ChemicalBook--->CAS DataBase List--->1309-37-1

1309-37-1

1309-37-1 Structure

1309-37-1 Structure
IdentificationMore
[Name]

Ferric oxide
[CAS]

1309-37-1
[Synonyms]

IRON(III) OXIDE DIHYDRATE
11554red
anchredstandard
anhydrousironoxide
anhydrousoxideofiron
armenianbole
bauxiteresidue
blackoxideofiron
blendedredoxidesofiron
burntislandred
burntsienna
c.i.pigmentred101
c.i.pigmentred101and102
c.i.pigmentred102
calcotonered
caputmortuum
colcothar
colloidalferricoxide
crocusmartisadstringens
deanox
[EINECS(EC#)]

215-168-2
[Molecular Formula]

Fe2O3
[MDL Number]

MFCD00748135
[Molecular Weight]

159.69
[MOL File]

1309-37-1.mol
Chemical PropertiesBack Directory
[Definition]

A high-grade red pigment used as a polishing agent for glass, jewelry, etc. (2) A cosmetic prepared from dried flowers of the saf- flower.
[Appearance]

Hematite is a noncombustible, black to black red or brick-red mineral (iron ore) composed mainly of ferric oxide, Fe2O3. Ferric oxide
[Melting point ]

1538°C
[density ]

5.24
[Fp ]

>230 °F
[storage temp. ]

2-8°C
[solubility ]

It is soluble In Warm Hydrochloric Acid, Slightly Soluble in Sulfuric Acid.
[form ]

pieces
[color ]

black
[Specific Gravity]

5.1~5.2
[PH]

3.7±0.3
[Stability:]

Stable.
[Water Solubility ]

INSOLUBLE
[Merck ]

14,4028
[Exposure limits]

ACGIH: TWA 5 mg/m3
OSHA: TWA 10 mg/m3; TWA 15 mg/m3; TWA 5 mg/m3
NIOSH: IDLH 2500 mg/m3; TWA 5 mg/m3
[Uses]

Ferric Oxide is a nutrient and dietary supplement that is a source of iron.
[CAS DataBase Reference]

1309-37-1(CAS DataBase Reference)
[IARC]

3 (Vol. 1, Sup 7) 1987
[NIST Chemistry Reference]

Iron(iii) oxide(1309-37-1)
[EPA Substance Registry System]

1309-37-1(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xi,F
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[WGK Germany ]

-
[RTECS ]

NO7400000
[TSCA ]

Yes
[HS Code ]

28211000
[Hazardous Substances Data]

1309-37-1(Hazardous Substances Data)
[IDLA]

2,500 mg Fe/m3
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Sodium hydroxide-->Hydrochloric acid-->Sulfuric acid-->Iron-->Ammonium bicarbonate-->Oxygen-->Ferrous sulfate heptahydrate-->Iron oxide-->PYRITE-->3-METHOXYPROPIONIC ACID-->Ferric nitrate-->Micaceous Iron Oxide-->Sodium oleate-->Complexing agent-->Mica-->FERROUS CARBONATE-->Iron Oxide Black-->Aniline sulfate-->Ferric oxalate-->Hematite
[Preparation Products]

Oleic acid-->Styrene-->PAINT-->o-Cresol-->Iron oxide red phenolic antirust paint-->Phenolic resin paint-->Triiron tetraoxide-->Various color nitrocellulose exterior enamel Q04-2-->Red lead alkyd antirust paint
Hazard InformationBack Directory
[Hazard]

Questionable carcinogen.
[Potential Exposure]

Hematite; as an iron ore composed mainly of ferric oxide, is a major source of iron and is used as a pigment for rubber, paints, paper, linoleum, ceramics, dental restoratives; and as a polishing agent for glass and pre cious metals. It is also used in electrical resistors, semiconduc tors, magnets, and as a catalyst. Human exposure to hematite from underground hematite mining is principally through inhalation and/or ingestion of dusts. No estimates are available concerning the number of underground miners exposed.
[First aid]

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, includ ing resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medi cal attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit.
[Incompatibilities]

Contact with hydrogen peroxide, ethyl ene oxide, calcium hypochlorite will cause explosion. Violent reaction with powdered aluminum; hydrazine, hydrogen trisulfide.
[Description]

Iron oxides are produced synthetically and consist essentially of anhydrous and/or hydrated iron oxides. The range of hues includesyellows, reds, browns and blacks. Food quality iron oxides are primarily distinguished from technical grades by the comparatively low levels of contamination by other metals. This is achieved by the selection and control of the source of iron and/or by the extent of chemical purification during the manufacturing process. Iron oxides have been used to color confectionery, fillings and decorations for pastry products, cheese products, fish paste, pet foods, cosmetics and pharmaceutical products.
[Chemical Properties]

Hematite is a noncombustible, black to black red or brick-red mineral (iron ore) composed mainly of ferric oxide, Fe2O3. Ferric oxide
[Occurrence]

Iron(III) oxide occurs in nature as the mineral hematite. It is the principal ore of iron from which the metal and its alloys are produced. Also, this oxide occurs in the mineral, limonite, 2Fe2O3?3H2O. An important application of this compound involves producing red, orange, and yellow pigments. Other applications are in coatings for metals, steel and rubber; in ceramics; and as a catalyst for oxidation reactions.
[Flammability and Explosibility]

Nonflammable
[Carcinogenicity]

Welders are typically exposed to a complex mixture of dust and fume of metallic oxides, as well as irritant gases, and are subject to mixeddust pneumoconiosis with possible loss of pulmonary function; this should not be confused with benign pneumoconiosis caused by iron oxide.1 Although an increased incidence of lung cancer has been observed among hematite miners exposed to iron oxide, presumably owing to concomitant radon gas exposure, there is no evidence that iron oxide alone is carcinogenic to man or animals.6
[storage]

Color Code- Green: General storage may be used.Prior to working with this chemical you should be trainedonits proper handling and storage. Store in tightly closedcontainers in a cool, well-ventilatedarea. .Where possible,automatically transfer material from other storage contain-ers to process containers A regulated, marked area shouldbe established where this chemical is handled, used, orstored in compliance with OSHA Standard 1910.1045.
[Properties and Applications]

TEST ITEMS

SPECIFICATION

APPEARANCE

DARK RED POWDER

SHADE

CLOSE TO STANDARD

CONTENT OF Fe 2 O 3

96% min

pH VALUE

3-7

OIL ABSORPTION

15-25%

RESIDUE ON 320 MESH

0.3% max

WATER SOLUBLE

0.3% max

VOLATITE 105 °C

1.0% max

TINTING STRENGTH

98-102 %

Questions And AnswerBack Directory
[Physical Properties]

Reddish-brown hexagonal crystal; refractive index 2.91; density 5.25g/cm3; Moh’s hardness 6.0; melts at 1565°C; insoluble in water; dissolves in acids.
red iron oxide powder
[Occurrence and Uses]

Ferric oxide occurs in nature as the mineral hematite. It is the principal ore of iron from which the metal and its alloys are produced. Also, this oxide occurs in the mineral, limonite, 2Fe2O3•3H2O. An important application of this compound involves producing red, orange, and yellow pigments. Other applications are in coatings for metals, steel and rubber; in ceramics; and as a catalyst for oxidation reactions.
[Preparation]

Ferric oxide is prepared as a reddish-brown hydrated precipitate by treating an aqueous solution of an iron(III) salt with caustic soda:
2FeCl3 + 6NaOH → Fe2O3•3H2O + 6NaCl
It also is obtained by thermal decomposition of iron(II) sulfate or the brown oxide hydroxide:
2FeSO4 → Fe2O3 + SO2 + SO3
2FeO(OH) → Fe2O3 + H2O
The oxide is prepared in industrial scale by first precipitating iron(II) hydroxide Fe(OH)2 by treating aqueous solutions of iron(II) sulfate and caustic soda. The Fe(OH)2 is then oxidized to iron(III) hydroxide by aeration. The latter is dehydrated by heating:
Fe2+ (aq) + OH¯ (aq) → Fe(OH)2(s) → 2Fe(OH)3 → Fe2O3 + 3H2O
It also is produced by ignition of iron(III) oxalate and iron carbonyls:
2Fe2(C2O4)3 +3O2 → 2Fe2O3 + 12CO
[Reactions]

Ferric oxide decomposes to its elements when heated at elevated temperatures:
2Fe2O3 → 4Fe + 3O2
The oxide is reduced by most reducing agents. Reaction with carbon monoxide at elevated temperatures (that occurs in the blast furnace) gives metallic iron. The overall reaction is mildly exothermic (ΔHrxn –113.4 kcal/mol):
2 Fe2O3 + 6CO → 4Fe + 6CO2
It also is reduced by powdered aluminum at elevated temperatures, forming aluminum oxide and metallic iron:
Fe2O3 + 2Al → Al2O3 + 2Fe
The reaction is highly exothermic and becomes self-sustaining after ignition.
When heated with sand in an electric furnace, iron(III) oxide forms ferrosilicon alloy. When heated in a vacuum at 1,000°C, it forms triiron tetroxide, Fe3O4.
Spectrum DetailBack Directory
[Spectrum Detail]

Ferric oxide(1309-37-1)IR1
Ferric oxide(1309-37-1)IR2
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Iron(III) oxide, 99.999%,-100 mesh(1309-37-1)
[Alfa Aesar]

Iron(III) oxide, Puratronic, 99.998% (metals basis)(1309-37-1)
[Sigma Aldrich]

1309-37-1(sigmaaldrich)
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