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
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
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
Edited
Fri Dec 15 15:10:52 UTC 2023
by
admin
on
Fri Dec 15 15:10:52 UTC 2023
|
Record UNII |
30Q7KI53AK
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
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 | ||
---|---|---|---|---|---|
|
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 | |||
|
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 | ||
|
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. | ||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | ||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 |
|