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638-38-0

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638-38-0 Usage

Description

Manganese (II) acetate is the chemical compound with the formula Mn(CH3COO)2. It is used as a desiccant, a catalyst, and as fertilizer.

Chemical Properties

Pale-red crystals.Soluble in water and alcohol. Combustible.

Uses

Different sources of media describe the Uses of 638-38-0 differently. You can refer to the following data:
1. Textile dyeing, oxidation catalyst, paint and varnish (drier, boiled oil manufacture), fertilizers, food packaging, feed additive.
2. Manganese(II) acetate is used as a dye mordant and varnish drier. It is also used in fertilizers, food packaging and feed additives. Further, it serves as a desiccant, catalyst, intermediate and ion exchange agent.

Reactions

Manganese (II) acetate can be formed by reacting acetic acid with either manganese (II,III) oxide or manganese (II) carbonate : Mn3O4 + 2CH3COOH → Mn(CH3COO)2 + Mn2O3+ H2O If manganese (II,III) oxide is used , manganese (III) oxide is produced as a byproduct. If the anhydrous form needs to be produced, manganese (II) nitrate can be reacted with acetic anhydride.

Purification Methods

Crystallise it from water acidified with acetic acid. [Beilstein 2 IV 120.]

Check Digit Verification of cas no

The CAS Registry Mumber 638-38-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 638-38:
(5*6)+(4*3)+(3*8)+(2*3)+(1*8)=80
80 % 10 = 0
So 638-38-0 is a valid CAS Registry Number.
InChI:InChI=1/2C2H3O.Mn/c2*1-2-3;/h2*1H3;/rC4H6MnO2/c1-3(6)5-4(2)7/h1-2H3

638-38-0 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (B23708)  Manganese(II) acetate, anhydrous, 98+%   

  • 638-38-0

  • 50g

  • 397.0CNY

  • Detail
  • Alfa Aesar

  • (B23708)  Manganese(II) acetate, anhydrous, 98+%   

  • 638-38-0

  • 250g

  • 1315.0CNY

  • Detail
  • Alfa Aesar

  • (B23708)  Manganese(II) acetate, anhydrous, 98+%   

  • 638-38-0

  • 1000g

  • 4661.0CNY

  • Detail
  • Aldrich

  • (330825)  Manganese(II)acetate  98%

  • 638-38-0

  • 330825-5G

  • 381.42CNY

  • Detail
  • Aldrich

  • (330825)  Manganese(II)acetate  98%

  • 638-38-0

  • 330825-25G

  • 1,070.55CNY

  • Detail
  • Aldrich

  • (330825)  Manganese(II)acetate  98%

  • 638-38-0

  • 330825-100G

  • 3,208.14CNY

  • Detail

638-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name MANGANESE(II) ACETATE

1.2 Other means of identification

Product number -
Other names manganousacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates,Ion exchange agents
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:638-38-0 SDS

638-38-0Relevant articles and documents

Oxidative Cyclization of Lithium 4-Ethoxy-1,1,1-trifluoro-4-oxobut-2-en-2-olate

Boltacheva,Slepukhin,Filyakova,Charushin

, p. 883 - 885 (2019/08/02)

Diethyl 2,5-dihydroxy-2,5-bis(trifluoromethyl)tetrahydrofuran-3,4-dicarboxylate has been synthesized for the first time by reaction of lithium 4-ethoxy-1,1,1-trifluoro-4-oxobut-2-en-2-olate with manganese(III) acetate. The structure of its (2S*3S*4S*5S*) stereoisomer has been confirmed by X-ray analysis.

Anomalous non-prussian blue structures and magnetic ordering of K 2MnII[MnII(CN)6] and Rb 2MnII[MnII(CN)6]

Her, Jae-Hyuk,Stephens, Peter W.,Kareis, Christopher M.,Moore, Joshua G.,Min, Kil Sik,Park, Jong-Won,Bali, Garima,Kennon, Bretni S.,Miller, Joel S.

, p. 1524 - 1534 (2010/04/25)

The reaction of MnII and KCN in aqueous and non-aqueous media leads to the isolation of three-dimensional (3-D) Prussian blue analogues, K2Mn[Mn(CN)6] (1a-d, 1e, respectively). Use of RbCN forms Rb2Mn[Mn(CN)6] (2). 1 and 2 are isomorphic {monoclinic, P21/n: 1 [a = 10.1786(1) A, b = 7.4124(1) A, c = 6.9758(1) A, β = 90.206(1)°]; 2 [a = 10.4101(1) A, b = 7.4492(1) A, c = 7.2132(1) A, β = 90.072(1)°]}, with a small monoclinic distortion from the face centered cubic (fcc) structure that is typical of Prussian blue structured materials that was previously reported for K2Mn[Mn(CN)6]. Most notably the average Mn-N-C angles are 148.8° and 153.3° for 1 and 2, respectively, which are significantly reduced from linearity. This is attributed to the ionic nature of high spin MnII accommodating a reduced M-CN-M0 angle and minimizing void space. Compounds 1a, b have a sharp, strong.OH band at 3628 cm-1, while 1e lacks a v OH absorption. The vOH absorption in 1a, b is attributed to surface water, as use of D2O shifts the.OH absorption to 2677 cm-1, and that 1a-e are isostructural. Also, fcc Prussian blue-structured Cs2Mn[Mn(CN)6] (3) has been structurally [Fm3hm: a = 10.6061(1) A] and magnetically characterized. The magnetic ordering temperature, Tc, increases as K+ (41 K) + (34.6 K) + (21 K) for A2Mn[Mn(CN)6] in accord with the increasing deviation for linearity of the Mn-N-C linkages [148.8 (K+) +)], decreasing Mn(II) · · · Mn(II) separations [5.09 (K+) > 5.19 (Rb+) > 5.30 A° (Cs+)], and decreasing size of the cation (increasing electrostatic interactions). Hence, the bent cyanide bridges play a crucial role in the superexchange mechanism by increasing the coupling via shorter Mn(II) 3 3 3 Mn(II) separations, and perhaps enhanced overlap. In addition, the temperature dependent magnetic behavior of K4[MnII(CN) 6] · 3H2O is reported.

Stabilizing Vegetable Oils And Methods Of Making Same

-

Page/Page column 7, (2008/06/13)

A method for modifying ethylenic unsaturation in a triglyceride. One or more unsaturated fatty acyl moieties present in the triglyceride are substituted with a lactone or ketone moiety via a electron donor mediated reaction. The resulting reaction products are useful, for example, as formulations for lubricants, hydraulic fluids, dielectric fluids, and intermediates for polymer synthesis.

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