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Merck
CN

261823

4-氨基嘧啶

98%

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关于此项目

经验公式(希尔记法):
C4H5N3
化学文摘社编号:
分子量:
95.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
Form:
solid
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Quality Level

assay

98%

form

solid

mp

154-156 °C (lit.)

SMILES string

Nc1ccncn1

InChI

1S/C4H5N3/c5-4-1-2-6-3-7-4/h1-3H,(H2,5,6,7)

InChI key

OYRRZWATULMEPF-UHFFFAOYSA-N

General description

The consequences of one-electron oxidation and one-electron reduction were studied for 4-aminopyrimidine.

Application

4-Aminopyrimidine has been used in the preparation of 1:4-dihydro-4-imino-1-methylpyrimidine hydriodide.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

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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G R Li et al.
The American journal of physiology, 274(3 Pt 1), C577-C585 (1998-04-08)
The threshold potential for the classical depolarization-activated transient outward K+ current and Cl- current is positive to -30 mV. With the whole cell patch technique, a transient outward current was elicited in the presence of 5 mM 4-aminopyridine (4-AP) and
K Takagi et al.
Cell structure and function, 11(3), 235-243 (1986-09-01)
We compared intracellular K+ and Na+ ion concentrations during cell growth and differentiation of a mouse myeloid leukemia M1 cell line. Cells undergoing mitosis had higher K+ concentrations than quiescent cells. Treatment with a K+ channel blocker and furosemide enhanced
Potential roles of the aminopyrimidine ring in thiamin catalyzed reactions.
F Jordan et al.
Annals of the New York Academy of Sciences, 378, 14-31 (1982-01-01)



全球贸易项目编号

货号GTIN
261823-1G04061826671399
261823-250MG04061833482100