Iron supplier | CasNO.7439-89-6

Name
Iron
EINECS 231-096-4
CAS No. 7439-89-6
Article Data1624
CAS DataBase
Density 1.05 g/mL at 20 °C
Solubility insoluble in water
Melting Point 1535 °C(lit.)
Formula Fe
Boiling Point 2750 °C(lit.)
Molecular Weight 55.847
Flash Point >230 °F
Transport Information UN 3264 8/PG 3
Appearance grey crystalline powder, rod or chips
Safety 26-16-33
Risk Codes 36/38-11-17
Molecular Structure
Hazard Symbols F, Xi
Synonyms Eisen;Ferrum;Hierro;Iron, elemental;
PSA 0.00000
LogP -0.00250

Synthetic route

: iron(III) oxide

: 7439-89-6
iron

Conditions

Conditions	Yield
With hydrogen In neat (no solvent) passing H2 over Fe2O3 at 350°C over period of 36 h, at 440°C 12 h or at 500°C in fast reaction;;	100%
With H2 In neat (no solvent) passing H2 over Fe2O3 at 350°C over period of 36 h, at 440°C 12 h or at 500°C in fast reaction;;	100%
With hydrogen In neat (no solvent) reduction of Fe2O3 at 600°C leads to formation of powdered Fe, at 1000°C formed Fe hardly fragile;;

: goethite

: 1333-74-0
hydrogen

: 7439-89-6
iron

Conditions

Conditions	Yield
In neat (no solvent) Isothermal heat treatment for 2 h at 400°C.;	100%

: iron(II) chloride

: 7439-89-6
iron

Conditions

Conditions	Yield
With 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclo-hexadiene In tetrahydrofuran at 20℃; for 6h; Inert atmosphere;	100%
With hydrogen In neat (no solvent) heated with H2 at approx. 350 °C; formation of pyrophoric Fe;;
With aluminium trichloride; 1-ethyl-3-methyl-1H-imidazol-3-ium chloride In melt Electrochem. Process; (He or Ar); dissoln. of FeCl2 in AlCl3/1-ethyl-3-methyimidazoline chloride ionic liquid (room temp.), chronoamperometric electrodeposition (tungsten electrode substrate, -0.35 V vs. Fe/Fe(II), 120 s, room temp.);

: 111496-23-2
LaFe(1+)

A: La(1+)

B: 7439-89-6
iron

Conditions

Conditions	Yield
In gas collision induced dissocn. reaction (argon) in a mass spectrometer; energy range 17-78 eV; total pressure: 4E-6 Torr; not isolated;	A 100% B 100%

: iron(III) oxide

: 7439-89-6
iron

Conditions

Conditions	Yield
With water; lithium chloride In melt at 660℃; for 5h; Inert atmosphere; Electrolysis;	98.4%

: 13463-40-6
iron pentacarbonyl

: 876938-53-3
Cyclohepta-1,3-diene

A: 40674-86-0
tricarbonyl(η-3-cyclohepta-1,3-diene)iron

B: 7439-89-6
iron

Conditions

Conditions	Yield
In dibutyl ether cycloheptadiene stirred in n-Bu2O while N2 bubbled through mixt. for 15h, Fe(CO)5 added, heated with stirring at 150°C for 44 h, cooled; filtered through Celite, evapd. in vac.;	A 93% B n/a

...Expand

: 7705-08-0
iron(III) chloride

: 22560-16-3
lithium triethylborohydride

: 7439-89-6
iron

Conditions

Conditions	Yield
In tetrahydrofuran FeCl3 in THF was added dropwise to stirring soln. of 12 ml LiBEt3H in THF (1.0 M), held at const. temp. under N2 atm.; forms of particles dependon dropping rate (1 drop/10s, 1/s, 2/s), stirring rate (200, 400, 1600 rpm) and temp.(0 - 60°C); vac. filtration, washed THF/EtOH (1:1), dried in vac.;	90%

: 1-trimethylsilyl-μ3-S,S'-ethylenedithiolatohexacarbonyldiiron

A: iron sulfide

B: (CH3)3SiC2H3S8Fe7

C: 7439-89-6
iron

D: 4-Trimethylsilanyl-[1,3]dithiolan-2-one

E: 754-05-2
ethenyltrimethylsilane

Conditions

Conditions	Yield
In decane byproducts: CH2CH2, CH3CHCH2, CO; Ar atmosphere; decompn. (165°C, 13 h); further products; GLC, chromato-mass spectroscopy;	A n/a B n/a C n/a D 5% E 75%

...Expand

: 14243-23-3
(μ-dithio)bis(tricarbonyliron)

: Fe3-μ-(o-C6H4CH2NPh)(CO)8

A: iron sulfide

B: Fe2-μ-(o-C6H4CH2NPh)(CO)6

C: Fe3(CO)9S2

D: 7439-89-6
iron

Conditions

Conditions	Yield
In n-heptane N2 atmosphere; stirring (70°C, 40 min); filtn., evapn., chromy. (silica gel);	A n/a B 66% C 25% D n/a

...Expand

: 12086-84-9
benzothiaferrole

A: 3986-98-9
2-thiocoumarin

B: 7439-89-6
iron

C: 95-15-8
Benzo[b]thiophene

Conditions

Conditions	Yield
flash vac. pyrolysis in a Pyrex tube connected with a cold trap (E-5 Torr, 285-315°C); coating of the hot zone by Fe, rinsing of trap with acetone, GC;	A <1 B n/a C 63%
With ceric ammonium nitrate In acetone addn. of (NH4)2Ce(NO3)6 to a stirred soln. of Fe-compound in acetone (5 min, air), stirring for 2 h; monitored by TLC (hexane), filtn. (Celite), dilution of filtrate with ether, filtn. and evapn. to dryness, GLC of white crystals in acetone, TLC (CH2Cl2/hexane=1:1), (1)H NMR, IR, elem. anal.;	A 35.5% B 36% C 4.4%

...Expand

: 13463-40-6
iron pentacarbonyl

: 7439-89-6
iron

Conditions

Conditions	Yield
In not given byproducts: CO; Sonication; soln. of Fe(CO)5 in diphenylmethane sonicated for 3 h under Ar at 30 °C to give iron nanoparticles; removed by centrifugation, washed with pentane, dried under vac., detd. by Moessbauer spectroscopy, XRD;	53%
In further solvent(s) under Ar; thermolysis of Fe(CO)5 using heterogeneous nucleation technique (Proc. Phys. Soc. A 1949, 62, 562); diluted 2 times with octyl ether; Fe(CO)5 added (100°C); heated (260°C); cooled; EtOH (3:1 volume ratio to octyl ether); collected with magnet;	40%
With cis-Octadecenoic acid In further solvent(s) under Ar; thermolysis of Fe(CO)5 using heterogeneous nucleation technique (Proc. Phys. Soc. A 1949, 62, 562); oleic acid:oleylamine 1:1 molar ratio; diluted 2 times with octyl ether; Fe(CO)5 added (100°C); heated (260°C); cooled; EtOH (3:1 volume ratio to octyl ether); collected with magnet;	40%

: lithiumpentamethylcyclopentadiene

: 75-08-1
ethanethiol

: iron(II) chloride

A: 12126-50-0
bis(pentamethylcyclopentadienyl)iron(II)

B: [(η5-pentamethylcyclopentadienyl)Fe(II)(μ2-SEt)3Fe(III)(η5-pentamethylcyclopentadienyl)]

C: 7439-89-6
iron

Conditions

Conditions	Yield
With n-BuLi In tetrahydrofuran; hexane under Ar; FeCl2 added at 0°C to stirred suspn. of (C5Me5)Li in THF; stirred (1 h); cooled to -78°C; suspn. prepared from n-BuLi inn-hexane and HSEt at 0°C added; 1 h at -78°C; warmed to r oom temp. with stirring overnight; evapd. to dryness; purified by column chromy. (neutral alumina, n-hexane); insol. solid washed with H2O (Fe); elem. anal.;	A 9% B 49% C 15%

...Expand

: 107339-80-0
(η4-1,3-butadiene)tris(triethylphosphine)iron(0)

A: 103835-78-5
bis(η4-1,3-butadiene)(triethylphosphino)iron(II)

B: 7439-89-6
iron

Conditions

Conditions	Yield
In tetrahydrofuran under Ar at 5°C;	A 40% B 40%

: 99611-53-7
iron(II) bromide dimethoxyethane adduct

: 1421320-35-5
potassium dimethylnopadienide

A: [Fe(η5-dimethylnopadienyl)2]

B: 7439-89-6
iron

Conditions

Conditions	Yield
In tetrahydrofuran; toluene at 20℃; for 4h; Inert atmosphere;	A 28% B n/a

...Expand

: Fe(CO)4(COCH2CH2O)

A: 646-06-0
1,3-DIOXOLANE

B: 7439-89-6
iron

Conditions

Conditions	Yield
With H2 In decalin High Pressure; 71.5 atm H2 at room temp., heated to 200°C and stirred for 24 h; pressure realesed, detn. by GC and GC-MS;	A 27% B n/a

: 13463-40-6
iron pentacarbonyl

A: 17685-52-8
triiron dodecarbonyl

B: 7439-89-6
iron

Conditions

Conditions	Yield
In n-heptane; decalin Sonication; 0°C (Ar); products identified IR, UV, mass spect., chromy.;	A 9.8% B n/a
In octane Sonication; 0°C (Ar); products identified IR, UV, mass spect., chromy.;	A 6.9% B n/a
In decalin Sonication; 0°C (Ar); 0.1 M Fe(CO)5; products identified IR, UV, mass spect., chromy.;	A 4.7% B n/a

: 13463-40-6
iron pentacarbonyl

: 1333-74-0
hydrogen

A: iron(II,III) oxide

B: 1345-25-1
iron(II) oxide

C: iron(III) oxide

D: cementite

E: 7439-89-6
iron

Conditions

Conditions	Yield
In neat (no solvent, gas phase) mixt. of vapor of Fe(CO)5 and H2 decomposed by plasma-chemical decomposition on Al2O3; monitored by XRD;	A n/a B n/a C n/a D 1% E n/a

...Expand

: 7782-61-8
ferric nitrate

: 7439-89-6
iron

Conditions

Conditions	Yield
Stage #1: ferric nitrate at 450℃; for 8h; Stage #2: With hydrogen at 500℃; for 16h;
In neat (no solvent) 15 min at 900°C under atomic hydrogen atmosphere;
With hydrogen In methanol Fe/MCM-41 prepd. by impregnation of MCM-41 with methanolic soln. of Fe(NO3)3 with stirring for 24 h under N2; catalyst filtered, washed with methanol, dried at 373 K and calcined at 773 K; catalyst reduced in H2 above 773 K;

: C26H28Br2N4O4

: 7439-89-6
iron

Conditions

Conditions	Yield
In tetrahydrofuran; methanol for 1h; Heating / reflux;

: ammonium tris(bi(tetrazolato)amine)ferrate(III)

: 7439-89-6
iron

Conditions

Conditions	Yield
Heating / reflux;

: 584-08-7
potassium carbonate

: potassium ferrocyanide

A: 590-28-3
potassium cyanate

B: potassium cyanide

C: 7439-89-6
iron

Conditions

Conditions	Yield
In melt at red heat; pression of KCN from iron sponge out;
In melt byproducts: N2; at red heat; extraction of KCN with H2O;
In melt at red heat; pression of KCN from iron sponge out;

...Expand

: ferrous(II) sulfate heptahydrate

: ammonium chloride

: 7439-89-6
iron

Conditions

Conditions	Yield
In water Electrolysis; electrolysis of aq. soln. of FeSO4*7H2O and NH3 leads to precipitation of light grey iron on cathode;;

: zinc ferrite

A: 7439-89-6
iron

B: 7440-66-6
zinc

Conditions

Conditions	Yield
With H2 In neat (no solvent) sample heating in TG apparatus in 25% H2/He (50 ml/min) at 5 K/min up to800°C; TG;

: iron(III) oxide

: 7439-89-6
iron

Conditions

Conditions	Yield
With hydrogen In neat (no solvent) Kinetics; byproducts: H2O; 300°C, carrier gas N2 or Ar + CH4 or CH4 + Ar + CO or air;
With hydrogen In gaseous matrix Kinetics; byproducts: H2O; sample redn. by 10% H2/Ar at 15 K/min up to 1000 K;
With hydrogen; gold In gaseous matrix Kinetics; byproducts: H2O; Au/Fe2O3 mixt. heating at 15 K/min in 10% H2/Ar (24 ml/min) up to 1260 K;
With hydrogen In gaseous matrix Kinetics; byproducts: H2O; sample heating at 15 K/min in 10% H2/Ar (24 ml/min) up to 1260 K;

: iron oxide

: 7439-89-6
iron

Conditions

Conditions	Yield
In sodium hydroxide aq. NaOH; Electrolysis; in 50 wt % NaOH/water electrolyte at 110°C using Pt cylinder counter electrode and steel/adsorbed hematite as cathode; at -1.2 V vs. Hg/HgO;
With hydrogen hematite redn. at 500°C under hydrogen;

: iron oxide

: 1333-74-0
hydrogen

: 7439-89-6
iron

Conditions

Conditions	Yield
In neat (no solvent) Kinetics; reduced at 252.5-383°C under conditions without an external diffusion effect; TEM;

: iron(II) metasilicate

: 7439-89-6
iron

Conditions

Conditions	Yield
In solid Electrolysis; electrolyzing molten FeSiO3 with addn. of either CaO or MgO leads to pptn. of Fe on cathode;;
In neat (no solvent) no redn. of feO to Fe in a stream of H at 850°C;;	0%
In neat (no solvent) no redn. of feO to Fe in a stream of H at 850°C;;	0%

: sodium iron(III) pyrophosphate

: 7439-89-6
iron

Conditions

Conditions	Yield
In not given Electrolysis; electrolyzing soln. of NaFeP2O7 with bath potential 4 V;; contains Fe2O3 and pyrophosphorous acid;;

: iron(II) chloride tetrahydrate

: 7439-89-6
iron

Conditions

Conditions	Yield
In water Electrolysis; electrolyzing soln. FeCl2*4H2O and NaCl (addn. of little HCl to clear soln.) at 50 to 70°C with current efficiency of 95 %;;
With ammonia In ethanol n-type Si(100) substrate coated with drop of soln. FeCl2*4H2O; dried; loaded on quartz boat into quartz tube reactor; heated under Ar; treated by NH3 with flow rate of 20 sccm for 1-10 min;
With sodium hydroxide In further solvent(s) heating FeCl2*4H2O and NaOH in propylene glycol; X-ray diffraction;

: 907994-35-8
4,4-dimethyl-3-(2-nitrobenzyl)-2-oxazolidinone

: 7439-89-6
iron

: 907993-76-4
4,4-dimethyl-3-(2-aminobenzyl)-2-oxazolidinone

Conditions

Conditions	Yield
With ammonium chloride In ethanol; water	100%

: 907994-36-9
5-methyl-3-(2-nitrobenzyl)-2-oxazolidinethione

: 7439-89-6
iron

: 907993-79-7
5-methyl-3-(2-aminobenzyl)-2-oxazolidinethione

Conditions

Conditions	Yield
With ammonium chloride In ethanol; water	100%

: 907994-37-0
5-ethyl-3-(2-nitrobenzyl)-2-oxazolidinone

: 7439-89-6
iron

: 907993-80-0
5-ethyl-3-(2-aminobenzyl)-2-oxazolidinone

Conditions

Conditions	Yield
With ammonium chloride In ethanol; water	100%

: 907994-43-8
5,5-dimethyl-3-(2-nitrobenzyl)thiazolidine-2-one

: 7439-89-6
iron

: 907994-20-1
3-(2-aminobenzyl)-5,5-dimethylthiazolidine-2-one

Conditions

Conditions	Yield
With ammonium chloride In ethanol; water	100%

: 280759-64-0
3-hexyl-6-methyl-6-(3-nitrophenyl)-3-azabicyclo[3.1.0]hexan-2-one

: 7439-89-6
iron

: 6-(3-Aminophenyl)-3-hexyl-6-methyl-3-azabicyclo[3.1.0]hexan-2-one

Conditions

Conditions	Yield
With calcium chloride In ethanol; water	100%

: 3-hexyl-6-isopropyl-6-(3-nitrophenyl)-3-azabicyclo[3.1.0]hexane

: 7439-89-6
iron

: 3-(3-hexyl-6-isopropyl-3-azabicyclo[3.1.0]hex-6-yl)aniline

Conditions

Conditions	Yield
With calcium chloride In ethanol; dichloromethane; water	100%

: 3-hexyl-6-(3-nitrophenyl)-6-propyl-3-azabicyclo[3.1.0]hexane

: 7439-89-6
iron

: 3-(3-hexyl-6-propyl-3-azabicyclo[3.1.0]hex-6-yl)aniline

Conditions

Conditions	Yield
With calcium chloride In ethanol; dichloromethane; water	100%

: 3-Hexyl-6-(3-nitrophenyl)-6-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexane-2,4-dione

: 7439-89-6
iron

: 3-Hexyl-6-(3-aminophenyl)-6-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexane-2,4-dione

Conditions

Conditions	Yield
With calcium chloride In ethanol; dichloromethane; water	100%

: 7647-01-0
hydrogenchloride

: 7732-18-5
water

: 7439-89-6
iron

: iron(II) chloride tetrahydrate

Conditions

Conditions	Yield
In water soln. of Fe in concd. HCl was refluxed; ppt. filtered off, washed with Et2O, dried in vac.;	100%
In hydrogenchloride evapn. a soln. of iron filings in dild. aq. HCl over iron filings until the hot soln. starts foaming; crystn. on cooling;; filtn.; crystn.; drying in a stream of dry air at 30-40°C;;
In hydrogenchloride evapn. a soln. of iron filings in dild. aq. HCl over iron filings until the hot soln. starts foaming; crystn. on cooling;; filtn.; crystn.; drying in a stream of dry air at 30-40°C;;
In water slight excess of 0.1 M hydrochloric acid added to iron powder, heated to dissolution; evapd.;
In hydrogenchloride iron powder and aq. HCl;

...Expand

: 64-18-6
formic acid

: 7732-18-5
water

: 7439-89-6
iron

: iron(II) formate dihydrate

Conditions

Conditions	Yield
at 250℃; for 16h; Inert atmosphere;	100%
In not given HCOOH was neutralized with Fe at 70-80°C; filtered, concd., cooled to room temp., recrystd. from water, dried in air;
Inert atmosphere;
Inert atmosphere;
In neat (no solvent) at 80℃;

...Expand

: 917-23-7
5,10,15,20-tetraphenyl-21H,23H-porphine

: 7439-89-6
iron

: 16591-56-3
5,10,15,20-tetraphenyl porphyrin iron

Conditions

Conditions	Yield
In toluene byproducts: H2; cocondensation of iron and toluene vapor at liq. nitrogen temp.; heating to -94.6°C; dropwise addn. of porphine soln. under nitrogen to the slurry (molar ratio Fe:porphine 4:1); gradually warming to 0°C, 1h; filtration; evapn. of filtrate;	100%
With Ag(111) In neat (no solvent) deposition of porphyrin deriv. onto silver by evapn. at 638 K, removing excess of porphyrin at 550 K, deposition of stoich. amount of iron; Buchner F., Schwald V., Cmanici K., Steinrueck H.-P., Marbach H. ChemPhysChem 2007, 8, 241-243; XPS and UPS;

: 7439-89-6
iron

: 132-42-3
picrolonic acid

: iron picrolonate*H2O

Conditions

Conditions	Yield
With HClO4 In water iron fillings dissolve in dilute HClO4, added aq. NaOH, resulting soln. added to aq. picrolonic acid at room temp.; ppt. filtered, washed with water, ethanol, ether, dried in vac. till constant weight, elem. anal.;	100%

: lithium nitride

: 7727-37-9
nitrogen

: 7439-89-6
iron

: Li2.7Fe0.3N

Conditions

Conditions	Yield
In neat (no solvent) Li3N fused in pure iron vessel; sealed under 300 kPa of N2; heated at 850-1050°C for 12 h; thermally quenched; detd. by X-ray powder diffraction;	100%

...Expand

: uranium

: 7782-49-2
selenium

: 7439-89-6
iron

: UFeSe3

Conditions

Conditions	Yield
In melt (Ar glovebox) U, Fe and Se were placed in fused-silica ampoule, evacuated to about 1E-4 Torr, sealed, heated to 1173 K in 30 h, maintained at 1173 K for 2 days, cooled to 773 K in 6 days, maintained at 773 K for 2 days, cooled to 298 K over 6 h; washed with water and dried with acetone, XRD;	100%

...Expand

: 1342835-29-3
1-(4-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)benzyl)pyrrolidin-2-one

: 7439-89-6
iron

: 1342835-31-7
1-(4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)benzyl)pyrrolidin-2-one

Conditions

Conditions	Yield
With ammonium chloride In water	100%

: 7647-01-0
hydrogenchloride

: 7439-89-6
iron

: Fe(57)Cl2

Conditions

Conditions	Yield
In water at 60℃; for 47h;	100%

: 557-34-6
zinc diacetate

: 373-02-4, 14998-37-9, 33025-09-1, 94044-50-5, 98268-31-6
nickel diacetate

: 144-62-7
oxalic acid

: 7439-89-6
iron

: (x)Ni(2+)*(1-x)Zn(2+)*2Fe(2+)*3C2O4(2-)*99H2O

Conditions

Conditions	Yield
In acetic acid heating of iron powder in a twofold excess of 1.5-2.0 M acetic acid under a N2 atmosphere; stirring; addn. of a soln. of Zn(2+) and Ni(2+) acetate; boilig; addn. of 3-5% excess 1 M oxalic acid; boiling for 1 h; filtration;; washing and drying at 100°C;;	99.8%
In acetic acid heating of iron powder in a twofold excess of 1.5-2.0 M acetic acid under a N2 atmosphere; stirring; addn. of a soln. of Zn(2+) and Ni(2+) acetate; boilig; addn. of 3-5% excess 1 M oxalic acid; boiling for 1 h;; frozen ppt. with liquid N2 (with total mother soln.) and then freeze dried;;

...Expand

: 118-69-4
2,6-dichlorotoluene

: 7439-89-6
iron

: 127049-87-0
2,4-dichloro-3-methylbromobenzene

Conditions

Conditions	Yield
With bromine; iodine In tetrachloromethane; (2S)-N-methyl-1-phenylpropan-2-amine hydrate	99.5%

: 3-allyl-6-methyl-6-(3-nitrophenyl)-3-azabicyclo[3.1.0]hexan-2-one

: 7439-89-6
iron

: 3-allyl-6-(3-aminophenyl)-6-methyl-3-azabicyclo[3.1.0]hexan-2-one

Conditions

Conditions	Yield
With calcium chloride In methanol; ethanol; dichloromethane; water	99%

: 98027-81-7
2,6-dibromo-4-nitro-pyridine 1-oxide

: 7439-89-6
iron

: 39771-34-1
4-amino-2,6-dibromopyridine

Conditions

Conditions	Yield
With acetic acid	99%

: ferrous(II) sulfate heptahydrate

: 131341-02-1
2,2,4-trimethyl-4-[5-nitro-3-(3-phenylprop-2-ynyloxy)phenyl]-1,3-dioxolane

: 7439-89-6
iron

: 4-[5-amino-3-(3-phenylprop-2-ynyloxy)phenyl]-2,2,4-trimethyl-1,3-dioxolane

Conditions

Conditions	Yield
With hydrogenchloride; triethylamine In methanol; water	99%

...Expand

sodium bicarbonate water: sodium bicarbonate water

: 875774-88-2
4-nitro-1-(4-trifluoromethoxyphenoxy)-2-trifluoromethylbenzene

: 7439-89-6
iron

: 875774-55-3
4-(4-trifluoromethoxyphenoxy)-3-trifluoromethyl-aniline

Conditions

Conditions	Yield
With hydrogenchloride In ethanol; water; ethyl acetate	99%

...Expand

: 1493-13-6
trifluorormethanesulfonic acid

: 7439-89-6
iron

: 67-68-5
dimethyl sulfoxide

: iron(III) triflate - dimethylsulfoxide (1/6.2)

Conditions

Conditions	Yield
With oxygen In dimethyl sulfoxide metal. Fe under O2 atm. treated with DMSO and triflic acid (3 equiv.) in3 portions, heated at 100°C for 24 h;	99%

...Expand

: 108-89-4
picoline

: 7439-89-6
iron

: 17356-08-0
thiourea

: [4-methylpyridinium]2[Fe(isothiocyanate)4(4-methylpyridine)2]*2(4-methylpyridine)

Conditions

Conditions	Yield
In further solvent(s) under Ar atm. using Schlenk techniques; metal powder, thiourea (excess),4-methylpyridine refluxed overnight; soln. refluxed for 4 ds; soln. coo led to room temp.; soln. layered (hexane); crystn.;	99%

...Expand

: 1493-13-6
trifluorormethanesulfonic acid

: 7439-89-6
iron

: iron(II) triflate

Conditions

Conditions	Yield
In water stoich., Fe powder dissolved in aq. soln. of CF3SO3H by heating; ppt. filtered, dried (air), elem. anal.;	99%
In water metal compd. dissolved in aq. soln. of triflic acid; filtered, cocd., crystd., dried at 200°C for several h;
In water mixed, warmed in water;

: 2175-90-8
6,6-Diphenylfulvene

: 7439-89-6
iron

: 1,1'-bis(diphenylmethyl)ferrocene

Conditions

Conditions	Yield
In acetonitrile Electrolysis; iron anode, 0.1 M tetraethylammonium bromide base electrolyte, inert atmosphere, 40°C, current density 5 mA/cm*2; pptn. on water diln., collection (filtn.), dissoln. (acetone), repptn. on hexane addn., recrystn. (acetone);	99%
In dimethyl sulfoxide Electrolysis; iron anode, sodium bromide base electrolyte, inert atmosphere, 40°C, current density 5 mA/cm*2; pptn. on water diln., collection (filtn.), dissoln. (acetone), repptn. on hexane addn., recrystn. (acetone);	<80

Iron History

The first wrought Iron used by mankind during prehistory came from meteors. The smelting of iron in bloomeries began in the second millennium BC. Artefacts from smelted iron occur in India from 1800-1200 BC.in the Levant from about 1500 BC.
Cast Iron was first produced in China about 550 BC, but not in Europe until the medieval period.

Iron Consensus Reports

Reported in EPA TSCA Inventory.

Iron Analytical Methods

For occupational chemical analysis use NIOSH: Elements (ICP), 7300; Metals in Urine (ICP), 8310.

Iron Specification

The IUPAC name of this chemical is Iron. With the CAS registry number 7439-89-6 and EINECS registry number 231-096-4, it is also named as Iron, elemental. In addition, the molecular formula is Fe and the molecular weight is 55.85. It is a kind of and belongs to the classes of Inorganics; Alphabetic; Analytical Standards; Application CRMs; ICertified Reference Materials (CRMs); Industrial Raw MaterialsReference/Calibration Standards; IRMM/BCR Certified Reference Materials; Matrix CRMs; Reactor DosimetryCertified Reference Materials (CRMs); Reactor Neutron Dosimetry; Reactor Neutron DosimetryCertified Reference Materials (CRMs).

Preparation of Iron: it can be prepared by iron hydroxide or iron oxide with hydrogen. It is a kind of reduction reaction. The equations are as follows: 2Fe(OH)₃ + 3H₂ → 2Fe + 6H₂O; Fe₂O₃ + 3H₂ → 2Fe + 3H₂O. Also it can be get by oxalic acidiron and ammonia. The reaction temperature is 400-500 °C. You should get the oxalic acidiron from sulfuric acidiron and sodium oxalate at first.

Uses of Iron: it can react with water to get iron oxide. The equations are as follows: Fe + H₂O → FeO + H₂; 2Fe + 3H₂O → Fe₂O₃ + 3H₂; 3Fe + 4H₂O → Fe₃O₄ + 4H₂. And it reacts with oxygen in the air to form various oxide and hydroxide compounds; the most common are iron(II,III) oxide (Fe₃O₄), and iron(III) oxide (Fe₂O₃). In addition, it is used as gel, catalyst, absorbent, reductant and sintering surfactant. Also it can be used for powder metallurgy products, mechanical parts products and hard alloy material products. Moreover, it can be used in preparation of magnets, drugs, ink, paint and abrasive.

You can still convert the following datas into molecular structure:
(1)SMILES: [Fe]
(2)InChI: InChI=1/Fe
(3)InChIKey: XEEYBQQBJWHFJM-UHFFFAOYAG

The toxicity data is as follows:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
child	TDLo	oral	77mg/kg (77mg/kg)	BEHAVIORAL: IRRITABILITY GASTROINTESTINAL: NAUSEA OR VOMITING BLOOD: NORMOCYTIC ANEMIA	Journal of Toxicology, Clinical Toxicology. Vol. 25, Pg. 251, 1987.
guinea pig	LD50	oral	20gm/kg (20000mg/kg)		Indian Journal of Pharmacy. Vol. 13, Pg. 240, 1951.
rabbit	LDLo	intraperitoneal	20mg/kg (20mg/kg)		National Technical Information Service. Vol. PB158-508,
rat	LD50	oral	30gm/kg (30000mg/kg)		Indian Journal of Pharmacy. Vol. 13, Pg. 240, 1951.

Product Name

Iron

Synthetic route

Iron History

Iron Consensus Reports

Iron Analytical Methods

Iron Specification

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