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Merck
CN

C79409

Cholesteryl stearate

96%

Synonym(s):

5-Cholesten-3β-yl octadecanoate

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About This Item

Empirical Formula (Hill Notation):
C45H80O2
CAS Number:
35602-69-8
Molecular Weight:
653.12
Beilstein:
2068492
EC Number:
252-637-0
MDL number:
MFCD00003639
UNSPSC Code:
12352108
PubChem Substance ID:
24892584
NACRES:
NA.22

Key Documents

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Quality Level

100

Assay

96%

form

powder

optical activity

[α]25/D −21°, c = 2 in chloroform

mp

79-83 °C (lit.)

transition temp

cholesteric phase to smectic phase 75.5 °C
isotropic phase to cholesteric phase 79.5 °C
crystalline phase to isotropic phase 83 °C

SMILES string

CCCCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@]2(C)C3CC[C@]4(C)C(CCC4C3CC=C2C1)[C@H](C)CCCC(C)C

InChI

1S/C45H80O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25-43(46)47-38-30-32-44(5)37(34-38)26-27-39-41-29-28-40(36(4)24-22-23-35(2)3)45(41,6)33-31-42(39)44/h26,35-36,38-42H,7-25,27-34H2,1-6H3/t36-,38+,39+,40-,41+,42+,44+,45-/m1/s1

InChI key

XHRPOTDGOASDJS-XNTGVSEISA-N

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General description

Cholesteryl stearate is a stearic acid ester of cholesterol. In solid-state, its autoxidation is higher than its free form.

Application

It can be used as a reference standard during the determination of tocopherols and sterols in vegetable oils by GC.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB4073
STBL0384
STBK1009
STBJ7564
STBJ4738

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Determination of tocopherols and sterols in vegetable oils by solid-phase extraction and subsequent capillary gas chromatographic analysis.
Lechner M, et al.
Journal of Chromatography A, 857(1), 231-238 (1999)
Autoxidation of cholesterol fatty acid esters in solid state and aqueous dispersion.
Korahani V, et al.
Lipids, 17(10), 703-708 (1982)
Laura Carreón-Palau et al.
Marine drugs, 18(12) (2020-12-03)
Triterpenoid biosynthesis is generally anaerobic in bacteria and aerobic in Eukarya. The major class of triterpenoids in bacteria, the hopanoids, is different to that in Eukarya, the lanostanoids, and their 4,4,14-demethylated derivatives, sterols. In the deep sea, the prokaryotic contribution
J Robin Harris et al.
Journal of structural biology, 139(2), 122-135 (2002-10-31)
The Vibrio cholerae cytolysin (VCC) 63-kDa monomer has been shown to interact in aqueous suspension with cholesterol microcystals to produce a ring/pore-like heptameric oligomer approximately 8 nm in outer diameter. Transmission electron microscopy data were produced from cholesterol samples adsorbed
Haiyang Feng et al.
Chemical biology & drug design, 90(5), 867-872 (2017-04-23)
In this study, rhein-SLNs were successfully produced by hot homogenization followed by ultrasonication. Precirol ATO5 in which rhein exhibited higher partition coefficient was selected for preparation of SLNs. In the dynamic light scattering, the rhein-SLNs showed a smaller size with
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