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Resorcinol

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

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:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material
TraceCERT®

Quality Level

vapor density

3.8 (vs air)

vapor pressure

1 mmHg ( 21.1 °C)

product line

TraceCERT®

autoignition temp.

1126 °F

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

storage condition

under inert gas

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

178 °C/16 mmHg (lit.)

mp

109-112 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

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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General description

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Resorcinol, a dihydric phenol or a phenyl derivative, is a versatile chemical compound, utilized extensively in a variety of applications including cosmetics, pharmaceuticals, agricultural chemicals, rubber/wood industries, flame retardants, manufacturing of specialty chemicals, antioxidants, etc.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

This compound is commonly found in plants of the genus: allium zingiber

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

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


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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
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
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
Maurizio Scaltriti et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 18(17), 4508-4513 (2012-06-22)
Many kinases and hormone receptors, important for cancer cell proliferation and survival, bind to and are dependent on the Hsp90 cycle for their folding and maturation. This provides the rationale for the development of small-molecule ATP competitors that, inhibiting Hsp90

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