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12320 Aldrich

p-Benzoquinone dioxime

technical, ≥90% (TLC)

  • CAS Number 105-11-3

  • Linear Formula C6H4(=NOH)2

  • Molecular Weight 138.12

  •  Beilstein Registry Number 2043234

  •  EC Number 203-271-5

  •  MDL number MFCD00063636

  •  PubChem Substance ID 24847527

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Properties

Related Categories Building Blocks, Chemical Synthesis, Nitrogen Compounds, Organic Building Blocks, Oximes More...
InChI Key   LNHURPJLTHSVMU-CGXWXWIYSA-N
grade   technical
assay   ≥90% (TLC)
mp   243 °C (dec.)(lit.)
solubility   dioxane: soluble0.1 g/10 mL, clear

Description

Packaging

250 g in poly bottle

Application

p-Benzoquinone dioxime was used in oxidative regeneration of a variety of carbonyl compounds from their oximes using superoxide ion generated in situ by the phase transfer reaction between potassium superoxide and 18-crown-6.

Biochem/physiol Actions

p-Benzoquinone dioxime is sex-specific rat carcinogen inducing tumours of the urinary bladder in female rats and is a direct-acting mutagen in Salmonella typhimurium TA982.

General description

The electrochemical behaviour of p-benzoquinone dioxime on modified Pt electrodes has been studied in aqueous HClO4 solutions by employing cyclic voltammetric and rotating-disc or ring-disc techniques.

Price and Availability

Suggested Laboratory Gloves


Laboratory GlovesThis substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.



Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3
RTECS 
DK4900000

Documents

Certificate of Analysis

Protocols & Articles

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Peer-Reviewed Papers
15

References

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