What is the DL-Carnitine?

DL-Carnitine is , while it's Molecular Formula is C 7 H 15 NO 3 . DL-Carnitine is a Chloride salt free form of D,L-Carnitine Chloride (C184100). Carnitine is a vitamin, essential cofactor of fatty acid metabolism. It is required for the transport of fatty acids through the inner mitochondrial membrane. Synthesized primarily in the liver and kidney; highest concentrations found in heart and skeletal muscle. Dietary sources include red meat, dairy products, beans, avocado.

What is the CAS number for DL-Carnitine?

The CAS number of DL-Carnitine is 406-76-8.

What is DL-Carnitine (406-76-8) used for?

DL-Carnitine, also known as D,L-Carnitine Chloride, is a vital compound that plays a crucial role in the metabolism of fatty acids. It functions as an essential cofactor, facilitating the transport of fatty acids across the inner mitochondrial membrane. This process is vital for energy production within the body. DL-Carnitine is primarily synthesized in the liver and kidneys, with the highest concentrations found in the heart and skeletal muscles. It can also be obtained through dietary sources such as red meat, dairy products, beans, and avocados.InChI:InChI=1/C7H15NO3/c1-8(2,3)5-6(9)4-7(10)11/h6,9H,4-5H2,1-3H3

Quality manufacturer supply Cardiogen 406-76-8 in stock with high standard

Molecular Formula:C₇H₁₅NO₃
Molecular Weight:161.201
Melting Point:197-198 °C (decomp)
PSA：60.36000
LogP:-1.80650

DL-Carnitine(Cas 406-76-8) Usage

InChI:InChI=1/C7H15NO3/c1-8(2,3)5-6(9)4-7(10)11/h6,9H,4-5H2,1-3H3

406-76-8 Relevant articles

Resolution of the racemates of DL-carnitine

Mueller,Strack

, p. 618 - 622 (1972)

On the preparation of carnitinbetaine

Strack,Lorenz

, p. 276 - 277 (1966)

PROCESS FOR THE PRODUCTION OF CARNITINE BY CYCLOADDITION

-

Page/Page column 10, (2012/02/03)

The invention relates to a method for th...

An efficient, highly enantioenriched route to L-carnitine and α-lipoic acid via hydrolytic kinetic resolution

Bose, D. Subhas,Fatima, Liyakat,Rajender, Salla

, p. 1863 - 1867 (2008/01/27)

A general and practical approach for the...

Retention and selectivity of teicoplanin stationary phases after copper complexation and isotopic exchange

Berthod,Valleix,Tizon,Leonce,Caussignac,Armstrong

, p. 5499 - 5508 (2007/10/03)

Teicoplanin is a macrocyclic glycopeptid...

Asymmetric synthesis of (S)-(+)-carnitine and analogs

Jain, Rajendra P,Williams, Robert M

, p. 6505 - 6509 (2007/10/03)

A general asymmetric route to enantiomer...

406-76-8 Process route

: 4-(chloromethyl)oxetane-2-one

: 75-50-3
trimethylamine

: 24587-49-3
(2E)-4-hydroxybut-2-enoic acid

: 541-15-1,44985-79-7
L-carnitine

: 406-76-8,461-06-3,541-14-0,541-15-1,44985-79-7
(S)-carnitin

Conditions

Conditions	Yield
With sodium hydroxide; In water; at 0 - 20 ℃; for 2h; Product distribution / selectivity;

tetrafluoroborate salt of L-carnitine: tetrafluoroborate salt of L-carnitine

: dichlorotetradecylphosphite

: (R)-3-carboxy-N,N,N-trimethyl-2-{[hydroxy(tetradecyloxy)phosphinyl]oxy}-1-propanaminium hydroxide

: 406-76-8,461-06-3,541-14-0,541-15-1,44985-79-7
(S)-carnitin

Conditions

Conditions	Yield
In 2,3,5-trimethyl-pyridine; methanol; water; acetonitrile;

406-76-8 Upstream products

461-06-3
CARNITINE
1116-95-6
(D)-(+)-carnitinenitrile chloride
133039-09-5
Toluene-4-sulfonate((S)-3-carboxy-2-hydroxy-propyl)-trimethyl-ammonium;
32224-01-4
(S)-4-bromo-3-hydroxy-butyric acid ethyl ester