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W296600

Sigma-Aldrich

吡啶

≥99%

别名:

吖嗪, 氮杂苯

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About This Item

经验公式（希尔记法）:
C5H5N
CAS号:
110-86-1
分子量:
79.10
FEMA號碼:
2966
Beilstein:
103233
EC號碼:
203-809-9
歐洲委員會號碼:
604
MDL號碼:
MFCD00011732
分類程式碼代碼:
12164502
PubChem物質ID:
24901424
NACRES:
NA.21

生物源

synthetic

品質等級

400

等級

Fragrance grade
Halal
Kosher

agency

follows IFRA guidelines

法律遵循

EU Regulation 1223/2009

蒸汽密度

2.72 (vs air)

蒸汽壓力

10 mmHg ( 13.2 °C)
20 mmHg ( 25 °C)

化驗

≥99%

形狀

liquid

自燃溫度

899 °F

expl. lim.

12.4 %

包裝

composite drum of 25 kg
glass bottle of 1 kg
steel drum of 10 kg

雜質

≤0.50% (water)

顏色

colorless

折射率

n20/D 1.509 (lit.)

pH值

8.5 (25 °C, 15.82 g/L)

bp

115 °C (lit.)

mp

−42 °C (lit.)

密度

0.978 g/mL at 25 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

香料過敏原

no known allergens

感官的

fishy; sour

SMILES 字串

C1=CN=CC=C1

InChI

1S/C5H5N/c1-2-4-6-5-3-1/h1-5H

InChI 密鑰

JUJWROOIHBZHMG-UHFFFAOYSA-N

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應用


  • Reactivity and Steric Parameters from 2D to 3D Bulky Pyridines: Increasing Steric Demand at Nitrogen with Chiral Azatriptycenes.: The research explores the reactivity and steric parameters of bulky pyridines, specifically chiral azatriptycenes, which have potential applications in asymmetric catalysis and pharmaceutical chemistry (Bensaida et al., 2024).

  • Piperidine and Pyridine Series Lead-Free Dion-Jacobson Phase Tin Perovskite Single Crystals and Their Applications for Field-Effect Transistors.: The study investigates the use of piperidine and pyridine series lead-free tin perovskite single crystals in field-effect transistors, highlighting their potential in electronic and optoelectronic applications (Liao et al., 2024).

  • Synthesis, evaluation of biological activity and SAR of new thioalkyl derivatives of pyridine.: This research focuses on the synthesis and biological activity of new thioalkyl derivatives of pyridine, providing insights into their structure-activity relationships (SAR) and potential pharmaceutical applications (Sh Dashyan et al., 2024).

免責聲明

仅供R&D或非EU食品使用不用于零售。

象形圖

FlameExclamation mark
GHS02,GHS07

訊號詞

Danger

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2

儲存類別代碼

3 - Flammable liquids

水污染物質分類（WGK）

WGK 2

閃點（°F）

68.0 °F - closed cup

閃點（°C）

20 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

分析证书(COA)

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Total syntheses of complanadines A and B.
Le Zhao et al.
Angewandte Chemie (International ed. in English), 52(6), 1722-1725 (2013-01-03)
Nathalie Ségaud et al.
Inorganic chemistry, 52(2), 691-700 (2013-01-11)
We report the synthesis, characterization, and solution chemistry of a series of new Fe(II) complexes based on the tetradentate ligand N-methyl-N,N'-bis(2-pyridyl-methyl)-1,2-diaminoethane or the pentadentate ones N,N',N'-tris(2-pyridyl-methyl)-1,2-diaminoethane and N,N',N'-tris(2-pyridyl-methyl)-1,3-diaminopropane, modified by propynyl or methoxyphenyltriazolyl groups on the amino functions. Six of
Ye Wei et al.
Journal of the American Chemical Society, 135(10), 3756-3759 (2013-02-27)
We describe here a [3+3]-type condensation reaction of O-acetyl ketoximes and α,β-unsaturated aldehydes that is synergistically catalyzed by a copper(I) salt and a secondary ammonium salt (or amine). This redox-neutral reaction allows modular synthesis of a variety of substituted pyridines
Jerri M Rook et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 40(3), 755-765 (2014-09-23)
Allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGlu5) have exciting potential as therapeutic agents for multiple brain disorders. Translational studies with mGlu5 modulators have relied on mGlu5 allosteric site positron emission tomography (PET) radioligands to assess receptor occupancy
Yuya Kodama et al.
Journal of medicinal chemistry, 56(22), 9342-9350 (2013-11-01)
In this study, we developed an assignment-free approach for rapid identification of ligand-binding sites in target proteins by using NMR. With a sophisticated cell-free stable isotope-labeling procedure that introduces (15)N- or (13)C-labels to specific atoms of target proteins, this approach
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