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Atomfair Cholesteryl chloride C27H45Cl CAS 910-31-6

Cholesteryl Chloride (CAS No. 910-31-6) is a high-purity sterol derivative with the molecular formula C27H45Cl . This compound, also known by its IUPAC name (3S,8S,9S,10R,13R,14S,17R)-3-chloro-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene , is a chlorinated analog of cholesterol. It is widely utilized in biochemical research, particularly in studies involving lipid membranes, sterol metabolism, and as a precursor for synthesizing other steroidal compounds. Our product is rigorously tested for purity and stability, ensuring optimal performance for laboratory applications. Available in various quantities to suit your research needs.

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Description

Cholesteryl Chloride (CAS No. 910-31-6) is a high-purity sterol derivative with the molecular formula C27H45Cl. This compound, also known by its IUPAC name (3S,8S,9S,10R,13R,14S,17R)-3-chloro-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene, is a chlorinated analog of cholesterol. It is widely utilized in biochemical research, particularly in studies involving lipid membranes, sterol metabolism, and as a precursor for synthesizing other steroidal compounds. Our product is rigorously tested for purity and stability, ensuring optimal performance for laboratory applications. Available in various quantities to suit your research needs.

Properties

  • CAS Number: 910-31-6
  • Complexity: 591
  • IUPAC Name: (3S,8S,9S,10R,13R,14S,17R)-3-chloro-17-[(1R)-1,5-dimethylhexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene
  • InChI: InChI=1S/C27H45Cl/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9,18-19,21-25H,6-8,10-17H2,1-5H3/t19-,21+,22+,23-,24+,25+,26+,27-/m1/s1
  • InChI Key: OTVRYZXVVMZHHW-DPAQBDIFSA-N
  • Exact Mass: 404.3209791
  • Molecular Formula: C27H45Cl
  • Molecular Weight: 405.1
  • SMILES: C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)Cl)C)C
  • Monoisotopic Mass: 404.3209791
  • Physical Description: Off-white powder;
  • Synonyms: Cholesteryl chloride, 910-31-6, Cholesterol chloride, 3-Chlorocholest-5-ene, Cholest-5-ene, 3-chloro-, (3.beta.)-, UNII-39EHZ05V39, NSC 2084, NSC-2084, EINECS 213-004-4, 5-Cholesten-3beta-chloride, Cholest-5-ene, 3beta-chloro, 5-Cholesten-3.beta.-chloride, AI3-24122, DTXSID90883602, 3.BETA.-CHOLESTERYL CHLORIDE, 3-Chlorocholest-5-ene-, (3.beta.)-, Cholest-5-ene, 3-chloro-, (3beta)-, 3Chlorocholestene, 3Chlorocholest5ene, (1R,3aS,3bS,7S,9aR,9bS,11aR)-7-chloro-9a,11a-dimethyl-1-((2R)-6-methylheptan-2-yl)-1H,2H,3H,3aH,3bH,4H,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta(a)phenanthrene, (1R,3aS,3bS,7S,9aR,9bS,11aR)-7-chloro-9a,11a-dimethyl-1-[(2R)-6-methylheptan-2-yl]-1H,2H,3H,3aH,3bH,4H,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthrene, 3betaChlorocholest5ene, cholesteryl beta-chloride, Cholest5ene, 3betachloro, Cholest5ene, 3chloro, (3beta), 3BETA-CHOLESTERYL CHLORIDE, Cholest5ene, 3betachloro (8CI), DTXCID201023116, CHOLESTERYL CHLORIDE [INCI], 96345-96-9, 3-Chlorocholest-5-ene-, (3beta)-, 213-004-4, otvryzxvvmzhhw-dpaqbdifsa-n, 3-Chlorocholestene, Cholest-5-ene, 3.beta.-chloro-, 3.beta.-Chlorocholest-5-ene, 39EHZ05V39, 3-beta-Chlorocholest-5-ene, (3S,8S,9S,10R,13R,14S,17R)-3-chloro-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene, Cholest-5-ene, 3-chloro-, (3b)-, 3beta-Chloro-5-cholestene, Cholesteryl chloride, 97%, 3I(2)-Chlorocholest-5-ene, SCHEMBL137414, Cholest-5-ene, 3beta-chloro-, NSC2084, Cholesteryl chloride from beef fat, MFCD00003632, AKOS025310592, DB14045, FC61962, C0610, NS00013457, Q5104323, 3-Chlorocholestene from beef fat;5-Cholesten-3b-chloride from beef fat, (3S,8S,9S,10R,13R,14S,17R)-3-Chloro-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene

Application

Cholesteryl chloride is primarily used in biochemical research as a cholesterol analog to study lipid bilayer properties and membrane dynamics. It serves as a key intermediate in the synthesis of modified sterols and other derivatives for pharmaceutical and material science applications. Researchers also employ it in investigations of sterol-protein interactions and metabolic pathways involving cholesterol.

Safety and Hazards

GHS Hazard Statements

  • Not Classified
  • Reported as not meeting GHS hazard criteria by 1 of 1 companies. For more detailed information, please visit ECHA C&L website.

Hazard Classes and Categories

  • Not Classified

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Disclaimer

Intended Use & Restrictions

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  • Strictly prohibited: Resale, repackaging, or formulation into commercial products.
  • Not approved for human/animal use, diagnostics, or manufacturing (including pharmaceuticals, agrochemicals, or consumer goods).

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