20344-49-4[Fe+3].[O-2].[OH-]IEECXTSVVFWGSE-UHFFFAOYSA-MAn antiferromagnetic material; constitutes the core of natural ferritin.
20344-49-4DTXSID3042057CHEMBL4802224Breast Feeding; Lactation; Milk, Human; Ferric Compounds; Hematinics; Iron Compounds
FDA approved drugs -> Active ingredient
FDA approved drugs -> Active ingredient
reddish-brown crystalline solid
안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.
This chemical does not meet GHS hazard criteria for 100% (1312 of 1312) of all reports.
Not Classified
Aggregated GHS information provided per 1312 reports by companies from 3 notifications to the ECHA C&L Inventory.
Chemical: Iron hydroxide oxide, (Fe(OH)O)
Iron hydroxide oxide (Fe(OH)O) is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Iron hydroxide oxide (Fe(OH)O) are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Ferric hydroxide: Does not have an individual approval but may be used under an appropriate group standard
24 [mg/m3]
260 [mg/m3]
1600 [mg/m3]
87PZU03K0K
FERRIC OXYHYDROXIDE
Established Pharmacologic Class [EPC] - Phosphate Binder
Mechanisms of Action [MoA] - Phosphate Chelating Activity
Ferric oxyhydroxide is a Phosphate Binder. The mechanism of action of ferric oxyhydroxide is as a Phosphate Chelating Activity.
Wholesale and Retail Trade
Iron hydroxide oxide (Fe(OH)O): ACTIVE
용도In purifying water; as absorbent in chemical processing; as pigment; as catalyst.
일반 설명contains varying amounts of MgO2, SiO2, CaO, Al2O3
A cold solution of 810 g of Fe(NO3)39H2O in two liters of water is poured slowly, with vigorous stirring, into an ammonia solution prepared by dissolving 120 g of gaseous NH3 in two liters of water (cooling necessary). The hydroxide which precipitates is amorphous to x-ray analysis. It is washed by stirring at least five times with eight-liter portions of cold water, each portion being decanted as completely as possible. The residual slurry is then stirred with sufficient cone. KOH solution to give a mixture approximately 2N and allowed to stand for 3-4 hours. Finally 100℃ steam is bubbled through for two hours. The precipitate is thereby transformed completely into bright-yellow α-FeO(OH), which shows a crystalline x-ray diffraction pattern.
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