5086-74-8

  • Product Name:Tetramisole hydrochloride
  • Molecular Formula:C11H12N2S.HCl
  • Purity:99%
  • Molecular Weight:
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Product Details

Appearance:white to pale cream crystalline powder

Hot Sale, top purity 5086-74-8 Tetramisole hydrochloride in bulk supply

  • Molecular Formula:C11H12N2S.HCl
  • Molecular Weight:240.757
  • Appearance/Colour:white to pale cream crystalline powder 
  • Melting Point:266-267 °C(lit.) 
  • Boiling Point:344.4 °C at 760 mmHg 
  • Flash Point:162.1 °C 
  • PSA:40.90000 
  • LogP:2.32160 

Tetramisole hydrochloride 5086-74-8 Usage

Tetraimidazole hydrochloride is a white to pale cream crystalline powder, bitter and astringent, easily soluble in water , Methanol, slightly soluble in ethanol, insoluble in acetone. acid solutions are stable. Combined oxyclozanide and tetramisole hydrochloride are used to control gastrointestinal helminths (Paramphistomidae and Haemonchus contortus) in sheep in Haryana, India, but recent reports suggest the development of drug resistance. Tetramisole hydrochloride is an inhibitor of alkaline phosphatases, is a high purity antiparasitic. It is a racemic mixture of (+) and (-) isomers. The (-) isomer (levamisole) accounts for most of the biological activity of tetramisole.Tetramisole has been used to inhibit alkaline phosphatase in the effective range of 0.4 – 2 mM. Inhibition of intestinal alkaline phosphate requires higher concentrations.  It is suitable for inhibition of various alkaline phosphatase (i.e., liver, kidney, placenta, bone and tumor)(Intestinal alkaline phosphatases are only slightly inhibited.). Tetramisole has biological response modifier with anthelmintic activity. Anthelmintic (nematodes); immunomodulator.

 

Definition

ChEBI: Tetramisole hydrochloride is an organic molecular entity. It is a broad-spectrum veterinary anthelmintic with high efficiency and low toxicity.

 

 

Mode of action

Tetramisole HCl inhibits parasitic worm growth by acting as an agonist to nicotinic acetylcholine receptors leading to paralysis. The mechanism of action for anticancer activity is unknown.

 

InChI:InChI=1/C11H12N2S.ClH/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10;/h1-5,10H,6-8H2;1H

5086-74-8 Relevant articles

Method for the treatment of plants with agrochemical tablet compositions

-

, (2008/06/13)

Novel method for applying agrochemicals to plants, which method consists in attaching to the surface of the plants tablets comprising at least one agrochemically active compound and at least one adjuvant, which is solid, liquid of pasty at room temperature, and optionally, one or more excipients optionally in admixture with one or more other additives and/or water.

Addition technology for tetramisole hydrochloride

Jin Feng, Jinsong Yang, Yaotian Jiang, Haitao Sheng, Hong Chen

, Jul 25, 2012

The invention discloses an addition technology for preparing tetramisole hydrochloride.

Optically active 1-oxyethyl-4-phenyl-2-imidazolidones

-

, (2008/06/13)

The new process also permits the direct manufacture of optically active 1-(2-alkoxyethyl)-4-phenyl-2-imidazolidone and their 3-acylated derivatives, optically active 1-(2-alkoxyethyl)-4-phenylimidazolidine-2-thiones, and levamisole, the levorotatory isomer of tetramisole, using catalytic amounts of a chiral reducing agent, with the elimination of conventional resolution procedures.

5086-74-8 Process route

tetramisole hydrochloride
5086-74-8,74191-78-9

tetramisole hydrochloride

Tetramisole
5036-02-2

Tetramisole

Conditions
Conditions Yield
 
 
phosphorous pentasulfide

phosphorous pentasulfide

1-(2-hydroxy-ethyl)-4-phenyl-imidazolidin-2-one
65329-72-8

1-(2-hydroxy-ethyl)-4-phenyl-imidazolidin-2-one

tetramisole hydrochloride
5086-74-8,74191-78-9

tetramisole hydrochloride

Conditions
Conditions Yield
With hydrogenchloride; sodium hydroxide; In ethanol; chloroform; toluene;
 
With hydrogenchloride; sodium hydroxide; In ethanol; chloroform; toluene;
 

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