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110485

Sigma-Aldrich

trans-5-Decene

98%

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About This Item

Fórmula lineal:
CH3(CH2)3CH=CH(CH2)3CH3
Número de CAS:
7433-56-9
Peso molecular:
140.27
EC Number:
231-080-7
MDL number:
MFCD00009508
UNSPSC Code:
12352100
PubChem Substance ID:
24846988
NACRES:
NA.22

assay

98%

refractive index

n20/D 1.424 (lit.)

bp

170 °C/750 mmHg (lit.)

density

0.74 g/mL at 25 °C (lit.)

SMILES string

[H]\C(CCCC)=C(\[H])CCCC

InChI

1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h9-10H,3-8H2,1-2H3/b10-9+

InChI key

UURSXESKOOOTOV-MDZDMXLPSA-N

Application

trans-5-Decene has been used to characterize the effect of cyclization and size on the stability of Criegee intermediates formed in ozonolysis. It has been added to phenoxathiin cation radical in acetonitrile solution to form bis(10-phenoxathiiniumyl) alkane adducts.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

114.8 °F - closed cup

flash_point_c

46 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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trans-2-Hexene 97%

Sigma-Aldrich

110892

trans-2-Hexene

cis-3-Hexene ≥95.0%

Sigma-Aldrich

52985

cis-3-Hexene

Keisean A J M Stevenson et al.
Journal of separation science, 42(11), 2013-2022 (2019-04-10)
Thermodynamics-based models have been demonstrated to be useful for predicting retention time and peak widths in gas chromatography and two-dimensional gas chromatography separations. However, the collection of data to train the models can be time consuming, which lessens the practical
Greg T Drozd et al.
The journal of physical chemistry. A, 115(17), 4381-4387 (2011-04-12)
Ozonolysis is a key reaction in atmospheric chemistry, although important details of the behavior of the ozonolysis intermediates are not known. The key intermediate in ozonolysis, the Criegee intermeiate (CI), is known to quickly isomerize, with the favored unimolecular pathway
Bing-Jun Zhao et al.
The Journal of organic chemistry, 72(16), 6154-6161 (2007-07-03)
Addition of phenoxathiin cation radical (PO*+) to acyclic alkenes in acetonitrile (MeCN) solution occurred stereospecifically to form bis(10-phenoxathiiniumyl)alkane adducts. Stereospecific trans addition is ascribed to the intermediacy of an episulfonium cation radical. The alkenes used were cis- and trans-2-butene, cis-

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