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Merck
CN

275875

4-氨基吡啶

≥99%

别名:

4-吡啶胺, 4AP, 对氨基吡啶, 氨吡啶

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关于此项目

经验公式(希尔记法):
C5H6N2
化学文摘社编号:
分子量:
94.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-987-9
Beilstein/REAXYS Number:
105782
MDL number:
Assay:
≥99%
Form:
solid
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Quality Level

assay

≥99%

form

solid

bp

273 °C (lit.)

mp

155-158 °C (lit.)

solubility

DMF: soluble(lit.), DMSO: soluble(lit.), THF: soluble(lit.), acetone: soluble(lit.), acetonitrile: soluble(lit.), ethanol: soluble(lit.), isopropanol: soluble(lit.), methanol: soluble(lit.), water: soluble(lit.)

SMILES string

Nc1ccncc1

InChI

1S/C5H6N2/c6-5-1-3-7-4-2-5/h1-4H,(H2,6,7)

InChI key

NUKYPUAOHBNCPY-UHFFFAOYSA-N

General description

4-氨基吡啶(4-AP)可阻断其他神经膜中的电压依赖型钾离子通道。4-AP是一种K+通道阻断剂,在体外实验中可引起癫痫样放电,并且是动物和人的强效惊厥剂

Application

4-氨基吡啶可用作:
  • 制备药理学上极为重要的4-氨基-N吡啶-4-乙基-丁酰胺盐酸盐的反应剂。
  • 制备肉桂酸衍生物作为强效胆碱酶抑制剂的反应剂。
  • 制备batracylin氮杂类似物——拓扑异构酶II抑制剂的起始物料。



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Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

312.8 °F

flash_point_c

156 °C

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

法规信息

危险化学品

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分析证书(COA)

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Design, synthesis and evaluation of novel cinnamic acid derivatives bearing N-benzyl pyridinium moiety as multifunctional cholinesterase inhibitors for Alzheimer′s disease
Lan J-S, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry, 32(1), 776-788 (2017)
H Bostock et al.
The Journal of physiology, 313, 301-315 (1981-01-01)
1. 4-Aminopyridine (4AP) and tetraethylammonium ions (TEA), which block voltage-dependent potassium channels in other nerve membranes, have been used to study nerve conduction in fibres of normal rat spinal roots and those demyelinated with diphtheria toxin. The pharmacological actions have
M B Gill et al.
British journal of pharmacology, 160(6), 1417-1429 (2010-07-02)
A new class of heterotricyclic glutamate analogues recently was generated by incorporating structural elements of two excitotoxic marine compounds, kainic acid and neodysiherbaine A. Rather than acting as convulsants, several of these 'IKM' compounds markedly depressed CNS activity in mice.



全球贸易项目编号

货号GTIN
275875-1G04061826177662
275875-5G04061835554867