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109835

Sigma-Aldrich

2-Methylpyridine

98%

Sinonimo/i:

2-Picoline, α-Picoline, 2-Methylpyridine, NSC 3409

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About This Item

Formula empirica (notazione di Hill):
C6H7N
Numero CAS:
109-06-8
Peso molecolare:
93.13
Beilstein:
104581
Numero CE:
203-643-7
Numero MDL:
MFCD00006332
Codice UNSPSC:
12352100
ID PubChem:
24846941
NACRES:
NA.22

Densità del vapore

3.2 (vs air)

Tensione di vapore

10 mmHg ( 24.4 °C)

Saggio

98%

Temp. autoaccensione

995 °F

Limite di esplosione

8.6 %

Indice di rifrazione

n20/D 1.500 (lit.)

P. eboll.

128-129 °C (lit.)

Punto di fusione

−70 °C (lit.)

Solubilità

H2O: freely soluble
alcohol: miscible
diethyl ether: miscible

Densità

0.943 g/mL at 25 °C (lit.)

Stringa SMILE

Cc1ccccn1

InChI

1S/C6H7N/c1-6-4-2-3-5-7-6/h2-5H,1H3
BSKHPKMHTQYZBB-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

2-Picoline (2-Methylpyridine) was used to study the electron and proton transfer reactions of lumiflavin using Fourier transform ion cyclotron resonance mass spectrometry.
2-Picoline was used in the synthetic pathway for the production of dearomatized, allylated and C-H bond activated pyridine derivatives.

Avvertenze

Danger

Indicazioni di pericolo

H226,H302 + H332,H311,H314,H335

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1C - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

84.2 °F - closed cup

Punto d’infiammabilità (°C)

29 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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2-Pyridinemethanol 98%

Sigma-Aldrich

P66602

2-Pyridinemethanol

J Christian Lennox et al.
The journal of physical chemistry. B, 121(46), 10530-10542 (2017-11-14)
A polypyridyl ruthenium complex with fluorinated bipyridine ligands and a covalently bound tyrosine moiety was synthesized, and its photo-induced proton-coupled electron transfer (PCET) reactivity in acetonitrile was investigated with transient absorption spectroscopy. Using flash-quench methodology with methyl viologen as an
Phillip Jochmann et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(43), 12115-12122 (2011-09-10)
A facile and general synthetic pathway for the production of dearomatized, allylated, and C-H bond activated pyridine derivatives is presented. Reaction of the corresponding derivative with the previously reported reagent bis(allyl)calcium, [Ca(C(3)H(5))(2)] (1), cleanly affords the product in high yield.
Tianlan Zhang et al.
The journal of physical chemistry. A, 117(44), 11136-11141 (2013-09-07)
Examination of electron transfer and proton transfer reactions of lumiflavin and proton transfer reactions of the lumiflavin radical anion by Fourier transform ion cyclotron resonance mass spectrometry is described. From the equilibrium constant determined for electron transfer between 1,4-naphthoquinone and
Malcolm E Tessensohn et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 18(16), 2250-2257 (2017-06-14)
The voltammetric behavior of 2,3,5,6-tetramethyl-1,4-phenylenediamine was found to be able to differentiate the hydrogen acceptor abilities of electroinactive pyridine compounds in acetonitrile. Weak and strong hydrogen acceptors were distinguished through the onset of a third oxidation process that came about
Nikolaos Kritikos et al.
Journal of chromatography. A, 1403, 70-80 (2015-06-06)
In the current study, quantitative structure-retention relationships (QSRR) were constructed based on data obtained by a LC-(ESI)-QTOF-MS/MS method for the determination of amino acid analogues, following their derivatization via chloroformate esters. Molecules were derivatized via n-propyl chloroformate/n-propanol mediated reaction. Derivatives
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