Amylmetacresol

Amylmetacresol Basic information
Product Name:Amylmetacresol
Synonyms:5-methyl-2-pentyl-pheno;5-methyl-2-pentylphenol;6-n-amyl-m-cresol;6-n-pentyl-m-cresol;6-pentyl-m-creso;6-PENTYL-M-CRESOL;6-AMYL-M-CRESOL;5-Methyl-2-(pent-1-yl)phenol 97%
CAS:1300-94-3
MF:C12H18O
MW:178.27
EINECS:215-094-0
Product Categories:
Mol File:1300-94-3.mol
Amylmetacresol Structure
Amylmetacresol Chemical Properties
Melting point 24°C
Boiling point 139°C/15mmHg(lit.)
density 0.9414 (estimate)
refractive index 1.5120 to 1.5160
storage temp. Inert atmosphere,Room Temperature
solubility Practically insoluble in water, very soluble in acetone and in ethanol (96 per cent).
form neat
pka10.55±0.35(Predicted)
color Yellow to Dark Orange
EPA Substance Registry SystemPhenol, 5-methyl-2-pentyl- (1300-94-3)
Safety Information
Hazard Codes Xn
Risk Statements 22
RIDADR UN 3145 8/PG III
RTECS GP3100000
HazardClass 8
PackingGroup III
HS Code 2907199090
MSDS Information
Amylmetacresol Usage And Synthesis
Chemical PropertiesClear or almost clear liquid, or solid crystalline mass, colourless or slightly yellow when freshly prepared. The substance changes colour during storage by darkening and/or discolouration to dark yellow, brownish-yellow or pink.
UsesAntiseptic. Amylmetacresol is an antiseptic available in Canada over-the-counter in a number of lozenges for the treatment of sore throat and minor mouth infections,. Amylmetacresol is often combined with dichlorobenzyl alcohol and menthol in the commonly used sore throat lozenges, known as Strepsils. The acute sore throat (pharyngitis) is one of the most common conditions for which children are seen in the primary care setting. Pharyngitis is normally caused by viruses and proves benign and self-limiting. Clinically proven, over-the-counter throat lozenges offer rapid and effective relief of acute sore throat symptoms, and are increasingly important in the management of this condition.
DefinitionChEBI: Amylmetacresol is a phenol having the structure of m-cresol substituted at the 6-position with an amyl group. It has a role as an antiseptic drug. It derives from a m-cresol.
Mode of actionThe mechanism of virucidal action is not fully elucidated, however it is suggested that denaturation of external protein spikes, a pH-induced rearrangement of the tertiary structure of attachment proteins, or a selective effect on viral lipid membranes/protein–lipid interaction is responsible for this action. Amylmetacresol is an antibacterial and antiviral agent, and blocks voltage-gated Na channels in a local anesthetic-like manner.
Amylmetacresol Preparation Products And Raw materials
Raw materials2'-Hydroxy-4'-Methylvalerophenone-->Valeryl chloride-->m-Cresol
DELTA9-TETRAHYDROCANNABINOL Adriamycin D-gamma-Tocopherol DL-ALPHA-TOCOPHEROL HYDROGEN SUCCINATE NOGALAMYCIN D-alpha-Tocopheryl acetate DL-α-Tocopherol Vitamin E nicotinate Cresol Vitamin E AMMONIUM CARMINATE DL-ALPHA-TOCOPHEROL ACETATE 7,8-Dimethyltocol (+/-)-11-NOR-9-CARBOXY-DELTA9-THC (+/-)-ALPHA-TOCOPHEROL PHOSPHATE DISODIUM SALT LABOTEST-BB LT00244777 D-α-Tocopherol succinate 3,5,6,8-TETRAHYDROXY-1-METHYL-9,10-DIOXO-7-((2S,3S,4S,5R,6S)-3,4,5-TRIHYDROXY-6-HYDROXYMETHYL-TETRAHYDRO-PYRAN-2-YL)-9,10-DIHYDRO-ANTHRACENE-2-CARBOXYLIC ACID

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