Pyrrole-3-carboxylic acid, 98+%, Thermo Scientific Chemicals

Name: Pyrrole-3-carboxylic acid, 98+%, Thermo Scientific Chemicals
SKU: ALFH55383.MD

CAS: 931-03-3 | C5H5NO2 | 111.1 g/mol

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250 mg

1 g

Catalog number ALFH55383.MD

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250 mg

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Specifications

Chemical Name or MaterialPyrrole-3-carboxylic acid

CAS931-03-3

Health Hazard 1H302-H315-H319-H335

Health Hazard 2GHS H Statement
H301-H315-H319-H335
Toxic if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

Health Hazard 3P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c

Pyrrole-3-carboxylic acid is useful for the synthesis of cholecystokinin antagonists, benzopyran antihypertensives and azepinediones. It is utilized for the preparation of a poly(pyrrole-3-carboxylic acid) modified pencil graphite electrode and its usage in the determination of serotonin (SER) in blood serum and urine samples.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Pyrrole-3-carboxylic acid is useful for the synthesis of cholecystokinin antagonists, benzopyran antihypertensives and azepinediones. It is utilized for the preparation of a poly(pyrrole-3-carboxylic acid) modified pencil graphite electrode and its usage in the determination of serotonin (SER) in blood serum and urine samples.

Solubility
Soluble in water.

Notes
Incompatible with strong bases, strong oxidizing agents, strong reducing agents.

RUO – Research Use Only

General References:

Lee, J. S.; Kim, M.; Oh, J.; Kim, J.; Cho, S.; Jun, J.; Jang, J. Platinum-decorated carbon nanoparticle/polyaniline hybrid paste for flexible wideband dipole tag-antenna application. J. Mater. Chem. A 2015, 3 (13), 7029-7035.
Estévez, V.; Villacampa, M.; Menéndez, C. J. Recent advances in the synthesis of pyrroles by multicomponent reactions. Chem. Soc. Rev. 2014, 43 (13), 4633-4657.