CAS 1062-96-0
:Cholesteryl caproate
Description:
Cholesteryl caproate, with the CAS number 1062-96-0, is an ester derived from cholesterol and caproic acid (hexanoic acid). It is characterized by its hydrophobic nature due to the long hydrocarbon chains present in both the cholesterol and caproic acid components. This substance typically appears as a white to off-white solid or waxy material at room temperature. Cholesteryl caproate is known for its role in lipid chemistry and is often studied for its potential applications in drug delivery systems and as a model compound in membrane studies. Its melting point and solubility characteristics are influenced by the balance between the cholesterol moiety and the caproic acid chain, which can affect its behavior in biological systems. Additionally, cholesteryl caproate can participate in various chemical reactions, including hydrolysis and transesterification, making it a subject of interest in both synthetic and analytical chemistry. Overall, its unique structural features contribute to its significance in biochemistry and pharmaceutical research.
Formula:C33H56O2
InChI:InChI=1S/C33H56O2/c1-7-8-9-13-31(34)35-26-18-20-32(5)25(22-26)14-15-27-29-17-16-28(24(4)12-10-11-23(2)3)33(29,6)21-19-30(27)32/h14,23-24,26-30H,7-13,15-22H2,1-6H3/t24-,26+,27+,28-,29+,30+,32+,33-/m1/s1
InChI key:InChIKey=FPBODWXATDKICU-FLFWOSPYSA-N
SMILES:C[C@@]12[C@@]3([C@]([C@]4([C@](C)(CC3)[C@@]([C@@H](CCCC(C)C)C)(CC4)[H])[H])(CC=C1C[C@@H](OC(CCCCC)=O)CC2)[H])[H]
Synonyms:- (3Beta)-Cholest-5-En-3-Yl Hexanoate
- 3-(Hexanoyloxy)cholest-5-ene
- 3β-(Caproyloxy)cholest-5-ene
- 5-Cholesten-3β-ol caproate
- Cholest-5-En-3-Yl Hexanoate
- Cholest-5-en-3-ol (3β)-, hexanoate
- Cholest-5-en-3β-ol caproate
- Cholesterol caproate
- Cholesterol n-hexanoate
- Cholesterol, hexanoate
- Cholesteryl caproate
- Cholesteryl hexanoate
- See more synonyms
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Cholesterol Hexanoate
CAS:Formula:C33H56O2Purity:>95.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:484.81Cholesterol hexanoate
CAS:Cholesterolhexanoate is an organic compound classified under esters. It is formed through the reaction between cholesterol and hexanoic acid. Cholesterolhexanoate has various applications in the pharmaceutical industry, particularly as a bioactive compound with potential research roles for improving conditions such as high cholesterol and inflammation-related diseases. Additionally, it may serve as a food additive to enhance texture and stability.Formula:C33H56O2Molecular weight:484.79655-Cholesten-3β-ol caproate
CAS:Formula:C33H56O2Purity:95%Color and Shape:SolidMolecular weight:484.7965Cholesterol hexanoate
CAS:Controlled ProductCholesterol Hexanoate is a fatty acid that is used as a chiral stationary phase in liquid chromatography. It has been shown to have the ability to form films with high stability and good optical properties. Cholesterol Hexanoate is typically used for the separation of fatty acids, but it can also be used for other purposes such as diagnostic testing.
Formula:C33H56O2Purity:Min. 95%Color and Shape:PowderMolecular weight:484.8 g/mol








