CAS 35602-69-8|Cholesterol Stearate

Introduction:Basic information about CAS 35602-69-8|Cholesterol Stearate, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameCholesterol Stearate
CAS Number35602-69-8Molecular Weight653.115
Density1.0±0.1 g/cm3Boiling Point671.7±34.0 °C at 760 mmHg
Molecular FormulaC45H80O2Melting Point79-83ºC
MSDSChineseUSAFlash Point360.6±13.2 °C

Names

Namecholesteryl stearate
SynonymMore Synonyms

Cholesterol Stearate BiologicalActivity

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

Chemical & Physical Properties

Density1.0±0.1 g/cm3
Boiling Point671.7±34.0 °C at 760 mmHg
Melting Point79-83ºC
Molecular FormulaC45H80O2
Molecular Weight653.115
Flash Point360.6±13.2 °C
Exact Mass652.615845
PSA26.30000
LogP19.21
Vapour Pressure0.0±2.1 mmHg at 25°C
Index of Refraction1.505
InChIKeyXHRPOTDGOASDJS-XNTGVSEISA-N
SMILESCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C)C(=CCC3C2CCC2(C)C(C(C)CCCC(C)C)CCC32)C1
Storage condition-20°C

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesT+
Safety PhrasesS24/25
RIDADRNONH for all modes of transport
WGK Germany3

Articles8

More Articles
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...

Synonyms

(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
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