10-undecenoic acid

undec-10-enoic acid

CAS: 112-38-9 C11 H20 O2 MW: 184.27880000

Identification

Name10-undecenoic acid
IUPACundec-10-enoic acid
CAS Number112-38-9
EINECS203-965-8
FDA UNIIK3D86KJ24N
Molecular FormulaC11 H20 O2
Molecular Weight184.27880000
MDL NumberMFCD00004442
Nikkaji NumberJ5.125J
Beilstein1762631
CoE Number689
XlogP33.90 (est)

Regulatory

JECFA Food Flavoring331 10-undecenoic acid
DG SANTE Food Flavourings08.039 undec-10-enoic acid
FEMA Number3247
FDANo longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF)112-38-9 ; 10-UNDECENOIC ACID

Physical Properties

Appearance colorless white solid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.91000 to 0.91300 @ 25.00 °C.
Pounds per Gallon - (est). 7.572 to 7.597
Refractive Index 1.44700 to 1.44800 @ 20.00 °C.
Melting Point 25.00 to 27.00 °C. @ 760.00 mm Hg
Boiling Point 137.00 °C. @ 2.00 mm Hg
Flash Point 300.00 °F. TCC ( 148.89 °C. )
logP (o/w) 3.860
Soluble in alcohol
Insoluble in water

Cosmetic Information

CosIng['cosmetic data2', 'cosmetic data']
Cosmetic Usescleansing agents

Organoleptic Properties

Odor Description at 100.00 %.

Safety Information

Preferred SDSView
European informationMost important hazard(s):
Oral/Parenteral Toxicitygavage-mouse LD50 8150 mg/kg
Dermal Toxicityskin-guinea pig LD50 50 mg/kg
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryflavor and fragrance agents
RIFM Fragrance Material Safety AssessmentSearch
Recommendation for 10-undecenoic acid usage levels up to0.2000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU)26.00 (μg/capita/day)
baked goods-
beverages(nonalcoholic)-
beverages(alcoholic)-
breakfast cereal-
cheese-
chewing gum-
condiments / relishes-
confectionery froastings-
egg products-
fats / oils-
fish products-
frozen dairy-
fruit ices-
gelatins / puddings-
granulated sugar-
gravies-
hard candy-
imitation dairy-
instant coffee / tea-
jams / jellies-
meat products-
milk products-
nut products-
other grains-
poultry-
processed fruits-
processed vegetables-
reconstituted vegetables-
seasonings / flavors-
snack foods-
soft candy-
soups-
sugar substitutes-
sweet sauces-

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Potential Uses

FR jasmin FR oriental FR woody

Natural Occurrence

castor oil elder black elder seed

Synonyms

declid 10- hendecenoic acid omega- hendecenoic acid renselin sevinon undec-10-enoic acid undecenoic acid omega- undecenoic acid undecyl-10-enic acid undecylenic acid 10- undecylenic acid undecylenic acid natural undecylenic acid U.S.P. grade PubMed: Regio- and stereoselective hydroxylation of 10-undecenoic acid with a light-driven P450 BM3 biocatalyst yielding a valuable synthon for natural product synthesis. PubMed: Three monofunctional copolymers into one multifunctional Micelle: Part 1. Preparation and properties. PubMed: Divergent dendrimer synthesis via the Passerini three-component reaction and olefin cross-metathesis. PubMed: Bio-based aliphatic polyurethanes through ADMET polymerization in bulk and green solvent. PubMed: Total synthesis and biological evaluation of clavaminol-G and its analogs. PubMed: Fluorescence quenching in luminescent porous silicon nanoparticles for the detection of intracellular Cu2+. PubMed: Biosynthesis and characterization of polyhydroxyalkanoates by Pseudomonas guezennei from alkanoates and glucose. PubMed: Development of a three-steps derivatization assay for the localization of double bond in monounsaturated monomers of poly-beta-hydroxyalkanoates by GC-MS. PubMed: Total synthesis and antifungal activity of (2S,3R)-2-aminododecan-3-ol. PubMed: Structurally diverse polyamides obtained from monomers derived via the ugi multicomponent reaction. PubMed: Oxidation of 10-undecenoic acid by cytochrome P450(BM-3) and its Compound I transient. PubMed: A pH dependent thermo-sensitive copolymer drug carrier incorporating 4-amino-2,2,6,6-tetramethylpiperidin-1-oxyl (4-NH2-TEMPO) residues for electron spin resonance (ESR) labeling. PubMed: Deoxycholate as an efficient coating agent for hydrophilic silicon nanocrystals. PubMed: Rapid approach to biobased telechelics through two one-pot thiol-ene click reactions. PubMed: Simultaneous biosynthesis of two copolymers in Pseudomonas putida GPo1 using a two-stage continuous culture system. PubMed: Undecylenic acid: a valuable and physiologically active renewable building block from castor oil. PubMed: Oxidation-triggered release of fluorescent molecules or drugs from mesoporous Si microparticles. PubMed: Polymerizable vesicles based on a single-tailed fatty acid surfactant: a simple route to robust nanocontainers. PubMed: Fed-batch production of unsaturated medium-chain-length polyhydroxyalkanoates with controlled composition by Pseudomonas putida KT2440. PubMed: Spectra and kinetic studies of the compound I derivative of cytochrome P450 119. PubMed: Topographical and functional characterization of the ssDNA probe layer generated through EDC-mediated covalent attachment to nanocrystalline diamond using fluorescence microscopy. PubMed: 3,3,5-Trimethylcyclohexanols and derived esters: green synthetic procedures, odour evaluation and in vitro skin cytotoxicity assays. PubMed: Covalent biofunctionalization of silicon nitride surfaces. PubMed: Self-assembled monolayers with latent aldehydes for protein immobilization. PubMed: Efficient production of (R)-3-hydroxycarboxylic acids by biotechnological conversion of polyhydroxyalkanoates and their purification. PubMed: Bio-functional micelles self-assembled from a folate-conjugated block copolymer for targeted intracellular delivery of anticancer drugs. PubMed: Self-assembled thermo- and pH responsive micelles of poly(10-undecenoic acid-b-N-isopropylacrylamide) for drug delivery. PubMed: UV photodissociation spectroscopy of oxidized undecylenic acid films. PubMed: EDC-mediated DNA attachment to nanocrystalline CVD diamond films. PubMed: Tailor-made olefinic medium-chain-length poly[(R)-3-hydroxyalkanoates] by Pseudomonas putida GPo1: batch versus chemostat production. PubMed: Bacterial poly(hydroxyalkanoates) as a source of chiral hydroxyalkanoic acids. PubMed: Synthesis, stereochemistry and biological activity of some novel long alkyl chain substituted thiazolidin-4-ones and thiazan-4-one from 10-undecenoic acid hydrazide. PubMed: X-ray studies of self-assembled organic monolayers grown on hydrogen-terminated Si(111). PubMed: One-pot sequences of reactions with sol-gel entrapped opposing reagents: an enzyme and metal-complex catalysts. PubMed: Mutations in erg4 affect the sensitivity of Saccharomyces cerevisiae to medium-chain fatty acids. PubMed: Convenient formation of 4-hydroxyalk-2-en-1-one functionality via A knoevenagel-type carbon chain elongation reaction of aldehyde with 1-arylsulfinylalkan-2-one. PubMed: Evaluation of various carbon substrates for the biosynthesis of polyhydroxyalkanoates bearing functional groups by Pseudomonas putida. PubMed: Enantioselective synthesis of (11E, 13S)-13-hydroxy-10-oxooctadecenoic acid, the cytotoxic principle of corn. PubMed: RNA synthesis using a universal, base-stable allyl linker. PubMed: Expedient Synthesis of (R)-Patulolide A.