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AMMONIUM SALICYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 31295-34-8 Structure
  • Basic information

    1. Product Name: AMMONIUM SALICYLATE
    2. Synonyms: AMMONIUM 2-HYDROXYBENZOATE;AMMONIUM SALICYLATE;Ai3-36572;Benzoic acid, 2-hydroxy-, ammonium salt;Einecs 250-553-9
    3. CAS NO:31295-34-8
    4. Molecular Formula: C7H9NO3
    5. Molecular Weight: 155.15
    6. EINECS: 250-553-9
    7. Product Categories: N/A
    8. Mol File: 31295-34-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 336.3°Cat760mmHg
    3. Flash Point: 144.5°C
    4. Appearance: /
    5. Density: g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: AMMONIUM SALICYLATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: AMMONIUM SALICYLATE(31295-34-8)
    11. EPA Substance Registry System: AMMONIUM SALICYLATE(31295-34-8)
  • 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: 31295-34-8(Hazardous Substances Data)

31295-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31295-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,9 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31295-34:
(7*3)+(6*1)+(5*2)+(4*9)+(3*5)+(2*3)+(1*4)=98
98 % 10 = 8
So 31295-34-8 is a valid CAS Registry Number.

31295-34-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name AMMONIUM SALICYLATE

1.2 Other means of identification

Product number -
Other names -

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:31295-34-8 SDS

31295-34-8Downstream Products

31295-34-8Relevant articles and documents

Transforming aspirin into novel molecular salts of salicylic acid

Andre, Vania,Martins, Ines,Quaresma, Silvia,Martins, Marta,Duarte, M. Teresa

, p. 707 - 714 (2014/06/09)

Aspirin is one of the most widely used analgesic, antipyretic, and anti-inflammatory drugs. Herein we disclose a way to transform aspirin into novel multicomponent crystal forms of salicylic acid, also a long-known analgesic with anti-inflammatory properties, among others, covering a broad spectrum of applications, including skin care products. A salicylic acid:salicylate ammonium salt and a salicylate:2-methyl-4-oxopentan-2-aminium molecular salt are concomitantly formed in acetone/ammonia solutions, resulting from aspirin decomposition. Furthermore the 2-methyl-4-oxopentan-2-aminium cation results from a sequence of in situ reactions: (i) imine formation, in which acetone is known to undergo under basic pH conditions; (ii) nucleophilic attack of α-carbon of the deprotonated acetone to the imine yielding 4-amino-4-methylpentan-2-one; and (iii) protonation of 4-amino-4-methylpentan-2- one. In the structures obtained for the novel multicomponent crystal forms, the strong charge-assisted N+-H···O/O- hydrogen bonds between the drug molecule and the co-former play a key function in the supramolecular arrangement. The typical R22(8) carboxylic···carboxylic homosynthon observed in salicylic acid was inhibited by the salt formation. These results are in agreement with the results of a careful survey on the Cambridge Structural Database. Graphical abstract: [Figure not available: see fulltext.]

Process for the hydrogenation of nitrated paraffins using a palladium on carbon catalyst characterized by a low ash and a low halide content

-

, (2008/06/13)

Nitrated hydrocarbons, such as nitroparaffins, are reduced to amines by use of palladium on a carbon catalyst characterized by low ash and low halide.

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