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R5645

Sigma-Aldrich

Resorcinol

BioXtra, ≥99%

Synonym(s):

1,3-Benzenediol

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About This Item

Linear Formula:
C6H4-1,3-(OH)2
CAS Number:
Molecular Weight:
110.11
Beilstein:
906905
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.31

vapor density

3.8 (vs air)

Quality Level

vapor pressure

1 mmHg ( 21.1 °C)

product line

BioXtra

Assay

≥99%

form

powder

autoignition temp.

1126 °F

impurities

≤0.005% Phosphorus (P)
≤0.1% Insoluble matter

ign. residue

≤0.1%

bp

178 °C/16 mmHg (lit.)

mp

109-112 °C (lit.)

solubility

H2O: 1 M at 20 °C, clear, faintly yellow

anion traces

chloride (Cl-): ≤0.05%
sulfate (SO42-): ≤0.05%

cation traces

Al: ≤0.0005%
Ca: ≤0.0005%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Mg: ≤0.0005%
NH4+: ≤0.05%
Na: ≤0.005%
Pb: ≤0.001%
Zn: ≤0.0005%

SMILES string

Oc1cccc(O)c1

InChI

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

InChI key

GHMLBKRAJCXXBS-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1B - STOT SE 1 Oral - STOT SE 2 Oral

Target Organs

Central nervous system,Blood, Respiratory system

Storage Class Code

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

WGK

WGK 2

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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Phosphate-functionalized carbon monoliths from deep eutectic solvents and their use as monolithic electrodes in supercapacitors.
Daniel Carriazo et al.
ChemSusChem, 5(8), 1405-1409 (2012-07-06)
Antonio B Fuertes et al.
Chemical communications (Cambridge, England), 48(49), 6124-6126 (2012-05-15)
Core@shell spheres made up of a thin layer of resorcinol-formaldehyde enveloping a silica core were prepared by means of a one-step method under Stöber conditions. These spheres are used as a platform for the synthesis of carbon or polymeric capsules
S L da Silva et al.
European journal of medicinal chemistry, 44(1), 312-321 (2008-04-22)
Phospholipases A(2) are enzymes responsible for the hydrolysis of membrane phospholipids that release arachidonic acid, which serves as substrate for pro-inflammatory mediators, such as prostaglandins and leucotriens. The design of specific inhibitors for PLA(2) might help in the development of
Anton V Gulevich et al.
Journal of the American Chemical Society, 134(12), 5528-5531 (2012-03-15)
The efficient Pd-catalyzed double-fold C-H oxygenation of arenes into resorcinols using the newly developed 2-pyrimidyldiisopropylsilyl (PyrDipSi) directing group is described. Its use allows for the sequential introduction of OAc and OPiv groups in a one-pot manner to produce orthogonally protected
Jinjun Li et al.
Environmental science & technology, 46(22), 12648-12654 (2012-10-25)
Graphitized carbons with mesoporous and macroporous structures were synthesized by a facile template-catalysis procedure using resorcinol and formaldehyde as carbon precursors and particulate hydrated metal oxides as both template and catalyst precursors. The materials were used as novel adsorbents for

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