636-13-5

Basic information

• Product Name: MANGANESE BENZOATE
• Synonyms: MANGANESE(II) BENZOATE TETRAHYDRATE;MANGANESE BENZOATE;benzoicacid,manganese(2++)salt;manganese dibenzoate;Bisbenzoic acid manganese(II) salt;Dibenzoic acid manganese(II) salt;Manganese Benzoate Tetrahydrate
• CAS NO: 636-13-5
• Molecular Formula: C₁₄H₁₀MnO₄
• Molecular Weight: 297.16
• EINECS: 211-251-2
• Mol File: 636-13-5.mol
• Article Data: 7

Chemical Properties

• Melting Point: 216 °C
• Appearance: /
• CAS DataBase Reference: MANGANESE BENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: MANGANESE BENZOATE(636-13-5)
• EPA Substance Registry System: MANGANESE BENZOATE(636-13-5)

Safety Data

• Hazardous Substances Data: 636-13-5(Hazardous Substances Data)

Usage

General Description

Manganese benzoate is a chemical compound composed of manganese and benzoate ions. It is commonly used as a catalyst in organic synthesis and as a coloring agent in porcelain and ceramics. Manganese benzoate has also been studied for its potential applications in pharmaceuticals, especially in cancer treatment and as an antioxidant. Additionally, it is used in industrial applications such as in the production of plastics, textiles, and rubber. Manganese benzoate is known for its high thermal stability and low solubility in water, making it suitable for a wide range of applications in various industries.

InChI:InChI=1/2C7H6O2.Mn.4H2O/c2*8-7(9)6-4-2-1-3-5-6;;;;;/h2*1-5H,(H,8,9);;4*1H2/q;;+2;;;;/p-2

Upstream product

• 7439-96-5 manganese 
• 65-85-0 benzoic acid 
• 75-05-8 acetonitrile 
• 638-38-0 manganese(II) acetate 
• 532-32-1 sodium benzoate 
• 16397-91-4 manganese(II) 
• 93-58-3 benzoic acid methyl ester 
• 7553-56-2 iodine 

Downstream Products

• 122723-60-8 Benzoic acid 4,6,6-trimethyl-2-oxo-cyclohex-3-enyl ester 
• 122723-65-3 Benzoic acid 17-hydroxy-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-2-yl ester 
• 552-16-9 ortho-nitrobenzoic acid 
• 121-92-6 3-nitrobenzoic acid 
• 62-23-7 4-nitro-benzoic acid 
• 1313-13-9 manganese(IV) oxide 

Relevant articles and documents

Trinuclear Complexes Derived from R/S Schiff Bases – Chiral Single-Molecule Magnets

The employment of enantiomerically pure Schiff bases in manganese chemistry is revealed to be an excellent method to obtain chiral single-molecule magnets and has allowed the characterization of several pairs of enantiomers, for which the magnetic properties were investigated. The reported systems consist of MnIII–MnII–MnIIIlinear trimers or MnIII3cations in a triangular arrangement including the first example of a μ3-Cl bridge in an isolated manganese triangle.

Efficient synthesis of manganese(ii) carboxylates: From a trinuclear cluster [Mn3(PhCO2)6(THF)4] to a unique [Mn(PhCO2)2]n chiral 3D network

An efficient synthetic procedure for obtaining manganese carboxylates including a trinuclear cluster [Mn3(PhCO2) 6(THF)4]2 and a unique [Mn(PhCO 2)2]n chiral 3D network is reported. The procedure involves a simple redox process, in which acidic protons are reduced to gaseous hydrogen by oxidizing metallic manganese under solvothermal conditions.

Manganese clusters derived from 2-pyridylcyanoxime: New topologies and a large spin ground state in pyridyloximate chemistry

Series of manganese clusters derived from 2-pyridylcyanoxime with Mn 3II (1), Mn4II (2a, b), Mn II4MnIII4 (3), MnII 2MnIII6MnIV2 (4) and MnII3MnIII6MnIV (5) cores have been characterized. Dc magnetic measurements reveal antiferromagnetic coupling for 1-4 and dominant ferromagnetic interactions for 5 which shows the largest ground state reported to date in pyridyloximate chemistry (S = 14).