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Carboxymethoxylamine hemihydrochloride

Carboxymethoxylamine hemihydrochloride structure

Carboxymethoxylamine hemihydrochloride 

structure
  • CAS No:

    2921-14-4

  • Formula:

    C2H5NO3.1/2ClH

  • Chemical Name:

    Carboxymethoxylamine hemihydrochloride

  • Synonyms:

    Acetic acid,2-(aminooxy)-,hydrochloride (2:1);Acetic acid,(aminooxy)-,hydrochloride (2:1);Acetic acid,(aminooxy)-,hemihydrochloride;Aminooxyacetic acid hemihydrochloride;Carboxymethoxyamine hemihydrochloride;O-Carboxymethylhydroxylamine hemihydrochloride;Carboxymethoxylamine hemihydrochloride;Aminooxyacetic acid hemichloride

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

Aminooxyacetic acid hemihydrochloride is a malate-aspartate shuttle (MAS) inhibitor which also inhibits the GABA degradating enzyme GABA-T.


(aminooxy)acetic acid hemihydrochloride is the hemihydrochloride salt of (aminooxy)acetic acid. It is a malate-aspartate shuttle (MAS) inhibitor which also inhibits the GABA degradating enzyme 4-aminobutyrate aminotransferase and cystathionine beta-synthetase. It contains an (aminooxy)acetate.

Carboxymethoxylamine hemihydrochloride Basic Attributes

127.53

218.031

220-862-3

5G5QI2GN7A

29280000

Characteristics

145

White to off-white Crystalline Powder or Crystals

1.7848 (rough estimate)

150-151 °C (decomp)

326.7°C at 760 mmHg

151.4ºC

Decomposes in water

-20°C Freezer

Safety Information

II

3

UN 1193 3/PG 2

3

36/37/38

26-36

AF3150000

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|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 40 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Carboxymethoxylamine hemihydrochloride Use and Manufacturing

Methods of Manufacturing

It is obtained by reacting O-carboxymethylacetone oxime with hydrochloric acid.

Uses

A bifunctional linking reagent

Acetic acid, 2-(aminooxy)-, hydrochloride (2:1): ACTIVE

Computed Properties

Molecular Weight:218.59
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:4
Exact Mass:218.0305638
Monoisotopic Mass:218.0305638
Topological Polar Surface Area:145
Heavy Atom Count:13
Complexity:52.8
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes

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