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Merck
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Key Documents

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27-0220

Sigma-Aldrich

Resorcinol

SAJ first grade, ≥98.0%

Sinónimos:

1,3-Bencenodiol

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About This Item

Fórmula lineal:
C6H4-1,3-(OH)2
Número de CAS:
108-46-3
Peso molecular:
110.11
Beilstein/REAXYS Number:
906905
EC Number:
203-585-2
MDL number:
MFCD00002269
UNSPSC Code:
12352002
PubChem Substance ID:
329752897

grade

SAJ first grade

vapor density

3.8 (vs air)

vapor pressure

1 mmHg ( 21.1 °C)

assay

≥98.0%

form

solid

autoignition temp.

1126 °F

availability

available only in Japan

bp

178 °C/16 mmHg (lit.)

mp

109-112 °C (lit.)

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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signalword

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

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

wgk_germany

WGK 2

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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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
Alastair B Ross
Journal of agricultural and food chemistry, 60(36), 8954-8962 (2012-08-14)
Alkylresorcinols are phenolic lipids, with homologues ranging from C17 to C25, found in high concentrations in whole grain wheat and rye, lower concentrations in barley, and negligible concentrations in refined wheat flour. The analysis of alkylresorcinols is of importance due
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)
Fotini Karavassili et al.
Acta crystallographica. Section D, Biological crystallography, 68(Pt 12), 1632-1641 (2012-11-16)
The effects of the ligands phenol and resorcinol on the crystallization of human insulin have been investigated as a function of pH. Powder diffraction data were used to characterize several distinct polymorphic forms. A previously unknown polymorph with monoclinic symmetry
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
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