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Merck
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Documenti

A75633

Sigma-Aldrich

2-Amino-3-methylpyridine

95%

Sinonimo/i:

2-Amino-3-picoline

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About This Item

Formula empirica (notazione di Hill):
C6H8N2
Numero CAS:
1603-40-3
Peso molecolare:
108.14
Beilstein:
107892
Numero CE:
216-501-4
Numero MDL:
MFCD00006320
Codice UNSPSC:
12352100
ID PubChem:
24891251
NACRES:
NA.22

Saggio

95%

Forma fisica

solid

Indice di rifrazione

n20/D 1.5823 (lit.)

P. eboll.

221-222 °C (lit.)

Punto di fusione

29-31 °C (lit.)

Densità

1.073 g/mL at 25 °C (lit.)

Stringa SMILE

Cc1cccnc1N

InChI

1S/C6H8N2/c1-5-3-2-4-8-6(5)7/h2-4H,1H3,(H2,7,8)
RGDQRXPEZUNWHX-UHFFFAOYSA-N

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Pittogrammi

Skull and crossbonesCorrosion
GHS06,GHS05

Avvertenze

Danger

Indicazioni di pericolo

H301 + H331,H310,H314,H412

Classi di pericolo

Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

244.4 °F - closed cup

Punto d’infiammabilità (°C)

118 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

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Sigma-Aldrich

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Sigma-Aldrich

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2-Aminopyridine-3-carboxylic acid

2-Amino-3-hydroxypyridine 98%

Sigma-Aldrich

122513

2-Amino-3-hydroxypyridine

3-Methylpyridine 99%

Sigma-Aldrich

P42053

3-Methylpyridine

3-Picolylamine ≥99%

Sigma-Aldrich

A65409

3-Picolylamine

T G Altuntas et al.
Anticancer research, 17(5A), 3485-3491 (1997-12-31)
The metabolism of the comutagen 2-amino-3-methylpyridine has been studied in vitro using rat and rabbit hepatic preparations. 2-Amino-3-methylpyridine-N-oxide, 2-amino-3-hydroxymethylpyridine and 2-amino-5-hydroxy-3-methylpyridine were formed by both rat and rabbit hepatic preparations. No evidence was obtained for the formation of the corresponding
J W Gorrod et al.
European journal of drug metabolism and pharmacokinetics, 22(4), 341-344 (1998-03-26)
The in vitro metabolism of 2-hydroxylamino-3-methylpyridine has been investigated using arochlor 1254 pretreated rat S9 mixtures. 2-Hydroxylamino-3-methylpyridine is rapidly converted to the parent amine 2-amino-3-methylpyridine. No further oxidation products of 2-hydroxylamino-3-methylpyridine (i.e. nitroso or nitro) were detected under the HPLC
T G Altuntas et al.
Xenobiotica; the fate of foreign compounds in biological systems, 27(11), 1103-1111 (1997-12-31)
1. The effects of various potential inhibitors, activators and inducers on the metabolism of the comutagen 2-amino-3-methylpyridine (2A3MP) by rabbit hepatic microsomes and S9 supernatants have been studied. 2. The 1-N-oxidation of 2A3MP to 2-amino-3-methylpyridine-1-N-oxide (2A3M-PNO) was inhibited by 2,4-dichloro-6-phenylphenoxyethylamine
Cengiz Yenikaya et al.
Journal of enzyme inhibition and medicinal chemistry, 26(1), 104-114 (2010-09-24)
Two novel proton transfer compounds were prepared between 2,4-dichloro-5-sulphamoylbenzoic acid (lasamide) (Hsba) and ethylenediamine (en), namely ethane-1,2-diaminium 2,4-dichloro-5-sulphamoylbenzoate (1), and also between Hsba and 2-amino-3-methylpyridine (2-amino-3-picoline) (amp), namely 2-amino-3-methylpyridinium 2,4-dichloro-5-sulphamoylbenzoate (2). All these were characterised by elemental, spectral (IR and
T G Altuntas et al.
Anticancer research, 17(6D), 4479-4482 (1998-03-12)
The metabolism of 2-amino-3-methylpyridine (2A3MP) in vitro has been investigated using the rat, rabbit, dog, marmoset, guinea pig and hamster hepatic microsomes and S9 supernatants (10,000 g fraction). Species differences were observed in the in vitro formation of 2-amino-3-methylpyridine-N-oxide (2A3MPNO)

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