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302589

2-Methylresorcinol

Name: 2-Methylresorcinol
Brand: ALDRICH

98%

Synonym(s):

2,6-Dihydroxytoluene

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About This Item

Linear Formula:

CH₃C₆H₃(OH)₂

CAS Number:

608-25-3

Molecular Weight:

124.14

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24858264

EC Number:

210-155-8

Beilstein/REAXYS Number:

2042177

MDL number:

MFCD00002271

Assay:

98%

Form:

solid

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Properties

Quality Level

100

assay

98%

form

solid

bp

264 °C (lit.)

mp

114-120 °C (lit.)

SMILES string

Cc1c(O)cccc1O

InChI

1S/C7H8O2/c1-5-6(8)3-2-4-7(5)9/h2-4,8-9H,1H3

InChI key

ZTMADXFOCUXMJE-UHFFFAOYSA-N

Description

General description

The reaction between 2-methylresorcinol and 2-alkenals was studied to investigate the scavenging ability of m-diphenols for the 2-alkenals formed during lipid oxidation.

Application

2-Methylresorcinol was used in the synthesis of:

C-5-bromo-2-hydroxyphenylcalix[4]-2-methylresorcinarene
tripyrrane analogs
series of novel aromatic benziporphyrins

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pictograms

GHS06,GHS05,GHS09

signalword

Danger

hcodes

H301,H317,H318,H400

pcodes

P261 - P273 - P280 - P301 + P310 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Sens. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

275.0 °F - closed cup

flash_point_c

135 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Synthesis, characterization, X-ray structure and biological activities of C-5-bromo-2-hydroxyphenylcalix[4]-2-methyl resorcinarene.

Hamza M Abosadiya et al.

Molecules (Basel, Switzerland), 18(11), 13369-13384 (2013-11-01)

C-5-bromo-2-hydroxyphenylcalix[4]-2-methylresorcinarene (I) was synthesized by cyclocondensation of 5-bromo-2-hydroxybenzaldehyde and 2-methylresorcinol in the presence of concentrated HCl. Compound I was characterized by infrared and nuclear magnetic resonance spectroscopic data. X-ray analysis showed that this compound crystallized in a triclinic system with

Preparation of tripyrrane analogues from resorcinol and 2-methylresorcinol for applications in the synthesis of new benziporphyrin systems.

Kae Miyake et al.

Chemical communications (Cambridge, England), (2)(2), 178-179 (2004-01-23)

Acid catalyzed condensation of resorcinol or 2-methylresorcinol with 2 equiv. of an acetoxymethylpyrrole gave bis(pyrrolylmethyl)benzene derivatives in moderate yields; these afforded a series of novel aromatic benziporphyrins using the MacDonald "3 + 1" methodology.

2-Alkenal-scavenging ability of m-diphenols.

Francisco J Hidalgo et al.

Food chemistry, 160, 118-126 (2014-05-07)

The reaction between m-diphenols (resorcinol, 2-methylresorcinol, 2,5-dimethylresorcinol, 3-methylphenol, orcinol, and phloroglucinol) and 2-alkenals (2-pentenal and 2-octenal) was studied in an attempt to understand the chemical pathways involved in the scavenging ability of m-diphenols for the 2-alkenals produced as a consequence

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Global Trade Item Number

SKU	GTIN
302589-100G	04061826665930
302589-25G	04061826665947