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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
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Quality Level

100

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.)

functional group

phenyl

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[1].

Biochem/physiol Actions

1-Phenyldodecane was degraded to phenylacetic acid by an oil-degrading bacterium[2].

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV3739
0000229665
MKCT7959
MKCS6580
MKCQ9218

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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
C Ruffo et al.
Ecotoxicology and environmental safety, 8(3), 275-279 (1984-06-01)
Pyridine and nitrilotriacetic acid sodium salt as models of soluble compounds and linear dodecylbenzene, branched dodecylbenzene, and stearic acid as models of insoluble compounds were compared for their biodegradability in three tests: the ODCE modified test and the Sturm and
O O Amund et al.
Antonie van Leeuwenhoek, 51(1), 45-56 (1985-01-01)
An oil-degrading bacterium identified as Acinetobacter lwoffi was isolated by elective culture on North Sea Forties crude oil from an activated sludge sample. It grew on a wide range of n-alkanes (C12-C28) and 1-phenylalkanes, including 1-phenyldodecane, 1-phenyltridecane and 1-phenyltetradecane. The
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
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