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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
Discovery of 8-hydroxyadenines as a novel type of interferon inducer.
2002 Dec 5
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 Sep 9
Microbial synthesis of (R)- and (S)-3,4-dimethoxyamphetamines through stereoselective transamination.
2003 Nov
Kinetic resolution of (R,S)-sec-butylamine using omega-transaminase from Vibrio fluvialis JS17 under reduced pressure.
2004 Sep 20
Chiral recognition by resorcin[4]arene receptors: intrinsic kinetics and dynamics.
2004 Sep 6
Synthesis and in vitro skin permeation of naproxen conjugates with alpha-alkylamino acids.
2005 Apr
Gas-phase enantioselectivity of chiral amido[4]resorcinarene receptors.
2006 Oct 25
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
Monosolvation of R-1-phenyl-2,2,2-trifluoroethanol with amines: configurational effects on the excitation, ionization, and fragmentation of diastereomeric complexes.
2007 Dec 13
Modelling amphetamine/receptor interactions: a gas-phase study of complexes formed between amphetamine and Some chiral amido[4]resorcinarenes.
2008
Induced-fit in the gas phase: conformational effects on the enantioselectivity of chiral tetra-amide macrocycles.
2008 Jan 16
A kinetic study of guest displacement reactions on a host-guest complex with a photoswitchable calixarene.
2008 Nov
4-{(Z)-(sec-Butyl-amino)(phen-yl)methyl-ene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one.
2009 Aug 8
Peripheral blood monocytes are responsible for gammadelta T cell activation induced by zoledronic acid through accumulation of IPP/DMAPP.
2009 Jan
Interaction of antitumor platinum complexes with human liver microsomal cytochromes P450.
2009 Jun
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:18:40 GMT 2023
Edited
by admin
on Fri Dec 15 18:18:40 GMT 2023
Record UNII
QAZ452YGSG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
FEMA NO. 4240
Code 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 Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
JECFA EVALUATION SEC-BUTYLAMINE
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
Code System Code Type Description
WIKIPEDIA
SEC-BUTYLAMINE
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY
ECHA (EC/EINECS)
237-732-7
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY
MERCK INDEX
m2816
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY Merck Index
CAS
13952-84-6
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY
FDA UNII
QAZ452YGSG
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY
MERCK INDEX
m2816
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY Merck Index
PUBCHEM
24874
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY
CHEBI
74526
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY
NSC
8030
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY
JECFA MONOGRAPH
1574
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY
HSDB
6312
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID4022284
Created by admin on Fri Dec 15 18:18:40 GMT 2023 , Edited by admin on Fri Dec 15 18:18:40 GMT 2023
PRIMARY