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

16-hydroxyhexadecanoic acid
juniperic acid

Supplier Sponsors

Name:16-hydroxyhexadecanoic acid
CAS Number: 506-13-8Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:208-028-7
FDA UNII: 7IPP3U0F3I
Nikkaji Web:J11.795A
Beilstein Number:1783998
MDL:MFCD00002750
XlogP3:4.80 (est)
Molecular Weight:272.42864000
Formula:C16 H32 O3
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
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
PubMed:Search
NCBI:Search
 
Physical Properties:
Appearance:white crystalline powder (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 94.00 to 98.00 °C. @ 760.00 mm Hg
Boiling Point: 414.00 to 415.00 °C. @ 760.00 mm Hg (est)
Flash Point: 425.00 °F. TCC ( 218.60 °C. ) (est)
logP (o/w): 4.904 (est)
Soluble in:
 water, 2.872 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
16-HYDROXYHEXADECANOIC ACID >97.0%(T)
Sigma-Aldrich: Aldrich
For experimental / research use only.
16-Hydroxyhexadecanoic Acid 98%
sds
TCI AMERICA
For experimental / research use only.
16-Hydroxyhexadecanoic Acid >98.0%(T)
sds
 
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:
natural substances and extractives
Recommendation for 16-hydroxyhexadecanoic acid usage levels up to:
 not for fragrance use.
 
Recommendation for 16-hydroxyhexadecanoic acid flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):506-13-8
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :10466
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
16-hydroxyhexadecanoic acid
Chemidplus:0000506138
 
References:
 16-hydroxyhexadecanoic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):10466
Pubchem (sid):134976476
 
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
KEGG (GenomeNet):C18218
HMDB (The Human Metabolome Database):HMDB06294
FooDB:FDB001611
Export Tariff Code:2918.19.9000
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 cherry sweet cherry
Search Trop Picture
 juniperus scopulorum
Search Trop Picture
 potato leaf
Search Trop Picture
 quercus suber cork
Search Trop Picture
 tomato fruit
Search Trop Picture
 wine
Search Picture
 
Synonyms:
 hexadecanoic acid, 16-hydroxy-
16-hydroxy-hexadecanoic acid
16-hydroxypalmitic acid
omega-hydroxypalmitic acid
 juniperic acid
 palmitic acid, 16-hydroxy-
 

Articles:

PubMed:Defective in cuticular ridges (DCR) of Arabidopsis thaliana, a gene associated with surface cutin formation, encodes a soluble diacylglycerol acyltransferase.
PubMed:Isolation and identification of oligomers from partial degradation of lime fruit cutin.
PubMed:Self-assembled monolayers of alkanoic acids on the native oxide surface of SS316L by solution deposition.
PubMed:Synthesis of a glycolipid for studying mechanisms of mitochondrial uncoupling proteins.
PubMed:Oxygenation cascade in conversion of n-alkanes to alpha,omega-dioic acids catalyzed by cytochrome P450 52A3.
PubMed:Cloning and expression of the cutinase A gene of Botrytis cinerea.
PubMed:Molecular modelling of human gastric alcohol dehydrogenase (class IV) and substrate docking: differences towards the classical liver enzyme (class I).
PubMed:Macrocyclic lactone synthesis by lipases in water-in-oil microemulsions.
PubMed:Kinetic properties of human liver alcohol dehydrogenase: oxidation of alcohols by class I isoenzymes.
PubMed:Biochemistry of Suberization: omega-Hydroxyacid Oxidation in Enzyme Preparations from Suberizing Potato Tuber Disks.
PubMed:Biosynthesis of Cutin: Enzymatic Conversion of omega-Hydroxy Fatty Acids to Dicarboxylic Acids by Cell-free Extracts of Vicia Faba Epidermis.
PubMed:Determination of structure and composition of suberin from the roots of carrot, parsnip, rutabaga, turnip, red beet, and sweet potato by combined gas-liquid chromatography and mass spectrometry.
PubMed:Structure and Biosynthesis of Cuticular Lipids: Hydroxylation of Palmitic Acid and Decarboxylation of C(28), C(30), and C(32) Acids in Vicia faba Flowers.
 
Notes:
None found
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