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10341-45-4

2,4-DIMETHYL-6-(METHYLTHIOMETHYL)PHENOL, commonly known as thymol, is a natural monoterpene phenol derived from thyme oil and other essential oils. It possesses antiseptic, antimicrobial, and antifungal properties, making it a versatile compound with applications in various industries.

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  • 10341-45-4 Structure

  • Basic information

    1. Product Name: 2,4-DIMETHYL-6-(METHYLTHIOMETHYL)PHENOL
    2. Synonyms: Mesitol, a2-(methylthio)- (8CI)
    3. CAS NO:10341-45-4
    4. Molecular Formula: C10H14OS
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10341-45-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: 1.576
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,4-DIMETHYL-6-(METHYLTHIOMETHYL)PHENOL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-DIMETHYL-6-(METHYLTHIOMETHYL)PHENOL(10341-45-4)
    11. EPA Substance Registry System: 2,4-DIMETHYL-6-(METHYLTHIOMETHYL)PHENOL(10341-45-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10341-45-4(Hazardous Substances Data)

10341-45-4 Usage

Uses

Used in Food Industry:
2,4-DIMETHYL-6-(METHYLTHIOMETHYL)PHENOL is used as a flavoring agent for its distinctive aromatic properties, enhancing the taste and aroma of various food products.
Used in Pharmaceutical Industry:
2,4-DIMETHYL-6-(METHYLTHIOMETHYL)PHENOL is used as an antiseptic and antimicrobial agent in pharmaceutical formulations, helping to prevent infections and promote healing.
Used in Oral Care Industry:
2,4-DIMETHYL-6-(METHYLTHIOMETHYL)PHENOL is used as an active ingredient in oral care products, such as mouthwashes and toothpastes, for its antiseptic and antimicrobial effects, promoting oral hygiene and preventing dental issues.
Used in Traditional Medicine:
2,4-DIMETHYL-6-(METHYLTHIOMETHYL)PHENOL is used in traditional medicine for its therapeutic benefits in treating respiratory and digestive disorders, as well as for its antioxidant and antinociceptive effects.
Used in Pesticide Industry:
2,4-DIMETHYL-6-(METHYLTHIOMETHYL)PHENOL is used as a pesticide and insect repellent due to its insecticidal and acaricidal properties, providing an effective solution for controlling pests in agricultural and household settings.

Check Digit Verification of cas no

The CAS Registry Mumber 10341-45-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10341-45:
(7*1)+(6*0)+(5*3)+(4*4)+(3*1)+(2*4)+(1*5)=54
54 % 10 = 4
So 10341-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H14OS/c1-7-4-8(2)10(11)9(5-7)6-12-3/h4-5,11H,6H2,1-3H3

10341-45-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethyl-6-(methylsulfanylmethyl)phenol

1.2 Other means of identification

Product number -
Other names 2,4-DI-TERT-BUTYLPHENOL-D18

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10341-45-4 SDS

10341-45-4Downstream Products

10341-45-4Relevant articles and documents

Convenient Preparation of N-Acylbenzoxazines from Phenols, Nitriles, and DMSO Initiated by a Catalytic Amount of (COCl)2

Wang, Hao,Xi, Zeyu,Huang, Shuai,Ding, Rui,Gao, Yang,Liu, Yongguo,Sun, Baoguo,Tian, Hongyu,Liang, Sen

, p. 4932 - 4943 (2021)

A convenient preparation method of N-acylbenzoxazines has been developed, in which phenols react with nitriles and dimethyl sulfoxide (DMSO) in the presence of a catalytic amount of (COCl)2 in CH3CN or chloroform to afford the corresponding N-acylbenzoxaz

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