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113239

Sigma-Aldrich

1-Phenyldodecane

97%

Sinónimos:

Dodecylbenzene

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About This Item

Fórmula lineal:
C6H5(CH2)11CH3
Número de CAS:
123-01-3
Peso molecular:
246.43
Beilstein/REAXYS Number:
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

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

228.2 °F - closed cup

flash_point_c

109 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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Sigma-Aldrich

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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
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
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
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