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129186

Sigma-Aldrich

1,4-Hexadiene, mixture of cis and trans

99%

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About This Item

Linear Formula:
CH3CH=CHCH2CH=CH2
CAS Number:
592-45-0
Molecular Weight:
82.14
EC Number:
209-756-8
MDL number:
MFCD00009298
UNSPSC Code:
12352100
PubChem Substance ID:
24847887
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.411 (lit.)

bp

64-66 °C (lit.)

density

0.71 g/mL at 25 °C (lit.)

functional group

allyl

storage temp.

2-8°C

SMILES string

CC=CCC=C

InChI

1S/C6H10/c1-3-5-6-4-2/h3-4,6H,1,5H2,2H3

InChI key

PRBHEGAFLDMLAL-UHFFFAOYSA-N

Application

1,4-Hexadiene was used to prepare OH-adducts.

accessory

Product No.
Description
Pricing

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-14.8 °F - closed cup

Flash Point(C)

-26 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM0473
MKCC6404
MKCB9679
MKCB7154
MKBZ4911V

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Mohamad Al-Sheikhly et al.
Environmental science & technology, 40(9), 3082-3088 (2006-05-25)
Pulse radiolysis with spectrophotometric and conductometric detection was utilized to study the formation and reactions of radicals from benzene and dienes in aqueous solutions. The benzene OH adduct, *C6H6OH, reacts with O2 (k = 3 x 10(8) L mol(-1) s(-1))
Hexadiene.
American Industrial Hygiene Association journal, 43(1), B89-B90 (1982-01-01)
A versatile hexadiene synthesis by decarboxylative sp(3)-sp(3) coupling/cope rearrangement.
Shelli R Waetzig et al.
Angewandte Chemie (International ed. in English), 45(30), 4977-4980 (2006-07-05)

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