Thymol

OtherC10H14OCAS: 89-83-8Shelf life: 60 mo
Thymol
Image: NEUROtikerPublic domain

Physical Properties

  • Molecular Weight: 150.22 g/mol

Also known as: 2-isopropyl-5-methylphenol, 5-methyl-2-isopropylphenol, thyme camphor, 3-hydroxy-p-cymene, IPMP

Thymol (2-isopropyl-5-methylphenol; C₁₀H₁₄O; CAS 89-83-8) is a naturally-occurring phenolic compound originally extracted from thyme oil. In photographic chemistry it serves a single but important niche role: antimicrobial preservative in hand-coated silver gelatin emulsions and in a handful of alternative-process working solutions where warm gelatin is an ideal bacterial/fungal culture medium.[1]

Photographic uses

  • Silver-gelatin emulsion preservative: A few crystals of thymol (dissolved in a drop or two of ethanol as a carrier, since thymol is nearly insoluble in water) added to a finished hand-coated emulsion prevents bacterial breakdown during the weeks-to-months of storage between batches. Without a preservative, gelatin at room temperature becomes a thin soup within days. Typical dose: 0.02–0.05 % w/v of the finished emulsion — a dose-by-crystals approach in practice.
  • Mordançage working-solution preservative: The copper-chloride / hydrogen-peroxide / acetic-acid mordançage bath is rapidly colonized by bacteria if reused; a pinch of thymol extends its working life from hours to days.
  • Gum bichromate coating preservative (humid climates): In warm humid darkrooms, gum-dichromate coatings can develop mold before exposure. Thymol-saturated ethanol misted over dried coatings prevents this.

Practical notes

Supplied as white-to-pale-yellow crystals or crystalline chunks with a strong, medicinal thyme odor. Melts at about 50 °C (so the solid can soften on warm darkroom shelves). Nearly insoluble in water (<1 g/L at 20 °C) — always dissolve first in a small volume of ethanol or isopropyl alcohol, then add the alcoholic solution to the emulsion or bath. A 1 % w/v stock in ethanol is a convenient working form — one or two drops is usually enough per 100 ml of emulsion.

The characteristic odor persists in finished coatings for days; some alternative-process practitioners prefer odorless alternatives in heavily-ventilated workspaces.

Related compounds

Phenol (carbolic acid) was the classical emulsion preservative before thymol displaced it; phenol is much more toxic and is no longer recommended. Formaldehyde works but is unacceptably toxic for routine use. Dichlorophen and Kathon CG are modern commercial alternatives sold specifically as photographic biocides.

References

  1. WEB Ross, Denise. The Light Farm thelightfarm.com. https://thelightfarm.com/
  2. WEB Sigma-Aldrich (Merck KGaA). Sigma-Aldrich Safety Data Sheets Sigma-Aldrich. https://www.sigmaaldrich.com/US/en/search/safety-data-sheets

Reference databases