Detail of > 28300-74-5
- MSDS Download

- CAS Number:
- 28300-74-5
- Name:
Antimonate(2-), bis[m-[2,3-di(hydroxy-kO)butanedioato(4-)-kO1:kO4]]di-, potassium, hydrate (1:2:3), stereoisomer
- Superlist Name:
- Potassium antimonyl tartrate sesquihydrate
- Formula:
- C8H4K2O12Sb2.3(H2O)
- Molecular Structure:
![Molecular Structure of 28300-74-5 (Antimonate(2-), bis[m-[2,3-di(hydroxy-kO)butanedioato(4-)-kO1:kO4]]di-, potassium, hydrate (1:2:3), stereoisomer)](http://www.lookchem.com/300w/2010/0620/28300-74-5.jpg)
- Synonyms:
- Antimonate(2-),bis[m-[2,3-di(hydroxy-kO)butanedioato(4-)-kO1:kO4]]di-, dipotassium, trihydrate, stereoisomer (9CI);Antimonate(2-), bis[m-tartrato(4-)]di-, dipotassium, trihydrate (8CI);Antimonate(1-),aqua[tartrato(4-)]-, potassium, sesquihydrate, dimer;Antimony potassium tartrate;Antimonyl potassium tartrate, sesquihydrate;Butanedioic acid, 2,3-dihydroxy- (2R,3R)-, antimony potassium salt;Potassium antimony tartrate;Tartaremetic;Tartox;
- Molecular Weight:
- 667.87
- EINECS:
- 234-293-3
- Density:
- 2.607 g/cm3
- Melting Point:
- ≥300 °C(lit.)
- Solubility:
- water: 8.3 g/100 mL
- Appearance:
- colourless crystals
- Hazard Symbols:
Xn,
N- Risk Codes:
- 20/22-51/53
- Safety:
- 61Details
- Transport Information:
- UN 1551 6.1/PG 3
- Deleted CAS:
- 12125-10-9|1332-41-8|1332-43-0|16039-64-8|26282-95-1|304-61-0|53318-72-2|8012-64-4
Related products
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Reference
- Liver monoamine oxidase (MAO) in liver homogenate of mice infected with Schistosoma mansoni and effect of certain therapeutic agents
- Liver monoamine oxidase (MAO) in liver homogenate of mice infected with Schistosoma mansoni and effect of certain therapeutic agents. Abdel Samad, M. M.; Guirgis, F. K.; Zeitoun, R.; El-Feki, R. F.; Awadalla, H. N. (Alexandria Univ., Alexandria, Egypt). Tropenmed. Parasitol., 28(4), 554-9 (English) 1977. CODEN: TMPRAD. ISSN: 0303-4208. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) Section cross-reference(s): 14 MAO [9001-66-5] activity in liver homogenates of mice infected with S. mansoni decreased starting the sixth wk following infection, reaching a min. by the eighth wk. These changes obviously denote progress of hepatic fibrosis. Treatment of the infected mice with tartar emetic [28300-74-5], stibophen [15489-16-4], niridazole [61-57-4] and hycanthone [3105-97-3] returned the enzyme level to almost normal value. This may indicate the ease with which the lesions in the liver, inclucing fibrosis, recover when the infection is successfully treated.
- Dyeing of leather substitutes containing an elastomer
- Dyeing of leather substitutes containing an elastomer. (Toray Industries, Inc., Japan). Jpn. Kokai Tokkyo Koho JP 59199878 A2 13 Nov 1984 Showa, 4 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: D06P005-00. APPLICATION: JP 83-68300 20 Apr 1983. DOCUMENT TYPE: Patent CA Section: 38 (Plastics Fabrication and Uses) Leather substitutes composed of polyamide fibers and an elastomer are dyed, then treated with mixts. contg. natural or semisynthetic tannic acid and tartar emetic (I) [28300-74-5] and finally treated with a surfactant to improve their colorfastness. Thus, a leather substitute prepd. from nylon fibers and a polyurethane, was dyed with a soln. of (NH4)2SO4, C.I. Acid Brown 226, and C.I. Acid Red 318. The dyed material was treated with a liquor contg. vegetable tannic acid, I, citric acid, and AcOH, washed, treated with aq. soln. of Bisnol A 30 [95078-07-2] (nonionic surfactant) washed, and dried to give a dark colored leather substitute having excellent fastness to washing.
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