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Sodium methoxyacetate, also known as sodium methoxide acetate, is an organic sodium salt that consists of equal numbers of sodium and methoxyacetate ions. It is a compound with potential applications in various industries due to its unique chemical properties.

50402-70-5

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50402-70-5 Usage

Uses

Used in Chemical Synthesis:
Sodium methoxyacetate is used as a reagent in the chemical synthesis industry for its ability to facilitate specific chemical reactions. Its sodium and methoxyacetate ions can participate in various chemical processes, making it a versatile compound for creating new molecules and materials.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, sodium methoxyacetate is used as an intermediate in the synthesis of various drugs. Its unique structure allows it to be a key component in the development of new medications, potentially contributing to the treatment of various diseases and conditions.
Used in Cosmetics:
Sodium methoxyacetate is also utilized in the cosmetics industry, where it serves as a stabilizing agent or emulsifier. Its ability to interact with other ingredients helps to create consistent and effective formulations for a range of cosmetic products.
Used in Food Industry:
In the food industry, sodium methoxyacetate may be used as a preservative or flavor enhancer. Its properties can help to improve the shelf life and taste of certain food products, making it a valuable addition to the industry.
Used in Environmental Applications:
Sodium methoxyacetate can be employed in environmental applications, such as water treatment or soil remediation. Its chemical properties may allow it to help remove contaminants or improve the quality of environmental resources.
These are just a few examples of the potential uses of sodium methoxyacetate based on its chemical properties and the provided definition. Further research and development may reveal additional applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 50402-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,0 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 50402-70:
(7*5)+(6*0)+(5*4)+(4*0)+(3*2)+(2*7)+(1*0)=75
75 % 10 = 5
So 50402-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H6O3.Na/c1-6-2-3(4)5;/h2H2,1H3,(H,4,5);/q;+1/p-1

50402-70-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,2-methoxyacetate

1.2 Other means of identification

Product number -
Other names sodium methoxyacetate

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:50402-70-5 SDS

50402-70-5Relevant academic research and scientific papers

Method for the production of esters

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Page column 6, (2008/06/13)

The present invention relates to a novel process for the preparation of esters of the general formula I from compounds of the general formula II contained in aqueous solutions which comprises a) extracting the compounds of the general formula II directly or after liberation from their salts in the presence of a C1-C8-alcohol and a water-immiscible solvent and b) then esterifying with the C1-C8-alcohol in the presence of a catalyst and of an entraining agent under the conditions of an azeotropic distillation, where the process steps (a) and (b) can be carried out separately in terms of time and space or else in a successive continuous or batchwise sequence and where the variables and substituents in the formulae I and II have the following meanings: R1=F, Cl, —OH, —OC1-C10-alkyl, R2=H, C1-C10-alkyl; R3=C1-C8-alkyl, Q=—OH, —O?K+, where K+is an alkali metal cation or alkaline earth metal cation, n=0, 1 or 2.

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