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

Details

Stereochemistry ACHIRAL
Molecular Formula C10H13NO2
Molecular Weight 179.2157
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTYL NICOTINATE

SMILES

CCCCOC(=O)C1=CN=CC=C1

InChI

InChIKey=DQULIMIQTCDUAN-UHFFFAOYSA-N
InChI=1S/C10H13NO2/c1-2-3-7-13-10(12)9-5-4-6-11-8-9/h4-6,8H,2-3,7H2,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Estimation of serum protein binding of compounds metabolized in serum using matrix inhibition.
2008-07
Inhibitory effect of 3-carboethoxypyridine and 3-carbobutoxypyridine on isolated rat uterus.
2007-08-02
Effect of drug lipophilicity on in vitro release rate from oil vehicles using nicotinic acid esters as model prodrug derivatives.
2001-03-23
Patents
Name Type Language
BUTYL NICOTINATE
Systematic Name English
BA-2674
Preferred Name English
NSC-53506
Code English
NSC-27863
Code English
N-BUTYL NICOTINATE
Common Name English
Code System Code Type Description
MESH
C029162
Created by admin on Mon Mar 31 19:04:01 GMT 2025 , Edited by admin on Mon Mar 31 19:04:01 GMT 2025
PRIMARY
ECHA (EC/EINECS)
230-064-7
Created by admin on Mon Mar 31 19:04:01 GMT 2025 , Edited by admin on Mon Mar 31 19:04:01 GMT 2025
PRIMARY
PUBCHEM
81353
Created by admin on Mon Mar 31 19:04:01 GMT 2025 , Edited by admin on Mon Mar 31 19:04:01 GMT 2025
PRIMARY
NSC
53506
Created by admin on Mon Mar 31 19:04:01 GMT 2025 , Edited by admin on Mon Mar 31 19:04:01 GMT 2025
PRIMARY
FDA UNII
LD3V8A23CV
Created by admin on Mon Mar 31 19:04:01 GMT 2025 , Edited by admin on Mon Mar 31 19:04:01 GMT 2025
PRIMARY
EPA CompTox
DTXSID4064509
Created by admin on Mon Mar 31 19:04:01 GMT 2025 , Edited by admin on Mon Mar 31 19:04:01 GMT 2025
PRIMARY
NSC
27863
Created by admin on Mon Mar 31 19:04:01 GMT 2025 , Edited by admin on Mon Mar 31 19:04:01 GMT 2025
PRIMARY
CAS
6938-06-3
Created by admin on Mon Mar 31 19:04:01 GMT 2025 , Edited by admin on Mon Mar 31 19:04:01 GMT 2025
PRIMARY