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24376-01-0

N,N-diethylglycine hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 24376-01-0 Structure

  • Basic information

    1. Product Name: N,N-diethylglycine hydrochloride
    2. Synonyms: N,N-diethylglycine hydrochloride
    3. CAS NO:24376-01-0
    4. Molecular Formula: C6H13NO2*ClH
    5. Molecular Weight: 167.63386
    6. EINECS: 246-211-3
    7. Product Categories: N/A
    8. Mol File: 24376-01-0.mol

  • Chemical Properties

    1. Melting Point: 125-126 °C
    2. Boiling Point: 203.2°Cat760mmHg
    3. Flash Point: 76.7°C
    4. Appearance: /
    5. Density: g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: Inert atmosphere,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: N,N-diethylglycine hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-diethylglycine hydrochloride(24376-01-0)
    11. EPA Substance Registry System: N,N-diethylglycine hydrochloride(24376-01-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 24376-01-0(Hazardous Substances Data)

24376-01-0 Usage

Chemical Properties

White crystal

Check Digit Verification of cas no

The CAS Registry Mumber 24376-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,7 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24376-01:
(7*2)+(6*4)+(5*3)+(4*7)+(3*6)+(2*0)+(1*1)=100
100 % 10 = 0
So 24376-01-0 is a valid CAS Registry Number.

24376-01-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(diethylamino)acetic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names DIETHYLGLYCINE HYDROCHLORIDE

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:24376-01-0 SDS

24376-01-0Relevant articles and documents

N,N′-Dialkylaminoalkylcarbonyl (DAAC) prodrugs and aminoalkylcarbonyl (AAC) prodrugs of 4-hydroxyacetanilide and naltrexone with improved skin permeation properties

Devarajan-Ketha,Sloan

scheme or table, p. 4078 - 4082 (2011/08/06)

N,N′-Dialkylaminoalkylcarbonyl (DAAC) and aminoalkylcarbonyl (AAC) prodrugs of phenolic drugs acetaminophen (APAP) and naltrexone (NTX) are reported. The effects of incorporation of a basic amine group into the promoiety of an acyl prodrug of a phenolic drug on its skin permeation properties are also presented. DAAC-APAP prodrugs were synthesized via a three-step procedure starting with haloalkylcarbonyl esters which were reacted with five different amines: dimethylamine, diethylamine, dipropylamine, morpholine, and piperidine. The spacing between the amino group and the carbonyl group of the acyl group was 1-3 CH2. After the hydrolysis of the ester, the carboxylic acid product was subsequently coupled with the parent drug via a dicyclohexyl carbodiimide (DCC) mediated coupling to yield the DAAC-APAP-HCl prodrugs in excellent yields. The AAC prodrugs were synthesized using commercially available Boc-protected amino acids using DCC or EDCI as coupling agents. The yields of the prodrugs synthesized using these two different methods have been compared. Half-lives (t1/2) of a few members of the DAAC and AAC series were measured in buffer (pH 6.0, 20 mM). The members evaluated in hydrolysis experiments exhibit a t1/2 range of 15-113 min. Among AAC-APAP prodrugs, the isopropyl group in valinate-APAP-HCl exerted a steric effect that increased the t1/2 value for this prodrug compared to alaninate-APAP-HCl or prolinate-APAP-HCl. The 2-morpholinylacetate-APAP prodrug was able to achieve twice the flux of APAP in in vitro diffusion cell experiments through hairless mouse skin.

Method for lowering total serum cholesterol and treating hypercholesterolemia with aminoacetylmercapto derivatives

-

, (2008/06/13)

The present invention relates to the use of certain aminoacetylmercapto derivatives in treating patients suffering from hypercholesterolemia.

AMINOACETYLMERCAPTO DERIVATIVES USEFUL AS INHIBITORS OF ENKEPHALINASE AND ACE

-

, (2008/06/13)

The present invention relates to novel aminoacetylmercapto derivatives useful as inhibitors of enkephalinase and ACE.

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