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Merck
CN

M80407

Sigma-Aldrich

2-Methylresorcinol

technical grade, 90%

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
Beilstein:
2042177
EC Number:
210-155-8
MDL number:
MFCD00002271
UNSPSC Code:
12352100
PubChem Substance ID:
24897216
NACRES:
NA.22

Key Documents

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grade

technical grade

Assay

90%

form

crystals

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

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Signal Word

Danger

Hazard Statements

H301,H317,H318,H400

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
1408526V
1396436V
MKBN3659V
BCBJ1868V
BCBF5192V

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T A Re et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 7(2), 287-292 (1986-08-01)
2-methylresorcinol (2-MR) was administered to groups of 40 male and 35 female Sprague-Dawley rats by admixture with diets at levels of 0.1, 0.4, and 1.5% for periods up to 6 months. Methemoglobin levels were determined after 6 weeks. After 90
T A Re et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 7(2), 293-298 (1986-08-01)
2-Methylresorcinol (2-MR) was administered to groups of 40 male and 35 female Sprague-Dawley rats by admixture with the diets at levels of 0.1, 0.4, and 1.5% (see Part I; T.H. Re, R.F. Loehr, S.C. Rodriguez, C.E. Gilmore, and C.M. Burnett
C Naumann et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 7(8), 1637-1645 (2001-05-15)
The preparation of cavitands composed of 4, 5, 6, and 7 aromatic subunits ([n]cavitands, n=4-7) is described. The simple, two-step synthetic procedure utilized readily available starting materials (2-methylresorcinol and diethoxymethane). The two cavitand products having 4 and 5 aromatic subunits
Hye Jung Choi et al.
Journal of microbiology and biotechnology, 22(9), 1214-1217 (2012-07-21)
One Helicosporium strain, isolated from a wilted chestnut tree, evidenced in vitro antimicrobial activity against various types of bacteria and fungi, and generated a diffusible pigment. The antimicrobial compounds and the diffusible pigment of the Helicosporium sp. isolate were purified
O K Davydova et al.
Mikrobiologiia, 75(5), 654-661 (2006-11-10)
We established that chemical analogues of alkylhydroxybenzenes (AHB), belonging to alkylresorcinols and functioning as microbial autoregulatory d1 factors, enhance the UV resistance of various DNA molecules of different origin and conformation. These include the linear DNA of the lambda phage
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