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Merck
CN

44150

Sigma-Aldrich

1-Dodecene

technical, ≥90% (GC)

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About This Item

Linear Formula:
CH3(CH2)9CH=CH2
CAS Number:
Molecular Weight:
168.32
Beilstein:
1699848
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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vapor density

5.8 (vs air)

vapor pressure

0.2 mmHg ( 20 °C)

grade

technical

Assay

≥90% (GC)

autoignition temp.

491 °F

expl. lim.

~4.7 %

refractive index

n20/D 1.429 (lit.)
n20/D 1.430

bp

214-216 °C (lit.)

mp

−35 °C (lit.)

density

0.758 g/mL at 20 °C (lit.)

SMILES string

CCCCCCCCCCC=C

InChI

1S/C12H24/c1-3-5-7-9-11-12-10-8-6-4-2/h3H,1,4-12H2,2H3

InChI key

CRSBERNSMYQZNG-UHFFFAOYSA-N

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Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Asp. Tox. 1

Supplementary Hazards

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

174.2 °F - No data available

Flash Point(C)

79 °C - No data available

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites.
Aslam W, et al.
Catalysis Today, 227, 187-197 (2014)
[Leukocytic infiltration in the pathogenesis of lesions of the kidney glomeruli in the Shwartzman phenomenon].
T Kokoszka et al.
Patologia polska, 30(1), 135-138 (1979-01-01)
Hydroformylation of 1-dodecene using Rh-TPPTS in a microemulsion.
Haumann M, et al.
Applied Catalysis A: General, 225(1), 239-249 (2002)
A Malumbres et al.
Nanoscale, 7(18), 8566-8573 (2015-04-22)
Stable, alkyl-terminated, light-emitting silicon nanoparticles have been synthesized in a continuous process by laser pyrolysis of a liquid trialkyl-silane precursor selected as a safer alternative to gas silane (SiH4). Stabilization was achieved by in situ reaction using a liquid collection
Melina Nisenbaum et al.
Journal of environmental sciences (China), 25(3), 613-625 (2013-08-08)
We report on the biodegradation of pure hydrocarbons and chemotaxis towards these compounds by an isolated chlorophenol degrader, Pseudomonas strain H. The biochemical and phylogenetic analysis of the 16S rDNA sequence identified Pseudomonas strain H as having 99.56% similarity with

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