Oxandrolone Oxandrolone
Structural formula
| Business number | 015Y |
|---|---|
| Molecular formula | C19H30O3 |
| Molecular weight | 306.44 |
| label |
(4aS,4bS,6aS,7R,9aS,9bR,11aS)-7-hydroxy-4a,6a,7-trimethyl-tetradecahydroindeno[4,5-h]isochromene-2(1H) -ketone, (4aS,4bS,6aS,7R,9aS,9bR,11aS)-7-hydroxy-4a,6a,7-trimethyl-tetradecahydroindeno[4,5-h]isochromen-2(1H)-one |
Numbering system
CAS number:53-39-4
MDL number:MFCD00198944
EINECS number:200-172-9
RTECS number:RN6800700
BRN number:None
PubChem ID:None
Physical property data
1. Character: White odorless crystalline powder
2. Density (g/mL,25/4℃): Undetermined
3. Relative vapor density (g/mL,AIR=1): Undetermined
4. Melting point (ºC):235-238
5. Boiling point (ºC,Normal pressure): Undetermined
6. Boiling point (ºC,5.2kPa): Undetermined
7. Refractive index: undetermined
8. Flashpoint (ºC): Undetermined
9. Specific optical rotation (º): Undetermined
10. Autoignition point or ignition temperature (ºC): Undetermined
11. Vapor pressure (kPa,25ºC): Undetermined
<P class=MsoNormal style="MARGIN: 0cm 0cm 0pt 72pt; TEXT-INDENT: -18pt; TEXT-ALIGN: left; mso-list: l0 level1 lfo100mg/kg, 30 days before mating
Ecological data
None
Molecular structure data
1. Molar refractive index: 85.10
2. Molar volume (m3/mol）：277.0
3. isotonic ratio(90.2K)：696.3
4. Surface Tension(dyne/cm)：39.8
5. Polarizability(10-24cm3)：33.73
Compute chemical data
1. Reference value for hydrophobic parameter calculation (XlogP): 3.7
2. Number of hydrogen bond donors: 1
3. Number of hydrogen bond acceptors: 3
4. Number of rotatable chemical bonds: 0
5. Number of tautomers: 2
6. Topological molecule polar surface area 46.5
7. Number of heavy atoms: 22
8. Surface charge: 0
9. Complexity: 503
10. Number of isotope atoms: 0
11. Determine the number of atomic stereocenters: 7
12. Uncertain number of atomic stereocenters: 0
13. Determine the number of chemical bond stereocenters: 0
14. Number of uncertain chemical bond stereocenters: 0
15. Number of covalent bond units: 1
Properties and stability
None
Storage method
Seal and store in a cool place away from light.
Synthesis method
With5-Androster-1-ene–3-17-二Keto or17β-Hydroxy-17-α-Methyl derivatives are used as raw materials.
Purpose
is a male hormone whose main function is protein assimilation. Used to treat high cholesterol and triglycerides.
�Number: 0
14. Number of uncertain chemical bond stereocenters: 0
15. Number of covalent bond units: 1
Properties and stability
None
Storage method
Seal and store in a cool place away from light.
Synthesis method
With5-Androster-1-ene–3-17-二Keto or17β-Hydroxy-17-α-Methyl derivatives are used as raw materials.
Purpose
is a male hormone whose main function is protein assimilation. Used to treat high cholesterol and triglycerides.