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W296600

Sigma-Aldrich

Piridina

≥99%

Sinonimo/i:

Aza benzene, Azine

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About This Item

Formula empirica (notazione di Hill):
C5H5N
Numero CAS:
110-86-1
Peso molecolare:
79.10
Numero FEMA:
2966
Beilstein:
103233
Numero CE:
203-809-9
N° CoE:
604
Numero MDL:
MFCD00011732
Codice UNSPSC:
12164502
ID PubChem:
24901424
NACRES:
NA.21

Origine biologica

synthetic

Livello qualitativo

400

Grado

Fragrance grade
Halal
Kosher

agenzia

follows IFRA guidelines

Conformità normativa

EU Regulation 1223/2009

Densità del vapore

2.72 (vs air)

Tensione di vapore

10 mmHg ( 13.2 °C)
20 mmHg ( 25 °C)

Saggio

≥99%

Forma fisica

liquid

Temp. autoaccensione

899 °F

Limite di esplosione

12.4 %

Confezionamento

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

Impurezze

≤0.50% (water)

Colore

colorless

Indice di rifrazione

n20/D 1.509 (lit.)

pH

8.5 (25 °C, 15.82 g/L)

P. eboll.

115 °C (lit.)

Punto di fusione

−42 °C (lit.)

Densità

0.978 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Allergene in fragranze

no known allergens

Organolettico

fishy; sour

Stringa SMILE

C1=CN=CC=C1

InChI

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

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Applicazioni


  • 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).

Esclusione di responsabilità

For R&D or non-EU Food use. Not for retail sale.

Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H225,H302 + H312 + H332,H315,H319

Classi di pericolo

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

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

68.0 °F - closed cup

Punto d’infiammabilità (°C)

20 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
SHBL9168
SHBL6341
MKCH6989
MKCB7707
MKCF2460

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Angewandte Chemie (International ed. in English), 52(6), 1722-1725 (2013-01-03)
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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
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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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