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Buflomedil hydrochloride

pharmaceutical raw materials
Buflomedil hydrochloride structure

Buflomedil hydrochloride 

structure
  • CAS No:

    35543-24-9

  • Formula:

    C17H25NO4.ClH

  • Chemical Name:

    Buflomedil hydrochloride

  • Synonyms:

    1-Butanone,4-(1-pyrrolidinyl)-1-(2,4,6-trimethoxyphenyl)-,hydrochloride (1:1);1-Butanone,4-(1-pyrrolidinyl)-1-(2,4,6-trimethoxyphenyl)-,hydrochloride;LL 1656;Buflomedil hydrochloride;Irrodan R;Fonzylane;Buflocit;Lofton;Buflan;Provas;Loftyl;Bufedil;Irrodan;Buflonat;1-[3-(2,4,6-Trimethoxybenzoyl)Propyl]PyrrolidiniumChloride

  • Categories:

    Active Pharmaceutical Ingredients  >  Circulatory System Drugs

Description

Buflomedil HCl is a vasodilator used to treat claudication or the symptoms of peripheral arterial disease.Target: OthersBuflomedil is a vasoactive drug used to treat claudication or the symptoms of peripheral arterial disease. In the EU, buflomedil, a vasoactive agent, was indicated for treatment of PAOD symptoms, specifically in patients with stage II PAOD who experience severe pain when walking even relatively short distances. Buflomedil is not currently approved by the US Food and Dru

Buflomedil hydrochloride Basic Attributes

343.85

343.155029

252-611-9

2933990090

Characteristics

48

3.51100

White or off-white crystalline powder

192-193 °C

454.5°C at 760 mmHg

228.7ºC

Oral-rat LD50: 410 mg/kg; Oral-Mouse LD50: 275 mg/kg

Thermal decomposition releases toxic nitrogen oxides and hydrogen chloride fumes

Safety Information

NONH for all modes of transport

3

EL9885000

The warehouse is ventilated, low temperature and dry; stored separately from food raw materials

P264, P270, P301+P312, P330, P501

H302

Toxicity

highly toxic

Buflomedil hydrochloride Use and Manufacturing

Methods of Manufacturing

In a separate dry reaction flask, 33.6 g of 1, 3, 5-trimethoxybenzene and 27.2 g of anhydrous zinc chloride were added.Dichloromethane 300mL, stirring and cooling to 0-5 degrees after dropping 36.5g 1-pyrrolidinoyl chloride, drops, The reaction was heated to reflux for 2 hours. After the reaction was complete, 15 mL of concentrated hydrochloric acid and 150 mL of pure water were added and washed.The resulting organic phase is washed with saturated sodium bicarbonate solution to a pH of 7-8, and the organic phase is dried over magnesium sulfate and then reduced to dryness.Add 100 mL of anhydrous ethanol to the concentrate.20percent hydrochloric acid ethanol100mLAfter stirring the reaction at 60-70°C for 1 hour, the ethanol is then reduced to dryness.After adding 400 mL of acetone to the residue and cooling and crystallizing, the white crystal was filtered to obtain 60.2 g of buflomedil hydrochloride.

Uses

Buflomedil is used as an vasodilator (peripheral).

Drug Function and Efficacy

It is an α-adrenergic receptor inhibitor and has a weak nonspecific calcium ion antagonist effect. It improves the microcirculation blood flow in the brain and limbs by inhibiting the spasm of the precapillary sphincter. It also has the function of inhibiting platelet aggregation and improving red blood cell deformability.

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

  • ISOCHEM

    France France
    Active
  • ISOCHEM Vert Le

    European Union European Union
    Active
  • AMDIPHARM LIMITED

    European Union European Union
    Inactive

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