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Catechol, 99%
GREENER_CHOICE

CAS: 120-80-9 | C6H6O2 | 110.11 g/mol

$61.21 - $626.38

Chemical Identifiers

CAS 120-80-9
Molecular Formula C6H6O2
Molecular Weight (g/mol) 110.11
MDL Number MFCD00002188
InChI Key YCIMNLLNPGFGHC-UHFFFAOYSA-N
Synonym pyrocatechol, catechol, 1,2-dihydroxybenzene, 1,2-benzenediol, pyrocatechin, 2-hydroxyphenol, o-benzenediol, pyrocatechine, o-dihydroxybenzene, o-dioxybenzeneShow MoreShow Less
PubChem CID 289
ChEBI CHEBI:18135
IUPAC Name benzene-1,2-diol
SMILES OC1=CC=CC=C1O
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Products 2
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Catalog Number Mfr. No. Quantity Price Quantity  
AAA1016430
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Thermo Scientific Chemicals
A1016430
250 g
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AAA101640I
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Thermo Scientific Chemicals
A101640I
5000 g
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Description

Description

Catechol is used as a developer for photographic films, dyes and an intermediate for antioxidants in rubber and lubricating oils. It is used in polymerization inhibitors and in pharmaceuticals. It is a building block in organic synthesis and involved in the preparation of flavors and fragrances. It is used as a replacement for sandalwood oil, which is prepared from catechol through guaiacol and camphor. Further, it is a precursor for the preparation of vanillin from guaiacol, which is obtained by methylation reaction with catechol.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Catechol is used as a developer for photographic films, dyes and an intermediate for antioxidants in rubber and lubricating oils. It is used in polymerization inhibitors and in pharmaceuticals. It is a building block in organic synthesis and involved in the preparation of flavors and fragrances. It is used as a replacement for sandalwood oil, which is prepared from catechol through guaiacol and camphor. Further, it is a precursor for the preparation of vanillin from guaiacol, which is obtained by methylation reaction with catechol.

Solubility
Soluble in water, pyridine, chloroform, benzene, carbon tetrachloride, ether and acetate.

Notes
Air and light sensitive. Incompatible with oxidizing agents, aluminum, bases, acid chlorides and acid anhydrides.
Specifications
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Safety and Handling

Safety and Handling

GHS H Statement
H301-H311-H318-H341-H351-H315

P201-P202-P261-P264b-P270-P271-P272-P280g-P281-P301+P310-P302+P352-P304+P340-P305+P351+P338-P308+P313-P310-P312-P330-P333+P313-P361-P363-P501c

H301+H311-H315-H317-H318-H332-H341-H350-H500

DOTInformation : Transport Hazard Class: 6.1; Packing Group: III; Proper Shipping Name: TOXIC SOLIDS, ORGANIC, N.O.S.

EINECSNumber : 204-427-5

RTECSNumber : UX1050000

TSCA : Yes

Recommended Storage : Ambient temperatures; Store under Argon

SDS
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RUO – Research Use Only