Cholesterol Stearate

Modify Date: 2025-08-25 15:18:13

Cholesterol Stearate structure	Common Name	Cholesterol Stearate
	CAS Number	35602-69-8	Molecular Weight	653.115
	Density	1.0±0.1 g/cm3	Boiling Point	671.7±34.0 °C at 760 mmHg
	Molecular Formula	C₄₅H₈₀O₂	Melting Point	79-83ºC
	MSDS	Chinese USA	Flash Point	360.6±13.2 °C

Use of Cholesterol Stearate

Cholesteryl stearate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Name	cholesteryl stearate
Synonym	More Synonyms

Description	Cholesteryl stearate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog	Research Areas >> Others

Density	1.0±0.1 g/cm3
Boiling Point	671.7±34.0 °C at 760 mmHg
Melting Point	79-83ºC
Molecular Formula	C₄₅H₈₀O₂
Molecular Weight	653.115
Flash Point	360.6±13.2 °C
Exact Mass	652.615845
PSA	26.30000
LogP	19.21
Vapour Pressure	0.0±2.1 mmHg at 25°C
Index of Refraction	1.505
Storage condition	-20°C

Cholesterol Stearate MSDS(Chinese)

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	T+
Safety Phrases	S24/25
RIDADR	NONH for all modes of transport
WGK Germany	3

Precursor 10
CAS#:638-08-4 Stearic Anhydride CAS#:6252-45-5 3β-[(Tetrahydro... CAS#:57-88-5 cholesterol CAS#:112-76-5 Stearoyl chloride
CAS#:57-11-4 stearic acid CAS#:112-61-8 Methyl stearate CAS#:555-43-1 Tristealin CAS#:303-43-5 Cholesteryl oleate
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DownStream 0

A rapid and precise method for quantification of fatty acids in human serum cholesteryl esters by liquid chromatography and tandem mass spectrometry.

J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 960 , 222-9, (2014)

We described a rapid and precise method for simultaneous quantification of eleven fatty acids in human serum cholesteryl esters (CEFAs) by liquid chromatography and tandem mass spectrometry (LC-MS/MS)...

Accelerated separation of GC-amenable lipid classes in plant oils by countercurrent chromatography in the co-current mode.

Anal. Bioanal. Chem 407 , 9019-28, (2015)

Triacylglycerols represent the major part (>90%) in most plant oils and have to be eliminated, when the minor compounds such as phytosterols or tocopherols should be analyzed. Here, we used an all liq...

Modification of composition of a nanoemulsion with different cholesteryl ester molecular species: effects on stability, peroxidation, and cell uptake.

Int. J. Nanomedicine 5 , 679-86, (2010)

Use of lipid nanoemulsions as carriers of drugs for therapeutic or diagnostic purposes has been increasingly studied. Here, it was tested whether modifications of core particle constitution could affe...

(3S,8S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-[(2R)-6-methyl-2-heptanyl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl stearate

Stéarate de (3S,8S,9S,10R,13R,14S,17R)-10,13-diméthyl-17-[(2R)-6-méthyl-2-heptanyl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tétradécahydro-1H-cyclopenta[a]phénanthrén-3-yle

Cholestryl stearate

(3β)-cholest-5-en-3-yl octadecanoate

Cholesterol, stearate (8CI)

(3β)-Cholest-5-en-3-yloctadecanoat

5-Cholesten-3beta-yl octadecanoate

EINECS 252-637-0

cholesterol n-octadecanoate

18:0-cholesterol

(3β)-Cholest-5-en-3-yl stearate

5-Cholesten-3β-ol stearate

cholesteryl stearate

18:0 Cholesteryl ester

MFCD00003639

Stearic Acid Cholesterol Ester

5-Cholesten-3b-ol stearate

Cholesteryl octadecanoate

Cholesterol, stearate

Stéarate de (3β)-cholest-5-én-3-yle

CE(18:0)

(3b)-Cholest-5-en-3-yl stearate

(3S,8S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-[(2R)-6-methyl-2-heptanyl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloctadecanoat

[(3S,8S,9S,10R,13R,14S,17R)-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]phenanthren-3-yl] octadecanoate

Cholesterol Stearate

Octadecanoic acid, (3β)-cholest-5-en-3-yl ester