H2132
DL-Hexanoylcarnitine chloride
别名:
DL-Caproylcarnitine chloride
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线性分子式:
C13H26NO4Cl
化学文摘社编号:
分子量:
295.80
MDL编号:
UNSPSC代码:
12352211
PubChem化学物质编号:
NACRES:
NA.25
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
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
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
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
Anthony O Odibo et al.
Prenatal diagnosis, 31(10), 990-994 (2011-07-12)
We tested the hypothesis that first-trimester metabolic biomarkers offered a unique profile in women with preeclampsia (PE) in the second half of pregnancy, compared with controls. We conducted a nested case-control study within a prospective cohort of pregnant women followed
Tiina Tyni et al.
Pediatric research, 52(1), 64-70 (2002-06-27)
Defects of mitochondrial fatty acid beta-oxidation are an important group of inherited metabolic disorders in children. Despite improved screening opportunities, diagnosis of these disorders is not often straightforward and requires enzyme analyses. Because therapy is effective in many of these
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