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Home > Encyclopedia > Betahistine mesylate

Betahistine mesylate

pharmaceutical raw materials
Betahistine mesylate structure

Betahistine mesylate 

structure
  • CAS No:

    54856-23-4

  • Formula:

    C8H12N2.2CH4O3S

  • Chemical Name:

    Betahistine mesylate

  • Synonyms:

    2-Pyridineethanamine,N-methyl-,methanesulfonate (1:2);2-Pyridineethanamine,N-methyl-,dimethanesulfonate;Betahistine mesylate;Merislon

  • Categories:

    Active Pharmaceutical Ingredients  >  Circulatory System Drugs

Description

White or almost white, crystalline powder, very hygroscopic.


Betahistine mesilate is an aralkylamine.|A histamine analog and H1 receptor agonist that serves as a vasodilator. It is used in MENIERE DISEASE and in vascular headaches but may exacerbate bronchial asthma and peptic ulcers.

Betahistine mesylate Basic Attributes

328.41

328.076263

259-377-7

X1L0E3R43Y

DTXSID1045588

2933399090

Characteristics

150.42000

2.40400

112°C

210.9ºC at 760 mmHg

96.7ºC

almost transparency

Oral-rat LD50: 3030 mg/kg; Oral-Mouse LD50: 500 mg/kg

Flammable; burning produces toxic nitrogen oxides and sulfur oxide fumes

Safety Information

UT2970200

Ventilated, low temperature and dry

P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Toxicity

moderately toxic

Drug Information

Drugs that bind to and activate histamine receptors. Although they have been suggested for a variety of clinical applications histamine agonists have so far been more widely used in research than therapeutically. (See all compounds classified as Histamine Agonists.)|Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)

Aequamen

Betahistine mesylate Use and Manufacturing

Vasodilatator;H1 agonist

Computed Properties

Molecular Weight:328.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:328.07627871
Monoisotopic Mass:328.07627871
Topological Polar Surface Area:150
Heavy Atom Count:20
Complexity:176
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes

Drug Function and Efficacy

1. Improvement of inner ear circulation disorders: In the marmot model, blood flow increased to 148% 30 minutes after intraperitoneal administration. 2. Increased cochlear blood flow in marmots with endolymphatic edema: Cochlear blood flow increased from 5.5ml/(100g·min) to 8.1ml/(100g·min), due to the relaxation of the smooth muscle of the radial arteries of the cochlea. 3. Improvement of brain blood flow: In the rhesus monkey experiment, after intravenous injection, the blood flow of the cerebral and cerebellar tissues increased from 70.4ml/(100g·min) to 81.1ml/(100g·min) and from 73.2ml/(100g·min) to 84.0ml/(100g·min), respectively.

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

  • China CHINO PHARMA Ltd

    China China
    Active
  • Xiamen Encheng Tragacanth Limited Company

    China China
    Active
  • Lanxiha Sanlian Pharmaceutical Co., Ltd.

    China China
    Active

Recommended Suppliers of Betahistine mesylate

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