1,3-Di(4-pyridyl)propane

Names

[ Name ]:
1,3-Di(4-pyridyl)propane

[Synonym ]:
1,3-di(pyridin-4-yl)propane
4-(3-pyridin-4-ylpropyl)pyridine
Pyridine, 4,4'-(1,3-propanediyl)bis-
MFCD00038046
Pyridine, 4,4'- (1,3-propanediyl)bis-
4,4'-Propane-1,3-diyldipyridine
1,3-Bis-(4-pyridyl)propane
4,4′-trimethylene dipyridine
1,3-bis(4-pyridyl)-propane
4,4'-(1,3-Propanediyl)dipyridine
EINECS 241-284-8
1,3-Di(4-pyridyl)propane
1,3-bis(4-pyridyl)propane

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
338.7±22.0 °C at 760 mmHg

[ Melting Point ]:
57-60 °C(lit.)

[ Molecular Formula ]:
C₁₃H₁₄N₂

[ Molecular Weight ]:
198.264

[ Flash Point ]:
128.2±14.0 °C

[ Exact Mass ]:
198.115692

[ PSA ]:
25.78000

[ LogP ]:
2.10

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.571

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302 + H312 + H332-H315-H319-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R20/21/22;R36/37/38

[ Safety Phrases ]:
S26-S28-S36/37/39-S45

[ RIDADR ]:
2811

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1(b)

[ HS Code ]:
2933399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

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

Two- and three-dimensional cadmium-organic frameworks with trimesic acid and 4,4'-trimethylenedipyridine.

Inorg. Chem. 43(13) , 3882-93, (2004)

Three novel cadmium-organic frameworks built-up from 1,3,5-benzenetricarboxylate anions (HXBTC(x-3)) and 4,4'-trimethylenedipyridine (TMD) have been hydrothermally synthesized, and characterized using...

Electron-transfer study and solvent effects on the formal potential of a redox-active self-assembling monolayer. Acevedo D and Abruna HD.

J. Phys. Chem. 95(23) , 9590-9594, (1991)