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
SMILES string
Cl.CCCCCC(=O)OC(CC(O)=O)C[N](C)(C)C
InChI key
AWUOLOICNWRXPY-UHFFFAOYSA-N
lipid type
saturated FAs
storage temp.
−20°C
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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
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
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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