U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C5H13N
Molecular Weight 87.1634
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ISOAMYLAMINE

SMILES

CC(C)CCN

InChI

InChIKey=BMFVGAAISNGQNM-UHFFFAOYSA-N
InChI=1S/C5H13N/c1-5(2)3-4-6/h5H,3-4,6H2,1-2H3

HIDE SMILES / InChI
Molecular Formula C5H13N
Molecular Weight 87.1634
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Structural and functional evolution of the trace amine-associated receptors TAAR3, TAAR4 and TAAR5 in primates.
2010-06-15
A new ultra-pressure liquid chromatography method for the determination of biogenic amines in cheese.
2010-05-07
Nakijiquinones J--R, sesquiterpenoid quinones with an amine residue from okinawan marine sponges.
2010-03-26
Trace amine-associated receptors are olfactory receptors in vertebrates.
2009-07
Cytotoxic aaptamines from Malaysian Aaptos aaptos.
2009
Ion-trap versus time-of-flight mass spectrometry coupled to capillary electrophoresis to analyze biogenic amines in wine.
2008-06-27
Biomass in the manufacture of industrial products--the use of proteins and amino acids.
2007-06
A second class of chemosensory receptors in the olfactory epithelium.
2006-08-10
Protection of originality of Tokaji Aszú: amines and organic acids in botrytized wines by high-performance liquid chromatography.
2005-12-28
Separation and conductimetric detection of C1-C7 aliphatic monocarboxylic acids and C1-C7 aliphatic monoamines on unfunctionized polymethacrylate resin columns.
2004-06-11
Application of polymethacrylate resin as stationary phase in liquid chromatography with UV detection for C1-C7 aliphatic monocarboxylic acids and C1-C7 aliphatic monoamines.
2004-06-11
High-precision position-specific isotope analysis of 13C/12C in leucine and methionine analogues.
2003-10-15
Seasonal changes in plasma concentrations of cecum-derived amines in clinically normal ponies and ponies predisposed to laminitis.
2003-09
Effects of monoamines formed in the cecum of horses on equine digital blood vessels and platelets.
2003-09
Identification and quantification of amines in the equine caecum.
2003-04
Uptake of 5-hydroxytryptamine by equine digital vein endothelial cells: inhibition by amines found in the equine caecum.
2003-03
Production of amines in equine cecal contents in an in vitro model of carbohydrate overload.
2002-10
Patents

Patents

05310902
2
05912252
2
05955548
16
06509366
2
07220880
6
07396943
2
07514582
2
07547698
2
07560569
13
07691863
3
07754711
7
07902372
4
07919496
2
08158638
7
08642801
3
20090137755
2
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:51:20 GMT 2025
Edited
by admin
on Mon Mar 31 18:51:20 GMT 2025
Record UNII
LPO0L33SHY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ISOPENTYLAMINE
FHFI  
Preferred Name English
ISOAMYLAMINE
MI  
Systematic Name English
1-BUTANAMINE, 3-METHYL-
Systematic Name English
PROPYLAMINE, 3,3-DIMETHYL-
Systematic Name English
ISOVALERYLAMINE
Systematic Name English
1-AMINO-3-METHYLBUTANE
Systematic Name English
NSC-7907
Code English
MONOISOAMYLAMINE
Systematic Name English
3-METHYLBUTYLAMINE
Systematic Name English
3-METHYLBUTANAMINE
Systematic Name English
MONOISOPENTYLAMINE
Systematic Name English
ISOAMYLAMINE [MI]
Common Name English
ISOPENTYLAMINE [FHFI]
Common Name English
LEUCAMINE
Common Name English
3-METHYL-1-BUTANAMINE
Systematic Name English
FEMA NO. 3219
Code English
3-METHYL-N-BUTYLAMINE
Systematic Name English
.GAMMA.-ISOAMYLAMINE
Common Name English
2-(2-ISOPROPYL)ETHYLAMINE
Common Name English
Classification Tree Code System Code
JECFA EVALUATION ISOPENTYLAMINE
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
Code System Code Type Description
CAS
107-85-7
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-526-0
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
PRIMARY
MESH
C025371
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
PRIMARY
NSC
7907
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
PRIMARY
PUBCHEM
7894
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
PRIMARY
EPA CompTox
DTXSID7059355
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
PRIMARY
JECFA MONOGRAPH
1577
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
PRIMARY
FDA UNII
LPO0L33SHY
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
PRIMARY
CHEBI
43689
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
PRIMARY
MERCK INDEX
m6427
Created by admin on Mon Mar 31 18:51:20 GMT 2025 , Edited by admin on Mon Mar 31 18:51:20 GMT 2025
PRIMARY Merck Index
Related Record Type Details
Structure of ISOAMYLAMINE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of ISOAMYLAMINE
ACTIVE MOIETY
NIH
NCATS
PRIVACY NOTICE
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966