4-Chlorophenylhydrazine hydrochloride, 97%, Thermo Scientific Chemicals
4-Chlorophenylhydrazine hydrochloride, 97%, Thermo Scientific Chemicals
4-Chlorophenylhydrazine hydrochloride, 97%, Thermo Scientific Chemicals
4-Chlorophenylhydrazine hydrochloride, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4-Chlorophenylhydrazine hydrochloride, 97%, Thermo Scientific Chemicals

CAS: 1073-70-7 | C6H8Cl2N2 | 179.044 g/mol
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Catalog NumberQuantity
ALFA14518.065 g
Catalog number ALFA14518.06
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Quantity:
5 g
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Specifications
Chemical Name or Material4-Chlorophenylhydrazine hydrochloride
CAS1073-70-7
Health Hazard 1H302+H312+H332
Health Hazard 2GHS H Statement
H301-H350-H315-H319-H335
Toxic if swallowed.
May cause cancer.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P312-P330-P363-P501c
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4-Chlorophenylhydrazine hydrochloride is used as a pharmaceutical intermediates.

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
4-Chlorophenylhydrazine hydrochloride is used as a pharmaceutical intermediates.

Solubility
Soluble in hot water, methanol.

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

General References:

  1. J P Mahy; S Gaspard; M Delaforge; D Mansuy. Reactions of prostaglandin H synthase with monosubstituted hydrazines and diazenes. Formation of iron(II)-diazene and iron(III)-sigma-alkyl or iron(III)-sigma-aryl complexes. European Journal of Biochemistry. 1994, 226 (2), 445-457.
  2. Ruoxi Lan; Qian Liu; Pusheng Fan; Sonyuan Lin; Susanthi R. Fernando; Deirdre McCallion; Roger Pertwee and Alexandros Makriyannis. Structure-Activity Relationships of Pyrazole Derivatives as Cannabinoid Receptor Antagonists. J. Med. Chem. 1999, 42 (4), 769-776.