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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H13NO3
Molecular Weight 183.2044
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Epinephrine, (+)-

SMILES

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

InChI

InChIKey=UCTWMZQNUQWSLP-SECBINFHSA-N
InChI=1S/C9H13NO3/c1-10-5-9(13)6-2-3-7(11)8(12)4-6/h2-4,9-13H,5H2,1H3/t9-/m1/s1

HIDE SMILES / InChI

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 Mon Mar 31 23:11:11 GMT 2025
Edited
by admin
on Mon Mar 31 23:11:11 GMT 2025
Record UNII
NA71GR3TNV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(+)-(S)-EPINEPHRINE
Preferred Name English
Epinephrine, (+)-
Common Name English
EPINEPHRINE, D-
Common Name English
(S)-ADRENALINE
Systematic Name English
(+)-Epinephrine
Common Name English
1,2-BENZENEDIOL, 4-(1-HYDROXY-2-(METHYLAMINO)ETHYL)-, (S)-
Systematic Name English
D(+)-ADRENALINE
Common Name English
4-((1S)-1-HYDROXY-2-(METHYLAMINO)ETHYL)-1,2-BENZENEDIOL
Systematic Name English
RACEPINEFRINE, (S)-
Common Name English
BENZYL ALCOHOL, 3,4-DIHYDROXY-.ALPHA.-((METHYLAMINO)METHYL)-, (+)-
Systematic Name English
(+)-ADRENALINE
Systematic Name English
(+)-1-(3,4-DIHYDROXYPHENYL)-2-METHYLAMINOETHANOL
Systematic Name English
1,2-BENZENEDIOL, 4-((1S)-1-HYDROXY-2-(METHYLAMINO)ETHYL)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID301047668
Created by admin on Mon Mar 31 23:11:11 GMT 2025 , Edited by admin on Mon Mar 31 23:11:11 GMT 2025
PRIMARY
CAS
150-05-0
Created by admin on Mon Mar 31 23:11:11 GMT 2025 , Edited by admin on Mon Mar 31 23:11:11 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-752-5
Created by admin on Mon Mar 31 23:11:11 GMT 2025 , Edited by admin on Mon Mar 31 23:11:11 GMT 2025
PRIMARY
PUBCHEM
247704
Created by admin on Mon Mar 31 23:11:11 GMT 2025 , Edited by admin on Mon Mar 31 23:11:11 GMT 2025
PRIMARY
FDA UNII
NA71GR3TNV
Created by admin on Mon Mar 31 23:11:11 GMT 2025 , Edited by admin on Mon Mar 31 23:11:11 GMT 2025
PRIMARY
CHEBI
40751
Created by admin on Mon Mar 31 23:11:11 GMT 2025 , Edited by admin on Mon Mar 31 23:11:11 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER