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Merck
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重要文件

H17082

Sigma-Aldrich

2-肼吡啶

97%

同義詞:

2-吡啶基肼

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About This Item

經驗公式(希爾表示法):
C5H7N3
CAS號碼:
分子量::
109.13
Beilstein:
109984
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

bp

90-92 °C/1 mmHg (lit.)

mp

41-44 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

NNc1ccccn1

InChI

1S/C5H7N3/c6-8-5-3-1-2-4-7-5/h1-4H,6H2,(H,7,8)

InChI 密鑰

NWELCUKYUCBVKK-UHFFFAOYSA-N

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應用

  • 增强金属去除功能:利用由2-肼吡啶衍生的希夫碱功能化双醛淀粉,在增强溶液中Cu(II)的去除方面显示出显著的潜力。该研究包括制备方法、性能评估和DFT计算,展示了其在水处理技术中的功效(Liang et al., 2024)。
  • 双感测探头发展:研制了一种新型的含2-肼吡啶的双氰异佛隆探针,用于近红外荧光双传感Zn(2+)和Cd(2+)。这一进步有助于检测和分析各种环境和生物样品中的重金属(Yan et al., 2023)。
  • 赖氨酸氧化酶活性位点分析:该研究深入了解了赖氨酸氧化酶样2活性位点组分的空间排列,包括2-肼吡啶的作用,这对于理解酶的机制和潜在的治疗应用至关重要(Meier et al., 2022)。
  • 赖氨酸氧化酶的结构分析:研究重点是预测赖氨酸氧化酶样2的胺氧化酶结构域的三维结构,探索2-肼吡啶促进的相互作用动力学。这对分子生物学和酶功能分析领域意义重大(Meier et al., 2022)。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

230.0 °F - closed cup

閃點(°C)

110 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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E S H El Ashry et al.
Nucleosides, nucleotides & nucleic acids, 23(3), 567-580 (2004-04-29)
Reaction of 2-hydrazinopyridine (1) with D-xylose, D-galactose, D-glucose and D-fructose afforded the corresponding hydrazones mainly in the acyclic forms 2, 3, 6 and 11 with minor amounts of the cyclic structures. Oxidative cyclization of the hydrazones with bromine in methanol
C M Wilmot et al.
Biochemistry, 36(7), 1608-1620 (1997-02-18)
The crystal structure of the complex between the copper amine oxidase from Escherichia coli (ECAO) and a covalently bound inhibitor, 2-hydrazinopyridine, has been determined to a resolution of 2.0 A. The inhibitor covalently binds at the 5 position of the
G De Matteis et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 4(3), 348-353 (1999-08-10)
Bovine serum amine oxidase (BSAO) reacts with 2-hydrazinopyridine, which binds the organic co-factor 2,4,5-trihydroxyphenylalanine quinone, forming a band at 435 nm. The band shifts to 526 nm around 60 degrees C, to 415 nm upon denaturation, but only shifts to
J M Murray et al.
Biochemistry, 40(43), 12808-12818 (2001-10-24)
Copper amine oxidases are homodimeric enzymes that catalyze two reactions: first, a self-processing reaction to generate the 2,4,5-trihydroxyphenylalanine (TPQ) cofactor from an active site tyrosine by a single turnover mechanism; second, the oxidative deamination of primary amine substrates with the
Minae Mure et al.
Biochemistry, 44(5), 1583-1594 (2005-02-03)
Adduct I (lambda(max) at approximately 430 nm) formed in the reaction of 2-hydrazinopyridine (2HP) and the TPQ cofactor of wild-type Escherichia coli copper amine oxidase (WT-ECAO) is stable at neutral pH, 25 degrees C, but slowly converts to another spectroscopically

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