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线性分子式:
C6H5(CH2)11CH3
化学文摘社编号:
分子量:
246.43
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
204-591-8
Beilstein/REAXYS Number:
1909107
MDL number:
InChI key
KWKXNDCHNDYVRT-UHFFFAOYSA-N
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
SMILES string
CCCCCCCCCCCCc1ccccc1
grade
analytical standard
assay
≥99.5% (GC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
Quality Level
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
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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.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
228.2 °F - closed cup
flash_point_c
109 °C - closed cup
ppe
Eyeshields, Gloves
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
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)
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
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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