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Details

Stereochemistry RACEMIC
Molecular Formula C4H11N
Molecular Weight 73.1368
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SEC-BUTYLAMINE

SMILES

CCC(C)N

InChI

InChIKey=BHRZNVHARXXAHW-UHFFFAOYSA-N
InChI=1S/C4H11N/c1-3-4(2)5/h4H,3,5H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C4H11N
Molecular Weight 73.1368
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of protein kinase C-driven nuclear factor-kappaB activation: synthesis, structure-activity relationship, and pharmacological profiling of pathway specific benzimidazole probe molecules.
2010-06-24
4-{(Z)-(sec-Butyl-amino)(phen-yl)methyl-ene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one.
2009-08-08
A functional gammadeltaTCR/CD3 complex distinct from gammadeltaT cells is expressed by human eosinophils.
2009-06-17
Interaction of antitumor platinum complexes with human liver microsomal cytochromes P450.
2009-06
Peripheral blood monocytes are responsible for gammadelta T cell activation induced by zoledronic acid through accumulation of IPP/DMAPP.
2009-01
A kinetic study of guest displacement reactions on a host-guest complex with a photoswitchable calixarene.
2008-11
Enantiomerically pure quaternary ammonium salts with a chiral alkyl chain N(CH3)(n-C3H7)2(sec-C4H9)I: synthesis and physical studies.
2008-11
Induced-fit in the gas phase: conformational effects on the enantioselectivity of chiral tetra-amide macrocycles.
2008-01-16
Modelling amphetamine/receptor interactions: a gas-phase study of complexes formed between amphetamine and Some chiral amido[4]resorcinarenes.
2008
Monosolvation of R-1-phenyl-2,2,2-trifluoroethanol with amines: configurational effects on the excitation, ionization, and fragmentation of diastereomeric complexes.
2007-12-13
Efficacy of a novel biofilter in hatchery sanitation: II. Removal of odorogenous pollutants.
2007
Review of sitagliptin phosphate: a novel treatment for type 2 diabetes.
2007
Gas-phase enantioselectivity of chiral amido[4]resorcinarene receptors.
2006-10-25
Microbial synthesis of chiral amines by (R)-specific transamination with Arthrobacter sp. KNK168.
2006-01
Synthesis and in vitro skin permeation of naproxen conjugates with alpha-alkylamino acids.
2005-04
Kinetic resolution of (R,S)-sec-butylamine using omega-transaminase from Vibrio fluvialis JS17 under reduced pressure.
2004-09-20
Chiral recognition by resorcin[4]arene receptors: intrinsic kinetics and dynamics.
2004-09-06
DNA interactions of new antitumor platinum complexes with trans geometry activated by a 2-metylbutylamine or sec-butylamine ligand.
2004-03-15
Microbial synthesis of (R)- and (S)-3,4-dimethoxyamphetamines through stereoselective transamination.
2003-11
Substitution reactions of 5-nitropyridine-2-sulfonic acid. A new pathway to 2,5-disubstituted pyridines.
2003-08-07
Discovery of 8-hydroxyadenines as a novel type of interferon inducer.
2002-12-05
The effect of ligand charge on the coordination geometry of an Fe(III)ion: five- and six-coordinate Fe(III) complexes of tris(2-benzimidazolylmethyl)amine.
2002-09-09
Comparison of the omega-transaminases from different microorganisms and application to production of chiral amines.
2001-08
Novel modified adenosine 5'-triphosphate analogues pharmacologically characterized in human embryonic kidney 293 cells highly expressing rat brain P2Y(1) receptor: Biotinylated analogue potentially suitable for specific P2Y(1) receptor isolation.
2001-05-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:10:13 GMT 2025
Edited
by admin
on Mon Mar 31 19:10:13 GMT 2025
Record UNII
QAZ452YGSG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 4240
Preferred Name English
SEC-BUTYLAMINE
FHFI   HSDB   MI  
Systematic Name English
2-AMINOBUTANE
Systematic Name English
2-BUTANAMINE
Systematic Name English
BUTYLAMINE [ISO]
Common Name English
1-METHYLPROPANAMINE
Systematic Name English
(RS)-SEC-BUTYLAMINE
Systematic Name English
DL-SEC-BUTYLAMINE
Common Name English
TUTANE
Common Name English
(±)-2-BUTYLAMINE
Systematic Name English
2-BUTYLAMINE
Systematic Name English
(±)-2-AMINOBUTANE
Systematic Name English
SEC-BUTYLAMINE [MI]
Common Name English
SEC-BUTYLAMINE [FHFI]
Common Name English
NSC-8030
Code English
BUTAFUME
Common Name English
(±)-SEC-BUTYLAMINE
Systematic Name English
SEC-BUTYLAMINE [HSDB]
Common Name English
SEC-BUTYLAMINE DL-FORM [MI]
Common Name English
1-METHYLPROPYLAMINE
Systematic Name English
DL-2-BUTYLAMINE
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 4214
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
JECFA EVALUATION SEC-BUTYLAMINE
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
Code System Code Type Description
WIKIPEDIA
SEC-BUTYLAMINE
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
237-732-7
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY
MERCK INDEX
m2816
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY Merck Index
CAS
13952-84-6
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY
FDA UNII
QAZ452YGSG
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY
MERCK INDEX
m2816
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY Merck Index
PUBCHEM
24874
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY
CHEBI
74526
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY
NSC
8030
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY
JECFA MONOGRAPH
1574
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY
HSDB
6312
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID4022284
Created by admin on Mon Mar 31 19:10:13 GMT 2025 , Edited by admin on Mon Mar 31 19:10:13 GMT 2025
PRIMARY