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1-Phenylsemicarbazide

1-Phenylsemicarbazide structure

1-Phenylsemicarbazide 

structure
  • CAS No:

    103-03-7

  • Formula:

    C7H9N3O

  • Chemical Name:

    1-Phenylsemicarbazide

  • Synonyms:

    Hydrazinecarboxamide,2-phenyl-;Semicarbazide,1-phenyl-;2-Phenylhydrazinecarboxamide;Cryogenine;Cryogenine (pharmaceutical);Phenylsemicarbazide;1-Phenylsemicarbazide;1-Carbamyl-2-phenylhydrazine;Phenicarbazide;Carbaphen;Febrimin;Phenicarbazid;Phenygenine;1-Carbamoyl-2-phenylhydrazine;Kryogenin;NSC 2763;(Phenylamino)urea

  • Categories:

    Active Pharmaceutical Ingredients  >  Antipyretic Analgesics

Description

Phenicarbazide is a member of phenylhydrazines.

1-Phenylsemicarbazide Basic Attributes

151.17

151.17

203-072-3

1LR2578324

2763

DTXSID9020245

29280090

Characteristics

67.2

1.84600

1.2100 (rough estimate)

172 °C

273.17°C (rough estimate)

1.5860 (estimate)

acetone: very soluble(lit.)

Peritoneal-mouse LD50: 198 mg/kg

Thermal decomposition to emit toxic nitrogen oxide fumes

Safety Information

NONH for all modes of transport

3

22

45-36/37/39-26

FD0575000

Xn

The warehouse is low-temperature, ventilated and dry

P201, P202, P261, P264, P270, P271, P280, P281, P301+P312, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501

H302

|Warning|H302 (88.64%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P261, P264, P270, P271, P280, P281, P301+P312, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 44 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Toxicity

moderately toxic

1-Phenylsemicarbazide Use and Manufacturing

Methods of Manufacturing

The preparation method is made by reacting phenylhydrazine and urea as raw materials. Add 136kg of phenylhydrazine hydrochloride, 98kg of urea and 240L of water into a 1000L reactor. Stir uniformly and raise the temperature to above 100°C for condensation reaction. After reacting for 6 hours, add 280L of water, cool to 5°C, and filter to obtain 1-phenyl semicarbazide with a content of 95% or more and a yield of 93% or more.

Uses

1-Phenyl semicarbazide is used to synthesize 1-phenyl-1,2,4-triazole alcohol, an intermediate of organophosphorus insecticide triazophos. In addition, it is also used to manufacture antipyretics in the pharmaceutical industry.

Hydrazinecarboxamide, 2-phenyl-: INACTIVE

Computed Properties

Molecular Weight:151.17
XLogP3:0.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:151.074561919
Monoisotopic Mass:151.074561919
Topological Polar Surface Area:67.2
Heavy Atom Count:11
Complexity:132
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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