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Details

Stereochemistry ACHIRAL
Molecular Formula C5H10O2
Molecular Weight 102.1317
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTYL FORMATE

SMILES

CCCCOC=O

InChI

InChIKey=NMJJFJNHVMGPGM-UHFFFAOYSA-N
InChI=1S/C5H10O2/c1-2-3-4-7-5-6/h5H,2-4H2,1H3

HIDE SMILES / InChI

Molecular Formula C5H10O2
Molecular Weight 102.1317
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Vaccination against Strongyloides venezuelensis with homologue antigens using new immunomodulators.
2010-06
Monoketone analogs of curcumin, a new class of Fanconi anemia pathway inhibitors.
2009-12-31
Hexa-arginine enhanced uptake and residualization of selective high affinity ligands by Raji lymphoma cells.
2009-04-22
Toxicities of 31 volatile low molecular weight compounds against Aedes aegypti and Culex quinquefasciatus.
2009-03
Effects of synthetic sphingosine-1-phosphate analogs on cytosolic phospholipase A2alpha-independent release of arachidonic acid and cell toxicity in L929 fibrosarcoma cells: the structure-activity relationship.
2009-03
Pathway, inhibition and regulation of methyl tertiary butyl ether oxidation in a filamentous fungus, Graphium sp.
2008-01
Heat capacity of associated systems. Experimental data and application of a two-state model to pure liquids and mixtures.
2007-02-08
[Synthesis of [1,6-bis(L-alpha, beta-diaminopropionic acid) oxytocin].
2006-08
Positive ion chemistry of esters of carboxylic acids in air plasma at atmospheric pressure.
2005-12
Biotic and abiotic transformations of methyl tertiary butyl ether (MTBE).
2005-11
Design of wide-spectrum inhibitors targeting coronavirus main proteases.
2005-10
Ultrasonic relaxation and internal rotation in butyl formate.
2005-05
A micellar electrokinetic capillary chromatography method for monitoring mycophenolic acid in serum of transplant recipients.
2005-02
A novel synthetic peptide derivative from lactoferrin exhibiting antimicrobial activity.
2004-12
Attenuation of methyl tert-butyl ether in water using sunlight and a photocatalyst.
2002-06-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:18:44 GMT 2025
Edited
by admin
on Mon Mar 31 19:18:44 GMT 2025
Record UNII
0Y9MZ7VM9P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTYL FORMATE
FHFI  
Systematic Name English
FEMA NO. 2196
Preferred Name English
BUTYL FORMATE [FHFI]
Common Name English
BUTYL METHANOATE
Systematic Name English
FORMIC ACID, BUTYL ESTER
Common Name English
N-BUTYL FORMATE
Common Name English
NSC-6969
Code English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
JECFA EVALUATION BUTYL FORMATE
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
Code System Code Type Description
SMS_ID
100000166396
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
PRIMARY
JECFA MONOGRAPH
256
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
PRIMARY
NSC
6969
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID2060468
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
PRIMARY
EVMPD
SUB180484
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
PRIMARY
PUBCHEM
11614
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
PRIMARY
CHEBI
88514
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
PRIMARY
CAS
592-84-7
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-772-5
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
PRIMARY
FDA UNII
0Y9MZ7VM9P
Created by admin on Mon Mar 31 19:18:44 GMT 2025 , Edited by admin on Mon Mar 31 19:18:44 GMT 2025
PRIMARY