83194-70-1 Usage
Description
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester, also known as methyl 2,6-dimethyl-4-hydroxybenzoate, is a chemical compound with the molecular formula C10H12O3. It is a methyl ester derivative of 2,6-dimethyl-4-hydroxybenzoic acid and is characterized by its white to yellowish crystalline powder form with a faint odor. 2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is soluble in most organic solvents and is known for its antimicrobial and antioxidant properties.
Uses
Used in Food Industry:
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is used as a food preservative and flavoring agent for its ability to extend the shelf life and enhance the taste of various food products.
Used in Personal Care and Cosmetics Industry:
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is used as an antimicrobial and antioxidant agent in the formulation of personal care products and cosmetics, helping to protect the products from microbial contamination and oxidation, thus ensuring their safety and efficacy.
Used in Pharmaceutical Industry:
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is used in the production of pharmaceuticals due to its antimicrobial and antioxidant properties, which can contribute to the stability and effectiveness of medications.
Used in Fragrance Industry:
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is used as a component in the production of fragrances, providing a unique scent and enhancing the overall aroma of perfumes and other scented products.
Used in Sunscreen Products:
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is used as a UV filter in sunscreen products, offering protection against harmful ultraviolet radiation and helping to prevent skin damage.
It is important to handle 2,6-diMethyl-4-hydroxybenzoic acid Methyl ester with care, as it can be harmful if swallowed, inhaled, or comes into contact with the skin. Proper safety measures should be taken during its use and production to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 83194-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,9 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83194-70:
(7*8)+(6*3)+(5*1)+(4*9)+(3*4)+(2*7)+(1*0)=141
141 % 10 = 1
So 83194-70-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-6-4-8(11)5-7(2)9(6)10(12)13-3/h4-5,11H,1-3H3
83194-70-1Relevant articles and documents
Facile Synthesis of Halogen Decorated para -/ meta -Hydroxybenzoates by Iridium-Catalyzed Borylation and Oxidation
Shahzadi, Tayyaba,Saleem, Rahman S. Z.,Chotana, Ghayoor A.
, p. 4336 - 4342 (2018/11/23)
Hydroxybenzoates are an important class of phenols that are widely used as preservatives and antiseptics in the food and pharmaceutical industries. In this report, a facile preparation of 2,6- and 2,3-disubstituted 4/5-hydroxybenzoates by iridium-catalyze
METHOD OF MANUFACTURING 4-HYDROXY-2-METHYLBENZOIC ACID DERIVATIVE
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Paragraph 0049, (2016/11/17)
PROBLEM TO BE SOLVED: To provide a method for manufacturing 4-hydroxy-2-methylbenzoic esters simply in a short time. SOLUTION: There is provided a method for manufacturing a 4-hydroxy-2-methylbenzoic acid derivative (1) by air oxidizing a 2-methyl-4-oxo-2
The use of Hagemann's Esters to prepare highly functionalized phenols and benzenes
Majetich, George,Allen, Scott
, p. 104 - 124 (2012/11/07)
Hagemann's esters can be converted into highly functionalized phenols or arenes. The systematic functionalization of Hagemann's ester derivatives permits the preparation of tri-and tetraalkyl-substituted phenols or tetra-, penta-, and hexaalkyl-substituted benzenes. Kotnis's aromatization procedure was found to be solvent dependent, and Suzuki couplings were found to be sensitive to steric hindrance. Wittig olefination and ortho-Claisen reactions were reliable means to introduce alkyl substituents at C-4 and/or C-5 positions, respectively. The acid-promoted dehydration of tertiary alcohol 46 to produce enone 47, followed by its selective alkylation (cf. 48) is new. ARKAT USA, Inc.