Skip to Content
Merck
All Photos(2)

Key Documents

447420

Sigma-Aldrich

Orcinol

97%

Synonym(s):

5-Methylresorcinol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3C6H3-1,3-(OH)2
CAS Number:
Molecular Weight:
124.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

106-112 °C (lit.)

SMILES string

Cc1cc(O)cc(O)c1

InChI

1S/C7H8O2/c1-5-2-6(8)4-7(9)3-5/h2-4,8-9H,1H3

InChI key

OIPPWFOQEKKFEE-UHFFFAOYSA-N

Application

Orcinol can be used to synthesize:
  • Orcinol-containing azacryptands for use in optical amplifiers and light-emitting devices.
  • Ternary co-crystal with 4,4′-bipyridine.
  • Low-density carbon aerogels in the presence of formaldehyde.
  • PEG-orcinol coumarins with potent tyrosinase inhibitory activity.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Karen J Marsh et al.
Ecology, 87(8), 2103-2112 (2006-08-30)
Most herbivores eat more and survive better when they have access to a variety of foods. One explanation involves the detoxification of plant secondary metabolites (PSMs). By feeding from a variety of plants that contain different classes of PSMs, animals
Shape and size mimicry in the design of ternary molecular solids: towards a robust strategy for crystal engineering
Tothadi S, et al.
Chemical Communications (Cambridge, England), 47(44), 12080-12082 (2011)
Mikkel Schultz-Johansen et al.
Frontiers in microbiology, 9, 839-839 (2018-05-19)
Marine microbes are a rich source of enzymes for the degradation of diverse polysaccharides. Paraglaciecola hydrolytica S66T is a marine bacterium capable of hydrolyzing polysaccharides found in the cell wall of red macroalgae. In this study, we applied an approach
PEG-immobilization of cardol and soluble polymer-supported synthesis of some cardol-coumarin derivatives: Preliminary evaluation of their inhibitory activity on mushroom tyrosinase
Tocco G, et al.
Bioorganic & Medicinal Chemistry Letters, 19(1), 36-39 (2009)
One-pot synthesis of new functionalized azacryptands from resorcinol derivatives for advanced photonic materials
Ka J-W and Kim HK
Tetrahedron Letters, 45(23), 4519-4523 (2004)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service