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ACETYL-DL-CARNITINE HYDROCHLORIDE, also known as (±)-Acetylcarnitine Chloride, is a chemical compound derived from the amino acid L-carnitine. It is a chiral molecule with both D and L forms, and it is commonly used as a pharmaceutical agent. ACETYL-DL-CARNITINE HYDROCHLORIDE has the ability to enhance the absorption of drugs in the gastrointestinal tract, making it a valuable component in the development of various medications.

2504-11-2

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  • 1-Propanaminium,2-(acetyloxy)-3-carboxy-N,N,N-trimethyl-, chloride (1:1)

    Cas No: 2504-11-2

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2504-11-2 Usage

Uses

Used in Pharmaceutical Industry:
ACETYL-DL-CARNITINE HYDROCHLORIDE is used as a drug absorption-enhancing agent for improving the bioavailability and effectiveness of medications in the gastrointestinal tract. Its ability to facilitate drug absorption can lead to better therapeutic outcomes and potentially reduce the required dosage of certain drugs, thereby minimizing side effects and improving patient compliance.

Biological Activity

(±)-acetylcarnitine chloride is an agonist for cholinergic.acetylcholine receptor (achr) is an integral membrane protein receptor for acetylcholine. there are two kinds of achrs: nicotinic acetylcholine receptors and muscarinic acetylcholine receptors.(±)-acetylcarnitine chloride is a cholinergic agonist and an intermediate in lipid metabolism [1]. in retinal ganglion cells, acetylcarnitine and acetylcholine inhibited gabaergic responses to exogenous gaba and gabaergic inhibitory postsynaptic currents [2].in dogs with coronary ligation, (-)-carnitine chloride (lcc) (300 mg/kg) and acetyl (-)-carnitine chloride (alcc) (300 mg/kg) inhibited the ventricular arrhythmia. also, lcc and alcc improved oxidative phosphorylation rate and the mitochondrial function [1]. in the mouse hot plate test, acetyl-l-carnitine (alcar) (100 mg/kg) exhibited analgesia. while, u-73122 and neomycin (the phospholipase c (plc) inhibitors) blocked the increase of the pain threshold induced by alcar. licl that impairing phosphatidylinositol synthesis antagonized the antinociception in a dose-dependent way. pma and pdbu (pkc activators) blocked the increase of the pain threshold in a dose-dependent way. these results suggested that alcar analgesia required the participation of the plc-ip3 pathway [3].

Biochem/physiol Actions

Weak cholinergic receptor agonist; intermediate in lipid metabolism.

Purification Methods

Recrystallise the chloride from isopropanol. Dry it over P2O5 under high vacuum. The S-betaine crystallises from EtOH/Et2O with m 145o(dec) and is hygroscopic; it has [] D -19.5o (c 6, H2O). [Krimberg & Wittandt Biochem Z 251 231 1932, Strack et al. Z Physiol Chem 238 191 1936, Beilstein 4 III 1630, 1632.]

Check Digit Verification of cas no

The CAS Registry Mumber 2504-11-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,0 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2504-11:
(6*2)+(5*5)+(4*0)+(3*4)+(2*1)+(1*1)=52
52 % 10 = 2
So 2504-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO4.ClH/c1-7(11)14-8(5-9(12)13)6-10(2,3)4;/h8H,5-6H2,1-4H3;1H

2504-11-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-acetyloxy-3-carboxypropyl)-trimethylazanium,chloride

1.2 Other means of identification

Product number -
Other names rac. Acetylcarnitinchlorid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2504-11-2 SDS

2504-11-2Downstream Products

2504-11-2Relevant articles and documents

Compositions and methods for enhanced drug delivery

-

, (2008/06/13)

The present invention relates to methods of delivering pharmaceutical agents across membranes, including the skin layer or mucosal membranes of a patient. A pharmaceutical agent is covalently bonded to a chemical modifier, via a physiologically cleavable bond, such that the membrane transport and delivery of the agent is enhanced.

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