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Sodium 2,5-dichlorobenzoate, with the chemical formula C7H3Cl2O2Na, is a sodium salt of 2,5-dichlorobenzoic acid. It is an organic compound that serves as a pesticide and herbicide, and is widely recognized for its preservative and antimicrobial properties. Sodium 2,5-dichlorobenzoate is valued for its ability to inhibit the growth of bacteria and fungi, making it a crucial ingredient in the preservation of various products.

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  • 63891-98-5 Structure
  • Basic information

    1. Product Name: Sodium 2,5-dichlorobenzoate
    2. Synonyms: Sodium 2,5-dichlorobenzoate
    3. CAS NO:63891-98-5
    4. Molecular Formula: C7H3Cl2O2*Na
    5. Molecular Weight: 212.99329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63891-98-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Sodium 2,5-dichlorobenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Sodium 2,5-dichlorobenzoate(63891-98-5)
    11. EPA Substance Registry System: Sodium 2,5-dichlorobenzoate(63891-98-5)
  • 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: 63891-98-5(Hazardous Substances Data)

63891-98-5 Usage

Uses

Used in Cosmetics Industry:
Sodium 2,5-dichlorobenzoate is used as a preservative for [application reason] its ability to inhibit the growth of bacteria and fungi, ensuring the longevity and safety of cosmetic products.
Used in Pharmaceuticals Industry:
In the pharmaceuticals industry, Sodium 2,5-dichlorobenzoate is used as an antimicrobial agent for [application reason] its effectiveness in preventing microbial contamination, thus maintaining the integrity and potency of pharmaceutical products.
Used in Personal Care Items:
Sodium 2,5-dichlorobenzoate is used as a preservative in personal care items for [application reason] its capability to prevent spoilage and microbial growth, ensuring the safety and efficacy of these products for consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 63891-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,9 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63891-98:
(7*6)+(6*3)+(5*8)+(4*9)+(3*1)+(2*9)+(1*8)=165
165 % 10 = 5
So 63891-98-5 is a valid CAS Registry Number.

63891-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,2,5-dichlorobenzoate

1.2 Other means of identification

Product number -
Other names Sodium 2,5-dichlorobenzoate

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:63891-98-5 SDS

63891-98-5Relevant articles and documents

CLEAVAGE OF THE PHENACYL ESTERS OF CARBOXYLIC AND THIOCARBOXYLIC ACIDS BY METAL ALKOXIDES

Morozov, A. A.

, p. 1138 - 1143 (2007/10/02)

During the cleavage of phenacyl esters with general formula XC6H4COCH2OCOR by metal alkoxides in alcohols and in ether-alcohol solutions the acids, esters, and ethers are formed as a result of cleavage of the C-C bond.The solvent participates in the formation of the ether and gives rise to transesterification of RCOOCH3 with catalytic participation of the metal alkoxide.The reactivity of the phenacyl esters of the thio acids is much higher.Before dissociation the esters of substituted benzoins C6H5COCH(OCOCH3).C6H4X-4 undergo irreversible rearrangement with the formation of isomeric products.

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