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

Details

Stereochemistry ACHIRAL
Molecular Formula C6H12O3
Molecular Weight 132.1577
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 6-HYDROXYHEXANOIC ACID

SMILES

OCCCCCC(O)=O

InChI

InChIKey=IWHLYPDWHHPVAA-UHFFFAOYSA-N
InChI=1S/C6H12O3/c7-5-3-1-2-4-6(8)9/h7H,1-5H2,(H,8,9)

HIDE SMILES / InChI

Molecular Formula C6H12O3
Molecular Weight 132.1577
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Growth of human fibroblasts in the presence of 6-hydroxyhexanoic acid.
2011-01-15
Enatiomerically pure hydroxycarboxylic acids: current approaches and future perspectives.
2010-06
Cartilage tissue engineering for auricular reconstruction: in vitro evaluation of potential genotoxic and cytotoxic effects of scaffold materials.
2010-04
Histone deacetylase inhibitor vorinostat suppresses the growth of uterine sarcomas in vitro and in vivo.
2010-03-04
Synthesis of polycaprolactone: a review.
2009-12
Biodegradation of poly(butylene succinate) powder in a controlled compost at 58°C evaluated by naturally-occurring carbon 14 amounts in evolved CO(2) based on the ISO 14855-2 method.
2009-11-20
Recent advances in synthetic bioelastomers.
2009-11-20
Origin of byproducts during the catalytic autoxidation of cyclohexane.
2008-02-28
[Biosynthesis of multicomponent polyhydroxyalkanoates by Wautersia eutropha].
2008-02-27
[Physicochemical properties of multicomponent polyhydroxyalkanoates].
2007-07-19
[Fungicidal activity of cellobiose lipids from cultural fluid of yeast Cryptococcus humicola and Pseudozyma fusiformata].
2007-03-23
Degradation and controlled release behavior of epsilon-caprolactone copolymers in biodegradable antifouling coatings.
2006-03
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry with size-exclusion chromatographic fractionation for structural characterization of synthetic aliphatic copolyesters.
2006
Effect of composition of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) on growth of fibroblast and osteoblast.
2005-03
Mild, solvent-free omega-hydroxy acid polycondensations catalyzed by candida antarctica lipase B.
2004-01-13
Qualitative and quantitative solid-phase microextraction gas chromatographic-mass spectrometric determination of the low-molecular-mass compounds released from poly(vinyl chloride)/polycaprolactone-polycarbonate during ageing.
2003-08-22
Electrospray ion-trap multistage mass spectrometry for characterisation of co-monomer compositional distribution of bacterial poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) at the molecular level.
2003
Identification of two gene clusters involved in cyclohexanone oxidation in Brevibacterium epidermidis strain HCU.
2002-05
A new type of thermoalkalophilic hydrolase of Paucimonas lemoignei with high specificity for amorphous polyesters of short chain-length hydroxyalkanoic acids.
2001-09-28
Biosynthesis of PHB tercopolymer by Bacillus cereus UW85.
2001-03
Synthesis of guanylhydrazones derived from 3-pyridinol and evaluation of their effect on serum thromboxane B2 and prostaglandin E2 production.
1986-11
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:34:48 GMT 2025
Edited
by admin
on Mon Mar 31 18:34:48 GMT 2025
Record UNII
3Y3OX37NM8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
6-HYDROCAPROIC ACID
Preferred Name English
6-HYDROXYHEXANOIC ACID
Systematic Name English
6-HYDROXYHEXANOATE
Systematic Name English
HEXANOIC ACID, 6-HYDROXY-
Common Name English
.EPSILON.-HYDROXYCAPROIC ACID
Systematic Name English
Code System Code Type Description
CHEBI
32383
Created by admin on Mon Mar 31 18:34:48 GMT 2025 , Edited by admin on Mon Mar 31 18:34:48 GMT 2025
PRIMARY
CAS
1191-25-9
Created by admin on Mon Mar 31 18:34:48 GMT 2025 , Edited by admin on Mon Mar 31 18:34:48 GMT 2025
PRIMARY
EPA CompTox
DTXSID00152316
Created by admin on Mon Mar 31 18:34:48 GMT 2025 , Edited by admin on Mon Mar 31 18:34:48 GMT 2025
PRIMARY
FDA UNII
3Y3OX37NM8
Created by admin on Mon Mar 31 18:34:48 GMT 2025 , Edited by admin on Mon Mar 31 18:34:48 GMT 2025
PRIMARY
PUBCHEM
14490
Created by admin on Mon Mar 31 18:34:48 GMT 2025 , Edited by admin on Mon Mar 31 18:34:48 GMT 2025
PRIMARY
CHEBI
17869
Created by admin on Mon Mar 31 18:34:48 GMT 2025 , Edited by admin on Mon Mar 31 18:34:48 GMT 2025
PRIMARY