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108448 Aldrich

Cyanoacetamide

99%

  • CAS Number 107-91-5

  • Linear Formula NCCH2CONH2

  • Molecular Weight 84.08

  •  Beilstein Registry Number 878221

  •  EC Number 203-531-8

  •  MDL number MFCD00008024

  •  PubChem Substance ID 24846668

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Properties

Related Categories Amides, Amines, Amides and Derivatives, Analytical Reagents, Analytical/Chromatography, Building Blocks,
InChI Key   DGJMPUGMZIKDRO-UHFFFAOYSA-N
assay   99%
mp   119-121 °C(lit.)
solubility   cold water: soluble 1gm in 6.5ml

Description

Packaging

100, 500 g in glass bottle

Application

Cyanoacetamide was used in spectrofluorimetric method for the determination of some antihistaminic H1 receptor antagonist drugs such as ebastine, cetirizine dihydrochloride and fexofenadine hydrochloride. It may be used in fluorometric determination of 3,4-dihydroxyphenylalanine. It was used as post column fluorigenic derivatizing agent for the bio-analysis and pharmacokinetics of chitosan ester in rabbit serum.

General description

Cyanoacetamide is the starting reagent for vitamin B6 synthesis. It reacts with reducing carbohydrates in borate buffer to give intense fluorescence andis useful for the automated analysis of carbohydrates as borate complexes.

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
2
RTECS 
AB5950000
Flash Point(F) 
419 °F
Flash Point(C) 
215 °C

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Protocols & Articles

Articles

Knoevenagel Condensation Reaction

The Knoevenagel Condensation Reaction is a classic organic synthesis, described by Emil Knoevenagel in the 1890’s. The Knoevenagel reaction is a modified Aldol Condensation with a nucleophilic additi...
Keywords: Aldol condensation, C-C bond formation, Condensations, Dehydration reaction, Knoevenagel Condensation, Nucleophilic additions, Organic synthesis

Peer-Reviewed Papers
15

References

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