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Merck
CN

C13408

O -(羧甲基)羟胺 半盐酸盐

98%

别名:

羧甲氧基胺半盐酸盐, (氨氧基)乙酸 半盐酸盐, (羧基甲氧基)胺 半盐酸盐, 羟胺-O-乙酸 半盐酸盐

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关于此项目

线性分子式:
NH2OCH2COOH · 0.5HCl
化学文摘社编号:
分子量:
109.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-862-3
Beilstein/REAXYS Number:
3680528
MDL number:
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产品名称

O -(羧甲基)羟胺 半盐酸盐, 98%

InChI key

KBXIJIPYZKPDRU-UHFFFAOYSA-N

InChI

1S/2C2H5NO3.ClH/c2*3-6-1-2(4)5;/h2*1,3H2,(H,4,5);1H

SMILES string

Cl.NOCC(O)=O.NOCC(O)=O

biological source

synthetic (organic)

assay

98%

form

crystalline powder
powder or crystals

mp

156 °C (dec.) (lit.)

solubility

water: 100 mg/mL, clear to slightly hazy, colorless to faintly yellow

storage temp.

2-8°C

Quality Level

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Application

O-(羧甲基)羟胺半盐酸盐可作为反应物通过与醛和酮缩合合成肟。它还可作为(吡哆醛 5’-磷酸) PLP-依赖性 β-裂解酶的有效抑制剂

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Tetrahedron Letters, 34, 4347-4347 (1993)
A Sala et al.
Farmaco (Societa chimica italiana : 1989), 46(7-8), 887-897 (1991-07-01)
The synthesis of new 2-(3-bromo-5-isoxazolylideneamino-oxy)acetic acids and their condensation derivatives with suitable beta-lactam nuclei is reported. Their antibacterial properties have been tested in vitro. An interesting activity against Gram-positive bacteria including beta-lactamase-producing microorganisms was found among the cephalosporanic acid derivatives.
Seon-Ae Choi et al.
Scientific reports, 6, 26203-26203 (2016-05-18)
Hydrogen sulfide (H2S) is an important biological messenger, but few biologically-compatible methods are available for its detection in aqueous solution. Herein, we report a highly water-soluble naphthalimide-based fluorescent probe (L1), which is a highly versatile building unit that absorbs and
Tissue distribution of cytosolic beta-elimination reactions of selenocysteine Se-conjugates in rat and human
Rooseboom M, et al.
Chemico-Biological Interactions, 140, 243-264 (2002)
Characterization of a 5'-aldehyde terminus resulting from the oxidative attack at C5 `of a 2-deoxyribose on DNA
Angeloff A, et al.
Chemical Research in Toxicology, 14, 1413-1420 (2001)

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