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Supelco

Resorcinol

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

Sinonimo/i:

1,3-Benzenediol

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About This Item

Formula condensata:
C6H4-1,3-(OH)2
Numero CAS:
108-46-3
Peso molecolare:
110.11
Beilstein:
906905
Numero CE:
203-585-2
Numero MDL:
MFCD00002269
Codice UNSPSC:
41116107
ID PubChem:
329757871
NACRES:
NA.24

Grado

certified reference material
TraceCERT®

Livello qualitativo

300

Densità del vapore

3.8 (vs air)

Tensione di vapore

1 mmHg ( 21.1 °C)

Nome Commerciale

TraceCERT®

Temp. autoaccensione

1126 °F

Durata

limited shelf life, expiry date on the label

Produttore/marchio commerciale

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Condizioni di stoccaggio

under inert gas

tecniche

HPLC: suitable
gas chromatography (GC): suitable

P. eboll.

178 °C/16 mmHg (lit.)

Punto di fusione

109-112 °C (lit.)

applicazioni

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Stringa SMILE

Oc1cccc(O)c1

InChI

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

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Descrizione generale

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

Applicazioni

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

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Altre note

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

Note legali

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

Avvertenze

Danger

Indicazioni di pericolo

H302,H315,H317,H318,H370,H371,H410

Classi di pericolo

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

Organi bersaglio

Central nervous system,Blood, Respiratory system

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

260.6 °F - closed cup

Punto d’infiammabilità (°C)

127 °C - closed cup

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG1973
BCBW1281
BCBN3032V
BCBJ8541V
BCBJ8541

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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
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
Claudia E Calderón et al.
Molecular plant-microbe interactions : MPMI, 26(5), 554-565 (2013-04-04)
To determine the genetic basis by which 2-hexyl, 5-propyl resorcinol (HPR) is produced by the biocontrol rhizobacterium Pseudomonas chlororaphis (formerly known as P. fluorescens) PCL1606, the presence and role of dar genes were investigated. To accomplish this aim, the pCGNOV-1
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
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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