Sodium thiosulfate

remove iodine stains, e.g. after the explosion of nitrogen triiodide.

In bacteriological water assessment.

In the tanning of leather.

To demonstrate the concept of reaction rate in chemistry classes. The thiosulfate ion can decompose into the sulfite ion and a colloidal suspension of sulfur, which is opaque. The equation for this acid-catalysed reaction is as follows:

S2O32(aq) SO32(aq) + S(s)

To demonstrate the concept of supercooling in physics classes. Melted sodium thiosulfate is very easy to overcool to room temperature and when crystallization is forced, the sudden temperature jump to 48.3C can be experienced by touch.

As part of patina recipes for copper alloys.

Often used in pharmaceutical preparations as an anionic surfactant to aid in dispersion.

It can also be used as a very interesting solute in supersaturation experiments.

References

^ a b Holleman, A. F.; Wiberg, E. “Inorganic Chemistry” Academic Press: San Diego, 2001. ISBN 0-12-352651-5

^ Charles Robert Gibson (1908). The Romance of Modern Photography, Its Discovery & Its Achievements. Seeley & Co. p. 37. http://books.google.com/books?id=whYaAAAAMAAJ&pg=PA37&dq=hyposulphite-of-soda+herschel+fixer+hypo&lr=&as_brr=1&as_pt=ALLTYPES&ei=czVdSaipAYWekwSc_vW5Dg. 

^ Aylmore, M. G.; Muir, D. M. “Thiosulfate Leaching of Gold – a Review”, Minerals Engineering, 2001, 14, 135-174

^ “Toxicity, Cyanide: Overview – eMedicine”. http://emedicine.medscape.com/article/814287-overview. Retrieved 2009-01-01. 

^ Hall AH, Dart R, Bogdan G (June 2007). “Sodium thiosulfate or hydroxocobalamin for the empiric treatment of cyanide poisoning?”. Ann Emerg Med 49 (6): 80613. doi:10.1016/j.annemergmed.2006.09.021. PMID 17098327. 

^ Cicone JS, Petronis JB, Embert CD, Spector DA (June 2004). “Successful treatment of calciphylaxis with intravenous sodium thiosulfate”. Am. J. Kidney Dis. 43 (6): 11048. doi:10.1053/j.ajkd.2004.03.018. PMID 15168392. 

^ Sodium thiosulfate at Dorland’s Medical Dictionary

v  d  e

  Sodium compounds

NaAlO2  NaBH3(CN)  NaBH4  NaBr  NaBrO4  NaCH3COO  NaCN  NaC6H5CO2  NaC6H4(OH)CO2  NaCl  NaClO  NaClO2  NaClO3  NaClO4  NaF  NaH  NaHCO3  NaHSO3  NaHSO4  NaI  NaIO3  NaIO4  NaMnO4  NaNH2  NaNO2  NaNO3  NaN3  NaOH  NaO2  NaPO2H2  NaReO4  NaSCN  NaSH  NaTcO4  NaVO3  Na2CO3  Na2C2O4  Na2CrO4  Na2Cr2O7  Na2MnO4  Na2MoO4  Na2O  Na2O2  Na2O(UO3)2  Na2S  Na2SO3  Na2SO4  Na2S2O3  Na2S2O4  Na2S2O5  Na2S2O6  Na2S2O7  Na2S2O8  Na2SeO3  Na2SeO4  Na2SiO3  Na2Te  Na2TeO3  Na2Ti3O7  Na2U2O7  NaWO4  Na2Zn(OH)4  Na3N  Na3P  Na3VO4  Na4Fe(CN)6   Na5P3O10

v  d  e

Antifungals (D01 and J02)

Wall/

membrane

Ergosterol

inhibitors

Azoles

(lanosterol 14

alpha-demethylase inhibitors)

Imidazoles

topical: Bifonazole, Clomidazole, Clotrimazole#, Croconazole, Econazole, Fenticonazole, Ketoconazole, Isoconazole, Miconazole#, Neticonazole, Oxiconazole, Sertaconazole, Sulconazole, Tioconazole

Triazoles

topical: (Fluconazole#, Fosfluconazole)

systemic: (Fluconazole, Itraconazole, Posaconazole, Voriconazole)

Benzimidazoles

topical: Thiabendazole

Polyene antimycotics

(ergosterol binding)

topical: (Natamycin, Nystatin#)

systemic: (Amphotericin B#)

Allylamines

(squalene monooxygenase

inhibitors)

topical: (Amorolfine, Butenafine, Naftifine, Terbinafine)

systemic: (Terbinafine)

-glucan synthase

inhibitors

echinocandins (Anidulafungin, Caspofungin, Micafungin)

Intracellular

Pyrimidine analogues/

Thymidylate synthase inhibitors

Flucytosine#

Mitotic inhibitors

Griseofulvin#

Others

Bromochlorosalicylanilide  Methylrosaniline  Tribromometacresol  Undecylenic acid  Polynoxylin  Chlorophetanol  Chlorphenesin  Ticlatone  Sulbentine  Ethyl hydroxybenzoate  Haloprogin  Salicylic acid  Selenium sulfide#  Ciclopirox  Amorolfine  Dimazole  Tolnaftate  Tolciclate  Sodium thiosulfate#  Whitfield’s ointment#  Potassium iodide#

Tea tree oil citronella oil lemon grass orange oil patchouli lemon myrtle

PCP: Pentamidine Dapsone Atovaquone

#WHO-EM. Withdrawn from market. CLINICAL TRIALS: hase III. Never to phase III

see also diseases

v  d  e

Antidotes (V03AB)

Nervous system

Nerve agent / Organophosphate poisoning

Atropine#  Biperiden  Diazepam#  Oximes (Pralidoxime, Obidoxime)  see also Cholinesterase

Opioid overdose

Diprenorphine  Doxapram  Nalorphine  Naloxone#  Naltrexone  Nalmefene

Barbiturate overdose

Bemegride  Ethamivan

Benzodiazepine overdose

Cyprodenate  Flumazenil

GHB overdose

Physostigmine  SCH-50911

Reversal of neuromuscular

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