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4-Ethylphenylhydrazine hydrochloride

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4-Ethylphenylhydrazine hydrochloride manufacturers

4-Ethylphenylhydrazine hydrochloride Basic information
Product Name:4-Ethylphenylhydrazine hydrochloride
Synonyms:3-BROMO-4-PYRIDINYLAMINE;3-BROMO-4-PYRIDINEAMINE;1-(4-ETHYLPHENYL)HYDRAZINE HYDROCHLORIDE;N'-(4-ETHYL-PHENYL)-HYDRAZINIUM, CHLORIDE;TIMTEC-BB SBB005537;1-Ethyl-4-hydrazinobenzene hydrochloride;IFLAB-BB F1371-0140;BIO-FARMA BF001075
CAS:53661-18-0
MF:C8H13ClN2
MW:172.66
EINECS:674-306-3
Product Categories:
Mol File:53661-18-0.mol
4-Ethylphenylhydrazine hydrochloride Structure
4-Ethylphenylhydrazine hydrochloride Chemical Properties
Melting point 67-71 °C
storage temp. Sealed in dry,Room Temperature
AppearanceWhite to off-white Solid
CAS DataBase Reference53661-18-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 37/39-26-24/25
Hazard Note Irritant
HazardClass IRRITANT, IRRITANT-HARMFUL
HS Code 29280000
MSDS Information
ProviderLanguage
ACROS English
ALFA English
4-Ethylphenylhydrazine hydrochloride Usage And Synthesis
Uses4-Ethylphenylhydrazine, HCl
Synthesis
4-Ethylaniline

589-16-2

4-Ethylphenylhydrazine hydrochloride

53661-18-0

The general procedure for the synthesis of 4-ethylphenylhydrazine hydrochloride from 4-ethylaniline is as follows: 150 mL of deionized water and 160 mL of 12 N hydrochloric acid were added to a reaction flask containing 24.2 g (0.2 mol) of 4-ethylaniline. After cooling the reaction mixture to 0°C, 14 g (0.2 mol) of sodium nitrite solution dissolved in 140 mL of water was added slowly and dropwise. The reaction temperature was maintained at 0 °C and after 1 h, 112 g (0.496 mol) of stannous chloride dihydrate solution pre-dissolved in 90 mL of 12 N hydrochloric acid was added to the reaction mixture, controlling the temperature of the reaction not to exceed 10 °C during the addition process. After the addition, the reaction was continued with stirring at 10 °C for 1.5 h. The reaction mixture was cooled to 0 °C and then filtered. Upon completion of the reaction, the reaction mixture was filtered and the brown solid product was collected with a measured melting point of 198°C and 95% yield.

References[1] Patent: US2004/43995, 2004, A1. Location in patent: Page 13
[2] Journal of Medicinal Chemistry, 1999, vol. 42, # 3, p. 526 - 531
[3] Journal of the Chinese Chemical Society, 2018, vol. 65, # 5, p. 538 - 547
[4] European Journal of Medicinal Chemistry, 2018, vol. 156, p. 137 - 147
4-Ethylphenylhydrazine hydrochloride Preparation Products And Raw materials
Raw materials4-Bromoethylbenzene-->1-Ethyl-4-iodobenzene-->4-Ethylaniline-->Sodium nitrite-->Stannous chloride-->Hydrochloric acid
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