113239
1-Phenyldodecane
97%
Synonym(s):
Dodecylbenzene
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About This Item
Linear Formula:
C6H5(CH2)11CH3
CAS Number:
Molecular Weight:
246.43
Beilstein:
1909107
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
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.
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
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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
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
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)
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