N-TriMethyl-γ-aMinobutyric Acid-d9 Chloride

Base Information

Chemical Name:N-TriMethyl-γ-aMinobutyric Acid-d9 Chloride
CAS No.:85806-17-3
Molecular Formula:C₇H₁₆NO₂*Cl
Molecular Weight:190.591
Hs Code.:
Mol file:85806-17-3.mol

Synonyms:

Suppliers and Price of N-TriMethyl-γ-aMinobutyric Acid-d9 Chloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
γ-Butyrobetaine-d9Hydrochloride
5mg
$ 185.00

Medical Isotopes, Inc.
N-(Carboxypropyl)-N,N,N-trimethyl-d9-ammoniumChloride
0.05 g
$ 835.00

Total 4 raw suppliers

Chemical Property of N-TriMethyl-γ-aMinobutyric Acid-d9 Chloride

Chemical Property:

Melting Point:214-216°C
Storage Temp.:Hygroscopic, Refrigerator, Under Inert Atmosphere
Solubility.:Methanol (Slightly), Water (Slightly)

Purity/Quality:

97% ^*data from raw suppliers

γ-Butyrobetaine-d9Hydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses Labelled analogue of γ-Butyrobetaine, a synthetic carnitine related compound used as a transporter substrate in the cloning and sequencing of human carnitine transporter 2 (CT2).

Technology Process of N-TriMethyl-γ-aMinobutyric Acid-d9 Chloride

There total 1 articles about N-TriMethyl-γ-aMinobutyric Acid-d9 Chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 865-50-9
iodomethane-d3

: 56-12-2
4-amino-n-butyric acid

: 85806-17-3
C₇H₇⁽²⁾H₉NO₂⁽¹⁺⁾*Cl^(1-)

Guidance literature:: 4-amino-n-butyric acid; With potassium hydrogencarbonate; In methanol; for 0.25h; Inert atmosphere;

iodomethane-d3; In methanol; at 20 ℃; for 66h; Inert atmosphere;

With hydrogenchloride; In water;
DOI:10.1021/ac801654h