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Merck
CN

44150

1-Dodecene

technical, ≥90% (GC)

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About This Item

Linear Formula:
CH3(CH2)9CH=CH2
CAS Number:
112-41-4
Molecular Weight:
168.32
EC Number:
203-968-4
UNSPSC Code:
12352100
PubChem Substance ID:
329756459
Beilstein/REAXYS Number:
1699848
MDL number:
MFCD00008961

Key Documents

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InChI key

CRSBERNSMYQZNG-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCCCCCCCC=C

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.)

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pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H304

Hazard Classifications

Asp. Tox. 1

supp_hazards

EUH066

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

174.2 °F - No data available

flash_point_c

79 °C - No data available

ppe

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

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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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