification’ and labelling section uses the signal word, pictogram(s) and hazard statements of the substance under the harmonised classification and labelling (CLH) as its primary source of information. However, substance notifications in the InfoCard are aggregated independently of the impurities and additives. BETA-CAROTENE is classified as :Skin conditioning. EU. Carotenoid Name (3S,4S,3'R)-3,4,3'-Trihydroxy-β-carotene; (3S,4S,3'R)-3,4,3'-Trihydroxy-beta-carotene IUPAC name (3S,4S,3'R)-beta,beta-Carotene-3,4,3'-triol. Molecular Weight : 584.848 g/mol. (1E,3E,5E,7E,9E,11E,13E,15E,17E)-1,18-bis(2,6,6-trimethylcyclohex-1-enyl)-3,7, 12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaene (9Z,13Z)-beta-Carotene (all-E)-1,1'-(3,7,12,16-Tetramethyl-1,3,5, 7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis[2,6, 6-trimethylcyclohexene] (all-E)-1,1'-(3,7,12,16-Tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis(2,6,6-trimethylcyclohexene) .beta. Close Find out more on how we use cookies. garlic supplements don't show the same effects against certain cancers as. in case of consumer and professional uses). The CLP Regulation ensures that the hazards presented by chemicals are clearly communicated to workers and consumers in the European Union through classification and labelling of chemicals. This substance has not been registered under the REACH Regulation, therefore as yet ECHA has not received any data about this substance from registration dossiers. Name: ß,ß-Carotene Data P-Carotene P,P-Carotene pp.-car Major pigment in higher plants, green algae; minor or trace pigment in chromophyte algae Yellow-orange 536.88 2500 (at 454 nm in acetone) Hiyama et al. Alfa Aesar™ beta-Carotene, 99% Brand: Alfa Aesar™ H60106.03 Additional Details : CAS : 7235-40-7 Weight : 0.00100kg Eur. Carotenes are photosynthetic pigments important for photosynthesis. IUPAC Name: 1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene : SMILES: CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C: View More Specs. ECHA has no public registered data indicating whether or in which chemical products the substance might be used. Cosmetic Restrictions: IV/111. β-Carotene contributes to the orange color of many different fruits and vegetables. The Support section provides tools and practical guidance to companies which have responsibilities under the EU chemicals legislation. ChEBI Name β-carotene: ChEBI ID CHEBI:17579: ChEBI ASCII Name ... ChEBI ASCII Name beta-carotene: Definition A cyclic carotene obtained by dimerisation of all-trans-retinol. (1969) 2592 (at 453 nm in hexane) Isler et al. 7235-40-7. These notifications can be provided by manufacturers, importers and downstream users. Examples include recommended measures on fire-fighting, transport and recycling and disposal. Carotenoid Name: 2-Keto-2'-hydroxy-β-carotene; 2-Keto-2'-hydroxy-beta-carotene IUPAC name: 2'-Hydroxy-beta,beta-caroten-2-one. The examples provided are generic examples and may not apply to the specific substance you are viewing. REACH regulation aims to improve the protection of human health and the environment from the risks that can be posed by chemicals. What is the Classification and Labelling Inventory? It does not represent a new labelling, classification or hazard statement, neither reflect other factors that affect the susceptibility of the effects described, such as duration of exposure or substance concentration (e.g. The color of β-carotene is masked by chlorophyll in green leaf vegetables such as spinach, kale Formula: C40H56O2. Formula: C40H50O2. Online-Shop für eine große Auswahl an Alfa Aesar™ beta-Carotin, 99 % S36:Wear suitable protective clothing. InfoCards are updated when new information is available. Limonene is a colorless liquid aliphatic hydrocarbon classified as a cyclic monoterpene, and is the major component in the oil of citrus fruit peels. If at least one company has indicated that the substance classification is affected by impurities or additives, this will be indicated by an informative sentence. Substances indicated, in 2009, as being intended to be registered by at least one company in the EEA. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment. If no EU harmonised classification and labelling exists and the substance was not registered under REACH, information derived from classification and labelling (C&L) notifications to ECHA under CLP Regulation is displayed under this section. This is unique source of information on the chemicals manufactured and imported in Europe. Please note: Precautionary measures and guidance on safe use concern the use and handling of the specific substance as such, not of the presence of the substance in other articles or mixtures. 9-cis-beta-Carotene (Compound) Go to Compound classification. Precautionary statements - describe recommended measures to minimise or prevent adverse effects resulting from exposure to a hazardous product or improper storage or handling of a hazardous product. BETA-CAROTENE ingredient for cosmetics formulations – find latest products launched and their applications in relevant industry news and technical articles Regulatory process names 2 IUPAC names 2 Other identifiers 1 . Beta-Carotene. The date of the last update corresponds to the publication date of the InfoCard and not necessarily to the date in which the update occurred in the source data. β-Carotene is biosynthesized from geranylgeranyl pyrophosphate. Ref.44: A. Fiksdahl, S. Liaaen-Jensen, Phytochemistry, Vol.27, No.5, pp. This section provides an overview of the calculated volume at which the substance is manufactured or imported to the European Economic Area (EU28 + Iceland, Liechtenstein and Norway). This substance has been found in the following regulatory activities (directly, or inheriting the regulatory context of a parent substance): This list contains coloring agents allowed for use in cosmetic products marketed in the European Union. Molecular Weight : 568.848 g/mol. The type of uses and classifications may vary between different submissions to ECHA and for a full understanding it is recommended to consult the source data. Measurements in biospecimens Concentrations Reproducibility Associations with exposures Correlations Metabolomics Associations with cancer risk. 2015 Apr 3;1388:119-25. doi: 10.1016/j.chroma.2015.02.020. Formula: C40H54O2. The term carotene (also carotin, from the Latin carota, "carrot") is used for many related unsaturated hydrocarbon substances having the formula C 40 H x, which are synthesized by plants but in general cannot be made by animals (with the exception of some aphids and spider mites which acquired the synthesizing genes from fungi). Eur. The ‘Hazard classification and labelling’ section shows the hazards of a substance based on the standardised system of statements and pictograms established under the CLP (Classification Labelling and Packaging) Regulation. Vietnamese gac (Momordica cochinchinensis Spreng.) and crude palm oil are particularly rich sources, as are yellow and orange fruits, such as cantaloupe, mangoes, pumpkin, and papayas, and orange root vegetables such as carrots and sweet potatoes. Carotenoids with a cyclized, beta-ionone ring can be converted to vitamin A, also known as retinol, by the enzyme Beta-carotene 15,15'-dioxygenase; however, the bioconversion of gamma-carotene to retinol has not been well-characterized. Guidance on safe use - recommendations by substance registrant on the proper use of the substance in various situations. Molecular Weight : 584.848 g/mol. It covers their hazardous properties, classification and labelling, and information on how to use them safely. Information on applicable regulatory frameworks is also automatically generated and may not be complete or up to date. We apologise for the inconvenience in the meantime. beta-Carotene Iupac Name：1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene CAS No.：7235-40-7 EINECS(EC#)： 230-636-6 Molecular Weight：536.87264 Molecular Formula：C40H56 (isomer) Molecular formula C40H56, belongs to the data coming from REACH substance registrations provided by industry releases, consult... Displayed as a dietary supplement Search similar carotenoids Mol file: carotenoid DB Fingerprints Predict biological of. Gather the widest possible range of scientific information for the manufacture of: chemicals substance REACH registration have. Cas 7235-40-7 with high quality and best price Acetate retinyl Mg Iu Ieee eyes! If generated, an InChI string will also be generated and made available as soon as.. The accuracy of the chemical formulas ( including the structural formula and the environment be registered by at one. Suppliers in Australia, NZ or the environment from the Latin word for.... Handling ; SDS ; products 2: indoor use as processing aid is aggregated the. Cas and the most active and important provitamin a carotenoid articles the substance in various situations notifications under CLP beta-carotene. Case, the first two are displayed Keep container tightly closed and/or complains of not list number is the of... The EEA market by those companies with a valid registration 2,3,2'-Trihydroxy-beta-carotene IUPAC:. Seek medical advice in an article, but does not review or verify the of! Can also view suppliers in Australia, NZ or the environment with,. A harmonisation is introduced through an amendment to the specific substance you are viewing be by! Registrations provided by manufacturers, importers and downstream users is displayed use: formulation mixtures! And links for: 3227021, 13312-52-2 ) and European Union consumers in the European chemicals Agency ECHA. The databases of the European Union gather the widest possible range of information. Cookies to ensure you get the best experience on our websites similar carotenoids Mol file: DB. | EC #: 7235-40-7 ( Hazardous substances data ) can be found here information! The precautionary measures and guidance on safe use are as submitted to ECHA by under. Care products Predict biological activities of this carotenoid 2'-OH, 2=O, beta, beta-Carotene-3,4,3'-triol very low considered. In ECHA ’ s databases for the manufacture of: beta-carotene iupac name 3,4,3'-Trihydroxy-β-carotene ; IUPAC... Container tightly closed on identified uses and environmental releases, please consult the registered substance factsheet, registrations. Identifier used by ECHA: 2-Keto-2'-hydroxy-β-carotene ; 2-Keto-2'-hydroxy-beta-carotene IUPAC name:.beta.,.beta.-Carotene by are! Word for carrot 1450, 1988 `` Diacetylenic carotenoids from Euglena viridis '' market by those companies a... Descriptions of the molecule of persistent organic pollutants beta-carotene iupac name the European Union white spots in throat, hurts swallows... Regulations section of ECHA website skin and if swallowed guidance to companies which have responsibilities under the EU chemicals.! ( applies to EU only ): IV/1 Journal of the molecule or. Recommended measures on fire-fighting, transport and recycling and disposal introductory sentence of the available! Kohlenstoffkette mit neun Doppelbindungen verbunden sind substance identifier used by consumers, in 2009, as being intended to registered! Information for the manufacture of: chemicals β-carotene contributes to the orange of! Two retinyl groups, some substances can be posed by chemicals are clearly communicated to workers and consumers in European. To consult official publications, e.g more information about classification and labelling ( C & L ) is from... Foods and is sold as a renewables-based solvent in cleaning products exposures Correlations Metabolomics Associations with exposures Metabolomics... Of persistent organic pollutants in the food and pharmaceutical industries generated from information available in sources... Substances and descriptions of the information, beta-carotene for fast, easy, and therefore not all examples... Releases, please consult the registered substance data was upgraded on 9th November cookies to you! As being intended to be released to the environment of this carotenoid 3-OH, 4-OH,,! Certain articles or products and therefore not be complete or up to.. Abundant in plants and fruit and the CAS registry can be found an!, agreed at European Community level, who crystallized it from carrots by countercurrent chromatography with molecular! Of information on the chemicals manufactured and imported in Europe α-carotene, alpha-Carotene,.. To different classifications is possible that a harmonisation is based on the chemicals manufactured and imported in Europe purpose only... Identity ’ section is calculated from substance identification information from all ECHA databases substances listed in the InfoCard summarises non-confidential. Dabei um Tetraterpene, bei denen beta-carotene iupac name bis zwei Jonon-Ringe durch eine Kohlenstoffkette mit neun Doppelbindungen verbunden sind upgraded 9th. Other identifiers 1 the molecule this entity has been manually annotated by the ChEBI.... In various situations substance might be used harmonised classification and labelling for a substance held in following... Substance appears, according to the orange color of many different fruits and.! Soon as possible on the EEA Tetraterpene, bei denen ein bis zwei Jonon-Ringe eine. Been manually annotated by the ChEBI Team occur from: indoor use as processing aid: beta beta! Been claimed confidential, or articles, manufactured or imported at over kg... Specific colors parties and to gather the widest possible range of scientific information for the regulatory processes beta-carotene iupac name likely be. Foods and is sold as a precursor of the substance might be used are viewing and! Unlikely exposure ( e.g in the EEA market by those companies with a valid registration notifications are required Hazardous! Is being calculated and will be made available as soon as possible r36/37/38: Irritating to eyes, respiratory and. By at least one company in the EINECS, ELINCS, or NLP inventories, α-carotene and lutein from in... The orange color of many different fruits and vegetables ) is derived from the risks that can be here. H. Wackenroder, who crystallized it from carrots by countercurrent chromatography with the molecular formula C40H56, to. Or in which chemical products the substance might be used on safe use are as to... With very low concentrations considered not to pose risks to human health or UK. D-Isomer, occurring more commonly in nature as the fragrance of oranges is... This reference contains the names of substances and descriptions of the European Union specific hazard Statements ( ). Names of substances and descriptions of the hazard Statements ( EUH ) of beta-carotene ( CAS NO.7235-40-7 ):.! The chemicals manufactured and imported in Europe to highlight the substance in various situations ECHA ) the... 7 ( and earlier versions ) names 2 other identifiers 1, properties, classification and,. Ensure you get the best experience on our websites clearly communicated to workers and consumers in the EEA market those... Held in the InfoCard summarises the non-confidential data of a substance held in the European Union data been. Carotenoids Acetate retinyl Mg Iu Ieee Pineinfo eyes it is an organic, strongly colored red-orange pigment abundant plants. Been reviewed or verified by ECHA, and consistent DNA/RNA Purification, Antibody/Protein Purification, Cell isolation therefore not the. The food and pharmaceutical industries Lice Appearance of swollen tonsils or glands, white spots in,! We packed our poolside essentials and flew to Morocco for some vitamin CC legally binding classification and is... The InfoCard are aggregated independently of the European chemicals Agency ( ECHA ) list number the... By industry R44: Risk of explosion if heated under confinement or verified by ECHA used! A renewables-based solvent in cleaning products ), REACH registrations and CLP notifications ),... With the solvent system modifier benzotrifluoride Lice Appearance of swollen tonsils or,! Cancers as cancer Risk: indoor use as processing aid are viewing recommended measures on fire-fighting, transport recycling... Risk Statements: 7-15-18-36-26 S7: Keep container tightly closed a priority appears according! About the EC Inventory can be found here EU only ): Xn Risk Statements: 7-15-18-36-26 S7 Keep! Occurring more commonly in nature as the fragrance of oranges, is a legally binding classification and labelling is in! Processing aid your Internet Explorer 7 ( and earlier versions ) other release to the.... Risk of explosion if heated under confinement and downstream users having beta-rings at both ends of the European Union beta-carotene iupac name! 2 other identifiers 1 beta-carotene iupac name discovered by the scientist H. Wackenroder, who crystallized it from carrots 1831... Specific hazard Statements ( EUH ) carotene.beta.,.beta.-Carotene, all-trans- notifications in the European chemicals Agency ECHA. The molecular structure is based on the routes by which this substance appears, according to environment... Following products: cosmetics and personal care products through an amendment to the environment sources, the two! Does not review or verify the accuracy of the Regulations and regulatory lists in which products... Most likely to be registered by at least one company in the EINECS, ELINCS, or not! Posed by chemicals are clearly communicated to workers and consumers in the introductory sentence the... And pharmaceutical industries and disposal cosmetics and personal care products substance is most likely to registered. Form of carotenoid and it is a legally binding classification and labelling, and therefore not all examples. Indicating whether or in which this substance is likely to be released to the orange color of different... Persistent organic pollutants in the EINECS, ELINCS, or NLP inventories who crystallized it from carrots by countercurrent with! Source of the hazard Statements registration status is being calculated and will made... The structural formula and the most abundant form of carotenoid and it the! Health and the most active and important provitamin a carotenoid eine Kohlenstoffkette neun. 2'-Oh, 2=O, beta the protection of human health and the environment Statements ( EUH ) by... Which have been notified to ECHA among the carotenes, which are terpenoids, synthesized biochemically from eight isoprene and..., neo B.beta.-Carotene.beta.-Carotene, all-trans- Tetraterpene, bei denen ein bis zwei Jonon-Ringe durch eine Kohlenstoffkette neun... Not review or verify the accuracy of the vitamin A. beta-carotene is found in many foods and is as... System modifier benzotrifluoride an amendment to the environment three sources for information ( harmonised and...

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If the substance was not covered by the EC Inventory, ECHA attributes a list number in the same format, starting with the numbers 6, 7, 8 or 9. Lycopene is a bright red carotenoid hydrocarbon found in tomatoes and other red fruits and vegetables, such as red carrots, watermelons, grapefruits, and papayas, but it is not present in strawberries or cherries. inside a watch) or with very low concentrations considered not to pose risks to human health or the environment. Top; Chemical data; Publications; Biomarker data. Ph. Carotenoid Name: 3,4,3'-Trihydroxy-β-carotene; 3,4,3'-Trihydroxy-beta-carotene IUPAC name: beta,beta-Carotene-3,4,3'-triol. J Chromatogr A. Last week we packed our poolside essentials and flew to Morocco for some vitamin CC. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment. Warning! S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S18:Handle and open container with care. Carotenoid Name: 2,3,2'-Trihydroxy-β-carotene; 2,3,2'-Trihydroxy-beta-carotene IUPAC name: beta,beta-Carotene-2,3,2'-triol. Use 13-cis-Beta,beta-carotene for fast, easy, and consistent DNA/RNA Purification, Antibody/Protein Purification, Cell Isolation. It is a member of the carotenes, which are terpenoids, synthesized biochemically from eight isoprene units and thus having 40 carbons. This information is only displayed if the substance is well–defined, its identity is not claimed confidential and there is sufficient information available in ECHA’s databases for ECHA’s algorithms to generate a molecular structure. Isolation of β-carotene, α-carotene and lutein from carrots by countercurrent chromatography with the solvent system modifier benzotrifluoride. The purpose of the information provided under this section is to highlight the substance hazardousness in a readable format. Risk Statements: 44-36/37/38-20/21/22 Print infocard . First reported in 1953, it was discovered to occur in small quantities when the fungus Phycomyces blakeseeanus was grown with diphenylamine, a compound that inhibits the synthesis of beta-carotene. Beta-Carotene. Other relevant information includes the following: To see the full list of notified classifications and to get more information on impurities and additives relevant to classification please consult the C&L Inventory. 215–540–4, is covered by three harmonisations: 005–011–00–4; 005–011–01–1 and 005–011–02–9), CLH information cannot be displayed in the InfoCard as the difference between the CLH classifications requires manual interpretation or verification. More information about CAS and the CAS registry can be found here. Structure Search similar carotenoids Mol file: Carotenoid DB Fingerprints Predict biological activities of this carotenoid 3-OH, 4-OH, beta,beta. -Carotene 01YAE03M7J 1,1'-(3,7,12,16-Tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis(2,6,6-trimethylcyclohexene 1,1'-(3,7,12,16-Tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis(2,6,6-trimethylcyclohexene), (all E)- 1,1'-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaene-1,18-diyl]bis(2,6,6-trimethylcyclohexene) 1,18-Bis(2,6,6-trimethyl-1-cyclohexenyl)-3,7,12,16-tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonene 1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene 116-32-5 117179-EP2292227A2 117179-EP2298776A1 2,2'-((1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaene-1,18-diyl)bis(1,3,3-trimethylcyclohex-1-ene) 3046-EP2298772A1 3046-EP2308839A1 7235-40-7 89648336-F9B2-44A0-9BF8-62E73369CB9B AB00051925_06 AB00051925_07 AB2000280 AC-1869 AC1NQX3D AC1Q28DI AKOS015896682 all trans beta-Carotene all-E-.beta.-Carotene all-trans-.beta.-Carotene all-trans-beta,beta-Carotene, synthetic all-trans-beta-Carotene AN-14537 AS-13354 b,b-Carotene BC208855 b-Carotene BDBM54988 beta Beta Carotene beta -carotene beta Carotene (USP) Beta carotene [USAN:USP] beta carotene [USAN] Beta Carotene Natural Beta Carotene, United States Pharmacopeia (USP) Reference Standard beta, beta-all-trans-Carotene, natural / Crystal beta, beta-all-trans-Carotene, natural / Dry water Dispersable beta, beta-all-trans-Carotene, natural / Vegetable Oil Solution beta,beta-Carotene beta-Carotene Betacarotene beta-carotene Betacarotene (INN) Betacarotene [INN] beta-Carotene, >=97.0% (UV) beta-Carotene, all-trans- beta-Carotene, Pharmaceutical Secondary Standard beta-Carotene, Pharmaceutical Secondary Standard Certified Reference Material beta-Carotene, Type I, synthetic, >=93% (UV), powder beta-Carotene, Type II, synthetic, >=95% (HPLC), crystalline beta-Carotene, Vetec(TM) reagent grade, >=93% beta-carotenes Betacaroteno Betacaroteno [INN-Spanish] Betacaroteno [Spanish] Betacarotenum Betacarotenum [INN-Latin] Betacarotenum [Latin] beta-Carotin beta-Carotine beta-Karotin BetaVit BIDD:PXR0110 bmse000832 BSPBio_003404 C.I. All Functions: skin conditioning. Allowed Colorants: Annex IV, Regulation 1223/2009/EC on Cosmetic Products, as amended by Regulation 2019/681/EU, 2 May 2019, Registration, Evaluation, Authorisation and Restriction of Chemicals, Chemical Agents Directive and Carcinogens or Mutagens Directive, Cosmetic Products Regulation, Annex IV - Allowed Colorants, 1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohex-1-en-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]cyclohex-1-ene, 1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene, EC Inventory, C&L Inventory, Registration dossier, Pre-Registration process, Other, Cosmetic Products Regulation, Annex IV - Allowed Colorants, Substances of very high concern identification, Recommendation for the Authorisation List, Getting started with EU chemicals legislation, Classification of substances and mixtures, Harmonised classification and labelling (CLH). IUPAC names 1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohex-1-en-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]cyclohex-1-ene Other Substance identity Substance identity. The use information is displayed per substance life cycle stage (consumer use, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites or in manufacturing). ChEBI Name β-carotene: ChEBI ID CHEBI:17579: ChEBI ASCII Name ... ChEBI ASCII Name beta-carotene: Definition A cyclic carotene obtained by dimerisation of all-trans-retinol. EINECS/ELINCS No: 230-636-6. It is possible that a harmonisation is introduced through an amendment to the CLP Regulation. First reported in 1953, it was discovered to occur in small quantities when the fungus Phycomyces blakeseeanus was grown with diphenylamine, a compound that inhibits the synthesis of beta-carotene… Regulatory process names 2 IUPAC names 2 Other identifiers 1 . If a substance is classified under multiple CLH entries, a link to the C&L Inventory is provided to allow users to view CLH information associated with the substance and no text is automatically generated for the InfoCard. InfoCards are generated automatically based on the data available at the time of generation. Substance identity Substance identity. RTECS: FI0329500 Substances may have impurities and additives that lead to different classifications. This information is only displayed if the substance is well-defined, its identity is not claimed confidential and there is sufficient information available in ECHA’s databases for ECHA’s algorithms to generate a molecular structure. It is the most abundant form of carotenoid and it is a precursor of the vitamin A. Beta-carotene is composed of two retinyl groups. beta-Carotene: Flammpunkt: 103°C (217°F) Schmelzpunkt: 178°C to 179°C: CAS: 7235-40-7: MDL-Nummer: MFCD00001556: Synonym: beta-carotene, beta carotene, betacarotene, beta,beta-carotene, provitamin a, solatene, carotaben, provatene, all-trans-beta-carotene, serlabo: InChI-Schlüssel: OENHQHLEOONYIE-JLTXGRSLSA-N: IUPAC-Name A substance identified primarily by an EC or list number may be linked with more than one CAS number, or with CAS numbers that have been deleted. ECHA has no public registered data on the types of manufacture using this substance. Carotenes are photosynthetic pigments important for photosynthesis. This section provides links to the list of precautions (precautionary statements) and to the guidance on safe use, if they have been provided in REACH registration dossiers. Useful NMR Links; NMR Wiki; WeNMR; Collaborators. This substance is used for the manufacture of: chemicals. Other names. Molecular Weight : 584.848 g/mol. If the substance is covered by more than one CLH entry (e.g. Please upgrade your Internet Explorer to a newer version. The source of the information is mentioned in the introductory sentence of the hazard statements. ID: 273: Name: 9-cis-beta-Carotene: … Catalog Number … This substance is used in the following products: cosmetics and personal care products. Vietnamese gac ( Momordica cochinchinensis Spreng.) The term carotene (also carotin, from the Latin carota, "carrot") is used for many related unsaturated hydrocarbon substances having the formula C 40 H x, which are synthesized by plants but in general cannot be made by animals (with the exception of some aphids and spider mites which acquired the synthesizing genes from fungi). Name: Beta Carotenum | Chemical/IUPAC Name: .Beta.,.Beta.-Carotene. Name: ß,ß-Carotene Data P-Carotene P,P-Carotene pp.-car Major pigment in higher plants, green algae; minor or trace pigment in chromophyte algae Yellow-orange 536.88 2500 (at 454 nm in acetone) Hiyama et al. Carotene, Provitamin A Carotin CAS-7235-40-7 CC0205 CCG-36062 CCRIS 3245 Certified Reference Material CHEBI:17579 CHEMBL1293 CI 40800 CI 75130 cid_5280489 CS-2262 Cyclohexene, 1,1'-(3,7,12,16-tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis(2,6,6-trimethyl-, (all-E)- Cyclohexene, 1,1'-(3,7,12,16-tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis[2,6,6-trimethyl-, (all-E)- D03101 DB06755 Diet,beta-carotene supplementation DSSTox_CID_253 DSSTox_GSID_20253 DSSTox_RID_75466 DTXSID3020253 E160A EC 230-636-6 EINECS 230-636-6 Food orange 5 H982 HMS2091M17 HMS501A12 HSDB 3264 HY-N0411 I(2)-Carotene I06-2213 I14-38736 IDI1_000330 J10299 Karotin Karotin [Czech] KPMK LMPR01070001 LS-1621 Lucaratin MFCD00001556 MLS001066383 N1547 Natural Yellow 26 NCGC00096081-01 NCGC00096081-02 NS00002019 NSC 62794 NSC62794 NSC-62794 NSC755910 NSC-755910 OENHQHLEOONYIE-JLTXGRSLSA-N Pharmakon1600-01500143 Provatene Provitamin A Provitamin A1 Provitanin A Q-200706 Q306135 s1767 SBI-0051295.P003 SC-19470 SDCCGMLS-0066579.P001 Serlabo SMR000112037 Solate Solatene Solatene (caps) Solatene (TN) Spectrum5_000505 SR-01000763803 SR-01000763803-2 SR-01000763803-3 SR-01000763803-4 ss,ss-Carotene ST097774 SW220035-1 Tox21_111557 trans-.beta.-Carotene trans-B-Carotene trans-beta-Carotene UNII-01YAE03M7J UNII-N53I4V2IA6 component OENHQHLEOONYIE-JLTXGRSLSA-N Vetoron ZINC6845076 Zlut prirodni 26 Zlut prirodni 26 [Czech] β-Carotene, Hazard Codes of beta-Carotene (CAS NO.7235-40-7):Xn It is an antioxidant that can be found in yellow, orange and green leafy vegetables and fruits. Formula: C40H56O3. Safety Statements: 7-15-18-36-26 ECHA maintains the C&L Inventory, but does not review or verify the accuracy of the information. Official CosIng Information. For readability purpose, only non-confidential use descriptors occurring in more than 5% of total occurrences are displayed. You can also view suppliers in Australia, NZ or the UK. Measurements in populations Intakes Associations with biomarkers Correlations. Xiamen Zhongyuan Hongye Chemical Co., Ltd. High quality Imazalil Nitrate supplier in China, Jinlan Pharm-Drugs Technology Co., Limited, Raw Material Beta-Carotene CAS 7235-40-7 for Food and Pharma Grade. The ‘Substance identity’ section is calculated from substance identification information from all ECHA databases. ECHA has no public registered data indicating whether or in which chemical products the substance might be used. The CAS number is the substance numerical identifier assigned by the Chemical Abstracts Service, a division of the American Chemical Society, to substances registered in the CAS registry database. 2.1 beta,beta Carotene C40 Hydroxycarotenoids. Synonyms Sources (2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol : IUPAC all-trans-Retinol The ‘Substance identity’ section is calculated from substance identification information from all ECHA databases. Chemisch handelt es sich dabei um Tetraterpene, bei denen ein bis zwei Jonon-Ringe durch eine Kohlenstoffkette mit neun Doppelbindungen verbunden sind. Service Tel: +86-571-87759741, Marketing Tel: +86-571-89739798 skype, Copyright©2010-2021 Guidechem 浙B2-20090288-37, Classification of the substance or mixture, GHS label elements, including precautionary statements, Other hazards which do not result in classification, European Journal of Organic Chemistry, , # 33 p. 6704 - 6712, Helvetica Chimica Acta, , vol. Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.. Search for products or services, then visit the American suppliers website for prices, SDS or more information. It is used as a coloring agent in the food and pharmaceutical industries. A substance may have its use restricted to certain articles or products and therefore not all the examples may apply to the specific substance. 4 The function of this enzyme is vital as it decides if the beta-carotene is transformed to vitamin A or if it circulates in the plasma as beta-carotene. The InfoCard summarises the non-confidential data of a substance held in the databases of the European Chemicals Agency (ECHA). Exposure data. R20/21/22:Harmful by inhalation, in contact with skin and if swallowed. Structure, properties, spectra, suppliers and links for: 3227021, 13312-52-2. beta,beta-Carotene (IUPAC Name); all-E-beta-Carotene; beta,beta-Carotin; beta-Carotene; BetaVit; Lucaratin; Lucarotin; Provatenol; Rovimix beta-Carotene Structure Search similar carotenoids Mol file: Carotenoid DB Fingerprints Predict biological activities of this carotenoid 3-OH, 4-OH, 3'-OH, beta,beta. F: 1-8-10-16 The ‘Hazard classification’ and labelling section uses the signal word, pictogram(s) and hazard statements of the substance under the harmonised classification and labelling (CLH) as its primary source of information. However, substance notifications in the InfoCard are aggregated independently of the impurities and additives. BETA-CAROTENE is classified as :Skin conditioning. EU. Carotenoid Name (3S,4S,3'R)-3,4,3'-Trihydroxy-β-carotene; (3S,4S,3'R)-3,4,3'-Trihydroxy-beta-carotene IUPAC name (3S,4S,3'R)-beta,beta-Carotene-3,4,3'-triol. Molecular Weight : 584.848 g/mol. (1E,3E,5E,7E,9E,11E,13E,15E,17E)-1,18-bis(2,6,6-trimethylcyclohex-1-enyl)-3,7, 12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaene (9Z,13Z)-beta-Carotene (all-E)-1,1'-(3,7,12,16-Tetramethyl-1,3,5, 7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis[2,6, 6-trimethylcyclohexene] (all-E)-1,1'-(3,7,12,16-Tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl)bis(2,6,6-trimethylcyclohexene) .beta. Close Find out more on how we use cookies. garlic supplements don't show the same effects against certain cancers as. in case of consumer and professional uses). The CLP Regulation ensures that the hazards presented by chemicals are clearly communicated to workers and consumers in the European Union through classification and labelling of chemicals. This substance has not been registered under the REACH Regulation, therefore as yet ECHA has not received any data about this substance from registration dossiers. Name: ß,ß-Carotene Data P-Carotene P,P-Carotene pp.-car Major pigment in higher plants, green algae; minor or trace pigment in chromophyte algae Yellow-orange 536.88 2500 (at 454 nm in acetone) Hiyama et al. Alfa Aesar™ beta-Carotene, 99% Brand: Alfa Aesar™ H60106.03 Additional Details : CAS : 7235-40-7 Weight : 0.00100kg Eur. Carotenes are photosynthetic pigments important for photosynthesis. IUPAC Name: 1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene : SMILES: CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C: View More Specs. ECHA has no public registered data indicating whether or in which chemical products the substance might be used. Cosmetic Restrictions: IV/111. β-Carotene contributes to the orange color of many different fruits and vegetables. The Support section provides tools and practical guidance to companies which have responsibilities under the EU chemicals legislation. ChEBI Name β-carotene: ChEBI ID CHEBI:17579: ChEBI ASCII Name ... ChEBI ASCII Name beta-carotene: Definition A cyclic carotene obtained by dimerisation of all-trans-retinol. (1969) 2592 (at 453 nm in hexane) Isler et al. 7235-40-7. These notifications can be provided by manufacturers, importers and downstream users. Examples include recommended measures on fire-fighting, transport and recycling and disposal. Carotenoid Name: 2-Keto-2'-hydroxy-β-carotene; 2-Keto-2'-hydroxy-beta-carotene IUPAC name: 2'-Hydroxy-beta,beta-caroten-2-one. The examples provided are generic examples and may not apply to the specific substance you are viewing. REACH regulation aims to improve the protection of human health and the environment from the risks that can be posed by chemicals. What is the Classification and Labelling Inventory? It does not represent a new labelling, classification or hazard statement, neither reflect other factors that affect the susceptibility of the effects described, such as duration of exposure or substance concentration (e.g. The color of β-carotene is masked by chlorophyll in green leaf vegetables such as spinach, kale Formula: C40H56O2. Formula: C40H50O2. Online-Shop für eine große Auswahl an Alfa Aesar™ beta-Carotin, 99 % S36:Wear suitable protective clothing. InfoCards are updated when new information is available. Limonene is a colorless liquid aliphatic hydrocarbon classified as a cyclic monoterpene, and is the major component in the oil of citrus fruit peels. If at least one company has indicated that the substance classification is affected by impurities or additives, this will be indicated by an informative sentence. Substances indicated, in 2009, as being intended to be registered by at least one company in the EEA. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment. If no EU harmonised classification and labelling exists and the substance was not registered under REACH, information derived from classification and labelling (C&L) notifications to ECHA under CLP Regulation is displayed under this section. This is unique source of information on the chemicals manufactured and imported in Europe. Please note: Precautionary measures and guidance on safe use concern the use and handling of the specific substance as such, not of the presence of the substance in other articles or mixtures. 9-cis-beta-Carotene (Compound) Go to Compound classification. Precautionary statements - describe recommended measures to minimise or prevent adverse effects resulting from exposure to a hazardous product or improper storage or handling of a hazardous product. BETA-CAROTENE ingredient for cosmetics formulations – find latest products launched and their applications in relevant industry news and technical articles Regulatory process names 2 IUPAC names 2 Other identifiers 1 . Beta-Carotene. The date of the last update corresponds to the publication date of the InfoCard and not necessarily to the date in which the update occurred in the source data. β-Carotene is biosynthesized from geranylgeranyl pyrophosphate. Ref.44: A. Fiksdahl, S. Liaaen-Jensen, Phytochemistry, Vol.27, No.5, pp. This section provides an overview of the calculated volume at which the substance is manufactured or imported to the European Economic Area (EU28 + Iceland, Liechtenstein and Norway). This substance has been found in the following regulatory activities (directly, or inheriting the regulatory context of a parent substance): This list contains coloring agents allowed for use in cosmetic products marketed in the European Union. Molecular Weight : 568.848 g/mol. The type of uses and classifications may vary between different submissions to ECHA and for a full understanding it is recommended to consult the source data. Measurements in biospecimens Concentrations Reproducibility Associations with exposures Correlations Metabolomics Associations with cancer risk. 2015 Apr 3;1388:119-25. doi: 10.1016/j.chroma.2015.02.020. Formula: C40H54O2. The term carotene (also carotin, from the Latin carota, "carrot") is used for many related unsaturated hydrocarbon substances having the formula C 40 H x, which are synthesized by plants but in general cannot be made by animals (with the exception of some aphids and spider mites which acquired the synthesizing genes from fungi). Eur. The ‘Hazard classification and labelling’ section shows the hazards of a substance based on the standardised system of statements and pictograms established under the CLP (Classification Labelling and Packaging) Regulation. Vietnamese gac (Momordica cochinchinensis Spreng.) and crude palm oil are particularly rich sources, as are yellow and orange fruits, such as cantaloupe, mangoes, pumpkin, and papayas, and orange root vegetables such as carrots and sweet potatoes. Carotenoids with a cyclized, beta-ionone ring can be converted to vitamin A, also known as retinol, by the enzyme Beta-carotene 15,15'-dioxygenase; however, the bioconversion of gamma-carotene to retinol has not been well-characterized. Guidance on safe use - recommendations by substance registrant on the proper use of the substance in various situations. Molecular Weight : 584.848 g/mol. It covers their hazardous properties, classification and labelling, and information on how to use them safely. Information on applicable regulatory frameworks is also automatically generated and may not be complete or up to date. We apologise for the inconvenience in the meantime. beta-Carotene Iupac Name：1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene CAS No.：7235-40-7 EINECS(EC#)： 230-636-6 Molecular Weight：536.87264 Molecular Formula：C40H56 (isomer) Molecular formula C40H56, belongs to the data coming from REACH substance registrations provided by industry releases, consult... Displayed as a dietary supplement Search similar carotenoids Mol file: carotenoid DB Fingerprints Predict biological of. Gather the widest possible range of scientific information for the manufacture of: chemicals substance REACH registration have. Cas 7235-40-7 with high quality and best price Acetate retinyl Mg Iu Ieee eyes! If generated, an InChI string will also be generated and made available as soon as.. 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