Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C10H15NO.ClH |
Molecular Weight | 201.693 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CN[C@@H](C)[C@H](O)C1=CC=CC=C1
InChI
InChIKey=BALXUFOVQVENIU-GNAZCLTHSA-N
InChI=1S/C10H15NO.ClH/c1-8(11-2)10(12)9-6-4-3-5-7-9;/h3-8,10-12H,1-2H3;1H/t8-,10-;/m0./s1
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C10H15NO |
Molecular Weight | 165.2322 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:38:04 UTC 2023
by
admin
on
Fri Dec 15 16:38:04 UTC 2023
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Record UNII |
NLJ6390P1Z
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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CFR |
21 CFR 341.20
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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NCI_THESAURUS |
C29747
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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CFR |
21 CFR 341.16
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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CFR |
21 CFR 349.18
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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Code System | Code | Type | Description | ||
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50-98-6
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admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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PRIMARY | |||
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m4933
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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PRIMARY | Merck Index | ||
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200-074-6
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admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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PRIMARY | |||
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CHEMBL211456
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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PRIMARY | |||
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SUB13686MIG
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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NLJ6390P1Z
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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NLJ6390P1Z
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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65326
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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91165
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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PRIMARY | RxNorm | ||
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759611
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admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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C75031
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admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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1235999
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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DTXSID1045825
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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EPHEDRINE HYDROCHLORIDE
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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PRIMARY | Description: Colourless crystals or a white, crystalline powder; odourless.Solubility: Soluble in 4 parts of water; soluble in ethanol (~750 g/l) TS; practically insoluble in ether R.Category: Antiasthmatic drug.Storage: Ephedrine hydrochloride should be kept in a well-closed container, protected from light.Additional information: Ephedrine hydrochloride darkens on exposure to light.RequirementsDefinition: Ephedrine hydrochloride contains not less than 99.0% and not more than 101.0% of C10H15NO,HCl, calculated withreference to the dried substance. | ||
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DBSALT001513
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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100000091342
Created by
admin on Fri Dec 15 16:38:04 UTC 2023 , Edited by admin on Fri Dec 15 16:38:04 UTC 2023
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Related Record | Type | Details | ||
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (TITRATION)
EP
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PARENT -> SALT/SOLVATE | |||
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (TITRATION)
USP
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Related Record | Type | Details | ||
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IMPURITY -> PARENT | |||
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IMPURITY -> PARENT |
For the calculation of contents, multiply the peak areas by 0.4
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |