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Phenidone

Phenidone structure

Phenidone 

structure
  • CAS No:

    92-43-3

  • Formula:

    C9H10N2O

  • Chemical Name:

    Phenidone

  • Synonyms:

    3-Pyrazolidinone,1-phenyl-;2-Pyrazolin-3-ol,1-phenyl-;1-Phenyl-3-pyrazolidinone;Phenidone;1-Phenyl-3-oxopyrazolidine;1-Phenyl-3-pyrazolidone;Fenidon;1-Phenylpyrazolidine-3-one;1-Phenyl-4,5-dihydro-1H-pyrazol-3-ol;4072-30-4

  • Categories:

    Active Pharmaceutical Ingredients  >  Other Chemical Drugs

Description

light beige powder or crystals


DryPowder

Phenidone Basic Attributes

162.19

162.19

202-155-1

H0U5612P6K

30306

DTXSID1049433

2933199090

Characteristics

32.3

0.9

DryPowder

1.2±0.1 g/cm3

126 °C

304.1ºC at 760 mmHg

137.7±23.2 °C

1.620

SOLUBLE IN HOT WATER

Keep containers tightly closed. Store protected from light. Store in a cool, dry area away from incompatible substances.

LD50 orl-rat: 200 mg/kg KODAK* -,-,71

Safety Information

6.1

2811

2

6.1

S61

UQ8750000

Xn:Harmful;N:Dangerousfortheenvironment;

Stable, but light sensitive. Incompatible with strong acids, strong oxidizing agents, strong bases.

P273

H302-H411

|Warning|H302: Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P273, P301+P312, P330, P391, and P501|H302 (98.39%): Harmful if swallowed [Warning Acute toxicity, oral]|Aggregated GHS information provided by 62 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Compounds or agents that combine with cyclooxygenase (PROSTAGLANDIN-ENDOPEROXIDE SYNTHASES) and thereby prevent its substrate-enzyme combination with arachidonic acid and the formation of eicosanoids, prostaglandins, and thromboxanes. (See all compounds classified as Cyclooxygenase Inhibitors.)|Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)|Compounds that bind to and inhibit that enzymatic activity of LIPOXYGENASES. Included under this category are inhibitors that are specific for lipoxygenase subtypes and act to reduce the production of LEUKOTRIENES. (See all compounds classified as Lipoxygenase Inhibitors.)

phenidone

Phenidone Use and Manufacturing

Uses

Phenidone is used as black and white photographic developer.


Intermediates

Photographic film paper, plate, and chemical manufacturing|3-Pyrazolidinone, 1-phenyl-: ACTIVE

Computed Properties

Molecular Weight:162.19
XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:162.079312947
Monoisotopic Mass:162.079312947
Topological Polar Surface Area:32.3
Heavy Atom Count:12
Complexity:175
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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