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About This Item
Linear Formula:
C7H16NO2Cl
CAS Number:
Molecular Weight:
181.66
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
MDL number:
Product Name
(3-Carboxypropyl)trimethylammonium chloride, technical grade
InChI
1S/C7H15NO2.ClH/c1-8(2,3)6-4-5-7(9)10;/h4-6H2,1-3H3;1H
SMILES string
[Cl-].C[N+](C)(C)CCCC(O)=O
InChI key
GNRKTORAJTTYIW-UHFFFAOYSA-N
grade
technical grade
mp
220 °C (dec.) (lit.)
Quality Level
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Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Lisa Adamiak et al.
ACS nano, 11(10), 9877-9888 (2017-10-04)
Cellular uptake by macrophages and ensuing clearance by the mononuclear phagocyte system stands as a significant biological barrier for nanoparticle therapeutics. While there is a growing body of work investigating the design principles essential for imparting nanomaterials with long-circulating characteristics
C J Gross et al.
Biochimica et biophysica acta, 886(3), 425-433 (1986-05-29)
Uptake and metabolism of L-carnitine, D-carnitine and acetyl-L-carnitine were studied utilizing isolated guinea-pig enterocytes. Uptake of the D- and L-isomers of carnitine was temperature dependent. Uptake of L-[14C]carnitine by jejunal cells was sodium dependent since replacement by lithium, potassium or
W J Thoma et al.
Biochimica et biophysica acta, 797(1), 136-139 (1984-01-24)
The effect of ascorbate deficiency on carnitine biosynthesis was investigated in young male guinea pigs. Liver and skeletal muscle carnitine levels were reduced in scorbutic animals. Heart and kidney concentrations remained unchanged. 14C-labeled 4-N-trimethylaminobutyrate was administered to control, pair-fed and
L M Henderson et al.
Federation proceedings, 41(12), 2843-2847 (1982-10-01)
The biosynthesis of carnitine proceeds from trimethyllysine (TML) by beta-hydroxylation by a liver or kidney mitochondrial enzyme, which requires oxygen, alpha-ketoglutarate, ferrous iron, and ascorbate. This dioxygenase is rapidly inactivated by preincubation with Fe2+, but not Fe3+. The evidence suggests
J S Serrano et al.
Methods and findings in experimental and clinical pharmacology, 5(4), 251-254 (1983-01-01)
The effects of GABA, its quaternary derivative N-trimethyl GABA and quinidine have been studied in a model of ventricular automaticity induced in the isolated right ventricle of the rat. GABA shows low anti-automatic activity. N-trimethyl GABA and quinidine were, however
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