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Methoxyammonium chloride
- NameMethoxyammonium chloride
- CAS593-56-6
- Purity99%
Product Details
Top Quality Chinese Manufacturer supply 593-56-6 Methoxyammonium chloride
- Molecular Formula:CH5NO.HCl
- Molecular Weight:83.5177
- Appearance/Colour:White to very faintly yellow crystalline powder
- Vapor Pressure:298mmHg at 25°C
- Melting Point:151-154 °C(lit.)
- Refractive Index:n20/D 1.4021
- Boiling Point:49.5 °C at 760 mmHg
- Flash Point:18.2 °C
- PSA:35.25000
- Density:0.854 g/cm3
- LogP:1.00880
Methoxyammonium chloride(Cas 593-56-6) Usage
|
Methoxyamine hydrochloride |
Methoxyamine hydrochloride (also known as O-methylhydroxylamine hydrochloride; Methoxyamine; Methoxyamine hydrochloride (OMHA), is an important medicine, pesticide intermediates. Its major applications are as follows: it can be used for color photography and film printing. it is used as a reducing agent in organic synthesis industry for preparation of oximes. the field of medicine: it can be used for the synthesis of second-generation cephalosporins antibiotics cefuroxime (ester), neopropene, norethindine and hydroxyurea. the field of pesticides: the synthesis of new efficient, low-toxicity bactericidal metominostrobin. It is mainly produced by sodium nitrite method in our country. The similar compound of methoxyamine hydrochloride, the ethoxylamine hydrochloride is mainly used for the production of herbicides, oxycarbazone, diltiazem and other herbicides. |
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Air & Water Reactions |
Water soluble. |
|
Reactivity Profile |
In aqueous solution, Methoxyammonium chloride behaves as an acid. Materials in this group are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions. |
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Fire Hazard |
Flash point data for Methoxyammonium chloride are not available. Methoxyammonium chloride is probably combustible. |
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Purification Methods |
Crystallise the hydrochloride from absolute EtOH or EtOH by addition of diethyl ether. [Kovach et al. J Am Chem Soc 107 7360 1985, Beilstein 1 IV 1252.] |
|
Application |
Used as a methoxyamine reagent, also used in the production of the side chain of Cefuroxime and other new drugs Used for pesticide synthesis. Use for pharmaceuticals production Used for the preparation of O-methyloxime together with aldehydes or ketones. |
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General Description |
Off-white crystals. |
InChI:InChI=1/CH5NO.ClH/c1-3-2;/h2H2,1H3;1H
593-56-6 Relevant articles
Preparation method of methoxyamine hydrochloride
-
Paragraph 0022; 0030; 0038, (2021/09/21)
The invention relates to the field of ch...
Preparation method O - alkyl substituted hydroxylamine salt
-
Paragraph 0078-0081, (2021/11/14)
The invention relates to a preparation m...
Preparation method of methoxyamine hydrochloride and preparation method of N-methoxyacetamide
-
Paragraph 0038-0052, (2021/05/29)
The invention relates to a preparation m...
Vinylogous Aza-Michael Addition of Urea Derivatives with p-Quinone Methides Followed by Oxidative Dearomative Cyclization: Approach to Spiroimidazolidinone Derivatives
Kaur, Navpreet,Singh, Priyanka,Banerjee, Prabal
supporting information, p. 2813 - 2824 (2021/04/21)
Herein, we report an efficient protocol ...
593-56-6 Process route
-
-
7647-01-0,15364-23-5
hydrogenchloride
-
-
29144-51-2
(MeON=C(Me)-CMe=NOMe)
-
-
593-56-6
N-methoxylamine hydrochloride
-
-
431-03-8
dimethylglyoxal
| Conditions | Yield |
|---|---|
|
|
-
-
1914-20-1
N-methoxyphthalimide
-
-
593-56-6
N-methoxylamine hydrochloride
| Conditions | Yield |
|---|---|
|
N-methoxyphthalimide;
With
methylhydrazine;
In
dichloromethane;
at 0 - 20 ℃;
for 2h;
With
hydrogenchloride;
In
1,4-dioxane;
at 0 ℃;
|
90% |
|
With
hydrogenchloride;
for 0.5h;
Heating;
|
|
|
With
methylhydrazine;
In
dichloromethane;
|
|
|
N-methoxyphthalimide;
With
hydrogenchloride; acetic acid;
In
water;
for 1.5h;
Reflux;
Inert atmosphere;
With
hydrogenchloride;
at 0 - 20 ℃;
for 1h;
Inert atmosphere;
|
593-56-6 Upstream products
-
2446-51-7
N-methoxybenzamide
-
7647-01-0
hydrogenchloride
-
29144-51-2
(MeON=C(Me)-CMe=NOMe)
-
1914-20-1
N-methoxyphthalimide
593-56-6 Downstream products
-
861367-95-5
hydroxy-methoxyamino-malonic acid amide-p-toluidide
-
861554-36-1
hydroxy-methoxyamino-malonic acid di-p-toluidide
-
103990-59-6
N,N-bis-[3-(4-methoxy-phenyl)-3-oxo-propyl]-O-methyl-hydroxylamine
-
98670-03-2
6-<(methoxyimino)methyl>-2,3-dimethoxybenzoic acid
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