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Resorcinol is an organic compound with the formula C₆H₄(OH)₂. It is one of three isomeric benzenediols, the 1,3-isomer (or meta-isomer). It is a white, water-soluble solid. Resorcinol crystallizes from benzene as colorless needles that are readily soluble in water, alcohol, and ether, but insoluble in chloroform and carbon disulfide.
Resorcinol is mainly used in the production of resins. As a mixture with phenol, it condenses with formaldehyde to afford adhesives.

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1,3-Dimethoxybenzene or Resorcinol (or resorcin) is an organic compound with the formula C₆H₄(OH)₂. It is one of three isomeric benzenediols, the 1,3-isomer (or meta-isomer). It is a white, water-soluble solid. 

It is produced in several steps from benzene, starting with dialkylation with propylene to give 1,3-diisopropylbenzene. Oxidation and Hock rearrangement of this disubstituted arene gives acetone and resorcinol.^[5]

Although of little commercial value, many additional routes exist for resorcinol. It can produced when any of a large number of resins (e.g., galbanum, asafoetida, etc.) are melted with potassium hydroxide, or by the distillation of Brazilwood extract. It may be prepared synthetically by melting 3-iodophenol, phenol-3-sulfonic acid, or benzene-1,3-disulfonic acid with potassium carbonate; by the action of nitrous acid on 3-aminophenol or on 1,3-diaminobenzene.^[6] Many ortho- and para-compounds of the aromaticseries (for example, the bromophenols, benzene-para-disulfonic acid) also yield resorcinol on fusion with potassium hydroxide.

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