1,4-PENTADIENE

1,4-PENTADIENE Basic information
Product Name:1,4-PENTADIENE
Synonyms:ALLYLETHYLENE;CH2=CHCH2CH=CH2;DIVINYLMETHANE;Pentadiene-1,4 (technical);1,4-PENTADIENE 99+%;1,4-Pentadiene,98+%;PENTADIENE-1,4: TECH.;1,4-PENTADIENE
CAS:591-93-5
MF:C5H8
MW:68.12
EINECS:209-736-9
Product Categories:Acyclic;Alkenes;Organic Building Blocks
Mol File:591-93-5.mol
1,4-PENTADIENE Structure
1,4-PENTADIENE Chemical Properties
Melting point -148 °C
Boiling point 26 °C(lit.)
density 0.659 g/mL at 25 °C(lit.)
vapor pressure 11.91 psi ( 20 °C)
refractive index n20/D 1.389(lit.)
Fp 40 °F
storage temp. 0-6°C
solubility Soluble in acetone, alcohol, benzene, and ether (Weast, 1986)
form Liquid
pka>14 (Schwarzenbach et al., 1993)
color Clear colorless
Water Solubility 558 mg/kg at 25 °C (shake flask-GC, McAuliffe, 1966)
BRN 1696934
Henry's Law Constant0.120 at 25 °C (Hine and Mookerjee, 1975)
Stability:Stable. Highly flammable. Note low boiling point and low flash point. Incompatible with strong oxidizing agents.
CAS DataBase Reference591-93-5(CAS DataBase Reference)
EPA Substance Registry System1,4-Pentadiene (591-93-5)
Safety Information
Hazard Codes F+,Xn
Risk Statements 12-65
Safety Statements 16-23-62
RIDADR UN 3295 3/PG 1
WGK Germany 3
HazardClass 3.1
PackingGroup II
HS Code 29012900
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
1,4-PENTADIENE Usage And Synthesis
Chemical Propertiescolourless liquid
Uses1,4-Pentadiene can be used to obtain bioinsecticidal composition.
General DescriptionA colorless liquid. Less dense than water and insoluble in water. Hence floats on water.
Air & Water ReactionsHighly flammable. Insoluble in water.
Reactivity Profile1,4-PENTADIENE may react vigorously with strong oxidizing agents. May react exothermically with reducing agents to release gaseous hydrogen. Can undergo exothermic polymerization reactions in the presence of various catalysts (such as acids) or initiators. May undergo autoxidation upon exposure to the air to form explosive peroxides. Violent explosions have occurred at low temperatures in ammonia synthesis gas units. These explosions have been traced to the decomposition of addition products between dienes such as this one and oxides of nitrogen [Bretherick, 1995].
Health HazardVapor may cause dizziness or suffocation. Contact may irritate skin and eyes.
Purification MethodsDistil it from NaBH4. Purify it by preparative gas chromatography or distillation and stabilize it with 0.1% of 2,6-di-tert-butyl-p-cresol. [Reimann et al. J Am Chem Soc 108 5527 1986, Beilstein 1 IV 998.]
Jasmone DIPHENYLFULVENE 1,4,5,8,9,10-Hexahydroanthracene 4-TRICHLOROMETHYL-4-METHYL-2,5-CYCLOHEXADIENONE 1,2,3,4,5,6-HEXAMETHYLBICYCLO[2.2.0]HEXA-2,5-DIENE 2,5-Dimethyl-3,4-diphenylcyclopentadienone 1-METHOXY-1,4-CYCLOHEXADIENE trans-1,3-Pentadiene (stabilized with TBC) 1-CHLORO-1,2-DIFLUORO-1,4-PENTADIENE, 97% MIN. 3-METHYL-1,3-PENTADIENE (CIS- AND TRANS- MIXTURE) 99+%,3-Methyl-1,3-pentadiene (cis- and trans- mixture) 1,3-Pentadiene-2,4-diol diacetate PIPERYLENE/BUTENE/PENTENE COPOLYMER 1,2,3,4-Tetrachloro-5,5-dimethoxycyclopentadiene 2-METHYL-1,3-PENTADIENE (CIS- AND TRANS- MIXTURE) TERPENE DICYCLOPENTADIENE/T-BUTYLCRESOL COPOLYMER 1,2,3,4-TETRAPHENYL-1,3-CYCLOPENTADIENE (CYCLOPENTADIENYLIDENE)TRIPHENYLPHOSPHORANE

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