Phenols

Aromatic organic compounds that consist of a phenyl functional group (−C6H5) bonded to a hydroxyl functional group (−OH). Includes compounds with more substitutions and derivatives.

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1,726 – 1,740 of 12,116 results

1,726

Medchemexpress LLC Hydroquinone diacetate | 1205-91-0 | MFCD00011643 | 98.3% | 194.19 g/mol | C10H10O4 | 50 MG

Hydroquinone diacetate is an acetylated derivative of hydroquinone used in organic and medicinal chemistry. Supplied as a high-purity research chemical, it is used in synthetic applications and as an ingredient in some skin-lightening formulations.

Acetylated hydroquinone derivative used in organic and medicinal chemistry.
High purity (98.3%) suitable for research applications.
Molecular formula C10H10O4; molecular weight ≈ 194.19 g/mol.
White to off-white solid; typically supplied as a powder.
Available in small research quantities (for example, 50 mg) and as pre-made DMSO solution for reconstitution.
CAS number 1205-91-0 for unambiguous identification.

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1,727

eMolecules Hydroquinone monosulfate potassium salt | 37067-27-9 | MFCD00059841 | 1g

Combi-Blocks | Hydroquinone monosulfate potassium salt | 1g | 267203280 | QG-9511 | 95.000 | 37067-27-9 | MFCD00059841 | 228.260 | C6H5KO5S

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1,728

Electron Microscopy Sciences Hydroquinone 2% 250 ML

References: Genta PM., Robason GO, Graham DY-Simultaneous Visualization of Helicobactor Pylon and Gastric Morphology A New Stain Hum Pathol. 25:22 1-226, 1994.

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1,729

eMolecules 3-Methoxycatechol | 934-00-9 | MFCD00002191 | 25g

Combi-Blocks | 3-Methoxycatechol | 25g | 415500301 | QC-7853 | 96.000 | 934-00-9 | MFCD00002191 | 140.138 | C7H8O3

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1,730

Cayman Chemical 3-Methoxycatechol 5g

A lignan-derived phenol; a GPR35 agonist (EC50 = 147 µM in a DMR assay) using HT-29 cells; promotes esophageal carcinogenesis in rats at 2% in the diet either alone or in a multiorgan model of nitrosamine-induced carcinogenesis; has been used as a precursor in the enzymatic synthesis of pyrogallol and purpurogallin; has been used as a precursor in the electro-organic synthesis of coumestan derivatives