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Merck
CN

284432

二十八酸

synthetic, ≥98%

别名:

褐煤酸

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关于此项目

线性分子式:
CH3(CH2)26CO2H
化学文摘社编号:
分子量:
424.74
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-041-8
Beilstein/REAXYS Number:
1801616
MDL number:
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InChI key

UTOPWMOLSKOLTQ-UHFFFAOYSA-N

InChI

1S/C28H56O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28(29)30/h2-27H2,1H3,(H,29,30)

SMILES string

CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O

assay

≥98%

form

powder

Quality Level

solubility

chloroform: soluble 50 mg/mL, clear, colorless

functional group

carboxylic acid

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General description

二十八烷酸是 沙棘果实的成分之一 。它也存在于 温郁金 的地上部分。

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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R Menéndez et al.
Pharmacological research, 44(4), 299-304 (2001-10-11)
The present study was undertaken to investigate the effects of D003, a mixture of very long chain saturated fatty acids isolated and purified from sugar cane wax, on cholesterol biosynthesis in cultured fibroblasts. Cholesterol biosynthesis is regulated through feedback regulation
M D Rodríguez et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 41(1), 89-93 (2002-11-28)
D-003 is a mixture of long-chain fatty acids isolated and purified from sugar cane wax, the major component of which is 1-octacosanoic acid and which possesses effective antiplatelet, antithrombotic and cholesterol-lowering effects. D-003 was suspended in 1% acacia gum solution
Effect of D-003 on a subconvulsive dose of kainic Acid in rats.
Daisy Carbajal et al.
Drugs in R&D, 5(6), 331-336 (2004-11-26)
Zheng-Ming Tao et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 32(24), 2604-2606 (2008-03-15)
To investigate the chemical constituents from aerial part of Curcuma wenyujin. Compounds were isolated by repeated column chromatography on silica gel. Their structures were elucidated on the basis of spectral analysis and comparison with literature data. Six compounds were isolated
[Simple quantitative method of direct transesterification of higher fatty acid in biological samples].
V Z Lankin et al.
Voprosy meditsinskoi khimii, 17(3), 331-335 (1971-05-01)

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