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4-Methoxyphenylhydrazine hydrochloride(CAS# 19501-58-7)

Chemical Property:

Molecular Formula C7H11ClN2O
Molar Mass 174.63
Melting Point 160-162°C (dec.)(lit.)
Boling Point 263.5°C at 760 mmHg
Flash Point 113.2°C
Water Solubility soluble
Vapor Presure 0.0103mmHg at 25°C
Appearance Grey yellow pink solid
Color Slightly pink to gray to purple
BRN 3566583
Storage Condition Keep Cold
MDL MFCD00012945
Physical and Chemical Properties Melting point 160-162°C (dec.)
water-soluble soluble
Use Applied to dyes and pharmaceutical intermediates.

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Risk and Safety

Risk Codes R20/21/22 – Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38 – Irritating to eyes, respiratory system and skin.
Safety Description S36/37 – Wear suitable protective clothing and gloves.
S36 – Wear suitable protective clothing.
S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
UN IDs 2811
WGK Germany 3
HS Code 29280090
Hazard Note Irritant/Harmful
Hazard Class IRRITANT, KEEP COLD
Packing Group III

 

 

4-Methoxyphenylhydrazine hydrochloride(CAS# 19501-58-7) Information

Use 4-methoxyphenylhydrazine hydrochloride is an intermediate, mainly used to produce phenylhydrazine compounds, and can also be used to produce other chemical products, such as 4-nitroindole and apixaban.
Applied to dyes and pharmaceutical intermediates
Preparation 4-methoxyphenylhydrazine hydrochloride can be prepared from aniline through diazotization reaction.
Take aniline, hydrochloric acid and sodium nitrite, the molar ratio between them is 1: 3.2: 1.0, first add hydrochloric acid, then add ammonium nitrite at 5 ℃, and react at 0~20 ℃ for 40 minutes to generate chlorinated diazobenzene; According to the molar ratio of aniline to 1: 3.5: 2.5, ammonium sulfite and hydrochloric acid are added, and reduction, hydrolysis and acidification are carried out in the reduction kettle, the reduction time is 60~70 minutes, and the hydrolysis and acidification time is 50 minutes. First, ammonium sulfite reacts with excess hydrochloric acid to produce ammonium bisulfite, ammonium bisulfite, ammonium sulfite reacts with chlorinated diazobenzene to form phenylhydrazine disulfonate, and then reacts with hydrochloric acid for hydrolysis and acid analysis The reaction, and after spin-drying, 4-methoxyphenylhydrazine hydrochloride is prepared.

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