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Merck

284432

Sigma-Aldrich

二十八酸

synthetic, ≥98%

别名:

褐煤酸

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About This Item

线性分子式:
CH3(CH2)26CO2H
CAS号:
分子量:
424.74
Beilstein:
1801616
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

≥98%

形狀

powder

mp

91-93 °C (lit.)

溶解度

chloroform: soluble 50 mg/mL, clear, colorless

SMILES 字串

CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O

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)

InChI 密鑰

UTOPWMOLSKOLTQ-UHFFFAOYSA-N

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一般說明

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。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Slide 1 of 4

1 of 4

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)
[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)
Rui-Xia Zheng et al.
Natural product research, 23(15), 1451-1456 (2009-10-08)
Ten compounds were isolated from the fruits of Hippophae rhamnoides. On the basis of spectroscopic and chemical methods, the structures of these compounds were elucidated as hippophae cerebroside (1), oleanolic acid (2), ursolic acid (3), 19-alpha-hydroxyursolic acid (4), dulcioic acid

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