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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H32O3
Molecular Weight 344.4877
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Testosterone propionate

SMILES

[H][C@@]12CC[C@H](OC(=O)CC)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CCC4=CC(=O)CC[C@]34C

InChI

InChIKey=PDMMFKSKQVNJMI-BLQWBTBKSA-N
InChI=1S/C22H32O3/c1-4-20(24)25-19-8-7-17-16-6-5-14-13-15(23)9-11-21(14,2)18(16)10-12-22(17,19)3/h13,16-19H,4-12H2,1-3H3/t16-,17-,18-,19-,21-,22-/m0/s1

HIDE SMILES / InChI
Molecular Formula C22H32O3
Molecular Weight 344.4877
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:21:20 UTC 2023
Edited
by admin
on Fri Dec 15 15:21:20 UTC 2023
Record UNII
WI93Z9138A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Testosterone propionate
EP   GREEN BOOK   MART.   MI   ORANGE BOOK   USP   VANDF   WHO-DD   WHO-IP  
Common Name English
TESTOSTERONE PROPIONATE [JAN]
Common Name English
TESTOSTERONE PROPIONATE [USP IMPURITY]
Common Name English
TESTOSTERONE PROPIONATE [MART.]
Common Name English
VIRORMONE
Common Name English
TESTOSTERONE PROPIONATE [GREEN BOOK]
Common Name English
TESTOSTERONE 17.BETA.-PROPIONATE
Common Name English
TESTOSTERONE PROPIONATE [ORANGE BOOK]
Common Name English
ORCHISTERONE
Common Name English
TESTOSTERONI PROPIONAS [WHO-IP LATIN]
Common Name English
TESTOSTERON 17-PROPIONATE
Common Name English
ANDROST-4-EN-3-ONE, 17-(1-OXOPROPOXY)-, (17.BETA.)-
Systematic Name English
TESTOSTERONE PROPIONATE [WHO-IP]
Common Name English
TESTOSTERONE PROPIONATE [VANDF]
Common Name English
TESTOSTERONE PROPIONATE CIII
USP-RS  
Common Name English
Testosterone propionate [WHO-DD]
Common Name English
TESTOSTERONE PROPIONATE [USP MONOGRAPH]
Common Name English
NSC-9166
Code English
NRB-03689
Code English
TESTOSTERONE PROPIONATE [MI]
Common Name English
TESTOSTERONE PROPIONATE [EP MONOGRAPH]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 522.842
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
CFR 21 CFR 556.710
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
FDA ORPHAN DRUG 57691
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
NCI_THESAURUS C862
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
Code System Code Type Description
SMS_ID
100000085255
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
RS_ITEM_NUM
1649007
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
DRUG CENTRAL
4146
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
CAS
57-85-2
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
DAILYMED
WI93Z9138A
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
TESTOSTERONE PROPIONATE
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY Description: Colourless or slightly yellowish crystals or a white or slightly yellowish powder; odourless. Solubility: Practically insoluble in water; freely soluble in ethanol (~750 g/l) TS and ether R; soluble in vegetable oils. Category: Androgen. Storage: Testosterone propionate should be kept in a well-closed container, protected from light. Definition: Testosterone propionate contains not less than 97.0% and not more than 102.0% of C22H32O3, calculated with reference to the dried substance.
EVMPD
SUB04743MIG
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
PUBCHEM
5995
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
NCI_THESAURUS
C863
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
FDA UNII
WI93Z9138A
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
IUPHAR
7100
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
DRUG BANK
DB01420
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
RXCUI
10382
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY RxNorm
WIKIPEDIA
Testosterone propionate
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
ChEMBL
CHEMBL1170
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
NSC
9166
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
MESH
D043343
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-351-1
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
EPA CompTox
DTXSID9036515
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY
MERCK INDEX
m10594
Created by admin on Fri Dec 15 15:21:20 UTC 2023 , Edited by admin on Fri Dec 15 15:21:20 UTC 2023
PRIMARY Merck Index
Related Record Type Details
Structure of Boldenone propionate
IMPURITY -> PARENT
Structure of TESTOSTERONE
IMPURITY -> PARENT
Structure of TESTOSTERONE ISOBUTYRATE
IMPURITY -> PARENT
Related Record Type Details
Structure of TESTOSTERONE
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