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Pyridine-3,5-dicarboxylic acid

Names

[ CAS No. ]:
499-81-0

[ Name ]:
Pyridine-3,5-dicarboxylic acid

[Synonym ]:
3,5-Pyridinedicarboxylic acid
DINICOTINIC ACID
3,5-Pyridinedicarboxylate
MFCD00006393
3,5-Dipyridinecarboxylicacid
3,5-Pyridinedicarboxylicacid
3,5-Pyridinedicarbox
EINECS 207-893-8
Pyridine-3,5-dicarboxylic acid
5-Pyridinedicarboxylic acid
5-Carboxynicotinic acid

Biological Activity

[Description]:

Pyridine-3,5-dicarboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
463.7±30.0 °C at 760 mmHg

[ Melting Point ]:
>300 °C(lit.)

[ Molecular Formula ]:
C7H5NO4

[ Molecular Weight ]:
167.12

[ Flash Point ]:
234.3±24.6 °C

[ Exact Mass ]:
167.021851

[ PSA ]:
87.49000

[ LogP ]:
-0.34

[ Vapour Pressure ]:
0.0±1.2 mmHg at 25°C

[ Index of Refraction ]:
1.628

[ Storage condition ]:
Refrigerator

[ Water Solubility ]:
insoluble

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

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

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

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S24/25-S36/37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29333999

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

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J. Chromatogr. A. 1383 , 18-24, (2015)

Three Ag(I)-organic frameworks, [Ag5(pydc)2(CN)]n, {[Ag4(pydc)2]CH3CN}n, and [Ag(4,4'-bpy)NO3]n, were synthesized and embedded into silica gels to form metal-organic-framework (MOF)-embedded gels for ...

Endocannabinoids mediate bidirectional striatal spike-timing-dependent plasticity.

J. Physiol. 593 , 2833-49, (2015)

Although learning can arise from few or even a single trial, synaptic plasticity is commonly assessed under prolonged activation. Here, we explored the existence of rapid responsiveness of synaptic pl...

Cosubstrate binding site of Pseudomonas sp. AK1 gamma-butyrobetaine hydroxylase. Interactions with structural analogs of alpha-ketoglutarate.

J. Biol. Chem. 266 , 1526, (1991)

Forty-one aromatic and aliphatic analogs of alpha-ketoglutarate were studied kinetically for their interaction with the alpha-ketoglutarate binding site of gamma-butyrobetaine hydroxylase obtained fro...


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Related Compounds