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Merck
CN

SMB00291

十八碳四烯酸

≥99%

别名:

十八碳四烯酸, 鰮油酸, (6Z,9Z,12Z,15Z)-十八碳四烯酸, 6Z,9Z,12Z,15Z-十八碳四烯酸, 顺-6,9,12,15-十八碳四烯酸

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关于此项目

经验公式(希尔记法):
C18H28O2
化学文摘社编号:
分子量:
276.41
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352211
MDL number:
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InChI key

JIWBIWFOSCKQMA-LTKCOYKYSA-N

SMILES string

CC\C=C/C\C=C/C\C=C/C\C=C/CCCCC(O)=O

InChI

1S/C18H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h3-4,6-7,9-10,12-13H,2,5,8,11,14-17H2,1H3,(H,19,20)/b4-3-,7-6-,10-9-,13-12-

assay

≥99%

form

liquid

functional group

carboxylic acid

lipid type

omega FAs

shipped in

ambient

storage temp.

−20°C

Quality Level

Biochem/physiol Actions

一种含 18 个碳原子、ω-3 的脂肪酸,是二十碳五烯酸 (EPA) 和二十二碳六烯酸 (DHA) 的膳食先驱物质。十八碳四烯酸在植物油中少量存在。
十八碳四烯酸是一种含 18 碳的多不饱和脂肪酸(PUFA)。它属于 ω-3 脂肪酸类,其是二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)的膳食前体。 十八碳四烯酸在种子油中少量存在。

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Angela Oboh et al.
Lipids, 52(10), 837-848 (2017-09-01)
Elongation of very long-chain fatty acid 4 (Elovl4) proteins participate in the biosynthesis of very long-chain (>C
P Prasad et al.
Journal of oleo science, 68(3), 209-223 (2019-02-15)
Buglossoides arvensis is indigenous to India and its seed oil is rich in unique and nutritionally important omega-3 fatty acid namely, stearidonic acid (SDA). It is a non-conventional oil seed plant and needs to be agronomically adapt for commercial utilization.
Zahid Rasul Niazi et al.
Hypertension research : official journal of the Japanese Society of Hypertension, 40(12), 966-975 (2017-09-08)
Eicosapentaenoic acid:docosahexaenoic acid (EPA:DHA) 6:1, an omega-3 polyunsaturated fatty acid formulation, has been shown to induce a sustained formation of endothelial nitric oxide (NO) synthase-derived NO, a major vasoprotective factor. This study examined whether chronic intake of EPA:DHA 6:1 prevents
J L Fidalgo Rodríguez et al.
Biochimica et biophysica acta. Biomembranes, 1861(8), 1428-1436 (2019-06-13)
Unsaturated fatty acids (UFAs) are known to lower the level of sterols in blood, which accounts for their cardioprotective effect. To understand the molecular basis of this effect, Langmuir monolayer studies have been performed. A series of UFAs differing in
Protein kinase inhibition by ω-3 fatty acids.
Mirnikjoo B, et al.
The Journal of Biological Chemistry, 276(14), 10888-10896 (2001)

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