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Merck
CN

H2132

Sigma-Aldrich

DL-Hexanoylcarnitine chloride

别名:

DL-Caproylcarnitine chloride

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关于此项目

线性分子式:
C13H26NO4Cl
CAS Number:
分子量:
295.80
MDL编号:
UNSPSC代码:
12352211
PubChem化学物质编号:
NACRES:
NA.25
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脂质类型

saturated FAs

储存温度

−20°C

SMILES字符串

Cl.CCCCCC(=O)OC(CC(O)=O)C[N](C)(C)C

InChI

1S/C13H26NO4.ClH/c1-5-6-7-8-13(17)18-11(9-12(15)16)10-14(2,3)4;/h11H,5-10H2,1-4H3,(H,15,16);1H

InChI key

AWUOLOICNWRXPY-UHFFFAOYSA-N

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Skin Sens. 1

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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H Caksen et al.
Genetic counseling (Geneva, Switzerland), 15(1), 9-17 (2004-04-16)
Lissencephaly or agyria refers to a rare disorder that is characterized by the absence of cerebral convolutions and a poorly formed sylvian fissure, giving the appearance of a 3-4 months old fetal brain. At present more than 25 dysmorphology syndromes
A K Bhuiyan et al.
Clinical and investigative medicine. Medecine clinique et experimentale, 18(2), 144-151 (1995-04-01)
A sensitive method of continuous on-line radio-high performance liquid chromatography (HPLC) was used to detect the specific radio-labelled acyl-carnitine esters derived from the oxidation of [U-14C]3-methyl-2-oxopentanoate by rat liver and muscle mitochondrial fractions. The recoveries of carnitine, acetyl-carnitine, propionyl-carnitine, 2-methylbutyryl-carnitine
E Schmidt-Sommerfeld et al.
Pediatric research, 31(6), 545-551 (1992-06-01)
To determine the sensitivity and specificity of detecting urinary medium-chain acylcarnitines for the diagnosis of MCAD deficiency, 114 urine specimens from 75 children with metabolic diseases and controls were analyzed in a blinded fashion using a radioisotopic exchange/HPLC method. All
Anelise M Tonin et al.
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience, 30(5), 383-390 (2012-04-05)
Medium-chain fatty acids and acylcarnitines accumulate in medium-chain acyl-CoA dehydrogenase deficiency (MCADD), the most frequent fatty acid oxidation defect clinically characterized by episodic crises with vomiting, seizures and coma. Considering that the pathophysiology of the neurological symptoms observed in MCADD
P E Minkler et al.
Analytical biochemistry, 212(2), 510-518 (1993-08-01)
This paper describes a method for the quantitative determination of free carnitine, acetylcarnitine, propionylcarnitine, hexanoylcarnitine, octanoylcarnitine, and total carnitine in plasma. Carnitine and acylcarnitines were extracted from 100 microliters of plasma with acetonitrile/methanol and isolated using 0.5-ml columns of silica

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