15686-33-6

Basic information

• Product Name: Biclotymol
• Synonyms: 6,6'-dichlor-2,2'-methylendithymol;4-chloro-2-[(5-chloro-2-hydroxy-6-methyl-3-propan-2-ylphenyl)methyl]-3-methyl-6-propan-2-ylphenol;2,2'-methylenebis(6-chlorothymole);biclotymol;Biclothymol;PHENOL, 2,2'-METHYLENEBIS[4-CHLORO-3-METHYL-6-(1-METHYLETHYL)-(BICLOTYMOL);2,2'-Methylenebis(3-methyl-4-chloro-6-isopropylphenol);2,2'-Methylenebis[4-chloro-3-methyl-6-(1-methylethyl)phenol]
• CAS NO: 15686-33-6
• Molecular Formula: C₂₁H₂₆Cl₂O₂
• Molecular Weight: 381.33594
• EINECS: 239-771-5
• Mol File: 15686-33-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 479°Cat760mmHg
• Flash Point: 243.5°C
• Appearance: /
• Density: 1.183g/cm³
• Vapor Pressure: 8.48E-10mmHg at 25°C
• Refractive Index: 1.579
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: Biclotymol(CAS DataBase Reference)
• NIST Chemistry Reference: Biclotymol(15686-33-6)
• EPA Substance Registry System: Biclotymol(15686-33-6)

Safety Data

• Hazardous Substances Data: 15686-33-6(Hazardous Substances Data)

Usage

General Description

Biclotymol is a chemical compound with antiseptic and anti-inflammatory properties. It is commonly used in pharmaceuticals and oral care products to treat conditions such as sore throat, mouth infections, and other inflammatory conditions of the throat and oral cavity. Biclotymol works by reducing the activity of certain enzymes that are involved in the inflammatory process, and also has antimicrobial properties that help to inhibit the growth of bacteria and other microorganisms in the affected area. Overall, Biclotymol is a powerful and effective treatment for various oral and throat infections, providing relief from pain and inflammation while combating the underlying microbial causes.

InChI:InChI=1/C21H26Cl2O2/c1-10(2)14-8-18(22)12(5)16(20(14)24)7-17-13(6)19(23)9-15(11(3)4)21(17)25/h8-11,24-25H,7H2,1-6H3

Upstream product

• 50-00-0 formaldehyd 
• 89-68-9 4-chloro-2-isopropyl-5-methylphenol 

Related news

Collective relaxation dynamics and crystallization kinetics of the amorphous Biclotymol (cas 15686-33-6) antiseptic09/01/2019

We employ dielectric spectroscopy to monitor the relaxation dynamics and crystallization kinetics of the Biclotymol antiseptic in its amorphous phase. The glass transition temperature of the material as determined by dielectric spectroscopy is Tg = 290 ± 1 K. The primary (α) relaxation dynamic...detailed

Relevant articles and documents

New aluminum 2,2′-methylenebis(4-chloro-3-methyl-6-(isopropyl) phenoxides): Structural characterization of an unusual ionic aluminum bisphenoxide [Al(THF)4(Cl)2]+[Al(mcmip) 2]-·x THF

The synthesis and X-ray structure determination of an uncommon ionic aluminum bisphenoxide [Al(THF)4(Cl)2] +[Al(mcmip)2]-·1.1 THF (1) and its neutral analogue (mcmip)Al(CH2CH3)(THF) (2) are reported (mcmipH2: 2,2′-methylenebis(4-chloro-3-methyl-6-(isopropyl) phenol). The ligand was reacted in THF with diethyl aluminum chloride, respectively triethyl aluminum, under liberation of ethane to yield crystalline aluminum bisphenoxides. Compound 2 exhibits the usual structural features found in neutral THF-aluminum bisphenoxides adducts whereas the ionic compound 1 consists of a cationic octahedral aluminum dichloride moiety, [Al(THF) 4(Cl)2], and an anionic di-bisphenoxide aluminate fragment [Al(mcmip)2] containing two 2,2′-methylenebis(4-chloro-3- methyl-6-(isopropyl)phenol) ligands. Both aluminum bisphenoxides were tested as catalysts in the copolymerization of cyclohexene oxide with CO2 and displayed similar good catalytic activities although the carbonate amounts present in the copolymer remain low.