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

(E)-4-octene
4-octene, (4E)-

Supplier Sponsors

Name:(E)-oct-4-ene
CAS Number: 14850-23-8Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:238-913-3
FDA UNII: FKZ5737B1W
Nikkaji Web:J87.935E
Beilstein Number:1719104
MDL:MFCD00009476
XlogP3-AA:3.60 (est)
Molecular Weight:112.21552000
Formula:C8 H16
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:colorless clear liquid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity:0.71400 to 0.71800 @ 20.00 °C.
Pounds per Gallon - (est).: 5.948 to 5.981
Refractive Index:1.41100 to 1.41400 @ 20.00 °C.
Boiling Point: 122.00 to 123.00 °C. @ 760.00 mm Hg
Vapor Pressure:17.800000 mmHg @ 25.00 °C.
Flash Point: 70.00 °F. TCC ( 21.11 °C. )
logP (o/w): 4.374 (est)
Soluble in:
 alcohol
 water, 10.69 mg/L @ 25 °C (est)
Insoluble in:
 water
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
trans-4-Octene 95%
Santa Cruz Biotechnology
For experimental / research use only.
trans-4-Octene
Sigma-Aldrich: Aldrich
For experimental / research use only.
trans-4-Octene 98%
sds
TCI AMERICA
For experimental / research use only.
trans-4-Octene >99.0%(GC)
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 (E)-4-octene usage levels up to:
 not for fragrance use.
 
Recommendation for (E)-4-octene flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :5357253
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
(E)-oct-4-ene
Chemidplus:0014850238
 
References:
 (E)-oct-4-ene
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5357253
Pubchem (sid):134977843
 
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
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2901.29.5000
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
 juniperus drupacea fruit
Search Trop Picture
 
Synonyms:
(4E)-oct-4-ene
(E)-oct-4-ene
trans-oct-4-ene
trans-4-octene
4-octene, (4E)-
4-octene, (E)-
 

Articles:

PubMed:Bis(imino)pyridine cobalt-catalyzed dehydrogenative silylation of alkenes: scope, mechanism, and origins of selective allylsilane formation.
PubMed:Demonstration of remote steric differentiation of cis/trans alkene coordination in copper(I) complexes of aryl-substituted bis(2-pyridyl)amine.
PubMed:Coordination of neutral, methylene bridged bis-guanidyls at palladium.
PubMed:A structural, theoretical and coordinative evaluation of the bicyclic guanidinate derived from 1,4,6-triazabicyclo[3.3.0]oct-4-ene.
PubMed:Addition of the phenoxathiin cation radical to alkenes and nonconjugated dienes. Formation of (E)- and (Z)-(10-phenoxathiiniumyl)alkenes and (E)- and (Z)-(10-phenoxathiiniumyl)dienes on basic alumina.
PubMed:Metal-ligand charge-transfer-promoted photoelectronic Bergman cyclization of copper metalloenediynes: photochemical DNA cleavage via C-4' H-atom abstraction.
PubMed:Synthesis and reactivity of trans-Tricyclo
 
Notes:
None found
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