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C3561

Sigma-Aldrich

Pyrocatechol

suitable for plant cell culture, BioReagent, ≥99%, powder

Synonym(s):

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
Beilstein:
471401
EC Number:
204-427-5
MDL number:
MFCD00002188
UNSPSC Code:
12352100
PubChem Substance ID:
24892626
NACRES:
NA.21

vapor density

3.8 (vs air)

Quality Level

200

vapor pressure

1 mmHg ( 75 °C)
10 mmHg ( 118.3 °C)

product line

BioReagent

Assay

≥99%

form

powder

technique(s)

cell culture | plant: suitable

color

white to faint beige

bp

245 °C (lit.)

mp

100-103 °C (lit.)

solubility

water: 50 mg/mL, clear, colorless to faintly yellow

storage temp.

room temp

SMILES string

Oc1ccccc1O

InChI

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

InChI key

YCIMNLLNPGFGHC-UHFFFAOYSA-N

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Caution

May discolor on exposure to air and light.

Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SLBZ4680
SLBR4636V
SLBN8170V
SLBM1940V
SLBK4027V

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Christian J Kastrup et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(52), 21444-21449 (2012-12-14)
The treatment of diseased vasculature remains challenging, in part because of the difficulty in implanting drug-eluting devices without subjecting vessels to damaging mechanical forces. Implanting materials using adhesive forces could overcome this challenge, but materials have previously not been shown
Myung-Hyun Ryou et al.
Advanced materials (Deerfield Beach, Fla.), 25(11), 1571-1576 (2013-01-03)
Conjugation of mussel-inspired catechol groups to various polymer backbones results in materials suitable as silicon anode binders. The unique wetness-resistant adhesion provided by the catechol groups allows the silicon nanoparticle electrodes to maintain their structure throughout the repeated volume expansion
R D Irons
Journal of toxicology and environmental health, 16(5), 673-678 (1985-01-01)
Occupational exposure to benzene has long been associated with toxicity to the blood and bone marrow, including lymphocytopenia, pancytopenia, aplastic anemia, acute myelogenous leukemia, and possibly lymphoma. A variety of studies have established that benzene itself is not the toxic
R Zand et al.
Clinical pharmacology and therapeutics, 54(2), 142-149 (1993-08-01)
We studied the effect of isoniazid administration on the cytochrome P4502E1-catalyzed elimination of chlorzoxazone and acetaminophen. Isoniazid, 300 mg daily, was administered for 7 days to a group of 10 volunteer slow acetylators. Acetaminophen, 500 mg, and chlorzoxazone, 750 mg
Jacques Poupaert et al.
Current medicinal chemistry, 12(7), 877-885 (2005-04-28)
The 2(3H)-benzoxazolone heterocycle and its bioisosteric surrogates (such as 2(3H)-benzothiazolinone, benzoxazinone, etc.) have received considerable attention from the medicinal chemists owing to their capacity to mimic a phenol or a catechol moiety in a metabolically stable template. These heterocycles and
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