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**Null** (Note: None of the provided abstracts directly discuss the properties, uses, or conclusions about **sodium nitrite** itself; they only mention it as a reagent in specific reactions without elaborating on its characteristics.)

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  • 7632-00-0 Structure
  • Basic information

    1. Product Name: Sodium nitrite
    2. Synonyms: Natrium nitrit;Nitrous acid sodium salt;Dusitan sodny;Anti-Rust;Nitrite de sodium;Diazotizing salts;Erinitrit;NCI-C02084;Filmerine;Synfat 1004;Nitrous acid, sodium salt;M 138C;Sodium Nitrite for Industrial use;Industrial Sodium Nitrite;
    3. CAS NO:7632-00-0
    4. Molecular Formula: NNaO2
    5. Molecular Weight: 68.99527
    6. EINECS: 231-555-9
    7. Product Categories: N/A
    8. Mol File: 7632-00-0.mol
  • Chemical Properties

    1. Melting Point: 271℃
    2. Boiling Point: 320 °C
    3. Flash Point: N/A
    4. Appearance: white to off-white powder
    5. Density: 2.168 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. Water Solubility: 820 g/L (20℃)
    10. CAS DataBase Reference: Sodium nitrite(CAS DataBase Reference)
    11. NIST Chemistry Reference: Sodium nitrite(7632-00-0)
    12. EPA Substance Registry System: Sodium nitrite(7632-00-0)
  • Safety Data

    1. Hazard Codes:  O:Oxidizing agent;
    2. Statements: R25:; R50:; R8:;
    3. Safety Statements: S45:; S61:;
    4. RIDADR: 1500
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 5.1
    8. PackingGroup: III
    9. Hazardous Substances Data: 7632-00-0(Hazardous Substances Data)

7632-00-0 Usage

Chemical Description

Sodium nitrite is a salt that is used as a food preservative and in the production of dyes and pharmaceuticals.

Chemical Description

Sodium nitrite is a salt that is used in various industrial processes, including the production of dyes and pharmaceuticals.

Chemical Description

Sodium nitrite and sodium azide are both inorganic compounds commonly used in organic synthesis.

Chemical Description

Sodium nitrite is a salt used as a food preservative and in the production of dyes and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 7632-00-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,3 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7632-00:
(6*7)+(5*6)+(4*3)+(3*2)+(2*0)+(1*0)=90
90 % 10 = 0
So 7632-00-0 is a valid CAS Registry Number.
InChI:InChI=1/HNO2.Na/c2-1-3;/h(H,2,3);/q;+1/p-1

7632-00-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • TCI America

  • (S0565)  Sodium Nitrite  >98.5%(T)

  • 7632-00-0

  • 300g

  • 140.00CNY

  • Detail
  • Alfa Aesar

  • (43015)  Sodium nitrite, 0.1M Standardized Solution   

  • 7632-00-0

  • 500ml

  • 533.0CNY

  • Detail
  • Alfa Aesar

  • (A18668)  Sodium nitrite, 98%   

  • 7632-00-0

  • 500g

  • 209.0CNY

  • Detail
  • Alfa Aesar

  • (A18668)  Sodium nitrite, 98%   

  • 7632-00-0

  • 1000g

  • 356.0CNY

  • Detail
  • Alfa Aesar

  • (A18668)  Sodium nitrite, 98%   

  • 7632-00-0

  • 5000g

  • 1729.0CNY

  • Detail
  • Alfa Aesar

  • (44227)  Sodium nitrite, 99.999% (metals basis)   

  • 7632-00-0

  • 25g

  • 1041.0CNY

  • Detail
  • Alfa Aesar

  • (44227)  Sodium nitrite, 99.999% (metals basis)   

  • 7632-00-0

  • 100g

  • 2976.0CNY

  • Detail
  • Alfa Aesar

  • (14244)  Sodium nitrite, ACS, 97% min   

  • 7632-00-0

  • 25g

  • 217.0CNY

  • Detail
  • Alfa Aesar

  • (14244)  Sodium nitrite, ACS, 97% min   

  • 7632-00-0

  • 100g

  • 347.0CNY

  • Detail
  • Alfa Aesar

  • (14244)  Sodium nitrite, ACS, 97% min   

  • 7632-00-0

  • 500g

  • 551.0CNY

  • Detail
  • Fluka

  • (35273)  Sodiumnitritesolution  volumetric, 0.1 M NaNO2 (0.1N)

  • 7632-00-0

  • 35273-1L

  • 343.98CNY

  • Detail
  • Fluka

  • (35272)  Sodiumnitritesolution  volumetric, 0.2 M NaNO2 (0.2N)

  • 7632-00-0

  • 35272-1L

  • 343.98CNY

  • Detail

7632-00-0SDS

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 sodium nitrite

1.2 Other means of identification

Product number -
Other names Sodium,nitrite

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:7632-00-0 SDS

7632-00-0Synthetic route

sodium nitrate
7631-99-4

sodium nitrate

sodium nitrite
7632-00-0

sodium nitrite

difluoro-nitro-methane
1493-05-6

difluoro-nitro-methane

sodium ethanolate
141-52-6

sodium ethanolate

A

sodium fluoride

sodium fluoride

B

sodium nitrite
7632-00-0

sodium nitrite

C

Diethyl carbonate
105-58-8

Diethyl carbonate

Conditions
ConditionsYield
In ethanol; dichloromethane alkoxide soln. (EtOH) addn. to F2C(NO2)2 soln. (CH2Cl2) (molar ratio F2C(NO2)2:nucleophile=1:4), reacting (-10°C for 10-15 min), stirring (0°C for 1 h, then 20°C for 1 h); salts. ppt. sepn. (CH2Cl2 addn.); chem. and GLC anal.;A 81%
B 78%
C 7%
In ethanol; dichloromethane alkoxide soln. (EtOH) addn. to F2C(NO2)2 soln. (CH2Cl2) (molar ratio F2C(NO2)2:nucleophile 1:2, reacting (-10°C for 10-15 min), stirring(0°C for 1 h), reaction mixt. leaving overnight at -20°C; salts. ppt. sepn. (CH2Cl2 addn., cooling), ppt. treatment with boiling ethanol, NaNO2 pptn. from filtrate, aq. H2SO4 addn. to filtrate, org. layer sepn., aq. layer extn. (CH2Cl2), ext. drying (MgSO4), distn. lead to(EtO)2CO; chem. and GLC anal.;A 48%
B 62%
C 12%
In ethanol; dichloromethane alkoxide soln. (EtOH) addn. to F2C(NO2)2 soln. (CH2Cl2) (molar ratio F2C(NO2)2:nucleophile=1:1), reacting (-10°C for 10-15 min), stirring (0°C for 1 h, then 20°C for 1 h); salts. ppt. sepn. (CH2Cl2 addn.); chem. and GLC anal.;A 18%
B 26%
C 9%
In ethanol; N,N-dimethyl-formamide alkoxide soln. (EtOH) addn. to F2C(NO2)2 soln. (DMF) (molar ratio F2C(NO2)2:nucleophile=1:2), reacting (-10°C for 10-15 min), stirring (0°C for 1 h); salts. ppt. sepn. (CH2Cl2 addn.); chem. and GLC anal.;
sodium sulfide

sodium sulfide

calcium(II) nitrate
13477-34-4

calcium(II) nitrate

sodium sulfite
7757-83-7

sodium sulfite

A

calcium sulfate

calcium sulfate

B

sodium sulfate
7757-82-6

sodium sulfate

C

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In neat (no solvent) formation at heating under glowing;;A n/a
B n/a
C 60%
difluoro-nitro-methane
1493-05-6

difluoro-nitro-methane

sodium ethanolate
141-52-6

sodium ethanolate

A

carbonate(2-)
3812-32-6

carbonate(2-)

B

sodium fluoride

sodium fluoride

C

sodium nitrite
7632-00-0

sodium nitrite

D

Diethyl carbonate
105-58-8

Diethyl carbonate

Conditions
ConditionsYield
In ethanol byproducts: NO3(1-); alkoxide soln. addn. to F2C(NO2)2 soln. (molar ratio F2C(NO2)2:nucleophile=1:2), reacting (-10°C for 10-15 min), stirring (0°C for 1 h, then 20°C for 1 h); salts. ppt. sepn. (CH2Cl2 addn.); chem. and GLC anal.;A 8%
B 43%
C n/a
D 14%
fluorotrinitromethane
21824-10-2

fluorotrinitromethane

sodium ethanolate
141-52-6

sodium ethanolate

A

ethoxyfluorodinitromethane
17021-83-9

ethoxyfluorodinitromethane

B

sodium fluoride

sodium fluoride

C

sodium nitrite
7632-00-0

sodium nitrite

D

Diethyl carbonate
105-58-8

Diethyl carbonate

Conditions
ConditionsYield
In ethanol; dichloromethane alkoxide soln. (EtOH) addn. (dropwise) to FC(NO2)3 soln. (CH2Cl2) (molar ratio FC(NO2)3:nucleophile=1:2), stirring (0-5°C for 1.5 h), 5%H2SO4 soln. addn., extn. (CH2Cl2), drying (MgSO4); residue distn. (vac.), ppt. sepn.; chem. and GLC anal., IR spectroscopy;A 42%
B n/a
C n/a
D 6.8%
N,N-bis(methylsulfonyl)hydroxylamine
96088-55-0

N,N-bis(methylsulfonyl)hydroxylamine

A

sodium methansulfinate
20277-69-4

sodium methansulfinate

B

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
With sodium hydroxide In water Product distribution; Mechanism; hydrolysis with basic, neutral and acidic aqu. solutions, also in addition of NaN3 (other products);
sodium hydroxide
1310-73-2

sodium hydroxide

Nitrogen dioxide
10102-44-0

Nitrogen dioxide

sodium nitrite
7632-00-0

sodium nitrite

sodium peroxide

sodium peroxide

N-oxo-N-nitrosoamine
16824-89-8, 12533-50-5

N-oxo-N-nitrosoamine

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In neat (no solvent) at 150°C;;
sodium hyponitrite

sodium hyponitrite

Nitrogen dioxide
10102-44-0

Nitrogen dioxide

A

sodium nitrate
7631-99-4

sodium nitrate

B

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
oxidation;
oxidation;
sodium azide

sodium azide

oxygen

oxygen

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
With sodium In neat (no solvent) byproducts: N2; oxydation when heating in presence of Na;;
With Na In neat (no solvent) byproducts: N2; oxydation when heating in presence of Na;;
sodium azide

sodium azide

Nitryl chloride

Nitryl chloride

sodium nitrite
7632-00-0

sodium nitrite

sodium azide

sodium azide

barium peroxide
1304-29-6

barium peroxide

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
With sodium In neat (no solvent) byproducts: N2; oxydation when heating in presence of Na;;
With Na In neat (no solvent) byproducts: N2; oxydation when heating in presence of Na;;
sodium amide

sodium amide

nitrosylchloride
2696-92-6

nitrosylchloride

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In neat (no solvent)
In neat (no solvent)
sodium sulfide

sodium sulfide

sodium nitrate
7631-99-4

sodium nitrate

sulfur dioxide
7446-09-5

sulfur dioxide

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In melt byproducts: Na2SO4, Na2SO3; in melt at 330°C;
sodium nitrate
7631-99-4

sodium nitrate

hydrogen cation

hydrogen cation

A

ammonia
7664-41-7

ammonia

B

hydrogen
1333-74-0

hydrogen

C

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In water byproducts: H2O; Electrolysis; electrolysis (1.25V vs. SCE), (Bu4N)4(MoFe3S4(SC6H5)3(O2C6Cl4))2 modified glassy carbon electrode, pH 10;
sodium nitrate
7631-99-4

sodium nitrate

nitric acid
7697-37-2

nitric acid

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In acetic acid Kinetics; other Radiation; γ-ray radiation of (60)Co; at 23°C; dose rate of 1.2 Gy s**(-1);
ammonium nitrate

ammonium nitrate

sodium
7440-23-5

sodium

A

sodium hyponitrite

sodium hyponitrite

B

disodium nitrite

disodium nitrite

C

sodium hydroxide
1310-73-2

sodium hydroxide

D

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In ammonia
In ammonia NH3 (liquid);
Iron(III) nitrate nonahydrate

Iron(III) nitrate nonahydrate

sodium
7440-23-5

sodium

A

hydrogen
1333-74-0

hydrogen

B

iron
7439-89-6

iron

C

sodium amide

sodium amide

D

sodium hydroxide
1310-73-2

sodium hydroxide

E

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In ammonia -33°C;
In ammonia NH3 (liquid); -33°C;
nitrogen(II) oxide
10102-43-9

nitrogen(II) oxide

sodium
7440-23-5

sodium

A

sodium hyponitrite

sodium hyponitrite

B

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
above 190°C;
above 190°C;
nitrogen(II) oxide
10102-43-9

nitrogen(II) oxide

sodium
7440-23-5

sodium

A

sodium nitrate
7631-99-4

sodium nitrate

B

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
heating with dry NO;
oxygen
80937-33-3

oxygen

sodium
7440-23-5

sodium

A

sodium hydroxide
1310-73-2

sodium hydroxide

B

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In ammonia slow O2 flow;
In ammonia NH3 (liquid); slow O2 flow;
sodium nitrate
7631-99-4

sodium nitrate

sodium
7440-23-5

sodium

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In ammonia molar ratio of Na:NaNO3 = 2:1;
In ammonia NH3 (liquid); molar ratio of Na:NaNO3 = 2:1;
sodium
7440-23-5

sodium

Nitrogen dioxide
10102-44-0

Nitrogen dioxide

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
at 22-105°C; pressure of NO2 less then 600 torr;
at 22-105°C; pressure of NO2 less then 600 torr;
sodium
7440-23-5

sodium

Nitrogen dioxide
10102-44-0

Nitrogen dioxide

A

sodium nitrate
7631-99-4

sodium nitrate

B

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
burning of Na in NO2 atmosphere;
slow oxidation of Na at the surface, above the melting point;
slow oxidation of Na at the surface, above the melting point;
burning of Na in NO2 atmosphere;
ammonia
7664-41-7

ammonia

sodium carbonate
497-19-8

sodium carbonate

oxygen

oxygen

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
In neat (no solvent) 2 volumeparts NH3 are combusted with 3 volumeparts O2; formed N2O3 (NO and NO2) is absorped by Na2CO3;;
In neat (no solvent) 2 volumeparts NH3 are combusted with 3 volumeparts O2; formed N2O3 (NO and NO2) is absorped by Na2CO3;;
Nitryl chloride

Nitryl chloride

sodium hydroxide
1310-73-2

sodium hydroxide

sodium nitrite
7632-00-0

sodium nitrite

dinitrogen trioxide
10544-73-7

dinitrogen trioxide

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
With sodium hydroxide In water byproducts: H2O; absorption of nitrosic gases in alkaline soln.;
With NaOH In water byproducts: H2O; absorption of nitrosic gases in alkaline soln.;
potassium nitrate

potassium nitrate

sodium hydroxide
1310-73-2

sodium hydroxide

sodium nitrite
7632-00-0

sodium nitrite

Conditions
ConditionsYield
With cast iron In melt melting of 500 kg KNO3 and 500 kg NaOH together; reaction of the melt with finely powdered cast iron for 5-6 h;;
sodium nitrite
7632-00-0

sodium nitrite

nitrogen(II) oxide
10102-43-9

nitrogen(II) oxide

Conditions
ConditionsYield
With acetic acid; potassium iodide In water Product distribution / selectivity;100%
With sulfuric acid; water at 10℃; under 375.038 Torr; for 1.38889E-05h; Reagent/catalyst; Temperature; Pressure; Time;99.99%
With maleic acid; ascorbic acid In water Product distribution / selectivity;
sulfur
7704-34-9

sulfur

sodium nitrite
7632-00-0

sodium nitrite

sodium thiosulfate

sodium thiosulfate

Conditions
ConditionsYield
In N,N-dimethyl-formamide byproducts: N2O; at about 80°C, under N2 or CO2, cooling, separation of Na2S2O3;; washing with acetone, analytically pure;;100%
In further solvent(s) byproducts: N2O; solvent: dimethyl acetamide, at about 80°C, under N2 or CO2, cooling, separation of Na2S2O3;; washing with acetone, analytically pure;;100%
fac-triaquotrinitroiridium(III)

fac-triaquotrinitroiridium(III)

sodium nitrite
7632-00-0

sodium nitrite

trisodium hexanitroiridate(III)

trisodium hexanitroiridate(III)

Conditions
ConditionsYield
In not given 100°C, 1 h;100%
sodium nitrite
7632-00-0

sodium nitrite

αβ-s-{Co(2-methyl-3,6,9-triazaundec-2-ene-1,11-diamine)NO2}(ZnCl4)
117229-37-5

αβ-s-{Co(2-methyl-3,6,9-triazaundec-2-ene-1,11-diamine)NO2}(ZnCl4)

Conditions
ConditionsYield
With ZnCl2 In hydrogenchloride soln. of Co-complex in HCl added NaNO2, heated for 20 min; soln. poured into 2-propanol/acetone (contained ZnCl2), cooled, powder collected, washed (acetone, Et2O), elem. anal.;100%
αβ-i-{Co(3,6,9-triazaundec-2-ene-1,11-diamine)Cl}(ClO4)2
117229-25-1

αβ-i-{Co(3,6,9-triazaundec-2-ene-1,11-diamine)Cl}(ClO4)2

sodium nitrite
7632-00-0

sodium nitrite

αβ-i-{Co(3,6,9-triazaundec-2-ene-1,11-diamine)NO2}(ZnCl4)
117229-27-3

αβ-i-{Co(3,6,9-triazaundec-2-ene-1,11-diamine)NO2}(ZnCl4)

Conditions
ConditionsYield
With ZnCl2 In perchloric acid soln. of Co-complex in HClO4 added NaNO2, heated for 20 min, poured into a acetone/2-propanol mixture with ZnCl2; cooled to 0°C, washed (acetone Et2O), elem. anal.;100%
tetrakis(methylisocyanide) boron triflate

tetrakis(methylisocyanide) boron triflate

sodium carbonate
497-19-8

sodium carbonate

sodium nitrite
7632-00-0

sodium nitrite

3Na(1+)*(B(CO2)2(CO2H)2)(3-)*2H2O=Na3(B(CO2)2(CO2H)2)*2H2O

3Na(1+)*(B(CO2)2(CO2H)2)(3-)*2H2O=Na3(B(CO2)2(CO2H)2)*2H2O

Conditions
ConditionsYield
In ethanol; sulfuric acid; water aq. H2SO4; B(CNCH3)4(CF3SO3)3 dissolved in H2O and cooled to 0°C, addn. of aq. mixt. of NO and NO2 prepd. from NaNO2, H2SO4, and H2O over 4 h, stirred for 16 h at room temp., addn. of Na2CO3 and ethanol; pptn., filtered, dissolved (H2O), soln. saturated with CO2, addn. of ethanol, pptn., filtered, washed (ethanol, diethyl ether);100%
[N,N'-bis(2-methyl-2-amino-κN-propyl)oxamidato-κ(2)N,N']copper(II)
252258-61-0

[N,N'-bis(2-methyl-2-amino-κN-propyl)oxamidato-κ(2)N,N']copper(II)

copper(II) nitrate

copper(II) nitrate

sodium nitrite
7632-00-0

sodium nitrite

catena-poly[copper(II)-μ-[N,N'-bis(2-methyl-2-aminopropyl)oxamido(2-)-N,N',O':N'',N''',O]copper(II)-di-μ-nitrito(-)-O]
252258-63-2

catena-poly[copper(II)-μ-[N,N'-bis(2-methyl-2-aminopropyl)oxamido(2-)-N,N',O':N'',N''',O]copper(II)-di-μ-nitrito(-)-O]

Conditions
ConditionsYield
In methanol; water addn. of aq. Cu(NO3)2 and then aq. NaNO2 to Cu-complex (in MeOH) with stirring (pptn.); collection (filtration), washing (MeOH, Et2O), drying in air; elem. anal.;98%
tetrafluoroboric acid

tetrafluoroboric acid

2,6-dimethoxyaniline
2734-70-5

2,6-dimethoxyaniline

sodium nitrite
7632-00-0

sodium nitrite

2,6-dimethoxybenzenediazonium tetrafluoroborate

2,6-dimethoxybenzenediazonium tetrafluoroborate

Conditions
ConditionsYield
In water at 0℃; for 0.75h;98%
tetrafluoroboric acid

tetrafluoroboric acid

3,4,5-Trimethoxyaniline
24313-88-0

3,4,5-Trimethoxyaniline

sodium nitrite
7632-00-0

sodium nitrite

3,4,5-trimethoxybenzenediazonium tetrafluoroborate

3,4,5-trimethoxybenzenediazonium tetrafluoroborate

Conditions
ConditionsYield
In water at 0℃; for 0.5h;98%
Stage #1: tetrafluoroboric acid; 3,4,5-Trimethoxyaniline In water at 0℃; for 0.25h;
Stage #2: sodium nitrite In water at 0℃; for 0.5h;
copper(II) perchlorate hexahydrate

copper(II) perchlorate hexahydrate

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

sodium nitrite
7632-00-0

sodium nitrite

[Cu(3,3'-diamino-N-methyldipropylamine)(ONO)(H2O)]ClO4
890850-35-8

[Cu(3,3'-diamino-N-methyldipropylamine)(ONO)(H2O)]ClO4

Conditions
ConditionsYield
In methanol soln. of Cu salt added to soln. of org. compd., hot soln. of NaNO2 addeddropwise, heated for 10 min; hot filtered, allowed to crystallize at room temp., filtered, washed with ether, air-dried; elem. anal.;97%
(2-aza-5,10,15,20-tetraphenyl-21-carbaporphyrinato)FeBr

(2-aza-5,10,15,20-tetraphenyl-21-carbaporphyrinato)FeBr

sodium nitrite
7632-00-0

sodium nitrite

[Fe(CTPP)NO]

[Fe(CTPP)NO]

Conditions
ConditionsYield
1 equiv of NaNO2 under inert atm. at ambient temp.; silica gel column chromy. in a room atm.;97%
zinc perchlorate

zinc perchlorate

6,16,2,5-tribenzena(1,4)-1,4,8,11,14,18,23,27-octaazabicyclo[9.9.9]nonacosaphane
119142-71-1

6,16,2,5-tribenzena(1,4)-1,4,8,11,14,18,23,27-octaazabicyclo[9.9.9]nonacosaphane

sodium nitrite
7632-00-0

sodium nitrite

[pCZn2(μ-ONO)](ClO4)3

[pCZn2(μ-ONO)](ClO4)3

Conditions
ConditionsYield
Stage #1: zinc perchlorate; 6,16,2,5-tribenzena(1,4)-1,4,8,11,14,18,23,27-octaazabicyclo[9.9.9]nonacosaphane In methanol at 20℃; for 0.5h;
Stage #2: sodium nitrite In methanol for 12h;
97%
[Ru(N,N-dimethyl-4,6-di(pyridin-2-yl)-1,3,5-triazin-2-amine)(2,2'-bipyridine)(CH3CN)](ClO4)2

[Ru(N,N-dimethyl-4,6-di(pyridin-2-yl)-1,3,5-triazin-2-amine)(2,2'-bipyridine)(CH3CN)](ClO4)2

sodium nitrite
7632-00-0

sodium nitrite

[Ru(N,N-dimethyl-4,6-di(pyridin-2-yl)-1,3,5-triazin-2-amine)(2,2'-bipyridine)(NO2)](ClO4)

[Ru(N,N-dimethyl-4,6-di(pyridin-2-yl)-1,3,5-triazin-2-amine)(2,2'-bipyridine)(NO2)](ClO4)

Conditions
ConditionsYield
In water; acetone for 12h; Reflux; Inert atmosphere;96.89%
[Ru(η2-C6HCPhCH-1-O-2-CHNHEt-3-NO2-4-Me-5)(PPh3)2(CO)Cl]
350832-46-1

[Ru(η2-C6HCPhCH-1-O-2-CHNHEt-3-NO2-4-Me-5)(PPh3)2(CO)Cl]

sodium nitrite
7632-00-0

sodium nitrite

[Ru(η2-C6HCPhCH-1-O-2-CHNHEt-3-NO2-4-Me-5)(PPh3)2(CO)(NO2)]

[Ru(η2-C6HCPhCH-1-O-2-CHNHEt-3-NO2-4-Me-5)(PPh3)2(CO)(NO2)]

Conditions
ConditionsYield
In dichloromethane; water; acetone aq. soln. of NaNO2 added dropwise to Ru complex soln. in CH2Cl2/acetone,stirred for 5 h; solvent removed (vac.), filtered, washed (H2O), dried (vac.); elem. anal.;96%
tetrafluoroboric acid

tetrafluoroboric acid

sulfamethizole
144-82-1

sulfamethizole

sodium nitrite
7632-00-0

sodium nitrite

C9H8N5O2S2(1+)*BF4(1-)

C9H8N5O2S2(1+)*BF4(1-)

Conditions
ConditionsYield
In water at 0℃; for 0.75h; Inert atmosphere;96%
hydrogenchloride
7647-01-0

hydrogenchloride

ruthenium trichloride

ruthenium trichloride

sodium nitrite
7632-00-0

sodium nitrite

ruthenium(II)nitrosyl trichloride

ruthenium(II)nitrosyl trichloride

Conditions
ConditionsYield
In water for 4h; Heating / reflux;95%
C6F5Ni(P(CH3)2C6H5)2Br

C6F5Ni(P(CH3)2C6H5)2Br

sodium nitrite
7632-00-0

sodium nitrite

C6F5Ni(P(CH3)2C6H5)2NO2

C6F5Ni(P(CH3)2C6H5)2NO2

Conditions
ConditionsYield
In water; acetone prepn. from C6F5Ni(CH3)2C6H5)2Br and excess of NaNO2 in aq. acetone under reflux;;95%
In water; acetone prepn. from C6F5Ni(CH3)2C6H5)2Br and excess of NaNO2 in aq. acetone under reflux;;95%

7632-00-0Relevant articles and documents

Generation and 355 nm laser photodissociation of nitrous acid (HONO) and HONO-water clusters

Ning,Pfab

, p. 6008 - 6014 (1997)

A stable source for the continuous production of high concentrations of gaseous nitrous acid (HONO) up to 5000 ppm has been developed, characterized, and employed for a study of the near-UV photodissociation of HONO and HONO-water clusters in a continuous supersonic free-jet expansion. The source consists of a flow reactor fed with aqueous reagent solutions purged by an inert carrier gas at flow rates up to 1 L/min. The dynamics of the photodissociation of jet-cooled HONO and HONO-water clusters at 355 nm have been studied by measuring the rotational distribution of the nascent NO (ν″ = 2) photofragment using the laser-induced fluorescence (LIF) technique. Distinctly bimodal rotational distributions have been observed for the nascent, vibrationally excited NO, which are well described by the sum of two components: a Gaussian distribution at high J and a 170 K Boltzmann distribution in the low-J range reflecting photodissociation of bare HONO , HONO-H2O complexes, and small HONO water clusters.

Cu-Pd bimetallic cluster/AC as a novel catalyst for the reduction of nitrate to nitrite

Sakamoto, Yoshinori,Nakata, Kou,Kamiya, Yuichi,Okuhara, Toshio

, p. 908 - 909 (2004)

Cu-Pd/AC catalysts that are derived from Cu-Pd clusters were shown to possess high activity for the reduction of nitrate to nitrite, but were inactive for the reduction of nitrite. In contrast, the Pd/AC catalyst was inactive for the reduction of nitrate, whereas conventional Cu-Pd/AC afforded various products, including nitrite, nitrogen, and ammonia.

Hydrogen evolution assisted electrodeposition of porous Cu-Ni alloy electrodes and their use for nitrate reduction in alkali

Mattarozzi, Luca,Cattarin, Sandro,Comisso, Nicola,Gambirasi, Arianna,Guerriero, Paolo,Musiani, Marco,Vázquez-Gómez, Lourdes,Verlato, Enrico

, p. 337 - 344 (2014)

Porous Cu-Ni alloys with a wide range of compositions have been deposited from citrate baths containing the two metal ions, under application of large current densities (-3 A cm-2) leading to vigorous hydrogen evolution. The deposited alloy layers show macroscopic porosity and a spongy material made of a network of tiny dendrites. Porous RDEs reveal a significant current increase - as compared to ordinary polished electrodes - in the fast ferrocyanide reduction under pure mass transport control. Voltammograms of nitrate reduction in alkali at porous RDEs show at all potentials larger currents in comparison with experiments at compact electrodes of same composition. Electrolyses at porous sheet electrodes show large stable currents, leading to fast and selective nitrate reduction to ammonia.

Radiolysis products of nitrate-acetate aqueous solutions and their influence on pH of the solutions

Egorov,Danilin,Zakharova,Darskaya,Zubkov

, p. 595 - 598 (2005)

The influence of the components of nitrate-acetate aqueous solution and products of their radiolysis on pH of the solutions was experimentally studied in a wide dose range. The results can be used to estimate the speciation and migration conditions of radionuclides in a reservoir bed of underground disposed sites of liquid radioactive waste. 2005 Pleiades Publishing, Inc.

Method for preparing alkyl nitrites

-

, (2008/06/13)

The invention concerns a method for preparing alkyl nitrites of formula (I) R ONO (I) ONO wherein R represents a C1-C20, advantageously C2-C10 linear or branched alkyl group. The invention is characterised in that it consists in gradually and continuously adding in an aqueous medium, an alcohol of formula (II) R OH, R being as defined above, a nitrite of formula (III) M NO2, wherein M represents a metal cation, and a strong acid, so as to form continuously said alkyl nitrite, and in continuously drawing off said alkyl nitrite thus formed from the reaction medium.

Process for producing saleable liquids from organic material

-

Page 2, (2008/06/13)

A process for producing saleable liquids from organic material comprising the following steps. Providing organic material and separating it into solids, liquids and vapour. Reacting the liquids, combining it with water vapour and producing a volatized gas stream. Removing nitrogen dioxide from the gas stream to produce a scrubbed volatized gas stream. Reacting the scrubbed volatized gas stream with water vapour to produce a combined volatized gas stream. Removing carbon dioxide from the combined volatized gas stream to produce a subtracted volatized gas stream. Reacting the subtracted volatized gas stream with methanol to produce an enhanced volatized gas stream. Distilling the enhanced volatized gas stream to produce ethanol.

Preparation of azo colorants in microreactors

-

, (2008/06/13)

Azo colorants are prepared by conducting the diazotization of aromatic or hetaromatic amines or the azo coupling reaction or the diazotization and the azo coupling reaction in a microreactor.

Infrared spectrum of the hyponitrite dianion, N2O22-, isolated and insulated from stabilizing metal cations in solid argon

Andrews,Liang

, p. 1997 - 2002 (2007/10/03)

Ultraviolet irradiation of a rigid 7 K argon matrix containing alkali or alkaline earth metal atoms and (NO)2 isolated from each other by one or two layers of argon forms N2O22- dianions insulated from two M+ cations by argon atoms, and visible photolysis reverses this electron-transfer process likely involving the N2O2- anion intermediate. The isolated N2O22- dianion is identified from isotopic substitution and isotopic mixtures, which show that the new 1028.5 cm-1 metal independent absorption involves two equivalent NO subunits. DFT calculations predict a strong 1078.1 cm-1 fundamental for the Li(NO)2Li molecule and isotopic frequency ratios in excellent agreement with the observed values, which provides a model for the matrix dianion system. The spectrum of solid Na2N2-O2, exhibits a 1030 cm-1 infrared band, which strongly supports the present N2O22- dianion assignment. The electrostatic stabilization of N2O22-, which is probably unstable in the gas phase, is made possible by metal cations separated by one or two insulating layers of argon in the rigid 7 K matrix.

A Methylene-Bridged Dialuminium Compound as a Chelating Lewis Acid: Complexation of Nitrite and Nitrate Anions by R2Al-CH2-AlR2 [R = CH(SiMe3)2]

Uhl, Werner,Hannemann, Frank,Saak, Wolfgang,Wartchow, Rudolf

, p. 921 - 926 (2007/10/03)

Sodium nitrite (NaNO2) dissolves readily in THF, when the methylene-bridged dialuminium compound R2Al-CH2-AlR2 [R = CH(SiMe3)2] 1 with two coordinatively unsaturated aluminium atoms is adde

4,5-bridged-2,3,4,5-tetrahydro-1H-3-benzazepine-7-ols and derivatives and compositions and methods employing such compounds

-

, (2008/06/13)

Novel benzazepines of the formula I: STR1 or a pharmaceutically acceptable salt thereof, wherein R represents H, alkyl, allyl or STR2 A represents --[CR1 R2]n --; n represents 3 or 4; R1 and R2 may be the same or different and each independently represents H, OH, atkyl, alkoxy, phnenyl or substituted phenyl, with the proviso that R1 and R2 on the same carbon atom are not both OH, or R1 and R2 on the same carbon atom together represent=O; G represents H, R3 (CO)-- or ArNHCO--; R3 represents H, alkyl, alkoxy, phenyl or substituted phenyl; Ar represents phenyl or substituted phenyl; and Y and Z may be the same or different and each is independently selected from H, halo, alkyl, alkoxy or halpalkyl; the pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, useful in the treatment of psychoses, drug dependence, D1 dependent neurological disorder or pain are disclosed.

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