trans-5-Decene

Name: <I>trans</I>-5-Decene
Brand: ALDRICH
Price: 146 USD

98%

Slide 1 of 1

Select a Size

5 G

$146.00

Check Cart for Availability

Need it sooner? View alternative products.

One Time Order

Request a Bulk Order

Subscriptions are currently unavailable.

About This Item

Linear Formula:

CH₃(CH₂)₃CH=CH(CH₂)₃CH₃

CAS Number:

7433-56-9

Molecular Weight:

140.27

NACRES:

NA.22

PubChem Substance ID:

24846988

UNSPSC Code:

12352100

EC Number:

231-080-7

MDL number:

MFCD00009508

Key Documents

View All Documentation

Product Name

trans-5-Decene, 98%

InChI key

UURSXESKOOOTOV-MDZDMXLPSA-N

InChI

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

SMILES string

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

assay

98%

refractive index

n20/D 1.424 (lit.)

bp

170 °C/750 mmHg (lit.)

density

0.74 g/mL at 25 °C (lit.)

Quality Level

100

Related Categories

Chemical Building Blocks

Organic Building Blocks

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item	593028	111244	545449
Sigma-Aldrich 110485 trans-5-Decene	Sigma-Aldrich 593028 trans-4-Octene	Sigma-Aldrich 111244 trans-3-Octene	Sigma-Aldrich 545449 5-Decyne
assay 98%	assay 98%	assay 98%	assay 98%
Quality Level 100	Quality Level 100	Quality Level 100	Quality Level 100
density 0.74 g/mL at 25 °C (lit.)	density 0.715 g/mL at 25 °C (lit.)	density 0.716 g/mL at 25 °C (lit.)	density 0.766 g/mL at 25 °C (lit.)
bp 170 °C/750 mmHg (lit.)	bp 122-123 °C (lit.)	bp 121-122 °C (lit.)	bp -
refractive index n20/D 1.424 (lit.)	refractive index n20/D 1.412 (lit.)	refractive index n20/D 1.413 (lit.)	refractive index n20/D 1.4340 (lit.)

Application

trans-5-Decene has been used to characterize the effect of cyclization and size on the stability of Criegee intermediates formed in ozonolysis[1]. It has been added to phenoxathiin cation radical in acetonitrile solution to form bis(10-phenoxathiiniumyl) alkane adducts[2].

pictograms

GHS02,GHS07

signalword

Warning

hcodes

H226,H315,H319,H335

pcodes

P210 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Thermodynamics-based modelling of gas chromatography separations across column geometries and systems, including the prediction of peak widths.

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

Pressure dependence of stabilized Criegee intermediate formation from a sequence of alkenes.

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

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.

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-

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service