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Benorylate

pharmaceutical raw materials
Benorylate structure

Benorylate 

structure
  • CAS No:

    5003-48-5

  • Formula:

    C17H15NO5

  • Chemical Name:

    Benorylate

  • Synonyms:

    Benzoic acid,2-(acetyloxy)-,4-(acetylamino)phenyl ester;Salicylic acid acetate,ester with 4′-hydroxyacetanilide;Acetanilide,4′-hydroxy-,salicylate (ester) acetate (ester);p-Acetamidophenyl acetylsalicylate;4-Acetamidophenyl 2-acetoxybenzoate;4-Acetaminophenyl 2-acetoxybenzoate;Benorylate;Aspirin acetaminophen ester;Fenasprate;Benoral;Acetylsalicylic acid paracetamol ester;p-N-Acetylaminophenyl acetylsalicylate;Benorilate;Win 11450;TO 125;Benortan;Quinexin;Salipran

  • Categories:

    Organic Chemistry  >  Amides

Description

Benorylate (Benoral) is the esterification product of paracetamol and acetylsalicylic acid. It has anti-inflammatory, analgesic and antipyretic properties. Benorylate could also inhibit prostaglandin (PG) synthesis.


Benorilate is a carbonyl compound.

Benorylate Basic Attributes

313.3

313.30

225-674-5

W1QX9DV96G

DTXSID5022649

N - Nervous system

2924299090

Characteristics

81.7

2.2

1.2±0.1 g/cm3

175 °C

537.8°C at 760 mmHg

263.1±32.9 °C

1.566

20mg/L(21 ºC)

LD50 in mice, rats (mg/ml): 2000, ~10000 orally; 1255, 1830 i.p. (Robertson)

Safety Information

VO0720000

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Drug Information

Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)

2-acetoxy-4'-acetaminophenylbenzoate

Benorylate Use and Manufacturing

Methods of Manufacturing

Acetylsalicylic acid chloride is generated from acetylsalicylic acid through acid chlorination, and then condensed with p-acetamidophenol to obtain benoxate.

Uses

Benorilate is a codrug of Acetylsalicylic Acid (A187780) and Acetaminophen (A161220) and is used as an anti-inflammatory and antipyretic medication.

Computed Properties

Molecular Weight:313.30
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:313.09502258
Monoisotopic Mass:313.09502258
Topological Polar Surface Area:81.7
Heavy Atom Count:23
Complexity:442
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

Drug Function and Efficacy

Extract from the above information

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • Shaanxi Xiyue Pharmaceutical (Fufeng) Co., Ltd.

    China China
    Active
  • Jiuquan Dadeli Pharmaceutical Co., Ltd.

    China China
    Active
  • Guangxi LMZ Yikang Pharmaceutical Co., Ltd.

    China China
    Active

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