N-(1-PYRENYL)MALEIMIDE

N-(1-PYRENYL)MALEIMIDE
  • CAS No.:42189-56-0
Other grades of this product :
N-(1-PYRENYL)MALEIMIDE Chemical Properties
Melting point 235-237 °C(lit.)
Boiling point 438.82°C (rough estimate)
density 1.2310 (rough estimate)
refractive index 1.5180 (estimate)
storage temp. Refrigerator
solubility Soluble in chloroform, N,Ndimethylformamide, dimethyl sulfoxide, ethanol, methanol
form Solid
pka–1.21±0.20, most basic, temperature: 25°C
color Yellow needles;Gold needles
λmax338nm, 325nm (MeOH)
BRN 1542661
Major ApplicationDendrimers; dye functionalized single-wall carbon nanotube (SWNT) conjugated polymer devices; photovoltaic cells; polymer-coated gold electrodes; fluorescent polymers; radio-fluorogenic gel; in sequencecontrolled polymerizations; rubber
Biological ApplicationsAnalyzing molecular aspects of muscle contraction; detecting nucleic acids, proteins; determining/evaluating cell activity; diagnosing/treating Parkinson’s disease; monitoring/studying ribosomal structure and conformation; studying nicotinic acetylcholine receptor (AChR) structure; sulfhydryl reagent
CAS DataBase Reference42189-56-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 1
8-10-21
HS Code 29251900
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
N-(1-PYRENYL)MALEIMIDE Usage And Synthesis
Chemical PropertiesN-(1-PYRENYL)MALEIMIDE is Yellow Solid
UsesReactant used in synthesis of: • ;Oligodeoxynucleotide derivatives1 • ;Polymer conjugates of immunogenic peptides2 • ;Modified oligonucleotides for biosensing applications3,Reactant: • ;Involved in synthesis of thermally stable fluorescent maleimide/isobutene alternating copolymers4• ;Used as derivitizing agent for determination of glutathione disulfide levels in biological samples5
UsesA fluorescent sulfhydryl reagent that can form excited-state dimers which emit at longer wavelenghts than the lone excited fluorophore.
UsesN-(1-PYRENYL)MALEIMIDE is a fluorescent sulfhydryl reagent that can form excited-state dimers which emit at longer wavelenghts than the lone excited fluorophore.
N-(1-PYRENYL)MALEIMIDE Preparation Products And Raw materials

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