Ephedrine

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C10H15NO
Molecular Weight	165.2322
Optical Activity	UNSPECIFIED
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of Ephedrine

Structure Search

SMILES

CN[C@@H](C)[C@H](O)C1=CC=CC=C1

InChI

InChIKey=KWGRBVOPPLSCSI-WPRPVWTQSA-N

InChI=1S/C10H15NO/c1-8(11-2)10(12)9-6-4-3-5-7-9/h3-8,10-12H,1-2H3/t8-,10-/m0/s1

HIDE SMILES / InChI

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 `Fri Dec 15 17:21:02 UTC 2023` Edited by `admin` on `Fri Dec 15 17:21:02 UTC 2023`
Record UNII	GN83C131XS
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

Ephedrine

Common Name

English

(R-(R*,S*))-.ALPHA.-(1-(METHYLAMINO)ETHYL)BENZENEMETHANOL [WHO-IP]

Systematic Name

English

EPHEDRINE, ANHYDROUS [WHO-IP]

Common Name

English

EPHEDRINE [USP MONOGRAPH]

Common Name

English

EPHEDRINE [VANDF]

Common Name

English

EPHEDRINE [EP MONOGRAPH]

Common Name

English

PSEUDOEPHEDRINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]

Common Name

English

EPHEDRINE [MI]

Common Name

English

NSC-170951

Code

English

(1R,2S)-2-METHYLAMINO-1-PHENYLPROPAN-1-OL

Systematic Name

English

EPHEDRINUM, ANHYDROUS [WHO-IP LATIN]

Common Name

English

NSC-8971

Code

English

EPHEDRINE [MART.]

Common Name

English

XENADRINE

Common Name

English

L-ERYTHRO-2-(METHYLAMINO)-1-PHENYLPROPAN-1-OL

Common Name

English

BENZENEMETHANOL, .ALPHA.-(1-(METHYLAMINO)ETHYL)-, (R-(R*,S*))-

Common Name

English

L-EPHEDRINE

Common Name

English

(-)-EPHEDRINE

Common Name

English

EPHEDRINE [HSDB]

Common Name

English

Ephedrine [WHO-DD]

Common Name

English

EPHEDRINE, ANHYDROUS

Common Name

English

Classification Tree Code System Code

WHO-ATC

S01FB02

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-ATC

R01AA03

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-VATC

QC01CA26

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-ATC

R03CA02

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

NDF-RT

N0000175552

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-ESSENTIAL MEDICINES LIST

1.2

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

CFR

21 CFR 119.1

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-VATC

QR01AA03

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

CFR

21 CFR 1315.13

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-ATC

C01CA26

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-VATC

QS01FB02

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

CFR

21 CFR 341.20

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

NCI_THESAURUS

C87053

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

NDF-RT

N0000175555

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-VATC

QG04BX90

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

NDF-RT

N0000192563

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

DEA NO.

8113

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

CFR

21 CFR 341.16

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-ATC

A08AA56

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

CFR

21 CFR 1314.20

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-VATC

QR03CA02

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-ATC

R01AB05

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

WHO-VATC

QR01AB05

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

Code System Code Type Description

NSC

170951

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

EVMPD

SUB13683MIG

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

DRUG BANK

DB01364

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

DRUG CENTRAL

1024

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

SMS_ID

100000088883

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

HSDB

3072

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

MESH

D004809

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

ECHA (EC/EINECS)

206-080-5

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

PUBCHEM

9294

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

WIKIPEDIA

EPHEDRINE

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

NSC

8971

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

EVMPD

SUB11936MIG

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

FDA UNII

GN83C131XS

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

NCI_THESAURUS

C472

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

MERCK INDEX

m4933

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

Merck Index

CAS

299-42-3

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

WHO INTERNATIONAL PHARMACOPEIA

EPHEDRINE

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

Description: Colourless crystals or a white, crystalline powder; odourless or with a slight, aromatic odour.Solubility: Soluble in water; very soluble in ethanol (~750 g/l) TS; freely soluble in ether R.Category: Antiasthmatic drug.Storage: Ephedrine should be kept in a well-closed container, protected from light.Labelling: The designation on the container should state whether the substance is the hemihydrate or is in the anhydrous form.Additional information. Solutions of Ephedrine in chloroform R may become turbid, especially when the substance contains morethan 10 mg of water per g. Even in the absence of light, Ephedrine is gradually degraded on exposure to a humid atmosphere,the decomposition being faster at higher temperatures. Anhydrous Ephedrine melts at about 38?C, whereas Ephedrinehemihydrate melts at about 42?C.

DAILYMED

GN83C131XS

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

RXCUI

3966

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

RxNorm

IUPHAR

556

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

EPA CompTox

DTXSID0022985

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

ChEMBL

CHEMBL211456

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

CHEBI

15407

Created by admin on Fri Dec 15 17:21:03 UTC 2023 , Edited by admin on Fri Dec 15 17:21:03 UTC 2023

PRIMARY

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EPHEDRINE CAMPHORATE

SALT/SOLVATE -> PARENT

Amount:


					TB6LCS628F

EPHEDRINE THIOCYANATE

SALT/SOLVATE -> PARENT

Amount:


					1M92VL7U3I

EPHEDRINE TANNATE

SALT/SOLVATE -> PARENT

Amount:


					386QA522QG

PARENT->PRECURSOR

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					7N83L68L6V

EPHEDRINE LACTATE

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EPHEDRINE ACEFYLLINATE

SALT/SOLVATE -> PARENT

Amount:


					03VRY66076

DIASTEREOISOMER -> DIASTEREOISOMER

Amount:


					7CUC9DDI9F

PSEUDOEPHEDRINE

DIASTEREOISOMER -> DIASTEREOISOMER

Amount:


					72087NSY56

EPHEDRINE, (+)-

DIASTEREOISOMER -> DIASTEREOISOMER

Amount:


					NLJ6390P1Z

Ephedrine hydrochloride

SALT/SOLVATE -> PARENT

Amount:


					HH60WD6JQS

EPHEDRINE HEMIHYDRATE

SOLVATE->ANHYDROUS

Amount:


					WT9D3J0JEU

EPHEDRINE TARTRATE

SALT/SOLVATE -> PARENT

Amount:


					92SI0I19T6

METHCATHINONE, (-)-

PARENT->PRECURSOR

Amount:


					HH60WD6JQS

EPHEDRINE HEMIHYDRATE

SALT/SOLVATE -> PARENT

Comments:

Definition. Ephedrine contains not less than 98.5% and not more than 101.0% of C10H15NO, calculated with reference to the anhydrous substance.

Amount:


					U6X61U5ZEG

EPHEDRINE SULFATE

SALT/SOLVATE -> PARENT

Amount:


					S76J9U46ST

PSEUDOEPHEDRINE, (-)-

DIASTEREOISOMER -> DIASTEREOISOMER

Amount:


					584L885IMR

EPHEDRA EQUISETINA STEM

PARENT -> CONSTITUENT ALWAYS PRESENT

Interaction Type:

ASSAY (HPLC)

Amount:

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					44RAL3456C

METHAMPHETAMINE

PARENT -> IMPURITY

Amount:

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					GN83C131XS

Ephedrine

ACTIVE MOIETY

Amount: