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111805

Sigma-Aldrich

trans-1,3-Pentadiene

90%

Synonym(s):

trans-Piperylene

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About This Item

Linear Formula:
CH3CH=CHCH=CH2
CAS Number:
2004-70-8
Molecular Weight:
68.12
Beilstein:
1523659
EC Number:
217-909-5
MDL number:
MFCD00009295
UNSPSC Code:
12352100
PubChem Substance ID:
24847043
NACRES:
NA.22

vapor pressure

6.56 psi ( 20 °C)

Assay

90%

refractive index

n20/D 1.430 (lit.)

bp

42 °C (lit.)

mp

−87 °C (lit.)

density

0.678 g/mL at 20 °C
0.683 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

C\C=C\C=C

InChI

1S/C5H8/c1-3-5-4-2/h3-5H,1H2,2H3/b5-4+

InChI key

PMJHHCWVYXUKFD-SNAWJCMRSA-N

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General description

Trans-1,3-Pentadiene spectra is recorded in the 5000-17500 cm(-1) region with conventional and intracavity laser photoacoustic spectroscopy. It can be determined by the spectrophotometric method based on the Diels-Alder reaction. In this reaction, cisoid 1,3-dienes and tetracyanoethylene (TCNE) react with an aromatic-TCNE pi-complex.

Application


  • Hydroxyl radical reactions with diolefins in atmospheric and combustion environments: This study provides insights into the reactions of hydroxyl radicals with diolefins such as trans-1,3-Pentadiene, highlighting their significance in both atmospheric chemistry and combustion processes. This research helps in understanding the reactive pathways and kinetics that could inform both environmental and industrial applications of trans-1,3-Pentadiene (Khaled et al., 2019).

accessory

Product No.
Description
Pricing

Signal Word

Danger

Hazard Statements

H225,H304,H315,H319,H335

Hazard Classifications

Asp. Tox. 1 - 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)

5.0 °F - closed cup

Flash Point(C)

-15 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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D A Williams et al.
Talanta, 20(11), 1085-1096 (1973-11-01)
An indirect spectrophotometric method, based on the rapid Diels-Alder reaction between cisoid 1,3-dienes and tetracyanoethylene (TCNE) and the destruction of an aromatic-TCNE pi-complex, was developed to determine eleven 1,3-dienes in the 0.05-1.00 x 10(-3)M range. These dienes were: cyclopentadiene; 1,3-cyclohexadiene;
Ruth J Waldrom et al.
The journal of physical chemistry. A, 110(3), 913-920 (2006-01-20)
The room-temperature vapor-phase overtone spectra of cis- and trans-1,3-pentadiene (piperylene) have been recorded in the 5000-17500 cm(-1) region with the use of conventional and intracavity laser photoacoustic spectroscopy. The presence of five nonequivalent olefinic CH bonds and one methyl group

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