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44178

Supelco

1-Phenyldodecane

analytical standard

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:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥99.5% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.482 (lit.)
n20/D 1.482

bp

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

mp

3 °C (lit.)

density

0.856 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

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

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

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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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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
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
Xue-you Shen et al.
Huan jing ke xue= Huanjing kexue, 26(1), 122-126 (2005-04-30)
Effect of surfactant on the evaporative loss of benzene, toluene and ethylbenzene from static water was researched and the mechanism of surfactant was studied, so as try to supply theoretical reference for the effect of surfactant on the evaporation of

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