MilliporeSigma
All Photos(3)

Documents

403245

Sigma-Aldrich

(3-Carboxypropyl)trimethylammonium chloride

technical grade

Sign Into View Organizational & Contract Pricing

Synonym(s):
γ-Butyrobetaine hydrochloride, Deoxycarnitine hydrochloride
Linear Formula:
C7H16NO2Cl
CAS Number:
Molecular Weight:
181.66
MDL number:
PubChem Substance ID:
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

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
1.2480204573T7947
Thiamine hydrochloride tested according to Ph. Eur.

04573

Thiamine hydrochloride

(R)-Tomoxetine hydrochloride solid

T7947

(R)-Tomoxetine hydrochloride

grade

technical grade

grade

-

grade

-

grade

-

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


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Documents related to the products that you have purchased in the past have been gathered in the Document Library for your convenience.

Visit the Document Library

Difficulty Finding Your Product Or Lot/Batch Number?

Product numbers are combined with Pack Sizes/Quantity when displayed on the website (example: T1503-25G). Please make sure you enter ONLY the product number in the Product Number field (example: T1503).

Example:

T1503
Product Number
-
25G
Pack Size/Quantity

Additional examples:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

enter as 1.000309185)

Having trouble? Feel free to contact Technical Service for assistance.

Lot and Batch Numbers can be found on a product's label following the words 'Lot' or 'Batch'.

Aldrich Products

  • For a lot number such as TO09019TO, enter it as 09019TO (without the first two letters 'TO').

  • For a lot number with a filling-code such as 05427ES-021, enter it as 05427ES (without the filling-code '-021').

  • For a lot number with a filling-code such as STBB0728K9, enter it as STBB0728 without the filling-code 'K9'.

Not Finding What You Are Looking For?

In some cases, a COA may not be available online. If your search was unable to find the COA you can request one.

Request COA

Customers Also Viewed

Slide 1 of 9

1 of 9

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
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
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service