EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

2-hydroxyoctanoic acid
octanoic acid, 2-hydroxy-

Supplier Sponsors

Name:2-hydroxyoctanoic acid
CAS Number: 617-73-2Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:210-524-3
FDA UNII:0R6X0G0S8A
Nikkaji Web:J94.836E
Beilstein Number:1760638
MDL:MFCD00014410
XlogP3-AA:2.00 (est)
Molecular Weight:160.21312000
Formula:C8 H16 O3
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome or firefox)
Category:cosmetic agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 70.00 °C. @ 760.00 mm Hg
Boiling Point: 289.00 °C. @ 760.00 mm Hg (est)
Flash Point: 289.00 °F. TCC ( 142.80 °C. ) (est)
logP (o/w): 1.960 (est)
Soluble in:
 water, 1.572e+004 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: skin conditioning
 
Suppliers:
BOC Sciences
For experimental / research use only.
2-hydroxyoctanoic acid 95%
Carbosynth
For experimental / research use only.
2-Hydroxyoctanoic Acid
Santa Cruz Biotechnology
For experimental / research use only.
(±)-2-Hydroxyoctanoic Acid ≥98%
Seqens
2-Hydroxy Octanoic Acid
Sigma-Aldrich: Sigma
For experimental / research use only.
(±)-2-Hydroxyoctanoic acid
TCI AMERICA
For experimental / research use only.
2-Hydroxy-n-octanoic Acid >98.0%(T)
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
cosmetic agents
Recommendation for 2-hydroxyoctanoic acid usage levels up to:
 not for fragrance use.
 
Recommendation for 2-hydroxyoctanoic acid flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :94180
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
2-hydroxyoctanoic acid
Chemidplus:0000617732
 
References:
 2-hydroxyoctanoic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):94180
Pubchem (sid):135142655
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
Metabolomics Database:Search
HMDB (The Human Metabolome Database):HMDB00711
FooDB:FDB022197
Export Tariff Code:2918.19.9000
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 hydroxycaprylic acid
 octanoic acid, 2-hydroxy-
 

Articles:

PubMed:Development of an intravitreal peptide (BQ123) sustained release system based on poly(2-hydroxyoctanoic acid) aiming at a retinal vasodilator response.
PubMed:Design and in vitro assessment of L-lactic acid-based copolymers as prodrug and carrier for intravitreal sustained L-lactate release to reverse retinal arteriolar occlusions.
PubMed:Solutions as solutions--synthesis and use of a liquid polyester excipient to dissolve lipophilic drugs and formulate sustained-release parenterals.
PubMed:Determination of the enantiomers of alpha-hydroxy- and alpha-amino acids in capillary electrophoresis with contactless conductivity detection.
PubMed:Poly(hexyl-substituted lactides): novel injectable hydrophobic drug delivery systems.
PubMed:Inhibition of a medium chain acyl-CoA synthetase involved in glycine conjugation by carboxylic acids.
PubMed:Stereospecific synthesis of a novel farnesyl protein transferase inhibitor, valinoctin A and its analogues.
 
Notes:
Hydroxyoctanoic acid medium chain substrate of the 2-hydroxy acid oxidases associated with the 3 distinct human 2-hydroxy acid oxidase genes, HAOX1, HAOX2, and HAOX3. (PMID: 10777549) [HMDB]
Please share your Comments.
Email Address:
Top of Page Home
Copyright © 1980-2021 The Good Scents Company (tgsc) ™ Disclaimer Privacy Policy