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W358908

Sigma-Aldrich

Resorcinol

≥98%, FG

Synonym(s):

1,3-Benzenediol

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About This Item

Linear Formula:
C6H4-1,3-(OH)2
CAS Number:
108-46-3
Molecular Weight:
110.11
FEMA Number:
3589
Beilstein:
906905
EC Number:
203-585-2
Council of Europe no.:
11250
MDL number:
MFCD00002269
UNSPSC Code:
12164502
PubChem Substance ID:
24901799
Flavis number:
4.047
NACRES:
NA.21

biological source

synthetic

grade

FG
Fragrance grade
Halal

Agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 110

vapor density

3.8 (vs air)

vapor pressure

1 mmHg ( 21.1 °C)

Assay

≥98%

form

flakes

autoignition temp.

1126 °F

bp

178 °C/16 mmHg (lit.)
178 °C/16 mmHg

mp

109-112 °C (lit.)

solubility

H2O: 5%, colorless to faintly yellow

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

fragrance allergen

no known allergens

Organoleptic

creamy; musty

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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Certificates of Analysis (COA)

Lot/Batch Number
SHBN9570
SHBN9552
SHBM2245
MKCJ1781
MKCJ3872

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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
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
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
Ahmed M Elkhatat et al.
Advanced materials (Deerfield Beach, Fla.), 23(26), 2887-2903 (2011-05-25)
An overview on the preparation and properties of resorcinol-formaldehyde (RF) organic and carbon gels reveals the fascinating and remarkably flexible properties of RF carbon and organic gels and how these properties are related to the synthesis and processing conditions. The
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