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Name: N-Methyliminodiacetic acid
CAS NO: 4408-64-4
Purity: 97% min
MF: C5H9NO4
MW:147.129
BP:332.8¡À27.0 ¡ãC at 760 mmHg
Density:1.4¡À0.1 g/cm3
Name: N-Methyliminodiacetic acid
CAS NO: 4408-64-4
Purity: 97% min
MF: C5H9NO4
MW:147.129
BP:332.8¡À27.0 ¡ãC at 760 mmHg
Density:1.4¡À0.1 g/cm3
MP: 220 ¡ãC (dec.)(lit.)
EINECS:224-557-6
Appearance: Cream powder
Package: 25g, 100g, 500g, bulk package
Application: Organic Synthesis intermediate
Other name:
2,2'-(Methylazanediyl)diacetic acid;
2-[carboxymethyl(methyl)amino]acetic acid;
Glycine, N-(carboxymethyl)-N-methyl-;
Process for recovering N-methyliminodiacetic acid CAS NO: 4408-64-4 from sodium sulfate
methyliminodiacetic acid is separated from mixtures of N-methyliminodiacetic acid CAS NO: 4408-64-4 and sodium sulfate formed by acidification of solutions of its disodium salt with sulfuric acid. Thus the disodium salt is acidified with sulfuric acid to a ph of about 2 and concentrated by evaporating water so as to crystallize sodium sulfate. The sodium sulfate is separated, and the resulting mother liquor is cooled to precipitate N-methyliminodiacetic acid, which is then separated.
Preparation of N-Methyliminodiacetic acid CAS NO: 4408-64-4
The sodium chloroacetate solution reacts with the methylamine solution below 50¡æ,a solution of barium chloride dihydrate is added to the reaction mixture,the barium salt of methyl diacetate was filtered.Then The barium salt of methyl diacetate was filtered.The filtrate was reduced pressure and concentrated. Anhydrous methanol was added, cooled, filtered, and washed with methanol,after drying at 100¡æ, the yield of methyl diacetic acid was 63-71%.
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