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Merck
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重要文件

M7531

Sigma-Aldrich

11-Methyllauric acid

≥98%

同義詞:

11-Methyldodecanoic acid, Isotridecanoic acid

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About This Item

經驗公式(希爾表示法):
C13H26O2
CAS號碼:
分子量::
214.34
MDL號碼:
分類程式碼代碼:
12352211
PubChem物質ID:
暫時無法取得訂價和供貨情況

化驗

≥98%

形狀

powder

官能基

carboxylic acid

脂質類型

saturated FAs

運輸包裝

ambient

儲存溫度

−20°C

SMILES 字串

CC(C)CCCCCCCCCC(O)=O

InChI

1S/C13H26O2/c1-12(2)10-8-6-4-3-5-7-9-11-13(14)15/h12H,3-11H2,1-2H3,(H,14,15)

InChI 密鑰

SIOLDWZBFABPJU-UHFFFAOYSA-N

生化/生理作用

11-Methyl-lauric (11-Methyldodecanoic) acid is a methylated 13-carbon analog of the 12-carbon chain saturated fatty acid lauric acid. 11-Methyllauric may be used in comparative studies of the ability of medium chain saturated fatty acids to modulate inflammatory processes and to enhance skin permeation (drug delivery) formulations.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析證明 (COA)

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Sunita Gupta et al.
Journal of neurochemistry, 120(6), 1060-1071 (2012-01-18)
This study describes the effects of long-chain fatty acids on inflammatory signaling in cultured astrocytes. Data show that the saturated fatty acid palmitic acid, as well as lauric acid and stearic acid, trigger the release of TNFα and IL-6 from
Effect of vehicle systems, pH and enhancers on the permeation of highly lipophilic aripiprazole from Carbopol 971P gel systems across human cadaver skin.
Hossain MA, Ahmed SU, Plakogiannis FM.
Drug Devel. Ind. Pharm., 38, 323-330 (2012)
Eric Soupene et al.
Scientific reports, 7(1), 15767-15767 (2017-11-19)
De novo lipid synthesis and scavenging of fatty acids (FA) are processes essential for the formation of the membrane of the human pathogen Chlamydia trachomatis (C.t.). Host FA are assimilated via esterification by the bacterial acyl-acyl carrier protein (ACP) synthase
Yosuke Toyotake et al.
Biochemical and biophysical research communications, 500(3), 704-709 (2018-04-22)
1-Acyl-sn-glycerol-3-phosphate O-acyltransferase (PlsC) plays an essential role in the formation of phosphatidic acid, a precursor of various membrane phospholipids (PLs), in bacteria by catalyzing the introduction of an acyl group into the sn-2 position of lysophosphatidic acid. Various bacteria produce

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