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151114

Sigma-Aldrich

Cholesteryl acetate

97%

Synonym(s):

3β-Acetoxy-5-cholestene, 3β-Hydroxy-5-cholestene 3-acetate, 5-Cholesten-3β-ol 3-acetate

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$121.00
100 G
$339.00

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25 G
$121.00
100 G
$339.00

About This Item

Empirical Formula (Hill Notation):
C29H48O2
CAS Number:
604-35-3
Molecular Weight:
428.69
Beilstein/REAXYS Number:
2064235
EC Number:
210-066-4
MDL number:
MFCD00003636
UNSPSC Code:
12352103
PubChem Substance ID:
24849092
NACRES:
NA.23

$121.00

Available to ship onApril 24, 2025Details

Request a Bulk Order

Quality Level

200

assay

97%

form

liquid crystal

optical activity

[α]24/D −44°, c = 2 in chloroform

mp

112-114 °C (lit.)

SMILES string

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)OC(C)=O

InChI

1S/C29H48O2/c1-19(2)8-7-9-20(3)25-12-13-26-24-11-10-22-18-23(31-21(4)30)14-16-28(22,5)27(24)15-17-29(25,26)6/h10,19-20,23-27H,7-9,11-18H2,1-6H3/t20-,23+,24+,25-,26+,27+,28+,29-/m1/s1

InChI key

XUGISPSHIFXEHZ-VEVYEIKRSA-N

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Related Categories

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW1374
MKCW6404
MKCT5293
MKCM9914
MKCJ0341

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André J Simpson et al.
Analytical chemistry, 80(1), 186-194 (2007-12-07)
A general technique is described that permits the extraction of a complete 1H NMR spectrum for components in organosoluble mixtures. The approach should find a wide range of applications considering that pure component spectra can be generated without the need
Chirality in liquid crystals
Goodby, J. W.
Journal of Materials Chemistry, 1(3), 307-318 (1991)
Ana Paula D M Espindola et al.
Journal of the American Chemical Society, 131(44), 15994-15995 (2009-10-23)
A new technique to deconvolute complex (1)H NMR spectra of small molecules has been developed that utilizes shape selective pulses to simultaneously decouple multiple protons. A limitation in the assignment of the relative configuration of small molecules is the ability
H P Weber et al.
Acta crystallographica. Section B, Structural science, 47 ( Pt 1), 116-127 (1991-02-01)
Cholesteryl acetate (C29H48O2) at 20 K is monoclinic, space group P2(1) with a = 16,521 (4), b = 9,220 (2), c = 17,620 (5) A, beta = 107.18 (2) degrees and Z = 4 (two molecules in the asymmetric unit).
Allylic nitration of 3 beta-sitosterol and cholesterol acetate: preparation of 7-nitro derivatives.
M Jiménez-Estrada et al.
Steroids, 62(6), 500-503 (1997-06-01)
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