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Merck
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重要文件

A41909

Sigma-Aldrich

4-氨基苯甲酰肼

95%

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About This Item

線性公式:
H2NC6H4C(O)NHNH2
CAS號碼:
分子量::
151.17
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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品質等級

化驗

95%

形狀

powder

mp

225-227 °C (lit.)

SMILES 字串

NNC(=O)c1ccc(N)cc1

InChI

1S/C7H9N3O/c8-6-3-1-5(2-4-6)7(11)10-9/h1-4H,8-9H2,(H,10,11)

InChI 密鑰

WPBZMCGPFHZRHJ-UHFFFAOYSA-N

應用

4-氨基苯甲酰肼可用作合成以下物质的反应物:
  • 通过与2-乙酰基吡啶的缩合反应制备的酰腙席夫碱配体。[1]
  • 适用于制造具有高效电学和光电特性的有机-无机杂化器件的低聚过渡金属配合物。[2]
  • 潜在自由基清除剂氧钒(IV)-酰肼络合物。[3]

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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G O Peelen et al.
Analytical biochemistry, 198(2), 334-341 (1991-11-01)
Analysis of oligosaccharides in complex biological matrices is hampered by the fact that oligosaccharides, closely related in structure, are difficult to separate from each other and that conventional detection procedures (refraction index and uv detection) are not specific enough for
Preparation of porous resin with Schiff base chelating groups for removal of heavy metal ions from aqueous solutions
Ceglowski M and Schroeder G
Chemical Engineering Journal, 263 (2015)
A J Kettle et al.
The Biochemical journal, 308 ( Pt 2), 559-563 (1995-06-01)
Myeloperoxidase is the most abundant protein in neutrophils and catalyses the conversion of H2O2 and chloride into HOCl. To help clarify the role of this enzyme in bacterial killing and inflammation, a specific and potent inhibitor needs to be identified.
U Burner et al.
The Journal of biological chemistry, 274(14), 9494-9502 (1999-03-27)
Myeloperoxidase is the most abundant protein in neutrophils and catalyzes the production of hypochlorous acid. This potent oxidant plays a central role in microbial killing and inflammatory tissue damage. 4-Aminobenzoic acid hydrazide (ABAH) is a mechanism-based inhibitor of myeloperoxidase that
Enzyme inhibition, radical scavenging, and spectroscopic studies of vanadium (IV)-hydrazide complexes
Ashiq U, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry, 24(6), 1336-1343 (2009)

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