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2,6-di-tert-butylpyridine

Names

[ CAS No. ]:
585-48-8

[ Name ]:
2,6-di-tert-butylpyridine

[Synonym ]:
2,6-DI-T-BUTYLPYRIDINE
Pyridine, 2,6-bis(1,1-dimethylethyl)-
2,6-Di(tert-butyl)pyridine
EINECS 209-557-6
2,6-Bis(2-methyl-2-propanyl)pyridine
MFCD00006306
2,6-ditert-butylpyridine
2,6-di-tert-butylpyridine

Chemical & Physical Properties

[ Density]:
0.9±0.1 g/cm3

[ Boiling Point ]:
208.5±0.0 °C at 760 mmHg

[ Molecular Formula ]:
C13H21N

[ Molecular Weight ]:
191.313

[ Flash Point ]:
72.2±0.0 °C

[ Exact Mass ]:
191.167404

[ PSA ]:
12.89000

[ LogP ]:
4.10

[ Vapour Pressure ]:
0.3±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.478

[ Storage condition ]:
2-8°C

[ Stability ]:
Stable. Combustible. Incompatible with strong acids, strong oxidizing agents.

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xn,Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S37/39-S26-S36/37/39

[ RIDADR ]:
3267

[ HS Code ]:
2933399090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Disproportionation of Iron(III) Porphyrin pi-Cation Radicals in the Presence of Sterically Hindered Pyridines. Spectroscopic Detection of Asymmetric Highly Oxidized Intermediates.

Inorg. Chem. 35(5) , 1136-1147, (1996)

The reactivity of iron(III) tetraphenylporphyrin pi-cation radical (TPP(*))Fe(III)(ClO(4))(2), (1-1) iron(III) tetra-p-tolylporphyrin pi-cation radical (TTP(*))Fe(III)(ClO(4))(2) (1-2) and iron(III) t...

Enantioselective organocatalytic singly occupied molecular orbital activation: the enantioselective alpha-enolation of aldehydes.

J. Am. Chem. Soc. 129 , 7004, (2007)

J. Macromol. Sci., Pure Appl. Chem. A29 , 639, (1992)


More Articles


Related Compounds

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