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Merck

135011

1,2-Dihydroxybenzene

≥99%, solid, ReagentPlus®

Synonym(s):

Pyrocatechol, 1,2-Benzenediol, 1,2-Dihydroxybenzene, 2-Hydroxyphenol, Catechol

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About This Item

Linear Formula:
C6H4-1,2-(OH)2
CAS Number:
120-80-9
Molecular Weight:
110.11
NACRES:
NA.21
PubChem Substance ID:
24848193
UNSPSC Code:
12352100
EC Number:
204-427-5
MDL number:
MFCD00002188
Beilstein/REAXYS Number:
471401
Assay:
≥99%
Form:
solid

Key Documents

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Product Name

1,2-Dihydroxybenzene, ReagentPlus®, ≥99%

vapor density

3.8 (vs air)

Quality Level

200

vapor pressure

1 mmHg ( 75 °C), 10 mmHg ( 118.3 °C)

product line

ReagentPlus®

assay

≥99%

form

solid

bp

245 °C (lit.)

mp

100-103 °C (lit.)

SMILES string

Oc1ccccc1O

InChI

1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H

InChI key

YCIMNLLNPGFGHC-UHFFFAOYSA-N

General description

1,2-Dihydroxybenzene (a phenolic compound) is a useful industrial chemical. It is an ortho isomeric form of dihydroxybenzene. It is commonly referred to as catechol or pyrocatechol. Its standard molar enthalpy of combustion and sublimation at 298.15K have been evaluated by static-bomb calorimetry and microcalorimetry, respectively.

Application

1,2-Dihydroxybenzene may be used as raw material for the industrial synthesis of rubber, dyes, plastics, pharmaceuticals and cosmetics.
1,2-Dihydroxybenzene in combination with amberlite XAD-2, can be used as a chelating resin in the determination of metal ions, using atomic absorption spectrophotometry (AAS).

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Carc. 1B - Eye Dam. 1 - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

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

wgk

WGK 3

flash_point_f

260.6 °F - closed cup

flash_point_c

127 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKAA0672
MKAA0673
10024AJ
10412ME
02504MH

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Carbon nanoparticle-chitosan composite electrode with anion, cation, and neutral binding sites: Dihydroxybenzene selectivity.
Amiri M, et al.
Sensors and Actuators B, Chemical, 162(1), 194-200 (2012)
Enthalpies of combustion of 1, 2-dihydroxybenzene and of six alkylsubstituted 1, 2-dihydroxybenzenes.
Da Silva MDMCR, et al.
The Journal of Chemical Thermodynamics, 16(12), 1149-1155 (1984)
Thiago C Canevari et al.
The Analyst, 138(1), 315-324 (2012-11-17)
This paper describes the development, characterization and application of an Nb(2)O(5) film formed on the surface of a carbon ceramic material, SiO(2)/C, obtained by a sol-gel method, using the spin-coating technique. The working electrode using this material will be designated
Catechol suppresses EGF-induced cell transformation by inhibiting ERK2 activity as confirmed by a crystallographic study.
Malakhova M, et al.
Cancer Research, 73(8), 2234-2234 (2013)
Synthesis, characterization and applications of pyrocatechol modified amberlite XAD-2 resin for preconcentration and determination of metal ions in water samples by flame atomic absorption spectrometry (FAAS)
Tewari KP and Singh KA
Talanta, 53(4), 823- 833 (2001)
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Global Trade Item Number

SKUGTIN
135011-3KG04061838730442
135011-500G04061835252749

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