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Merck

360570

Pyridine

ACS reagent, ≥99.0%

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A propos de cet article

Formule empirique (notation de Hill) :
C5H5N
Numéro CAS:
Poids moléculaire :
79.10
UNSPSC Code:
12352005
NACRES:
NA.07
PubChem Substance ID:
EC Number:
203-809-9
Beilstein/REAXYS Number:
103233
MDL number:
Assay:
≥99.0%
Grade:
ACS reagent
Vapor pressure:
10 mmHg ( 13.2 °C), 20 mmHg ( 25 °C)
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grade

ACS reagent

Quality Level

vapor pressure

10 mmHg ( 13.2 °C), 20 mmHg ( 25 °C)

assay

≥99.0%

form

liquid

autoignition temp.

899 °F

dilution

(for analytical testing)

impurities

Reducing substances, passes test, ≤0.002% NH3, 0.1% water

evapn. residue

≤0.002%

refractive index

n20/D 1.509 (lit.)

pH

8.5 (25 °C, 15.82 g/L)

mp

−42 °C (lit.)

solubility

water: soluble

anion traces

chloride (Cl-): ≤0.001%, sulfate (SO42-): ≤0.001%

cation traces

Cu: ≤5 ppm

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General description

Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.

Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.

Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.

Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.
Pyridine (Pyr) is a nitrogen containing six membered heterocyclic compound commonly used as a base. It is a colorless liquid with a fishy odor. Pyridine moiety is present as a major component in a number of compounds like pyridine nucleotides, pyridine alkaloids, pyridine-based polymers and pyridine-containing macrocycles. It has wide application as a solvent, catalyst and as an intermediate for synthesis. IR, Raman and UV spectra of pyridine has been analyzed and the values obtained were used to calculate its thermodynamic properties. Photodegradation and bacterial degradation of Pyr has been studied.

Application

Pyridine may be used in the synthesis of the following:
  • complexes with cobalt(II) halides
  • pyridine-d5, a deuterated form of pyridine
  • ionic liquid matrices (ILMs)

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

Classe de stockage

3 - Flammable liquids

wgk

WGK 2

flash_point_f

68.0 °F - closed cup

flash_point_c

20 °C - closed cup


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Consulter la Bibliothèque de documents

Nickel (II) and copper (II) complexes with pyridine-containing macrocycles bearing an aminopropyl pendant arm: synthesis, characterization, and modifications of the pendant amino group.
Herrera AM, et al.
Dalton Transactions, 5, 846-856 (2003)
Pyridine coenzymes of subcellular tissue fractions.
Jacobson KB and Kaplan NO.
The Journal of Biological Chemistry, 226(2), 603-613 (1957)
Cyclostellettamines AF, pyridine alkaloids which inhibit binding of methyl quinuclidinyl benzilate (QNB) to muscarinic acetylcholine receptors, from the marine sponge, Stelletta maxima.
Fusetani N, et al.
Tetrahedron Letters, 35(23), 3967-3970 (1994)
The vibrational spectrum of pyridine and the thermodynamic properties of pyridine vapors.
Kline Jr CH and Turkevich J.
J. Chem. Phys. , 12(7), 300-309 (1944)
The thermal decomposition of metal complexes-III: The decomposition of some pyridine and substituted-pyridine complexes of cobalt (II) halides.
Allan JR, et al.
J. Inorg. Nucl. Chem., 26(11), 1895-1902 (1964)

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