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线性分子式:
[(CH3)2CH(CH2)3CH(CH3)(CH2)3CH(CH3)CH2CH2-]2
化学文摘社编号:
分子量:
422.81
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
776019
MDL number:
产品名称
角鲨烷, analytical standard
SMILES string
CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C
InChI
1S/C30H62/c1-25(2)15-11-19-29(7)23-13-21-27(5)17-9-10-18-28(6)22-14-24-30(8)20-12-16-26(3)4/h25-30H,9-24H2,1-8H3
InChI key
PRAKJMSDJKAYCZ-UHFFFAOYSA-N
grade
analytical standard
CofA
current certificate can be downloaded
packaging
ampule of 1000 mg
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
refractive index
n20/D 1.452 (lit.)
bp
176 °C/0.05 mmHg (lit.)
mp
−38 °C (lit.)
density
0.81 g/mL at 25 °C (lit.)
application(s)
environmental
food and beverages
format
neat
storage temp.
room temp
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Other Notes
产品442784已停产。可使用产品PHR1417进行替代。
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
424.4 °F - closed cup
flash_point_c
218 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Squalane is in the midplane of the lipid bilayer: implications for its function as a proton permeability barrier.
Hau? T, et al.
Biochimica et Biophysica Acta - Bioenergetics, 1556(2-3), 149-154 (2002)
Biological importance and applications of squalene and squalane.
Advances in Food and Nutrition Research, 65(2-3), 223-233 (2012)
Alexander M Zolot et al.
The Journal of chemical physics, 129(19), 194705-194705 (2008-11-26)
Exothermic chemical reaction dynamics at the gas-liquid interface have been investigated by colliding a supersonic beam of F atoms [E(com)=0.7(3) kcalmol] with a continuously refreshed liquid hydrocarbon (squalane) surface under high vacuum conditions. Absolute HF(v,J) product densities are determined by
Yueying Ren et al.
Journal of chromatography. A, 1155(1), 105-111 (2007-05-01)
A novel approach is described for the prediction of gas chromatographic Kováts retention indices of 150 acyclic C5-C8 alkenes on two stationary phases (polydimethylsiloxane, PDMS, and squalane, SQ). The heuristic method was used to build multiple linear regression models using
L Harivardhan Reddy et al.
Molecular pharmaceutics, 6(5), 1526-1535 (2009-07-29)
Gemcitabine (2',2'-difluorodeoxyribofuranosylcytosine) is an anticancer nucleoside analogue active against a wide variety of solid tumors. However, following intravenous administration, this drug is rapidly inactivated by enzymatic deamination and displays a short biological half-life necessitating the administration of high doses leading
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