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22041-23-2

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22041-23-2 Usage

General Description

ETHYL 4-(DIMETHYLAMINO)BUTANOATE is a chemical compound with the molecular formula C8H17NO2. It is a clear, colorless liquid with a fruity odor, commonly used in the production of flavors and fragrances. ETHYL 4-(DIMETHYLAMINO)BUTANOATE is commonly found in various food and cosmetic products as a flavoring agent. It is also used in the synthesis of pharmaceuticals and as an intermediate in organic synthesis. ETHYL 4-(DIMETHYLAMINO)BUTANOATE is known for its mild anesthetic effects and is used in some topical anesthetic products. It is important to handle this chemical with caution and follow proper safety protocols due to its potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 22041-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,4 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22041-23:
(7*2)+(6*2)+(5*0)+(4*4)+(3*1)+(2*2)+(1*3)=52
52 % 10 = 2
So 22041-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO2/c1-4-11-8(10)6-5-7-9(2)3/h4-7H2,1-3H3

22041-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-(dimethylamino)butanoate

1.2 Other means of identification

Product number -
Other names DF 491

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:22041-23-2 SDS

22041-23-2Relevant articles and documents

Formulation optimization of an ephrin A2 targeted immunoliposome encapsulating reversibly modified taxane prodrugs

Huang, Zhaohua Richard,Tipparaju, Suresh Kumar,Kirpotin, Dmitri B.,Pien, Christine,Kornaga, Tad,Noble, Charles O.,Koshkaryev, Alexander,Tran, Jimmy,Kamoun, Walid S.,Drummond, Daryl C.

, p. 47 - 57 (2019/08/20)

Ephrin A2 targeted immunoliposomes incorporating pH-sensitive taxane prodrugs were developed for sustained delivery of active drug to solid tumors. Here we describe the systematic formulation development and characterization of these immunoliposomes. We s

Targeting carnitine biosynthesis: Discovery of new inhibitors against γ-butyrobetaine hydroxylase

Tars, Kaspars,Leitans, Janis,Kazaks, Andris,Zelencova, Diana,Liepinsh, Edgars,Kuka, Janis,Makrecka, Marina,Lola, Daina,Andrianovs, Viktors,Gustina, Daina,Grinberga, Solveiga,Liepinsh, Edvards,Kalvinsh, Ivars,Dambrova, Maija,Loza, Einars,Pugovics, Osvalds

, p. 2213 - 2236 (2014/04/17)

γ-Butyrobetaine hydroxylase (BBOX) catalyzes the conversion of gamma butyrobetaine (GBB) to l-carnitine, which is involved in the generation of metabolic energy from long-chain fatty acids. BBOX inhibitor 3-(1,1,1-trimethylhydrazin-1-ium-2-yl)propanoate (

4-[(HALOALKYL)(DIMETHYL)AMMONIO]BUTANOATES AND USE THEREOF IN THE TREATMENT OF CARDIOVASCULAR DISEASE

-

Page/Page column 9, (2012/11/13)

4-[(Haloalkyl)(dimethyl)ammonio]butanoates of formula (I) wherein Hal is Cl or F, n=1 or 2, method for preparing thereof and use thereof for treating cardiovascular disease.

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