4,5-Dichloro-o-phenylenediamine, 98%, Thermo Scientific Chemicals
4,5-Dichloro-o-phenylenediamine, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4,5-Dichloro-o-phenylenediamine, 98%, Thermo Scientific Chemicals

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Quantity:
100 g
5 g
25 g
Catalog number A17738.22
also known as A17738-22
Price (USD)/ Each
921.65
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1024.00 
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Quantity:
100 g
Request bulk or custom format
Price (USD)/ Each
921.65
Online exclusive
1024.00 
Save 102.35 (10%)
Add to cart
4,5-Dichloro-o-phenylenediamine, 98%, Thermo Scientific Chemicals
Catalog numberA17738.22
Price (USD)/ Each
921.65
Online exclusive
1024.00 
Save 102.35 (10%)
-
Add to cart
Chemical Identifiers
CAS5348-42-5
IUPAC Name4,5-dichlorobenzene-1,2-diamine
Molecular FormulaC6H6Cl2N2
InChI KeyIWFHBRFJOHTIPU-UHFFFAOYSA-N
SMILESNC1=CC(Cl)=C(Cl)C=C1N
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥97.5%
FormCrystals or powder or crystalline powder or lumps
Appearance (Color)Dark brown to brown or dark purple to purple
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

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
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Solubility
Soluble in methanol and Dimethyl sulfoxide. Insoluble in water.

Notes
Store in a tightly closed container in a cool, dry, well-ventilated area. Store away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Peter Zöllner; Annette Lienau; Klaus Albert; Wolfgang Lindner. Derivatization reaction of the mycotoxin moniliformin with 1,2-diamino-4,5-dichlorobenzene: structure elucidation of an unexpected reaction product by liquid chromatography/tandem mass spectrometry and liquid chromatographyuclear magnetic resonance spectroscopy. Journal of Mass Spectrometry, 2003 38 (7), 709-714 .
  2. G. W. H. Cheeseman. 223. Quinoxalines and related compounds. Part VI. Substitution of 2,3-dihydroxyquinoxaline and its 1,4-dimethyl derivative. J. Chem. Soc, 1962, 1170-1176 .