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113239

Sigma-Aldrich

1-Phenyldodecane

97%

Synonym(s):

Dodecylbenzene

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About This Item

Linear Formula:
C6H5(CH2)11CH3
CAS Number:
123-01-3
Molecular Weight:
246.43
Beilstein:
1909107
EC Number:
204-591-8
MDL number:
MFCD00008974
UNSPSC Code:
12352100
PubChem Substance ID:
24846872
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.482 (lit.)

bp

185-188 °C/15 mmHg (lit.)
331 °C (lit.)

mp

3 °C (lit.)

density

0.856 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCc1ccccc1

InChI

1S/C18H30/c1-2-3-4-5-6-7-8-9-10-12-15-18-16-13-11-14-17-18/h11,13-14,16-17H,2-10,12,15H2,1H3

InChI key

KWKXNDCHNDYVRT-UHFFFAOYSA-N

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Application

1-Phenyldodecane acts as a pseudo-stationary phase (PSP) marker in the preparation of microemulsion.

Biochem/physiol Actions

1-Phenyldodecane was degraded to phenylacetic acid by an oil-degrading bacterium.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

228.2 °F - closed cup

Flash Point(C)

109 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Shaoqiang Hu et al.
Journal of chromatography. A, 1216(45), 7932-7940 (2009-09-29)
A novel procedure for in situ assembling a complex chiral selector, di-n-butyl l-tartrate-boric acid complex, by the reaction of di-n-butyl l-tartrate with boric acid in a running buffer was reported and its application in the enantioseparation of beta-blockers and structural
Studies of the carcinogenesis and tumorigenesis of skin applications of dodecylbenzene on hairless mice.
C B Assogne
British journal of industrial medicine, 47(5), 356-358 (1990-05-01)
J Campos-García et al.
Applied and environmental microbiology, 65(8), 3730-3734 (1999-07-31)
Pseudomonas aeruginosa W51D is able to grow by using branched-chain dodecylbenzene sulfonates (B-DBS) or the terpenic alcohol citronellol as a sole source of carbon. A mutant derived from this strain (W51M1) is unable to degrade citronellol but still grows on
Honghua Rao et al.
The Journal of organic chemistry, 70(20), 8107-8109 (2005-11-10)
[Chemical reaction: See text] We have developed a general, efficient, and inexpensive catalyst system for arylation of amines by using 10 mol % of CuI as the copper source, 20 mol % of diphenyl pyrrolidine-2-phosphonate (DPP) as the ligand, K3PO4
Ding-xi Cheng et al.
Guang pu xue yu guang pu fen xi = Guang pu, 27(1), 104-107 (2007-03-30)
There is a self-polymerization equilibrium system between the cation of the fluorescent dye-safranine T and its dimer. In the presence of appropriate amounts of anionic surfactant SDBS, the above mentioned equilibrium can be adjusted by a quantitative addition of protein
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