Product Name

  • Name

    Nitrogen

  • EINECS 231-783-9
  • CAS No. 7727-37-9
  • Article Data2195
  • CAS DataBase
  • Density 0.875 g/cm3
  • Solubility Soluble in hot sulfuric acid, nitric acid, aqua regia, slowly soluble in hot hydrochloric acid, insoluble in water
  • Melting Point 63.15 K, -210.00 °C, -346.00 °F
  • Formula N2
  • Boiling Point 77.36 K, -195.79 °C, -320.33 °F
  • Molecular Weight 28.0134
  • Flash Point
  • Transport Information UN 1066 2.2
  • Appearance Colorless odorless gas
  • Safety 38
  • Risk Codes
  • Molecular Structure Molecular Structure of 7727-37-9 (Nitrogen)
  • Hazard Symbols
  • Synonyms Diatomicnitrogen;Dinitrogen;Molecular nitrogen;Nitrogen (N2);Nitrogen gas;Nitrogennutrition (plant);Nitrogen-14;CHEBI:17997;HSDB 5060;
  • PSA 47.58000
  • LogP 0.03016

Synthetic route

nitrogen(II) oxide
10102-43-9

nitrogen(II) oxide

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
With Pd supported ZrO2-CeO2 catalyst at 175 - 400℃; for 1h; Reagent/catalyst; Temperature; Inert atmosphere;100%
With H2; O2; catalyst: 0.1 wtpercent Pt/La0.7Sr0.2Ce0.1FeO3 In neat (no solvent, gas phase) Kinetics; NO:H2:O2 = 1:0.25:5% gas mixt. with 5% H2O added in feed stream; at 140°C for 20 h; H2O as reagent; detd. by mass spectrometry, gas chromy.;93%
With (Y0.90Pr0.10)2O(3+x) at 900℃; Temperature; Inert atmosphere;79%
ammonia
7664-41-7

ammonia

oxygen
80937-33-3

oxygen

A

nitrogen
7727-37-9

nitrogen

B

nitrogen(II) oxide
10102-43-9

nitrogen(II) oxide

C

dinitrogen monoxide
10024-97-2

dinitrogen monoxide

Conditions
ConditionsYield
With oxygen In neat (no solvent) Fe-ZSM-5 catalyst prepared by ion exchange and heat-treated at 400, 425or 450 °C, 100 % NH3 conversion, 100 % N2 selectivity, 1000 ppm NH3 in 2 % O2-contg. He;A 100%
B 0%
C 0%
With catalyst:Fe-mordenite In neat (no solvent) Fe-mordenite catalyst prepared by ion exchange and heat-treated at 425 °C, 92 % NH3 conversion, 99 % N2 selectivity, 1000 ppm NH3 in 2 %O2-contg. He;A 92%
B n/a
C 0%
With catalyst:Fe-ZSM-5 In neat (no solvent) Fe-ZSM-5 catalyst prepared by ion exchange and heat-treated at 375 °C, 90 % NH3 conversion, 99 % N2 selectivity, 1000 ppm NH3 in 2 % O2-contg. He;A 90%
B n/a
C 0%
mercury(II) fulminate

mercury(II) fulminate

phenylhydrazine
100-63-0

phenylhydrazine

A

nitrogen
7727-37-9

nitrogen

B

mercury

mercury

Conditions
ConditionsYield
at room temperature;A n/a
B 100%
at room temperature;A n/a
B 100%
hydroxylamine
7803-49-8

hydroxylamine

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
silver (I) ion In water catalytic oxydation in presence of AgCl at pH=7.2;;100%
silver (I) ion In water catalytic oxydation in presence of AgI at pH=12.7;;91%
silver (I) ion In water catalytic oxydation in presence of (Ag(S2O3)2)(3-) at pH=12.7;;89%
barium hydrazine disulfinate

barium hydrazine disulfinate

A

barium sulfite

barium sulfite

B

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
5 d;A 100%
B n/a
5 d;A 100%
B n/a
(dinitrogen)bis(1,2-bis(diehylphosphino)ethane)iron(0)

(dinitrogen)bis(1,2-bis(diehylphosphino)ethane)iron(0)

A

nitrogen
7727-37-9

nitrogen

B

oxygen
80937-33-3

oxygen

Conditions
ConditionsYield
With HCl In tetrahydrofuran acidolysis (excess of HCl);A 100%
B 96%
In sulfuric acid aq. H2SO4;A 77%
B 90%
poly(sulfur nitride)
12033-56-6

poly(sulfur nitride)

A

(S3N3)
79796-30-8

(S3N3)

B

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
In neat (no solvent, gas phase) by heating to 130-150°C at low pressure; at temp. > 450°CS2, N2, S2N2 are produced; at temp. < 130°C S4N2, S4N4, S2N2 areproduced; various product ratio for various conditions; further products; detected by He I photoelectron spectroscopy and quadrupole mass specrometry;A 100%
B <1
(PPh3)3CoH(N2)
21373-88-6, 16920-54-0

(PPh3)3CoH(N2)

2,2,2-trifluoroethyl benzoate
1579-72-2

2,2,2-trifluoroethyl benzoate

A

(trifluoroethoxo)tris(triphenylphosphine)cobalt(I)
99668-73-2

(trifluoroethoxo)tris(triphenylphosphine)cobalt(I)

B

benzoic acid benzyl ester
120-51-4

benzoic acid benzyl ester

C

nitrogen
7727-37-9

nitrogen

D

hydrogen
1333-74-0

hydrogen

E

benzene
71-43-2

benzene

Conditions
ConditionsYield
In toluene PhCOOCH2CF3 added to toluene soln. of CoH(N2)(PPh3)3, evacuated, stirred at 20°C for 2 days;A n/a
B 28%
C 100%
D 17%
E 32%
strontium nitride diazenide

strontium nitride diazenide

A

strontium nitride diazenide

strontium nitride diazenide

B

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
In neat (no solvent) loading and unloading carried out in inert gas; heated at 920 K and pressure of 9 bar; elem. anal.;A 100%
B n/a
strontium diazenide

strontium diazenide

A

strontium nitride diazenide

strontium nitride diazenide

B

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
In neat (no solvent) High Pressure; loading and unloading carried out in inert gas; heated at 920 K and pressure of 400 bar; elem. anal.;A 100%
B n/a
strontium diazenide

strontium diazenide

A

strontium nitride

strontium nitride

B

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
In neat (no solvent) loading and unloading carried out in inert gas; heated at 618 K and pressure of 1E-5 bar; elem. anal.;A 100%
B n/a
ferrocenium trifluoromethanesulfonate

ferrocenium trifluoromethanesulfonate

Na(1+)*[Mo(N(C((2)H3C)2CH3)((CH3)2C6H3))3(N2)](1-)*99C4H8O=Na[Mo(N(C((2)H3C)2H3C)((CH3)2C6H3))3N2]*99C4H8O

Na(1+)*[Mo(N(C((2)H3C)2CH3)((CH3)2C6H3))3(N2)](1-)*99C4H8O=Na[Mo(N(C((2)H3C)2H3C)((CH3)2C6H3))3N2]*99C4H8O

A

Mo(N(C(CD3)2CH3)-3,5-C6H3Me2)3

Mo(N(C(CD3)2CH3)-3,5-C6H3Me2)3

B

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
In tetrahydrofuran -35°C or 25°C; followed by IR and NMR spectroscopy;A 100%
B n/a
ammonia
7664-41-7

ammonia

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
With oxygen In gaseous matrix 450°C; (NH3) = 1000 ppm; (O2) = 2%; He = balance; total flow rate = 500 ml/min; space velocity = 2.3 10**5 1/h;99%
With oxygen In gaseous matrix 450°C; (NH3) = 1000 ppm; (O2) = 2%; He = balance; total flow rate = 500 ml/min; space velocity = 2.3 10**5 1/h;97%
With oxygen In gaseous matrix byproducts: N2O, NO; 400°C; (NH3) = 1000 ppm; (O2) = 2%; He = balance; total flow rate = 500 ml/min; space velocity = 2.3 10**5 1/h;93%
ammonia
7664-41-7

ammonia

A

nitrogen
7727-37-9

nitrogen

B

nitrogen(II) oxide
10102-43-9

nitrogen(II) oxide

C

dinitrogen monoxide
10024-97-2

dinitrogen monoxide

Conditions
ConditionsYield
With oxygen In neat (no solvent) Fe-mordenite catalyst prepared by ion exchange and heat-treated at 450 °C, 99 % NH3 conversion, 100 % N2 selectivity, 1000 ppm NH3 in 2 % O2-contg. He;A 99%
B 0%
C 0%
With oxygen; platinum high excess O2,500 °C;A <1
B n/a
C n/a
With oxygen; platinum at 300 °C;A n/a
B <9
C n/a
ammonia
7664-41-7

ammonia

oxygen
80937-33-3

oxygen

A

nitrogen
7727-37-9

nitrogen

B

nitrogen(II) oxide
10102-43-9

nitrogen(II) oxide

Conditions
ConditionsYield
Sr0.22La0.78CoO2.843 In neat (no solvent) byproducts: H2O; 800°C;A n/a
B 98.6%
Sr0.42La0.68CoO2.80 In neat (no solvent) byproducts: H2O; 800°C;A n/a
B 98.1%
Sr0.46La0.54CoO2.79 In neat (no solvent) byproducts: H2O; 800°C;A n/a
B 98%
tetrabutylammonium dimethylaurate(I)
228118-52-3

tetrabutylammonium dimethylaurate(I)

A

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
With ClC6H4N2(1+) In tetrahydrofuran byproducts: ClC6H5, CH4, C2H6; -78°C;A 98%
B n/a
With 2,4,6-trichlorobenzenediazonium PF6 In acetonitrile byproducts: 2,4,6-trichlorobenzene, CH4, C2H6; -78°C;A 96%
B n/a
With CH3OC6H4N2(1+) In tetrahydrofuran byproducts: CH3OC6H5, C2H6; -78°C;A 96%
B n/a
ammonium nitrate

ammonium nitrate

A

nitrogen
7727-37-9

nitrogen

B

nitrogen(II) oxide
10102-43-9

nitrogen(II) oxide

C

Nitrogen dioxide
10102-44-0

Nitrogen dioxide

D

dinitrogen monoxide
10024-97-2

dinitrogen monoxide

Conditions
ConditionsYield
at 220-260°C, nearly 98% N2O, 2% N2; troces of NO and NO2 (0.001%);A 2%
B n/a
C n/a
D 98%
potassium cyanide

potassium cyanide

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
With copper(II) oxide In neat (no solvent) heating in a stream of CO2, ratio KCN:CuO=2:10, gegin of react. at 115°C, formation of 98% N2 at 420°C;;98%
With CuO In neat (no solvent) heating in a stream of CO2, ratio KCN:CuO=2:10, gegin of react. at 115°C, formation of 98% N2 at 420°C;;98%
heating; exclusion of air; anhydrous KCN;
(PPh3)3CoH(N2)
21373-88-6, 16920-54-0

(PPh3)3CoH(N2)

2,2,2-trifluoroethyl acetate
406-95-1

2,2,2-trifluoroethyl acetate

A

methane
34557-54-5

methane

B

(trifluoroethoxo)tris(triphenylphosphine)cobalt(I)
99668-73-2

(trifluoroethoxo)tris(triphenylphosphine)cobalt(I)

C

nitrogen
7727-37-9

nitrogen

D

hydrogen
1333-74-0

hydrogen

E

ethyl acetate
141-78-6

ethyl acetate

Conditions
ConditionsYield
In toluene CH3COOCH2CF3 added to toluene soln. of CoH(N2)(PPh3)3, evacuated, stirred at room temp. for 2 days; hexane added, solid recrystd. from toluene-hexane; elem. anal.;A 1%
B 40%
C 98%
D 23%
E 30%
hydrogen
1333-74-0

hydrogen

nitrogen(II) oxide
10102-43-9

nitrogen(II) oxide

Nitrogen dioxide
10102-44-0

Nitrogen dioxide

A

nitrogen
7727-37-9

nitrogen

B

ammonia
7664-41-7

ammonia

Conditions
ConditionsYield
With catalyst: industrial nickel methanation catalyst In neat (no solvent) reduction of mixt. of NO/NO2 in gas mixt. of N2/H2 on zeolite catalyst (pretreated in H2 at 550°C, 200°C reaction temp.); gas chromy. (dimethylsulfolane coated diatomite);A 96%
B 0%
With catalyst: industrial nickel methanation catalyst In neat (no solvent) reduction of mixt. of NO/NO2 in gas mixt. of N2/H2 on zeolite catalyst (pretreated in H2 at 300°C, 200°C reaction temp.); gas chromy. (dimethylsulfolane coated diatomite);A 92.5%
B 7.5%
With catalyst: industrial nickel methanation catalyst In neat (no solvent) reduction of mixt. of NO/NO2 in gas mixt. of N2/H2 on zeolite catalyst (pretreated in H2 at 300°C, 150°C reaction temp.); gas chromy. (dimethylsulfolane coated diatomite);A 91%
B 0%
1,3-di-tert-butyl-2,2-dimethyl-1,3,2,4-diazasilagermaetidine
84806-15-5

1,3-di-tert-butyl-2,2-dimethyl-1,3,2,4-diazasilagermaetidine

Phenyl azide
622-37-7

Phenyl azide

A

1,3,7,9-tetra-tert-butyl-2,2,8,8-tetramethyl-5,10-diphenyl-1,3,5,7,9,10-hexaaza-2,8-disila-4,6-digermadispiro{3.1.3.1}decane
138174-58-0

1,3,7,9-tetra-tert-butyl-2,2,8,8-tetramethyl-5,10-diphenyl-1,3,5,7,9,10-hexaaza-2,8-disila-4,6-digermadispiro{3.1.3.1}decane

B

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
In tetrahydrofuran under Ar, dropwise addn. of THF soln. of diaminogermylene to THF soln. of phenyl azide at -25.degreeC, 3h; pptn., recrystn. (THF), elem. anal.;A 64%
B 96%
In tetrahydrofuran under Ar, dropwise addn. of THF soln. of diaminogermylene to THF soln. of phenyl azide at 25.degreeC, 3h; pptn., recrystn. (THF), elem. anal.;A 64%
B 83%
tetra-n-butylammonium tetramethylaurate(III)

tetra-n-butylammonium tetramethylaurate(III)

trimethyl(triphenylphosphine)gold(III)

trimethyl(triphenylphosphine)gold(III)

B

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
With 4-chlorobenzenediazonium hexafluorophosphate byproducts: CH4, ClC6H5;A 91%
B 96%
tetra-n-butylammonium tetramethylaurate(III)

tetra-n-butylammonium tetramethylaurate(III)

A

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
With CH3OC6H4N2(1+) In tetrahydrofuran byproducts: CH3OC6H5, C2H6, CH4; -78°C;A 95%
B n/a
With 2,4,6-trichlorobenzenediazonium PF6 In tetrahydrofuran byproducts: 2,4,6-trichlorobenzene, CH4, C2H6; -78°C;A 94%
B n/a
With 2,4,6-trichlorobenzenediazonium PF6 In acetonitrile byproducts: 2,4,6-trichlorobenzene, CH4, C2H6; -78°C;A 94%
B n/a
(NaCl(C9H5CH(CH3)2CH3)2Zr)2N2

(NaCl(C9H5CH(CH3)2CH3)2Zr)2N2

iodine
7553-56-2

iodine

A

(C9H5CH(CH3)2CH3)2ZrI2
1072431-21-0, 1072431-11-8

(C9H5CH(CH3)2CH3)2ZrI2

B

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
A 95%
B n/a
ammonia
7664-41-7

ammonia

A

nitrogen
7727-37-9

nitrogen

B

dinitrogen monoxide
10024-97-2

dinitrogen monoxide

Conditions
ConditionsYield
With oxygen In gaseous matrix byproducts: NO; 0.2 g of catalyst, 1000 ppm NH3, 2% O2, He as balance, GHSV=2.0E+5 h**-1, at 450°C; mass spect.;A 94%
B 0%
With oxygen In gaseous matrix byproducts: NO; 0.2 g of catalyst, 1000 ppm NH3, 2% O2, He as balance, GHSV=2.0E+5 h**-1, at 400°C; mass spect.;A 93%
B 0%
With oxygen In gaseous matrix byproducts: NO; 0.2 g of catalyst, 1000 ppm NH3, 2% O2, He as balance, GHSV=2.0E+5 h**-1, at 400°C; mass spect.;A 92%
B 0%
ammonia
7664-41-7

ammonia

chlorine
7782-50-5

chlorine

A

chloroamine
12190-75-9

chloroamine

B

nitrogen
7727-37-9

nitrogen

C

ammonium chloride

ammonium chloride

Conditions
ConditionsYield
In neat (no solvent) NH3:Cl2 = 39; at ambient temp.;;A 94%
B n/a
C n/a
In neat (no solvent) NH3:Cl2 = 9; at ambient temp.;;A 5%
B n/a
C n/a
In neat (no solvent) Cl2:NH3 = 1:10-50; reaction of Cl2 and NH3 dild. with N2 below 180°C under pressure;;
In neat (no solvent) Cl2:NH3:N2 = 1:20:8; at 100°C;;
(dinitrogen)bis(1,2-bis(diehylphosphino)ethane)iron(0)

(dinitrogen)bis(1,2-bis(diehylphosphino)ethane)iron(0)

nitrogen
7727-37-9

nitrogen

Conditions
ConditionsYield
In neat (no solvent, solid phase) thermolysis (150°C, 3 h);94%
nitrogen
7727-37-9

nitrogen

magnesium
7439-95-4

magnesium

magnesium nitride

magnesium nitride

Conditions
ConditionsYield
In neat (no solvent) Mg (purity: 99.5%) was heated in N2 (free of O2) at 800-850 °C for 4-5 h;;100%
In neat (no solvent) Mg was heated in a stream of N2 at 900 °C;;95%
nitrogen
7727-37-9

nitrogen

barium
7440-39-3

barium

barium nitride

barium nitride

Conditions
ConditionsYield
260-560°C, then 0.5h at 600°C;100%
In neat (no solvent) exothermic formation out of the elements at temperatures under the melting point of Ba; after heating cooling to keeping the necessary temperature;;
above 190°C; 96.15% Ba3N2;
nitrogen
7727-37-9

nitrogen

barium
7440-39-3

barium

barium subnitride

barium subnitride

Conditions
ConditionsYield
In neat (no solvent) loading and unloading carried out in inert gas; Ba metal loaded in tungsten crucible, which palced in a steel tube before loaded in quartz glasstube; evacuated (p<1E-6 bar); heated in stream of nitrogen at 1120 K fo r 24 h; evacuated again (p<1E-6 bar) for 24 h at 900 K; elem. anal.;100%
In further solvent(s) absence of air and moisture; passing N2 through soln. of Ba in liquid Naat 573 K (pptn.); filtration; reaction followed by resistivity measurements;
In further solvent(s) under inert atmosphere; Ba submerged in molten Na in stainless steel crucible; sealed; evacuated; filled with N2; heated at 973 K for 48 h; cooled under vac.; heated at 723 K for 24 h; cooled to room temp.; opened in Ar filled glovebox; detd. by X-ray powder diffraction;
bismuth
7440-69-9

bismuth

nitrogen
7727-37-9

nitrogen

bismuth nitride

bismuth nitride

Conditions
ConditionsYield
In neat (no solvent) Electrochem. Process; cothodic pulverization within 10 hours of Bi under pure N2 (0.1 - 0.3 Torr), glow-discharge at 1000-1500 V; anode Fe; description of the aparatus given;; 359.8 mg BiN; deposition of 12.1 weight % on cathode, of 45.4 weight % on anode, 25.2 weight % on glass parts of the aparatus, 17.3 weight % on Fe- (or Al-) protecting ring of the aparatus;;100%
In further solvent(s) Electric Arc; between Bi-cathode and Cu-anode in a liquid mixture of argon and nitrogen;;
In further solvent(s) Electric Arc; between Bi-cathode and Cu-anode in a liquid mixture of argon and nitrogen;;
In neat (no solvent) cathodic pulverization of Bi during glow discharge under N2 (0.1 - 0.3 torr);;
nitrogen
7727-37-9

nitrogen

strontium

strontium

strontium nitride

strontium nitride

Conditions
ConditionsYield
In neat (no solvent) loading and unloading carried out in inert gas; Sr metal loaded in tungsten crucible, which palced in a steel tube before loaded in quartz glasstube; evacuated (p<1E-6 bar); heated in stream of nitrogen at 1120 K fo r 24 h; evacuated again (p<1E-6 bar); for 24 h at 900 K; elem. anal.;100%
In gas other Radiation; strontium deposited on MgO substrate at temp. 673 K under irradn. of nitrogen radicals (RF power 350 W, N2 feed 3.0 cm**+3(STP)min**-1); annealed in vac. at 673 K or continuous nitrogen radical irradn. for 30 min; cooled;
In neat (no solvent) Fresh Sr filings are loaded into a Al2O3 jacket which is itself placed in a quartz tube. The assembly is evacuated to E-5 Torr. N2 is introduced into the vacuum line to a total pressure of 100 Torr. The temp. is slowly increased to 750°C.;
nitrogen
7727-37-9

nitrogen

ammonia
7664-41-7

ammonia

benzene
71-43-2

benzene

hydrogen cyanide
74-90-8

hydrogen cyanide

Conditions
ConditionsYield
With catalyst: Pt-oxide at 1000°C;100%
platinum at 1000°C;100%
platinum at 800°C;62.8%
With catalyst: Pt-oxide at 800°C;62.8%
Mo(N(C(CD3)2CH3)-3,5-C6H3Me2)3

Mo(N(C(CD3)2CH3)-3,5-C6H3Me2)3

nitrogen
7727-37-9

nitrogen

sodium triethylborohydride

sodium triethylborohydride

[Mo(N(C((2)H3C)2CH3)((CH3)2C6H3))3N]
163929-87-1

[Mo(N(C((2)H3C)2CH3)((CH3)2C6H3))3N]

Conditions
ConditionsYield
In tetrahydrofuran; toluene stirring (25°C, N2 atmosphere, 24 h); evapn. (vac.);100%
strontium nitride diazenide

strontium nitride diazenide

nitrogen
7727-37-9

nitrogen

strontium diazenide

strontium diazenide

Conditions
ConditionsYield
In neat (no solvent) High Pressure; loading and unloading carried out in inet gas; SrN loaded in a Mo boat, which placed in an autoclave; evacuated; filled up with N2; heated at 920 K for 24 h at 5500 bar; elem. anal.;100%
Mo(N(C(CD3)2CH3)-3,5-C6H3Me2)3

Mo(N(C(CD3)2CH3)-3,5-C6H3Me2)3

nitrogen
7727-37-9

nitrogen

[Mo(N(C((2)H3C)2CH3)((CH3)2C6H3))3N]
163929-87-1

[Mo(N(C((2)H3C)2CH3)((CH3)2C6H3))3N]

Conditions
ConditionsYield
With sodium amalgam In tetrahydrofuran stirring (28°C, 1 atm. N2);100%
With 1-methyl-1H-imidazole In diethyl ether 25°C, ether, 1 atm. of N2, 1 equiv of 1-methylimidazole, 6 h; evapd., extd. with pentane, filtered, evapd., recrystd. from pentane at -35°C;91%
With dmap In diethyl ether 25°C, ether, 1 atm. of N2, 4-dimethylaminopyridine, 24 h; evapd., extd. with pentane, filtered, evapd., recrystd. from pentane at -35°C;85%
Mo(N[((t)Bu)(3,5-C6H3Me2)])3

Mo(N[((t)Bu)(3,5-C6H3Me2)])3

nitrogen
7727-37-9

nitrogen

A

Na(1+)*[Mo(N(C(CH3)3)((CH3)2C6H3))3(N2)](1-)*99C4H8O=Na[Mo(N(C(CH3)3)((CH3)2C6H3))3(N2)]*99C4H8O

Na(1+)*[Mo(N(C(CH3)3)((CH3)2C6H3))3(N2)](1-)*99C4H8O=Na[Mo(N(C(CH3)3)((CH3)2C6H3))3(N2)]*99C4H8O

B

[Mo(N(C((2)H3C)2CH3)((CH3)2C6H3))3N]
163929-87-1

[Mo(N(C((2)H3C)2CH3)((CH3)2C6H3))3N]

Conditions
ConditionsYield
With sodium amalgam In tetrahydrofuran addn. of soln. of Mo-complex to stirred suspn. of amalgam (syringe pump,10 h); decantation, filtration (Celite), evapn. (vac.), dissoln. (pentane), filtration (Celite), evapn. (vac.);A 100%
B 1%
strontium nitride diazenide

strontium nitride diazenide

nitrogen
7727-37-9

nitrogen

strontium nitride diazenide

strontium nitride diazenide

Conditions
ConditionsYield
In neat (no solvent) High Pressure; loading and unloading carried out in inet gas; Sr4N3 loaded in a Mo boat, which placed in an autoclave; evacuated; filled up with N2; heated at 920 K for 24 h at 400 bar; elem. anal.;100%
strontium nitride

strontium nitride

nitrogen
7727-37-9

nitrogen

strontium diazenide

strontium diazenide

Conditions
ConditionsYield
In neat (no solvent) High Pressure; loading and unloading carried out in inet gas; Sr2N loaded in a Mo boat,which placed in an autoclave; evacuated; filled up with N2; heated at 9 20 K for 24 h at 5500 bar; elem. anal.;100%
High Pressure; under N2 pressure of 5500 bar; heated at 920 K in Mo-boat for 72 h; initial pressure about 2720 bar; X-ray and neutron diffraction; TG/DTA; elem. anal.;
lithium nitride

lithium nitride

nitrogen
7727-37-9

nitrogen

Li2.7Fe0.3N

Li2.7Fe0.3N

Conditions
ConditionsYield
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%
(RuH(μ-Cl)(triisopropylphosphine)2
262359-17-1

(RuH(μ-Cl)(triisopropylphosphine)2

nitrogen
7727-37-9

nitrogen

RuHCl(triisopropylphosphine)2(N2)
262359-18-2

RuHCl(triisopropylphosphine)2(N2)

Conditions
ConditionsYield
In benzene-d6 (Ar); soln. of Ru-complex in benzene-d6 added to NMR tube, sample degassed, benzene frozen in ice, tube filled with N2 to ca. 1 atm., tube agitated for 5 min;100%
Sr0992Eu0.008(Al0.5Si0.5)2

Sr0992Eu0.008(Al0.5Si0.5)2

nitrogen
7727-37-9

nitrogen

SrAlSiN3#dotEu(2+)

SrAlSiN3#dotEu(2+)

Conditions
ConditionsYield
In neat (no solvent) alloy powder transferred into boron nitride crucible, loaded into hot isostatic pressing with graphite heater, N2 pressure raised to 190 MPa at room temp., heated to 2173 K, held for 2 h, temp. reduced to ca. 473 K, pressure to 70 MPa; cooled to room temp.; detd. by XRD;100%
Ca(0.2-x)Sr0.8Eu(x)(Al0.5Si0.5)2

Ca(0.2-x)Sr0.8Eu(x)(Al0.5Si0.5)2

nitrogen
7727-37-9

nitrogen

Sr0.8Ca0.2AlSiN3#dotEu(2+)

Sr0.8Ca0.2AlSiN3#dotEu(2+)

Conditions
ConditionsYield
In neat (no solvent) alloy powder transferred into boron nitride crucible, loaded into hot isostatic pressing with graphite heater, N2 pressure raised to 50 MPa at room temp., heated to 2173 K, held for 2 h, temp. reduced to ca. 473 K, pressure to 70 MPa; cooled to room temp.; detd. by XRD;100%
Ca(0.5-x)Sr0.5Eu(x)(Al0.5Si0.5)2

Ca(0.5-x)Sr0.5Eu(x)(Al0.5Si0.5)2

nitrogen
7727-37-9

nitrogen

Sr0.5Ca0.5AlSiN3#dotEu(2+)

Sr0.5Ca0.5AlSiN3#dotEu(2+)

Conditions
ConditionsYield
In neat (no solvent) alloy powder transferred into boron nitride crucible, loaded into hot isostatic pressing with graphite heater, N2 pressure raised to 50 MPa at room temp., heated to 2173 K, held for 2 h, temp. reduced to ca. 473 K, pressure to 70 MPa; cooled to room temp.; detd. by XRD;100%

Nitrogen History

 Nitrogen (Latin nitrogenium, where nitrum (from Greek nitron) means "saltpetre" , and genes means "forming") is formally considered to have been discovered by Daniel Rutherford in 1772, who called it noxious air or fixed air. That there was a fraction of air that did not support combustion was well known to the late 18th century chemist. Nitrogen was also studied at about the same time by Carl Wilhelm Scheele, Henry Cavendish, and Joseph Priestley, who referred to it as burnt air or phlogisticated air. Compounds of nitrogen were known in the Middle Ages.

Nitrogen Consensus Reports

Reported in EPA TSCA Inventory.

Nitrogen Standards and Recommendations

DOT Classification:  2.2; Label: Nonflammable Gas

Nitrogen Specification

The Nitrogen with CAS registry number of 7727-37-9 is also known as Nitrogen gas. The IUPAC name is Molecular nitrogen. It belongs to product categories of Refrigerants; Compressed and Liquefied GasesMicro/Nanoelectronics; Chemical Synthesis; Electronic Chemicals; Gases; Synthetic Reagents; Compressed and Liquefied Gases. Its EINECS registry number is 231-783-9. In addition, the formula is N2 and the molecular weight is 28.01. Besides, this chemical is a colorless odorless gas and should be sealed in cool, ventilated place away from heat, fire at the temperature below 30 °C. In case of insufficient ventilation wear suitable respiratory equipment.

Physical properties about Nitrogen are: (1)ACD/BCF (pH 5.5): 1; (2)ACD/BCF (pH 7.4): 1; (3)#H bond acceptors: 2; (4)Polar Surface Area: 47.58Å2; (5)Index of Refraction: 1.189; (6)Molar Refractivity: 3.871 cm3; (7)Molar Volume: 31.997 cm3; (8)Polarizability: 1.535×10-24cm3; (9)Surface Tension: 23.691 dyne/cm; (10)Density: 0.875 g/cm3; (11)Enthalpy of Vaporization: 5.56 kJ/mol; (12)Vapour Pressure: 431351.344 mmHg at 25 °C.

Preparation of Nitrogen: it is prepared by the fractional distillation of liquid air in industry or by mechanical means using gaseous air. The mechanical means needs low-pressure. Firstly, clear the air of dust and mechanical impurities. Then compressing and removing carbon dioxide. Secondly, dried compressed air is separated into oxygen and nitrogen after liquefaction and distillation. At last, compressed nitrogen is filled into bottle.

Uses of Nitrogen. It has a variety of applications, including serving as an inert replacement for air where oxidation is undesirable. It can be used as a modified atmosphere, an inexpensive alternative to argon,  a safety measure on top of liquid explosives and it also can be used as a dielectric gas for high-voltage equipment. Besides, it can be used for the manufacturing of stainless steel and used in military aircraft fuel systems to reduce fire hazard. Nitrogen is commonly used during sample preparation procedures for chemical analysis for concentrating and reducing the volume of liquid samples. What's more, nitrogen tanks are also replacing carbon dioxide as the main power source for paintball guns.

You can still convert the following datas into molecular structure:
1. SMILES: N#NCopyCopied
2. InChI: InChI=1/N2/c1-2
3. InChIKey: IJGRMHOSHXDMSA-UHFFFAOYAF
4. Std. InChI: InChI=1S/N2/c1-2
5. Std. InChIKey: IJGRMHOSHXDMSA-UHFFFAOYSA-N

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