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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:
207-988-4
Beilstein/REAXYS Number:
105785
MDL number:
Assay:
99%
Form:
crystals
产品名称
2-氨基吡啶, 99%
InChI key
ICSNLGPSRYBMBD-UHFFFAOYSA-N
InChI
1S/C5H6N2/c6-5-3-1-2-4-7-5/h1-4H,(H2,6,7)
SMILES string
Nc1ccccn1
assay
99%
form
crystals
bp
204-210 °C (lit.)
mp
54-58 °C (lit.)
Quality Level
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Application
2-Aminopyridine has been used as a reactant in the synthesis of 2-(2-aminopyridinium)acetyl starch with antioxidant property.
It can also be used:
It can also be used:
- As a reactant in the synthesis of 3-aroylimidazopyridines from chalcones by aerobic oxidative amidation using copper acetate catalyst.
- In the synthesis of crystalline Cu(II) complex, di-μ-(2-aminopyridine(N,N′))-bis[(2,6 pyridinedicarboxylate)aquacopper(II)] tetrahydrate using 2,6-pyridinedicarboxylic acid and Cu(CH3COO)2.H2O.
- As an imprinting molecule for the preparation of poly(methacrylic acid–ethylene glycol dimethacrylate) polymer. It is packed in micro-column for selective solid phase extraction of 2-aminopyridine.
- As a reactant in the synthesis of 2-aryl-3-(pyridin-2-yl)-1,3-thiazolidin-4-ones in the presence of Lewis acid catalysts.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
197.6 °F - closed cup
flash_point_c
92 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
危险化学品
此项目有
Synthesis of aminopyridinium-grafted starch derivatives and evaluation of their antioxidant property
Tan W, et al.
Starch, 69(7-8), 1600259-1600259 (2017)
Synthesis, characterization and biological evaluation of a novel Cu (II) complex with the mixed ligands 2, 6-pyridinedicarboxylic acid and 2-aminopyridine
Yenikaya C, et al.
Polyhedron, 28(16), 3526-3532 (2009)
A 2-aminopyridine molecularly imprinted polymer surrogate micro-column for selective solid phase extraction and determination of 4-aminopyridine
Mullett WM, et al.
Analytica Chimica Acta, 414(1-2), 123-131 (2000)
Copper (II)-Catalyzed Aerobic Oxidative Coupling between Chalcone and 2-Aminopyridine via C-H Amination: An Expedient Synthesis of 3-Aroylimidazo [1, 2-a] pyridines
Monir K, et al.
advanced synthesis and catalysis, 356(5), 1105-1112 (2014)
Tadasu Urashima et al.
Advances in nutrition (Bethesda, Md.), 3(3), 473S-482S (2012-05-16)
Human milk and colostrum contain ∼12-13 g/L and ∼22-24 g/L of oligosaccharides, respectively. The chemical structures of >100 human milk oligosaccharides (HMO) have been characterized to date. We determined the concentrations of 10 neutral and 9 acidic colostrum HMO collected
实验方案
Explore mass spectrometry analysis of glycans for glycomic & glycoproteomic neutral & acidic glycan analysis. See a general mass spec glycan analysis procedure.
该聚糖质谱分析方案,被称之为干液滴法,基于原始的MALDI实验并依然是MS领域中最常用的方法。
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