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1,3-BenzenediMethanol, 5-Methyl, commonly known as "5-Methylresorcinol," is a derivative of resorcinol (1,3-dihydroxybenzene) with a methyl group attached at the fifth position. It has the chemical formula C7H8O2 and appears as yellow solid crystals with a sweet smell. This biodegradable chemical possesses antioxidant, antiseptic, and preservative properties. It is slightly soluble in water and fully soluble in ethanol, ether, and several other organic solvents. Due to its potential to cause skin and eye irritation, it should be handled with care.

27711-63-3

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27711-63-3 Usage

Uses

Used in Cosmetic Industry:
1,3-BenzenediMethanol, 5-Methyl is used as a skin lightening agent for its ability to reduce the production of melanin, leading to a lighter skin complexion.
Used in Pharmaceutical Industry:
1,3-BenzenediMethanol, 5-Methyl is used as an antiseptic and preservative due to its antimicrobial properties, which help prevent the growth of bacteria and other microorganisms in various pharmaceutical products.
Used in Antioxidant Applications:
1,3-BenzenediMethanol, 5-Methyl is used as an antioxidant to protect against oxidative stress and damage, which can be beneficial in various health and wellness products.

Check Digit Verification of cas no

The CAS Registry Mumber 27711-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,7,1 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27711-63:
(7*2)+(6*7)+(5*7)+(4*1)+(3*1)+(2*6)+(1*3)=113
113 % 10 = 3
So 27711-63-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2/c1-7-2-8(5-10)4-9(3-7)6-11/h2-4,10-11H,5-6H2,1H3

27711-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(hydroxymethyl)-5-methylphenyl]methanol

1.2 Other means of identification

Product number -
Other names 11.31-Dioxy-1.3.5-trimethyl-benzol

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:27711-63-3 SDS

27711-63-3Relevant academic research and scientific papers

AMINOGUANIDINE HYDRAZONES AS RETROMER STABILIZERS USEFUL FOR TREATING NEUROLOGICAL DISEASES

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Page/Page column 20-21; 45-47; 50, (2020/10/20)

The present invention relates to novel aminoguanidine hydrazone-derivatives of Formula (I) which are effective as retromer stabilizers and useful as neuroprotecting drugs. The invention also relates to pharmaceutical compositions comprising the compounds and their use in therapy and diagnostic.

Synthesis of monodeoxycalix[4]arene and its dimer structure in solution

Fukazawa,Deyama,Usui

, p. 5803 - 5806 (2007/10/02)

Monodeoxycalix[4]arene (3) has been synthesized by a stepwise condensation method. It forms dimer in solution, the structure of which has an arrangement of the two cone of 3 facing the respective narrower rim with each other. A cyclic hydrogen bonding array of six hydroxyl groups in the dimer was suggested from the thermodynamic parameters of the monomer-dimer equilibrium.

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