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CAS

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Cobalt is a chemical element with the symbol Co and atomic number 27. It is a hard, lustrous, silvery-gray metal that is commonly found in minerals such as cobaltite, smaltite, and erythrite. Cobalt is widely used in various applications due to its unique properties, making it a versatile and important chemical element.

7440-48-4

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7440-48-4 Usage

Uses

Used in Magnetic Alloys Industry:
Cobalt is used as a component in magnetic alloys for its high magnetic permeability and resistance to demagnetization. This makes it suitable for applications such as high-performance magnets, magnetic sensors, and magnetic storage devices.
Used in Ceramics and Glass Industry:
Cobalt is used as a pigment in ceramics and glass for its intense blue color. It imparts a deep, rich hue to these materials, making it a popular choice for decorative and functional applications.
Used in Rechargeable Batteries Industry:
Cobalt is used in rechargeable batteries, particularly in lithium-ion batteries, for its high energy density and ability to maintain a stable voltage. This makes it an essential component in portable electronic devices, electric vehicles, and renewable energy storage systems.
Used in Human Nutrition and Animal Health:
Cobalt is an essential trace element for humans and other animals, playing a key role in the functioning of vitamin B12 and cobalamins. It is used in dietary supplements and animal feed to ensure adequate intake and support overall health.
However, it is important to note that cobalt can be toxic in high doses, causing health issues such as respiratory problems, heart failure, and dermatitis. Therefore, proper handling and regulation of cobalt exposure are crucial to ensure its safe and beneficial use.

Check Digit Verification of cas no

The CAS Registry Mumber 7440-48-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,4 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7440-48:
(6*7)+(5*4)+(4*4)+(3*0)+(2*4)+(1*8)=94
94 % 10 = 4
So 7440-48-4 is a valid CAS Registry Number.
InChI:InChI=1/2Co/rCo2/c1-2

7440-48-4 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (46347)  Cobalt nanopowder, APS 25-30nm, 99.8% (metals basis)   

  • 7440-48-4

  • 5g

  • 1313.0CNY

  • Detail
  • Alfa Aesar

  • (46347)  Cobalt nanopowder, APS 25-30nm, 99.8% (metals basis)   

  • 7440-48-4

  • 25g

  • 2978.0CNY

  • Detail
  • Alfa Aesar

  • (42355)  Cobalt slug, 3.175mm (0.125in) dia x 3.175mm (0.125in) length, 99.95% (metals basis)   

  • 7440-48-4

  • 5g

  • 627.0CNY

  • Detail
  • Alfa Aesar

  • (42355)  Cobalt slug, 3.175mm (0.125in) dia x 3.175mm (0.125in) length, 99.95% (metals basis)   

  • 7440-48-4

  • 25g

  • 2385.0CNY

  • Detail
  • Alfa Aesar

  • (42355)  Cobalt slug, 3.175mm (0.125in) dia x 3.175mm (0.125in) length, 99.95% (metals basis)   

  • 7440-48-4

  • 100g

  • 10053.0CNY

  • Detail
  • Alfa Aesar

  • (42354)  Cobalt slug, 3.175mm (0.125in) dia x 6.35mm (0.25in) length, 99.95% (metals basis)   

  • 7440-48-4

  • 5g

  • 553.0CNY

  • Detail
  • Alfa Aesar

  • (42354)  Cobalt slug, 3.175mm (0.125in) dia x 6.35mm (0.25in) length, 99.95% (metals basis)   

  • 7440-48-4

  • 25g

  • 2351.0CNY

  • Detail
  • Alfa Aesar

  • (42354)  Cobalt slug, 3.175mm (0.125in) dia x 6.35mm (0.25in) length, 99.95% (metals basis)   

  • 7440-48-4

  • 100g

  • 9589.0CNY

  • Detail
  • Alfa Aesar

  • (42353)  Cobalt slug, 6.35mm (0.25in) dia x 12.7mm (0.50in) length, 99.95% (metals basis)   

  • 7440-48-4

  • 25g

  • 1077.0CNY

  • Detail
  • Alfa Aesar

  • (42353)  Cobalt slug, 6.35mm (0.25in) dia x 12.7mm (0.50in) length, 99.95% (metals basis)   

  • 7440-48-4

  • 100g

  • 3165.0CNY

  • Detail
  • Alfa Aesar

  • (43227)  Cobalt slug, 6.35mm (0.25in) dia x 12.7mm (0.50in) length, Puratronic?, 99.995% (metals basis)   

  • 7440-48-4

  • 1slug

  • 423.0CNY

  • Detail
  • Alfa Aesar

  • (43227)  Cobalt slug, 6.35mm (0.25in) dia x 12.7mm (0.50in) length, Puratronic?, 99.995% (metals basis)   

  • 7440-48-4

  • 5slug

  • 1714.0CNY

  • Detail

7440-48-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name cobalt atom

1.2 Other means of identification

Product number -
Other names Cobalt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Inorganic substances, Radionuclides (radioactive materials)
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7440-48-4 SDS

7440-48-4Synthetic route

cobalt(II) chloride
7646-79-9

cobalt(II) chloride

A

chlorine
7782-50-5

chlorine

B

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
In acetonitrile Electrolysis; Ag-anode;;A n/a
B 100%
In acetonitrile Electrolysis; Ag-anode;;A n/a
B 100%
In neat (no solvent) Electrolysis; Cl2 is formed on anode, Co on cathode;;
In neat (no solvent) decompn. of CoCl2 at 600 ° C;
In neat (no solvent) Electrolysis; Cl2 is formed on anode, Co on cathode;;
{Co(NH3)6}(2+)*SO4(2-)={Co(NH3)6}SO4
65459-62-3

{Co(NH3)6}(2+)*SO4(2-)={Co(NH3)6}SO4

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
With hydrogen In ammonia pptn. of 100.0% metallic Co out of NH3-containing (Co(NH3)6)SO4-solution with H2 (50-75 atm) at 200°C after 2 h;;100%
With H2 In ammonia aq. ammonia=NH3; pptn. of 100.0% metallic Co out of NH3-containing (Co(NH3)6)SO4-solution with H2 (50-75 atm) at 200°C after 2 h;;100%
With hydrogen In ammonia pptn. of 95.5% metallic Co out of NH3-containing (Co(NH3)6)SO4-solution with H2 (50-75 atm) at 190°C after 2 h;;95.5%
(η6-toluene)bis(η1-pentafluorophenyl)cobalt(II)
60528-58-7

(η6-toluene)bis(η1-pentafluorophenyl)cobalt(II)

A

decafluorobiphenyl
434-90-2

decafluorobiphenyl

B

cobalt
7440-48-4

cobalt

C

toluene
108-88-3

toluene

Conditions
ConditionsYield
In neat (no solvent, solid phase) pyrolysis at 150°C;A 93%
B n/a
C 100%
cobalt(II) sulfate

cobalt(II) sulfate

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
With NH4-sulfate In ammonia Electrolysis; electrolysis at pH=8-12 with 5-10 mg metal in the electrolyt;;99%
With ammonium sulfate; triethanolamine In not given Electrolysis; electrolyte contains 5-10mg metal, triethanolamin and (NH4)2SO4;;99%
With ammonium sulfate In not given Electrolysis; electolyte: 8% educt, 2.5% (NH4)2SO4, 3.7-4.5V, 2.5A/dm(2), pH=5.0;;85%
dichloromethane
75-09-2

dichloromethane

water
7732-18-5

water

Dimethyl(phenyl)phosphine
672-66-2

Dimethyl(phenyl)phosphine

cobalt(II) chloride
7646-79-9

cobalt(II) chloride

A

ZnCl4(2-)*2(C6H5)(CH3)3P(1+)=[(C6H5)(CH3)3P]2[ZnCl4]

ZnCl4(2-)*2(C6H5)(CH3)3P(1+)=[(C6H5)(CH3)3P]2[ZnCl4]

B

cobalt
7440-48-4

cobalt

C

zinc(II) chloride
7646-85-7

zinc(II) chloride

D

zinc(II) hydroxide

zinc(II) hydroxide

Conditions
ConditionsYield
In dichloromethaneA n/a
B 99%
C n/a
D n/a
dichloromethane
75-09-2

dichloromethane

tributylphosphine
998-40-3

tributylphosphine

water
7732-18-5

water

cobalt(II) chloride
7646-79-9

cobalt(II) chloride

A

ZnCl4(2-)*2(C4H9)3(CH3)P(1+)=[(C4H9)3(CH3)P]2[ZnCl4]

ZnCl4(2-)*2(C4H9)3(CH3)P(1+)=[(C4H9)3(CH3)P]2[ZnCl4]

B

cobalt
7440-48-4

cobalt

C

zinc(II) chloride
7646-85-7

zinc(II) chloride

D

zinc(II) hydroxide

zinc(II) hydroxide

Conditions
ConditionsYield
In dichloromethaneA n/a
B 99%
C n/a
D n/a
bis(salicylidene)cobalt(II)
14220-65-6, 922735-20-4, 41139-17-7

bis(salicylidene)cobalt(II)

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
With oleylamine; Ph3P In neat (no solvent) (Ar); Co complex was reacted with oleylamine; heated to 100°C for90 min; soln. was injected to Ph3P at 220°C; aged at 210° C for 45 min; cooled to room temp.; EtOH added; centrifuged;70%
[((Co(CO)3)2)2(HCCC6H4C)2]
252329-39-8

[((Co(CO)3)2)2(HCCC6H4C)2]

graphite

graphite

B

carbon dioxide
124-38-9

carbon dioxide

C

carbon monoxide
201230-82-2

carbon monoxide

D

hydrogen
1333-74-0

hydrogen

E

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
In solid byproducts: CH4; below 200°C, then graphitization (800°C, 6 h);A 60%
B n/a
C n/a
D n/a
E n/a
[(CC6H4CC((Co(CO)3)2)CCC6H4C(Co(CO)3))2]
252329-37-6

[(CC6H4CC((Co(CO)3)2)CCC6H4C(Co(CO)3))2]

graphite

graphite

B

carbon dioxide
124-38-9

carbon dioxide

C

carbon monoxide
201230-82-2

carbon monoxide

D

hydrogen
1333-74-0

hydrogen

E

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
In solid byproducts: CH4; below 200°C, then graphitization (800°C, 6 h);A 60%
B n/a
C n/a
D n/a
E n/a
(hydridotris(3-tert-butyl-5-methylpyrazolyl)borato)cobalt(II)(N2)

(hydridotris(3-tert-butyl-5-methylpyrazolyl)borato)cobalt(II)(N2)

hydrogen
1333-74-0

hydrogen

A

hydrido(hydridotris(3-tert-butyl-5-methylpyrazolyl)borato)cobalt(II)

hydrido(hydridotris(3-tert-butyl-5-methylpyrazolyl)borato)cobalt(II)

B

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
In toluene 60°C (overnight); filtering, evapn. (vac.), recrystn. (toluene); elem. anal.;A 59%
B n/a
(hydridotris(3-tert-butyl-5-methylpyrazolyl)borato)cobalt(II)(N2)

(hydridotris(3-tert-butyl-5-methylpyrazolyl)borato)cobalt(II)(N2)

deuterium
16873-17-9

deuterium

A

deuterido(hydridotris(3-tert-butyl-5-methylpyrazolyl)borato)cobalt(II)

deuterido(hydridotris(3-tert-butyl-5-methylpyrazolyl)borato)cobalt(II)

B

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
In (2)H8-toluene 60°C (overnight); filtering, evapn. (vac.), recrystn. (toluene);A 58%
B n/a
Conditions
ConditionsYield
In 1,2-dimethoxyethane Irradiation (UV/VIS); under Ar; mole ratios NaBPh4 : CoCl2 : CuBr2 = 4 : 1 : 1; irradn. (254 nm) for 10 h gave deposition of Co and Cu;A 47%
B 48%
cobaltocene
1277-43-6

cobaltocene

CoBr2*DME

CoBr2*DME

tetraphenylborate anion
4358-26-3

tetraphenylborate anion

1,5-dicyclooctadiene
5259-72-3, 10060-40-9, 111-78-4

1,5-dicyclooctadiene

A

cobalt(II) oxide
1307-96-6

cobalt(II) oxide

B

(η5-cyclopentadienyl)-η4-cycloocta-1,5-dienecobalt(I)
12184-35-9

(η5-cyclopentadienyl)-η4-cycloocta-1,5-dienecobalt(I)

C

[(cyclopentadienyl)2Co][tetraphenylborate]

[(cyclopentadienyl)2Co][tetraphenylborate]

D

cobalt(II)

cobalt(II)

E

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
With C5H5Na In tetrahydrofuran; water; pentane under N2, CoBr2*DME, NaCp, CoCp2 and COD mixed in THF in molar ratio of2/2.06/0.5/1.16 (CoCp2 added at -80°C prior to NaCp), warmed to room temp. during 3 h, evapd., pentane ext. passed through Al2O3/4% H2O and CuCl powder; concd., cooled to -80°C, CpCoCOD filtered off; CuCl washed with water, CoCp2(1+) pptd. with BPh4(1-) from aq. soln., filtered off; pentane-insol. residue treated with water, Co and CoO mixt. filtered, Co(2+) determined complexometrically;A n/a
B 45.3%
C n/a
D n/a
E n/a
With C5H5Na In tetrahydrofuran; water; pentane under N2, CoBr2*DME, NaCp, CoCp2 and COD mixed in THF in molar ratio of2/2.06/0.5/1.16 (CoCp2 added at -80°C after NaCp), warmed to room temp. during 3 h, evapd., pentane ext. passed through Al2O3/4% H2O andCuCl powder; concd., cooled to -80°C, CpCoCOD filtered off; CuCl washed with water, CoCp2(1+) pptd. with BPh4(1-) from aq. soln., filtered off; pentane-insol. residue treated with water, Co and CoO mixt. filtered, Co(2+) determined complexometrically;A n/a
B 43%
C n/a
D n/a
E n/a
With C5H5Na In tetrahydrofuran; water; pentane under N2, CoBr2*DME, NaCp, CoCp2 and COD mixed in THF in molar ratio of2/2.06/0.5/1.16 (CoCp2 added at 0°C prior to NaCp at -80°C), warmed to room temp. during 3 h, evapd., pentane ext. passed throughAl2O3/4% H2O and CuCl powder; concd., cooled to -80°C, CpCoCOD filtered off; CuCl washed with water, CoCp2(1+) pptd. with BPh4(1-) from aq. soln., filtered off; pentane-insol. residue treated with water, Co and CoO mixt. filtered, Co(2+) determined complexometrically;A n/a
B 37.5%
C n/a
D n/a
E n/a
With C5H5Na In tetrahydrofuran; water; pentane under N2, CoBr2*DME, NaCp, CoCp2 and COD mixed in THF in molar ratio of2/3/0.5/1.16, warmed to room temp. during 3 h, evapd., pentane ext. passed through Al2O3/4% H2O and CuCl powder; concd., cooled to -80°C, CpCoCOD filtered off; CuCl washed with water, CoCp2(1+) pptd. with BPh4(1-) from aq. soln., filtered off; pentane-insol. residue treated with water, Co and CoO mixt. filtered, Co(2+) determined complexometrically;A n/a
B 11.5%
C n/a
D n/a
E n/a
With C5H5Na In hexane; water; pentane under N2, CoBr2*DME, NaCp, CoCp2 and COD mixed in molar ratio of 2/3/0.5/1.16 in hexane at -80°C, warmed to room temp. during 3 h, evapd., pentane ext. passed through Al2O3/4% H2O and CuCl powder; concd., cooled to -80°C, CpCoCOD filtered off; CuCl washed with water, CoCp2(1+) pptd. with BPh4(1-) from aq. soln., filtered off; pentane-insol. residue treated with water, Co and CoO mixt. filtered, Co(2+) determined complexometrically;A n/a
B 8.6%
C n/a
D n/a
E n/a
Co4(CO)10C6F4

Co4(CO)10C6F4

A

1,2,3,4,5,6,7,8-Octafluoro-9-fluorenone
19925-96-3

1,2,3,4,5,6,7,8-Octafluoro-9-fluorenone

B

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
In neat (no solvent) byproducts: CO; in vac., thermic decompn.;A 45%
B n/a
In neat (no solvent) byproducts: CO; in vac., thermic decompn.;A 45%
B n/a
(η6-toluene)bis(η1-pentafluorophenyl)cobalt(II)
60528-58-7

(η6-toluene)bis(η1-pentafluorophenyl)cobalt(II)

A

Pentafluorobenzene
363-72-4

Pentafluorobenzene

B

decafluorobiphenyl
434-90-2

decafluorobiphenyl

C

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
In toluene refluxing under N2 for 3 d;A 135 %
B 30%
C n/a
cobaltocene
1277-43-6

cobaltocene

CoBr2*DME

CoBr2*DME

tetraphenylborate anion
4358-26-3

tetraphenylborate anion

cyclopentadienyllithium
16733-97-4

cyclopentadienyllithium

1,5-dicyclooctadiene
5259-72-3, 10060-40-9, 111-78-4

1,5-dicyclooctadiene

A

cobalt(II) oxide
1307-96-6

cobalt(II) oxide

B

(η5-cyclopentadienyl)-η4-cycloocta-1,5-dienecobalt(I)
12184-35-9

(η5-cyclopentadienyl)-η4-cycloocta-1,5-dienecobalt(I)

C

[(cyclopentadienyl)2Co][tetraphenylborate]

[(cyclopentadienyl)2Co][tetraphenylborate]

D

cobalt(II)

cobalt(II)

E

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
In tetrahydrofuran; water; pentane under N2, CoBr2*DME, LiCp, CoCp2 and COD mixed in THF in molar ratio of2/2.06/0.5/1.16, warmed to room temp. during 3 h, evapd., pentane ext. passed through Al2O3/4% H2O and CuCl powder; concd., cooled to -80°C, CpCoCOD filtered off; CuCl washed with water, CoCp2(1+) pptd. with BPh4(1-) from aq. soln., filtered off; pentane-insol. residue treated with water, Co and CoO mixt. filtered, Co(2+) determined complexometrically;A n/a
B 18%
C n/a
D n/a
E n/a
Trioxalatcobaltat-(III)

Trioxalatcobaltat-(III)

tin(II)

tin(II)

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
presence of V(5+);2%
cobalt(II) chloride
7646-79-9

cobalt(II) chloride

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
for 0.0833333h;
In not given Electrolysis; deposition potential given; influence of electrolyte concn. and acidifying addtives (12% H3BO3, 0.003 n-HCl) investigated);;
chloride In N,N-dimethyl-formamide Electrochem. Process; electrodeposition;
Reaxys ID: 15738947

Reaxys ID: 15738947

cobalt
7440-48-4

cobalt

Conditions
ConditionsYield
In water at 60℃; for 0.5h;
water
7732-18-5

water

cobalt
7440-48-4

cobalt

5-(4-chlorophenylazo)-3-cyano-4,6-dimethyl-pyridine-2-(1H)-thione

5-(4-chlorophenylazo)-3-cyano-4,6-dimethyl-pyridine-2-(1H)-thione

Co(ClC6H4NNC5N(CH3)2(CN)(S))2(H2O)2

Co(ClC6H4NNC5N(CH3)2(CN)(S))2(H2O)2

Conditions
ConditionsYield
In acetone byproducts: H2; Electrolysis; Pt-cathode, Co-anode, 40 mA, 35 min, Et4NClO4, two drops of water; ppt. was filtered, washed with Et2O, elem. anal.;100%
cobalt
7440-48-4

cobalt

5-(4-methylphenylazo)-3-cyano-4,6-dimethyl-pyridine-2-(1H)-thione
147675-09-0

5-(4-methylphenylazo)-3-cyano-4,6-dimethyl-pyridine-2-(1H)-thione

Co(CH3C6H4NNC5N(CH3)2(CN)(S))2

Co(CH3C6H4NNC5N(CH3)2(CN)(S))2

Conditions
ConditionsYield
In acetone byproducts: H2; Electrolysis; Pt-cathode, Co-anode, 40 mA, 30 min, Et4NClO4, two drops of water; ppt. was filtered, washed with Et2O;100%
lanthanum(III) oxide

lanthanum(III) oxide

tungsten(VI) oxide

tungsten(VI) oxide

cobalt
7440-48-4

cobalt

sulfur
7704-34-9

sulfur

tungsten
7440-33-7

tungsten

La3CoS3(6+)*WO6(6-)=La3CoWS3O6

La3CoS3(6+)*WO6(6-)=La3CoWS3O6

Conditions
ConditionsYield
In melt stoich. amts. of La2O3, S, W, WO3, Co mixed with KCl flux; sealed in carbon coated SiO2 ampoule under vac.; heated from 200 to 400°C in 24 h; held for 48 h; heated to 950°C in 12 h; held for 120 h; cooled to room temp. within 24 h; soaked in H2O overnight; washed with H2O; detn. by EDX, XRD;100%
Conditions
ConditionsYield
In acetone Electrolysis; 2 h, initial voltage 32 V; washed with acetonitrile and dried in vacuo for 3-4 h at room temp.;elem.anal;98%
water
7732-18-5

water

cobalt
7440-48-4

cobalt

5-(4-chlorophenylazo)-3-cyano-4-methyl-6-phenylpyridine-2-(1H)-thione
147675-15-8

5-(4-chlorophenylazo)-3-cyano-4-methyl-6-phenylpyridine-2-(1H)-thione

Co(ClC6H4NNC5N(CH3)(C6H5)(CN)(S))2(H2O)2*H2O

Co(ClC6H4NNC5N(CH3)(C6H5)(CN)(S))2(H2O)2*H2O

Conditions
ConditionsYield
In acetone byproducts: H2; Electrolysis; Pt-cathode, Co-anode, 40 mA, 30 min, Et4NClO4, two drops of water; ppt. was filtered, washed with Et2O, elem. anal.;98%
water
7732-18-5

water

hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

cobalt
7440-48-4

cobalt

tetrazol-1-yl-tris(hydroxymethyl)methane
103518-51-0

tetrazol-1-yl-tris(hydroxymethyl)methane

Co(tetrazol-1-yl-tris(hydroxymethyl)methane)2Br2*2H2O
1363414-20-3

Co(tetrazol-1-yl-tris(hydroxymethyl)methane)2Br2*2H2O

Conditions
ConditionsYield
In methanol metal, tetrazol compd., 35% HBr added to MeOH. heated in air to 50-60°C for 2-3 h, cooled to 18-20°C, stored in air for a week (slow evapn.); filtered, dried (air); elem. anal., metal content by colorimetry or complexonometric titration, halide content by Volhard's method;98%
1-phenyl-3-methyl-4-[4-methyl-2-(4-methylphenylazophenyl)hydrazono]-5H-pyrazol-5-one
1609350-31-3

1-phenyl-3-methyl-4-[4-methyl-2-(4-methylphenylazophenyl)hydrazono]-5H-pyrazol-5-one

cobalt
7440-48-4

cobalt

C48H42CoN12O2

C48H42CoN12O2

Conditions
ConditionsYield
With tetraethylammonium perchlorate In methanol for 1h; Electrochemical reaction;97%
1,2-dimethoxyethane
110-71-4

1,2-dimethoxyethane

bromine
7726-95-6

bromine

cobalt
7440-48-4

cobalt

cobalt dibromide*1,2-dimethoxyethane

cobalt dibromide*1,2-dimethoxyethane

Conditions
ConditionsYield
at 0 - 20℃; for 24h; Inert atmosphere;96%
cobalt
7440-48-4

cobalt

cyclohexanol
108-93-0

cyclohexanol

2(C6H11O)(1-)*Co(2+)=Co(C6H11O)2

2(C6H11O)(1-)*Co(2+)=Co(C6H11O)2

Conditions
ConditionsYield
With tetraethylammonium chloride In acetonitrile Electrolysis; cyclohexanol soln. is electrolyzed in presence of Et4NCl at -2.5 V withstirring in a electrolyzer without diaphragma with Co as electrodes; ppt. is filtered off, washed with hot CH3CN and dried at 1-2 mm, elem. anal.;95.7%
cobalt
7440-48-4

cobalt

acetylacetone
123-54-6

acetylacetone

cobalt(III) acetylacetonate

cobalt(III) acetylacetonate

Conditions
ConditionsYield
With tert-butylammonium hexafluorophosphate(V) In acetylacetone Electrochem. Process; tetra-n-butylammonium hexafluorophosphate added to dry acetylacetone, Coelectrode; evapd. under vac., oily residue dissolved in CHCl3, evapd.;95.1%
cobalt
7440-48-4

cobalt

isopropyl alcohol
67-63-0

isopropyl alcohol

cobalt(II) isopropoxide

cobalt(II) isopropoxide

Conditions
ConditionsYield
With carbon monoxide; tetrabutylammomium bromide In isopropyl alcohol Electrochem. Process; CO 10 bar, electrolysis (Co-anode, Bu4NBr, 293 K, 30 mA, 7.5 V, 44 h);95%
1,10-Phenanthroline
66-71-7

1,10-Phenanthroline

cobalt
7440-48-4

cobalt

4-Phenyl-3-thiosemicarbazide
5351-69-9

4-Phenyl-3-thiosemicarbazide

Cu(PTS)*phen

Cu(PTS)*phen

Conditions
ConditionsYield
In acetone Electrolysis; electrolysis of Cu into a soln. of thiosemicarbazide, 1,10-phenanthroline and Et2NClO4 in acetone, 30V, 40 mA, 1h; crystn.; filtration; washing (acetone, ether); elem. anal.;95%
potassium sulfide

potassium sulfide

cobalt
7440-48-4

cobalt

sulfur
7704-34-9

sulfur

10K(1+)*Co4Sn4S17(10-)=K10Co4Sn4S17

10K(1+)*Co4Sn4S17(10-)=K10Co4Sn4S17

Conditions
ConditionsYield
In neat (no solvent) heating (50°C/h.) of a mixt. of Sn, Co, K2S, S (stoich. mol. ratio 5:4:4:12) in a quartz tube sealed under vac. to 650°C, heating at this temp. for 60 h; cooling to room temp. at 5°C/h.;95%
In neat (no solvent, solid phase) all manipulations under N2 atm.; calcd. amts. of elements and K2S sealedunder vac. in silica tube and heated to 650°C (50°C/h) fo r 60 h, cooled to room temp. (5°C/h); excess flux (K2S) removed with MeOH; elem. anal.;90%
In melt byproducts: CoS2; heating (50°C/h.) of a mixt. of Sn, Co, K2S, S (mol. ratio 1:1:3:12) in a quartz tube sealed under vac. to 650°C for 60 h; cooling to room temp. at 5°C/h.;0%
2,6-bis(1-[2-(tosylamino)phenylimino]ethyl)pyridine
660394-39-8

2,6-bis(1-[2-(tosylamino)phenylimino]ethyl)pyridine

cobalt
7440-48-4

cobalt

Co(2+)*C5H3N(C(CH3)NC6H4NSO2C6H4CH3)2(2-)*H2O=[Co(C5H3N(C(CH3)NC6H4NSO2C6H4CH3)2)](H2O)
660394-36-5

Co(2+)*C5H3N(C(CH3)NC6H4NSO2C6H4CH3)2(2-)*H2O=[Co(C5H3N(C(CH3)NC6H4NSO2C6H4CH3)2)](H2O)

Conditions
ConditionsYield
With (CH3)4NClO4; Pt In acetone Electrolysis; suspn. of ligand in warm acetone (contained Me4NClO4 as supporting electrolyte) electrolysed for 2.5 h (10 mA) using metal plate as anode and Ptwire as cathode; solid washed with Et2O, dried in vac., elem. anal.;95%
pyridine-2-formaldehyde N4-methyl thiosemicarbazone
6839-88-9

pyridine-2-formaldehyde N4-methyl thiosemicarbazone

water
7732-18-5

water

cobalt
7440-48-4

cobalt

Co(4-N-methylthiosemicarbazone-2-pyridinecarboxaldehyde(-H))2(H2O)3.3

Co(4-N-methylthiosemicarbazone-2-pyridinecarboxaldehyde(-H))2(H2O)3.3

Conditions
ConditionsYield
With tetraethylammonium perchlorate In acetonitrile Electrochem. Process; soln. of thiosemicarbazone in CH3CN contg. Et4NClO4 electrolysed for 1.3h using Pt cathode and Co platelet anode and a current of 10 mA; solid filtered off; washed with diethyl ether; dried under vac.; elem. anal.;95%
cobalt
7440-48-4

cobalt

(2-hydrazinyl-2-oxoethyl)benzamide
2443-68-7

(2-hydrazinyl-2-oxoethyl)benzamide

acetone
67-64-1

acetone

Co(C9H10N3O2)2*(CH3)2CO = Co(C9H10N3O2)2(CH3)2CO

Co(C9H10N3O2)2*(CH3)2CO = Co(C9H10N3O2)2(CH3)2CO

Conditions
ConditionsYield
With Et4NClO4 In acetone byproducts: H2; Electrolysis; electrolysis (20 V, 3 h); elem. anal.;95%

7440-48-4Relevant articles and documents

Synthesis, characterisation and catalytic performance of nanocrystalline Co3O4 for gas-phase chlorinated VOC abatement

De Rivas, Beatriz,Lopez-Fonseca, Ruben,Jimenez-Gonzalez, Cristina,Gutierrez-Ortiz, Jose I.

, p. 88 - 97 (2011)

Several nanocrystalline Co3O4 catalysts were investigated for their activity and selectivity during the oxidation of 1,2-dichloroethane, which was selected as a model chlorinated volatile organic compound. A wide number of synthesis routes starting from cobalt(II) nitrate were examined, namely calcination of the precursor salt, solid-state reaction, precipitation and sol-gel. The catalysts prepared by precipitation decomposed the chlorinated feed at the lowest temperatures. Activity was observed to be chiefly governed by a small crystallite size which may give rise to more easily accessible active sites (oxygen -O- or O2-- species), which were not present on the more highly crystalline Co3O 4 catalysts. Additionally, surface Lewis acidity played a relevant catalytic role. Interestingly, the behaviour of some of the nanocrystalline oxides was superior to that of supported noble metal catalysts and other bulk oxide catalysts. Conversion to deep oxidation products was complete (CO 2, HCl and Cl2), and no appreciable deactivation with time on stream was noticed.

Thermogravimetric study of the kinetics of Co3O4 reduction by hydrogen

Tomi?-Tucakovi?, Biljana,Majstorovi?, Divna,Jeli?, Dijana,Mentus, Slavko

, p. 15 - 24 (2012)

Cobalt(II,III) oxide (Co3O4), synthesized by gel-combustion method, thermally treated in air at temperatures 400, 600 and 800 °C, was subjected to the reduction to metallic state in hydrogen atmosphere. The reduction was carried out

Co nanoparticles embedded in a 3D CoO matrix for electrocatalytic hydrogen evolution

Liu, Xiangye,Dong, Chenlong,Dong, Wujie,Wang, Xin,Yuan, Xiaotao,Huang, Fuqiang

, p. 38515 - 38520 (2016)

Earth-abundant and highly efficient electrocatalysts for the hydrogen evolution reaction (HER) are desired for hydrogen production from water-splitting. Here, Co nanoparticles were embedded in the 3D CoO matrix via a template-free method, including cobalt hydroxy-carbonate nanowire arrays grown on Ni foam and the following non-contact Al-reduction process. The as-prepared 3D hierarchical structured Co/CoO nanowires possess good charge transfer and mass transport properties, and a synergistic effect at the Co/CoO interface can hugely facilitate the HER kinetics. A suitable balance between Co and CoO in the catalyst is crucial for high catalytic activity. And the optimal Co/CoO array exhibited outstanding HER activities in 1 M NaOH, achieving nearly zero onset potential, and a current density of 100 mA cm-2 with a small overpotential of 167 mV. They also showed good long-term stabilities. This hybrid Co/CoO nanowire array is a promising material for large-scale hydrogen production from water-splitting.

Electrochemical deposition of co under the influence of high magnetic fields

Uhlemann,Krause,Chopart,Gebert

, p. C817-C826 (2005)

The effect of uniform, vertically oriented high magnetic fields up to 13 T on the electrodeposition of Co has been investigated in dependence on the cell and electrode geometry as well as the orientation and strength of the magnetic flux density by means of cyclic voltammetry, chronoamperometric measurements, and atomic force microscopy investigations. In the majority of cases, the limiting current density ilim increases with increasing magnetic flux densities independent of the cell geometry and orientation. The current efficiency of Co increases with increasing magnetic flux densities only in magnetic fields aligned parallel to the electrodes due to the magnetohydrodynamic (MHD) effect. The morphology of the deposits exhibits randomly oriented round-shaped grains. The electrochemical behavior of horizontal electrodes with magnetic fields oriented perpendicular to the surface is strongly dependent on the electrode geometry. The current efficiency of the Co deposition on flat electrodes increases for low magnetic flux densities and keeps constant for high magnetic fields. In contrast, for wall electrodes the current efficiency decreases strongly even for low magnetic fields. These results are caused by overlapping effects of two types of convection, macro-MHD- and micro-magneto convection due to gradients of the concentration and the magnetic susceptibility. This leads to a modified morphology.

Highly crystalline anisotropic superstructures via magnetic field induced nanoparticle assembly

Park, Jong-Il,Jun, Young-Wook,Choi, Jin-Sil,Cheon, Jinwoo

, p. 5001 - 5003 (2007)

A magnetic field is successfully utilized to induce the fabrication of size controllable one-dimensional (1-D) supercrystals which are composed of a highly crystalline assembly of fcc-packed cobalt nanoparticles; the anisotropy associated supercrystal magnetism is enhanced with four times higher coercivity than that of randomly aggregated nanoparticles. The Royal Society of Chemistry.

Synthesis, characterization, and tunable optical properties of hollow gold nanospheres

Schwartzberg, Adam M.,Olson, Tammy Y.,Talley, Chad E.,Zhang, Jin Z.

, p. 19935 - 19944 (2006)

Nearly monodisperse hollow gold nanospheres (HGNs) with tunable interior and exterior diameters have been synthesized by sacrificial galvanic replacement of cobalt nanoparticles. It is possible to tune the peak of the surface plasmon band absorption betwe

Effect of temperature on Co electrodeposition in the presence of boric acid

Santos,Matos,Trivinho-Strixino,Pereira

, p. 644 - 649 (2007)

The electrodeposition of cobalt from sulphate solutions containing boric acid was investigated using EQCM technique coupled with potentiostatic measurements. The boric acid was added to electrolyte as a buffer to avoid the local pH rise caused by parallel hydrogen evolution reaction (HER). The results showed that the buffer contribution of boric acid is effective in the cobalt electrodeposition at 25 °C; however, cobalt hydroxide is formed simultaneously with cobalt deposition at 48 °C. The M/z values calculated using the Sauerbrey equation and the Faraday Law showed that in the initial stages of deposition at 48 °C, only cobalt deposits were detected, but after 2 s, an important amount of Co(OH)2 started to be formed.

Paramagnetic alkyl, hydride, and alkene complexes of the Tpt-Bu,MeCo moiety

Jewson, Jennifer D.,Liable-Sands, Louise M.,Yap, Glenn P. A.,Rheingold, Arnold L.,Theopold, Klaus H.

, p. 300 - 305 (1999)

The paramagnetic 15-electron alkyls Tpt-Bu,MeCo(R) (R = Me, Et, n-Bu) have been prepared, and the closely related Tpt-BuCo(Me) has been structurally characterized. Hydrogenation of Tpt-Bu,MeCo(N2) produced the a

Preparation and Properties of Cobalt(II) Hydroxide-(Sodium Fluoride Tetrasilicic Mica) Intercalation Complexes and of Highly Dispersed Cobalt on Mica

Ohtsuka, Kunio,Koga, Johji,Suda, Mitsuru,Ono, Mikiya,Takahashi, Minoru

, p. 2843 - 2848 (1987)

Cobalt(II) hydroxide-(sodium fluoride tetrasilicic mica) intercalation complexes were prepared by titrating cobalt(II) nitrate solutions in the presence of mica with sodium hydroxide under oxygen-free conditions.These complexes were characterized by chemical analysis, XRD, DTA-TGA, IR, and surface area measurements.These confirmed that the brucite-like cobalt(II) hydroxyde sheet developed within the interlayer of the silicate.Cobalt atoms reduced at 400-700 deg C by H2 migrated from the interlayer of the silicate to the external surface of these where highly dispersed cobalt particles were formed.Ultra-fine cobalt metals (50-200 Angstroem) with a hexagonal close-packed form were prepared at 400 deg C by H2.The degree of reduction and the grain diameter of cobalt increased with an increase of the reducing temperature and/or the reducing time.

Effects of heat treatments on the ductility of cobalt electrodeposits

Dille,Charlier,Winand

, p. 2771 - 2779 (1998)

The effects of annealing treatments on the structure and mechanical properties of cobalt electrodeposits have been studied. Annealing temperatures range from 250-800°C, i.e. below, as well as above, the allotropic α-h c p ? β-f c c transformation temperature (417°C). The structural characterization included hydrogen content measurement, relative volume fraction of α and β phases determination by X-ray diffraction, and microstructural investigations by optical and electron microscopy. The results showed that an annealing is a very effective means to optimize the ductility of cobalt electrodeposits. The increase of ductility observed after annealing is essentially due to a decrease of the stacking fault density in the deposits. Annealing treatment above the allotropic transformation temperature also produces, in some deposits, an increase of the ductile β-f c c phase content, but this fact does not lead to supplementary improvements of ductility. This is due to the detrimental influence of hydrogen that always exists in these deposits.

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