Formohydroximic acid

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Company Name: Henan Tianfu Chemical Co.,Ltd.
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Products Intro: Product Name:Formohydroximic acid
CAS:4312-87-2
Purity:99% Package:25KG;5KG;1KG
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Products Intro: Product Name:N-hydroxyformamide
CAS:4312-87-2
Purity:98% Package:100mg; 250mg;500mg; 1g; 5g;10g;25g;100g;
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Formohydroximic acid Basic information
Product Name:Formohydroximic acid
Synonyms:Formohydroximic acid;formohydroxamic acid;FORMHYDROXAMICACID;Hydroxyaminomethanone;Hydroxyformaldehydeoxime;Hydroxyiminomethanol;Hydroxymethanoneoxime;N-Hydroxyformamide
CAS:4312-87-2
MF:CH3NO2
MW:61.04
EINECS:
Product Categories:
Mol File:4312-87-2.mol
Formohydroximic acid Structure
Formohydroximic acid Chemical Properties
Melting point 81.5-82.0 °C
Boiling point 97.79°C (rough estimate)
density 1.253±0.06 g/cm3(Predicted)
refractive index 1.4400 (estimate)
pka9.13±0.23(Predicted)
Safety Information
MSDS Information
Formohydroximic acid Usage And Synthesis
Preparation(a) Preparation of hydroxylamine solution. Thirty grams (0.43 mole) of hydroxylamine hydrochloride is dissolved in 150 ml of boiling methanol. The solution is cooled somewhat and a solution of 9.9 gm (0.43 gm-atom) of sodium in 150 ml of methanol is added cautiously. The mixture is cooled and then placed in an ice-salt bath until the sodium chloride formed has been precipitated as completely as possible. After the sodium chloride has been filtered off, approximately 200 ml of the methanol is distilled off under reduced pressure. The still residue is again filtered and then used directly in the next step.
(b) Preparation of formohydroxamic acid. The hydroxylamine solu­tion, prepared as above, is cooled at 0°C. Then 31 gm (0.42 mole) of ethyl formate is added. During this addition an increase in temperature is observed. This is moderated by cooling in a stream of running water. After the addition has been completed, the reaction mixture is allowed to stand at room temperature for several hours.
Preparation of Formohydroxamic Acid
The excess methanol is evaporated from the reaction mixture under reduced pressure. The crystalline residue is contaminated with a small amount of an oily substance and some sodium chloride. The oily material is removed by pressing the crude product on an unglazed clay plate. The yield is 17.9 gm (70%). The product is crystallized from ethyl acetate. During this process, the remaining sodium chloride is separated by filtra­tion of the hot solution. The final product melts at 81-82°C.
Formohydroximic acid Preparation Products And Raw materials
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