(Z+E)-cyclododecene

cyclododecene, mixture of cis and trans

CAS: 1501-82-2 C12 H22 MW: 166.30734000

Identification

Name(Z+E)-cyclododecene
IUPACcyclododecene
CAS Number1501-82-2
EINECS216-117-7
FDA UNIISearch
Molecular FormulaC12 H22
Molecular Weight166.30734000
MDL NumberMFCD00003721
Beilstein2037841

Regulatory

Physical Properties

Appearance colorless clear liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.87300 to 0.87600 @ 20.00 °C.
Pounds per Gallon - (est). 7.273 to 7.298
Refractive Index 1.48400 to 1.48700 @ 20.00 °C.
Boiling Point 237.00 to 239.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.066000 mmHg @ 25.00 °C. (est)
Flash Point 201.00 °F. TCC ( 93.90 °C. ) (est)
logP (o/w) 6.281 (est)
Soluble in alcohol
Insoluble in water

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

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

Safety in Use

Categoryflavoring agents
Recommendation for (Z+E)-cyclododecene usage levels up tonot for fragrance use.

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Potential Uses

None Found

Natural Occurrence

beef fat overheated PMC passiflora alata

Synonyms

cyclododec-1-ene cyclododecene cyclododecene, mixture of cis and trans PubMed: Surface-initiated ring-opening metathesis polymerization in the vapor phase: an efficient method for grafting cyclic olefins with low strain energies. PubMed: Facile synthesis and preferred conformation analysis of cyclododeceno[b]indene. PubMed: Toward less dependence on platinum group metal catalysts: the merits of utilizing tin. PubMed: Synthesis, characterization, electronic structure and catalytic performance of bimetallic and trimetallic nanoparticles containing tin. PubMed: Bimetallic Ru-Sn nanoparticle catalysts for the solvent-free selective hydrogenation of 1,5,9-cyclododecatriene to cyclododecene. PubMed: Conformational Study of trans-Cyclododecene by Dynamic NMR Spectroscopy and Computational Methods. PubMed: 1,2-Epoxycycloalkanes: substrates and inhibitors of microsomal and cytosolic epoxide hydrolases in mouse liver. PubMed: Effects of cyclic 12-, 8-, and 6-carbon compounds on glutathione S-transferase activity.