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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H13NO3.C4H6O6
Molecular Weight 333.2913
Optical Activity ( - )
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EPINEPHRINE BITARTRATE

SMILES

O[C@H]([C@@H](O)C(O)=O)C(O)=O.CNC[C@H](O)C1=CC=C(O)C(O)=C1

InChI

InChIKey=YLXIPWWIOISBDD-NDAAPVSOSA-N
InChI=1S/C9H13NO3.C4H6O6/c1-10-5-9(13)6-2-3-7(11)8(12)4-6;5-1(3(7)8)2(6)4(9)10/h2-4,9-13H,5H2,1H3;1-2,5-6H,(H,7,8)(H,9,10)/t9-;1-,2-/m01/s1

HIDE SMILES / InChI

Molecular Formula C4H6O6
Molecular Weight 150.0868
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula C9H13NO3
Molecular Weight 183.2044
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:10:52 UTC 2023
Edited
by admin
on Fri Dec 15 15:10:52 UTC 2023
Record UNII
30Q7KI53AK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EPINEPHRINE BITARTRATE
JAN   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD  
Common Name English
ADRENALINE (AS TARTRATE)
Common Name English
EPINEPHRINE BITARTRATE COMPONENT OF LIGNOSPAN FORTE
Common Name English
EPINEPHRINE BITARTRATE [JAN]
Common Name English
EPINEPHRINE D-BITARTRATE [MI]
Common Name English
ADRENALIN TARTRATE [WHO-IP]
Common Name English
(-)-3,4-DIHYDROXY-.ALPHA.-((METHYLAMINO)METHYL)BENZYL ALCOHOL (+)-TARTRATE (1:1) SALT.
Common Name English
ADRENALINE TARTRATE [EP MONOGRAPH]
Common Name English
ADRENALINE ACID TARTRATE [MART.]
Common Name English
MEDIHALER-EPI
Brand Name English
Epinephrine bitartrate [WHO-DD]
Common Name English
EPINEPHRINE BITARTRATE [ORANGE BOOK]
Common Name English
1,2-BENZENEDIOL, 4-(1-HYDROXY-2-(METHYLAMINO)ETHYL)-, (R)-, (R-(R*,R*))-2,3-DIHYDROXYBUTANEDIOATE (1:1) (SALT)
Common Name English
EPINEPHRINE HYDROGEN TARTRATE [WHO-IP]
Common Name English
NSC-756755
Code English
EPINEPHRINE BITARTRATE [VANDF]
Common Name English
ADRENALINE TARTRATE
EP  
Systematic Name English
LIGNOSPAN FORTE COMPONENT EPINEPHRINE BITARTRATE
Common Name English
EPINEPHRINI HYDROGENOTARTRAS [WHO-IP LATIN]
Common Name English
BRONITIN
Brand Name English
EPINEPHRINE TARTRATE
Common Name English
ADRENALINE ACID TARTRATE
MART.  
Common Name English
EPINEPHRINE BITARTRATE [USP MONOGRAPH]
Common Name English
EPINEPHRINE BITARTRATE [USP-RS]
Common Name English
ADRENALINE BITARTATE
Common Name English
L-EPINEPHRINE HYDROGEN TARTRATE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 341.16
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
NCI_THESAURUS C87053
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
Code System Code Type Description
NSC
756755
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
MERCK INDEX
m4944
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY Merck Index
WHO INTERNATIONAL PHARMACOPEIA
EPINEPHRINE BITARTRATE
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY Other name: Adrenalin tartrate. (In certain countries the name Adrenalin is a trademark: In those countries this name may beused only when applied to the product issued by the owners of the trademark.)Description: A white to greyish white, crystalline powder; odourless.Solubility: Soluble in 3 parts of water; slightly soluble in ethanol (~750 g/l) TS; practically insoluble in ether R.Category. Sympathomimetic.Storage: Epinephrine hydrogen tartrate should be kept in a tightly closed container, protected from light.Additional information: Epinephrine hydrogen tartrate gradually darkens in colour on exposure to air and light. Even in theabsence of light, Epinephrine hydrogen tartrate is gradually degraded on exposure to a humid atmosphere, the decompositionbeing faster at higher temperatures.Definition: Epinephrine hydrogen tartrate contains not less than 98.0% and not more than 101.0% of C9H13NO3,C4H6O6,calculated with reference to the dried substance.
ECHA (EC/EINECS)
200-097-1
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
DRUG BANK
DBSALT000788
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
FDA UNII
30Q7KI53AK
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
CAS
51-42-3
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
EVMPD
SUB01911MIG
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
RXCUI
203180
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY RxNorm
SMS_ID
100000087265
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
EVMPD
SUB72751
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
EPA CompTox
DTXSID3049415
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
RS_ITEM_NUM
1237000
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
ChEMBL
CHEMBL679
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
DAILYMED
30Q7KI53AK
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
NCI_THESAURUS
C48021
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
PUBCHEM
5815
Created by admin on Fri Dec 15 15:10:52 UTC 2023 , Edited by admin on Fri Dec 15 15:10:52 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE
Related Record Type Details
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity D = 0.7; impurity E = 0.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity D = 0.7; impurity E = 0.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY