Dihydrocholesterol structure
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Common Name | Dihydrocholesterol | ||
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CAS Number | 80-97-7 | Molecular Weight | 388.669 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 455.5±13.0 °C at 760 mmHg | |
Molecular Formula | C27H48O | Melting Point | 140-142ºC | |
MSDS | USA | Flash Point | 190.7±12.3 °C | |
Symbol |
GHS06, GHS08 |
Signal Word | Danger |
Use of Dihydrocholesterol5α-Cholestan-3β-ol is a derivitized steroid compound, which is isolated from the testes of White Carneau pigeons. |
Name | (5α)-cholestan-3β-ol |
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Synonym | More Synonyms |
Description | 5α-Cholestan-3β-ol is a derivitized steroid compound, which is isolated from the testes of White Carneau pigeons. |
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Related Catalog | |
Target |
Human Endogenous Metabolite |
In Vitro | 5α-Cholestan-3β-ol is derived from cholesterol by the action of intestinal microorganisms. It is known to induce the formation of gall stones in rabbits in the presence of sodium ions. 5α-Cholestan-3β-ol is used as a standard in lipid analysis using HPLC. |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 455.5±13.0 °C at 760 mmHg |
Melting Point | 140-142ºC |
Molecular Formula | C27H48O |
Molecular Weight | 388.669 |
Flash Point | 190.7±12.3 °C |
Exact Mass | 388.370514 |
PSA | 20.23000 |
LogP | 10.22 |
Vapour Pressure | 0.0±2.5 mmHg at 25°C |
Index of Refraction | 1.504 |
Storage condition | room temp |
Stability | Stable. Combustible. Incompatible with strong oxidizing agents. |
Water Solubility | chloroform: 0.1 g/mL, clear, colorless |
Symbol |
GHS06, GHS08 |
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Signal Word | Danger |
Hazard Statements | H302-H315-H319-H331-H336-H351-H361d-H372 |
Precautionary Statements | P261-P281-P305 + P351 + P338-P311 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
Hazard Codes | Xn: Harmful; |
Risk Phrases | R22 |
Safety Phrases | S22-S24/25 |
RIDADR | UN 1888 6 |
WGK Germany | 3 |
RTECS | FZ6350000 |
Precursor 8 | |
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DownStream 9 | |
Synthesis of steryl ferulates with various sterol structures and comparison of their antioxidant activity.
Food Chem. 169 , 92-101, (2014) Steryl ferulates synthesised from commercial sterols as well as commercial oryzanol were used to better understand how structural features affect antioxidant activity in vitro by the ABTS(+) radical d... |
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Novel and efficient synthesis and antifungal evaluation of 2,3-functionalized cholestane and androstane derivatives
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An integrated evaluation of molecular marker indices and linear alkylbenzenes (LABs) to measure sewage input in a subtropical estuary (Babitonga Bay, Brazil).
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b-Cholestanol |
5a-Cholestan-3b-ol |
(5α)-cholestan-3β-ol |
5a-Dihydrocholesterol |
3.β.-Hydroxy-5.α.-cholestane |
(5alpha)-cholestan-3beta-ol |
(3S,5S,8R,9S,10S,13R,14S,17R)-10,13-Dimethyl-17-[(2R)-6-methyl-2-heptanyl]hexadecahydro-1H-cyclopenta[a]phenanthren-3-ol |
5α-Cholestan-3β-ol |
(3β,5α)-Cholestan-3-ol |
β-Cholestanol |
3b-Hydroxy-5a-cholestane |
3β-Hydroxy-5α-cholestane |
Cholestan-3-ol, (3β,5α)- |
5α-Dihydrocholesterol |
Cholestan-3-ol |
cholestanol |
EINECS 201-315-8 |
MFCD00066413 |
(3b,5a)-Cholestan-3-ol |
Cholestanol (VAN) |
(3S,5S,8R,9S,10S,13R,14S,17R)-10,13-Diméthyl-17-[(2R)-6-méthyl-2-heptanyl]hexadécahydro-1H-cyclopenta[a]phénanthrén-3-ol |
beta-cholrestanol |