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Home > Encyclopedia > Propanedioic acid, 1-methyl ester, potassium salt (1:1)

Propanedioic acid, 1-methyl ester, potassium salt (1:1)

Propanedioic acid, 1-methyl ester, potassium salt (1:1) structure

Propanedioic acid, 1-methyl ester, potassium salt (1:1) 

structure
  • CAS No:

    38330-80-2

  • Formula:

    C4H6O4.K

  • Chemical Name:

    Propanedioic acid, 1-methyl ester, potassium salt (1:1)

  • Synonyms:

    Propanedioic acid,1-methyl ester,potassium salt (1:1);Propanedioic acid,monomethyl ester,potassium salt;Potassium methyl malonate;Potassium (carbomethoxy)acetate;Methyl potassium malonate;Monomethyl malonate potassium salt;Potassium monomethyl malonate;Methyl malonate potassium salt;Potassium methoxycarbonylacetate;Potassium 3-methoxy-3-oxopropanoate;131645-60-8;875479-57-5

  • Categories:

    Pharmaceutical Intermediates  >  Blood Glucose Regulators

Description

White crystalline powder

Propanedioic acid, 1-methyl ester, potassium salt (1:1) Basic Attributes

156.18

155.982498

253-886-8

DTXSID90191698

29171910

Characteristics

66.4

White Crystalline Powder

201-205 °C

232.1°C at 760 mmHg

103.7ºC

soluble in methanol.

Refrigerator

Safety Information

NONH for all modes of transport

3

36/37/38

37/39-26

Xi

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]|P264, P280, P305+P351+P338, and P337+P313|Aggregated GHS information provided by 43 companies from 4 notifications to the ECHA C&L Inventory.

Propanedioic acid, 1-methyl ester, potassium salt (1:1) Use and Manufacturing

Methods of Manufacturing

General procedure: According to the literature procedure, To the reaction flask was added 100 g of dimethyl malonate (0.757 mol) and 350.0 g of anhydrous methanol, and the mixture was completely mixed and dissolved, and a methanol solution of potassium hydroxide was slowly added dropwise at 10 to 35 ° C (potassium hydroxide: 42.3 G (0.754 mol), methanol: 350.0 g), Gradually there is a white solid precipitation process. After dripping, The reaction solution was further stirred at 10 to 35 ° C for about 3.5 hours.The temperature was raised to 65 to 68 ° C. The system was refluxed and filtered while hot to remove dipotassium malonate. The resulting filtrate was cooled to 0 ° C and filtered to give the monomethyl methyl malonate salt.After the filtrate was concentrated and further about 550 g of methanol was distilled off, the resulting concentrate was cooled to 0 ° C and filtered, and the resulting two partsPotassium monoglyceride potassium salt combined, vacuum drying, the final monomethyl methacrylate potassium salt 98.78g (HPLC purity:99.1percent yield: 82.80percent).Comparison To a water-cooled solution of dimethylmalonate (132 g, 1 mol) in MeOH (500 mL) was added KOH (56 g, 1 mol) portionwise. The reaction mixture was stirred for 16 h, the solid was filtered off, and the filtrate was condensed TO-100 mL. Ether was added to precipitate out the solid, which was filtered and washed with ether, then dried to yield a white solid (102 g, 65percent).

Uses

A protein advanced glycosylation inhibitor.

Computed Properties

Molecular Weight:156.18
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:155.98249012
Monoisotopic Mass:155.98249012
Topological Polar Surface Area:66.4
Heavy Atom Count:9
Complexity:111
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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