Sodium malonate hydrate (2:1:1)

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Names

[ CAS No. ]:
26522-85-0

[ Name ]:
Sodium malonate hydrate (2:1:1)

[Synonym ]:
Sodium malonate hydrate (2:1:1)
Propanedioic acid,sodium salt,hydrate (1:2:1)
DISODIUM MALONATE MONOHYDRATE
Malonic acid disodium salt monohydrate
Malonsaeure,Dinatrium-Verbindung
EINECS 205-514-0
Disodium Propanedioate Hydrate
malonic acid,disodium-compound
Propanedioic acid, sodium salt, hydrate (1:2:1)
MFCD00149114

Chemical & Physical Properties

[ Boiling Point ]:
386.8ºC at 760 mmHg

[ Molecular Formula ]:
C3H4Na2O5

[ Molecular Weight ]:
166.040

[ Flash Point ]:
201.9ºC

[ Exact Mass ]:
165.985413

[ PSA ]:
89.49000

[ Vapour Pressure ]:
4.66E-07mmHg at 25°C

[ Storage condition ]:
Store at RT.

[ Water Solubility ]:
H2O: 1 M at 20 °C, clear, colorless

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2917190090

Customs

[ HS Code ]: 2917190090

[ Summary ]:
2917190090 acyclic polycarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with carboxylates.

Bioorg. Med. Chem. Lett. 15 , 573-8, (2005)

A detailed inhibition study of five carbonic anhydrase (CA, EC 4.2.1.1) isozymes with carboxylates including aliphatic (formate, acetate), dicarboxylic (oxalate, malonate), hydroxy/keto acids (l-lacta...

Carbonic anhydrase inhibitors. Inhibition of the beta-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with aliphatic and aromatic carboxylates.

Bioorg. Med. Chem. 17 , 2654-7, (2009)

The inhibition of the beta-carbonic anhydrases (CAs, EC 4.2.1.1) from the pathogenic fungi Cryptococcus neoformans (Can2) and Candida albicans (Nce103) with carboxylates such as the C1-C5 aliphatic ca...

Effect of enzymatic pretreatment of various lignocellulosic substrates on production of phenolic compounds and biomethane potential.

Bioresour. Technol. 192 , 696-702, (2015)

Pretreatment of lignocellulosic biomass is necessary to enhance the hydrolysis, which is the rate-limiting step in biogas production. Laccase and versatile peroxidase are enzymes known to degrade lign...


More Articles


Related Compounds

  • Sodium 5'-O-phosphonatouridine hydrate (2:1:1)
  • Sodium 5'-O-phosphonatoinosine hydrate (2:1:1)
  • Sodium 5'-O-phosphonatoinosine hydrate (2:1:1)
  • Disodium Etidronate Hydrate
  • Sodium hexachloro palladate(IV)
  • sodium,hydrate
  • N-(4-isopropylphenyl)-2-(2-(3-(m-tolyl)ureido)thiazol-4-yl)acetamide
  • 5-Chloro-3-[(4-chlorophenyl)thio]-6-cyano-2-methyl-1h-indole-1-acetic acid
  • N-(2-methoxyphenyl)-2-(2-(3-(m-tolyl)ureido)thiazol-4-yl)acetamide
  • N-(4-ethoxyphenyl)-2-(2-(3-(m-tolyl)ureido)thiazol-4-yl)acetamide
  • N-(3,4-dichlorophenyl)-2-(2-(3-(m-tolyl)ureido)thiazol-4-yl)acetamide
  • N-(3-chloro-4-fluorophenyl)-2-(2-(3-(m-tolyl)ureido)thiazol-4-yl)acetamide
  • N-(2,3-dimethylphenyl)-2-(2-(3-(m-tolyl)ureido)thiazol-4-yl)acetamide
  • N-(2,6-dimethylphenyl)-2-(2-(3-(m-tolyl)ureido)thiazol-4-yl)acetamide
  • N-(3,5-dimethylphenyl)-2-(2-(3-(m-tolyl)ureido)thiazol-4-yl)acetamide
  • 2-(2-(3-(4-chlorophenyl)ureido)thiazol-4-yl)-N-(2,4-dimethoxyphenyl)acetamide
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