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Merck
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403245

Sigma-Aldrich

(3-Carboxypropyl)trimethylammonium chloride

technical grade

Sinónimos:

γ-Butyrobetaine hydrochloride, Deoxycarnitine hydrochloride

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About This Item

Fórmula lineal:
C7H16NO2Cl
Número de CAS:
6249-56-5
Peso molecular:
181.66
MDL number:
MFCD00011905
UNSPSC Code:
12352116
PubChem Substance ID:
24864895
NACRES:
NA.22

grade

technical grade

mp

220 °C (dec.) (lit.)

SMILES string

[Cl-].C[N+](C)(C)CCCC(O)=O

InChI

1S/C7H15NO2.ClH/c1-8(2,3)6-4-5-7(9)10;/h4-6H2,1-3H3;1H

InChI key

GNRKTORAJTTYIW-UHFFFAOYSA-N

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Categorías relacionadas

Storage Class

11 - Combustible Solids

wgk_germany

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
Carnitine synthesis in scorbutic guinea pigs.
Nutrition reviews, 43(6), 185-187 (1985-06-01)
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
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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