447420
Orcinol
97%
Synonym(s):
5-Methylresorcinol
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About This Item
Linear Formula:
CH3C6H3-1,3-(OH)2
CAS Number:
Molecular Weight:
124.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
207-984-2
MDL number:
Product Name
Orcinol, 97%
InChI key
OIPPWFOQEKKFEE-UHFFFAOYSA-N
InChI
1S/C7H8O2/c1-5-2-6(8)4-7(9)3-5/h2-4,8-9H,1H3
SMILES string
Cc1cc(O)cc(O)c1
assay
97%
form
solid
mp
106-112 °C (lit.)
Quality Level
Related Categories
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Dibenzofurans from the marine sponge-derived ascomycete Super1F1-09.
Rateb ME, et al.
Botanica Marina, 53(6), 499-506 (2010)
Preparation of carbon aerogels from 5-methylresorcinol-formaldehyde gels
Perez-Caballero F, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 108(1-3), 230-236 (2008)
Yong-qi Tian et al.
Natural product research, 29(9), 820-826 (2014-12-30)
A new citromycetin analogue, ascomycotin A (1), together with eight known compounds, wortmannilactone E (2), orcinol (3), orsellinic acid (4), isosclerone (5), (3R,4S)-( - )-4-hydroxymellein (6), diorcinol (7), chaetocyclinone B (8) and 2,5-dimethoxy-3,6-di(p-methoxypheny1)-1,4-benzoquinone (9), was isolated from the fungal strain Ascomycota sp.
Goutam Ghosh et al.
Pharmacognosy research, 7(1), 110-113 (2015-01-20)
Clerodendrum viscosum is commonly found in India and Bangladesh. Previously, various parts of this plant were reported for treatment of different types of diseases and there was no report on GC-Ms analysis. To analyze and characterize the phytochemical compounds of
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)
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