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Details

Stereochemistry ABSOLUTE
Molecular Formula 2C13H21NO3.H2O4S
Molecular Weight 576.7
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVALBUTEROL SULFATE

SMILES

OS(O)(=O)=O.CC(C)(C)NC[C@H](O)C1=CC(CO)=C(O)C=C1.CC(C)(C)NC[C@H](O)C2=CC(CO)=C(O)C=C2

InChI

InChIKey=BNPSSFBOAGDEEL-NMFAMCKASA-N
InChI=1S/2C13H21NO3.H2O4S/c2*1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15;1-5(2,3)4/h2*4-6,12,14-17H,7-8H2,1-3H3;(H2,1,2,3,4)/t2*12-;/m00./s1

HIDE SMILES / InChI
Molecular Formula H2O4S
Molecular Weight 98.078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula C13H21NO3
Molecular Weight 239.3107
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
149124
Patents

Patents

JP2003221335A
5
JP2005525177A
1
JP2010235617A
1
JP3908269B2
8
JP4722295B2
105
JP4827296B2
6
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:39:39 GMT 2025
Edited
by admin
on Mon Mar 31 18:39:39 GMT 2025
Record UNII
71TH42O2CQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOSALBUTAMOL SULFATE
MART.   WHO-DD  
Preferred Name English
LEVALBUTEROL SULFATE
USAN  
USAN  
Official Name English
Levosalbutamol sulfate [WHO-DD]
Common Name English
LEVOSALBUTAMOL SULFATE [MART.]
Common Name English
LEVALBUTEROL SULPHATE
Common Name English
(R)-.ALPHA.(SUP 1)-((TERT-BUTYLAMINO)METHYL)-4-HYDROXY-M-XYLENE-.ALPHA.,.ALPHA.'-DIOL SULPHATE (2:1)
Common Name English
(R)-.ALPHA.(SUP 1)-((TERT-BUTYLAMINO)METHYL)-4-HYDROXY-M-XYLENE-.ALPHA.,.ALPHA.'-DIOL SULFATE (2:1)
Common Name English
LEVALBUTEROL SULFATE [USAN]
Common Name English
Classification Tree Code System Code
EU-Orphan Drug EU/3/07/481
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
NCI_THESAURUS C48149
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID10164006
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
PRIMARY
USAN
JJ-49
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
PRIMARY
EVMPD
SUB14354MIG
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
PRIMARY
NCI_THESAURUS
C83873
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
PRIMARY
ChEMBL
CHEMBL1002
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
PRIMARY
PUBCHEM
11505167
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
PRIMARY
FDA UNII
71TH42O2CQ
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
PRIMARY
CAS
148563-16-0
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
PRIMARY
SMS_ID
100000077091
Created by admin on Mon Mar 31 18:39:39 GMT 2025 , Edited by admin on Mon Mar 31 18:39:39 GMT 2025
PRIMARY
Related Record Type Details
Structure of LEVALBUTEROL
PARENT -> SALT/SOLVATE
NIH
NCATS
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