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Merck

A78209

Sigma-Aldrich

3-氨基吡啶

99%

别名:

3-吡啶胺

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About This Item

经验公式(希尔记法):
C5H6N2
CAS号:
分子量:
94.11
Beilstein:
105692
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

99%

形狀

flakes

bp

248 °C (lit.)

mp

60-63 °C (lit.)

SMILES 字串

Nc1cccnc1

InChI

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

InChI 密鑰

CUYKNJBYIJFRCU-UHFFFAOYSA-N

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象形圖

Skull and crossbonesHealth hazard

訊號詞

Danger

危險分類

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

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

水污染物質分類(WGK)

WGK 3

閃點(°F)

190.4 °F - closed cup

閃點(°C)

88 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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分析证书(COA)

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Nitric oxide synthase inhibitor facilitates aminopyridine induced neocortical seizure.
B Boda et al.
Neurobiology (Budapest, Hungary), 4(1-2), 103-104 (1996-01-01)
Daniel Cappel et al.
Journal of chemical information and modeling, 51(10), 2581-2594 (2011-09-16)
The model binding site of the cytochrome c peroxidase (CCP) W191G mutant is used to investigate the structural and dynamic properties of the water network at the buried cavity using computational methods supported by crystallographic analysis. In particular, the differences
Pierre Garcia et al.
Organic letters, 13(8), 2030-2033 (2011-03-19)
Bimolecular cobalt-catalyzed [2 + 2 + 2] cycloadditions between yne-ynamides and nitriles afford bicyclic 3- or 4-aminopyridines in up to 100% yield. The high regioselectivity observed depends on the substitution pattern at the starting ynamide. Aminopyridines bearing TMS and Ts
Jaslin Ikhsan et al.
Journal of colloid and interface science, 284(2), 383-392 (2005-03-23)
The sorption of 2-, 3-, and 4-aminopyridine on K-saturated Wyoming (SWy-K) and Texas (STx-K) and Ca-enriched Texas (STx-Ca) montmorillonite was measured at 25 degrees C with 10 mM KNO(3) or 3.3 mM Ca(NO(3))(2) as the background electrolyte. The aminopyridines adsorbed
E O'Hearn et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 17(22), 8828-8841 (1997-11-14)
Ibogaine, an indole alkaloid that causes hallucinations, tremor, and ataxia, produces cerebellar neurotoxicity in rats, manifested by degeneration of Purkinje cells aligned in narrow parasagittal bands that are coextensive with activated glial cells. Harmaline, a closely related alkaloid that excites

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