CAS No.10102-43-9,Nitric oxide Suppliers,MSDS download

Dayang Chem (Hangzhou) Co.,Ltd.

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Hebei yanxi chemical co.,LTD.

D - glucuronic acid and N - acetyl glucosamine disaccharides unit composed of hyaluronic acid (Hyaluronan), also called uronic acid, hyaluronic acid, basic structure is made up of two disaccharides unit D - glucuronic acid and N - acetyl glucosamin

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high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea

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Zhuozhou Wenxi import and Export Co., Ltd

Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard

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Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

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Nitric Monoxide Application:Nitric Monoxide

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Nitric MonoxideAppearance:appearance White powder Storage:Dry and ventilated Package:1000 g/aluminum foil bag Application:Widely used in cosmetics, medicine, beauty health food and other industries Transportation:By express (Door to door) such as FED

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Zhengzhou Kingorgchem Chemical Technology Co., Ltd.

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HuBei Ipure Biotech CO.,ltd

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WUJI XINHUI CHEMICAL CO.,LTD

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Shanghai united Scientific Co.,Ltd.

United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat

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Shanghai Run-Biotech Co., Ltd.

Shanghai, Run-Biotech Co., Ltd is a leading domestic pharmaceutical, biopharmaceutical, and health care products R & D outsourcing services company. As an innovation-driven and customer-focused company, Run Biotech provides a broad and integrated por

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Hebei Minshang Biotechnology Co., Ltd

Nitric Monoxide Application:Widely used in cosmetics, medicine, beauty health food and other industries

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Nanjing Raymon Biotech Co., Ltd.

nitric oxide Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen

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Hangzhou Fenjun Chemical Co Ltd.

Nitric Monoxide Application:Nitric Monoxide

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Hebei Ruishun Trade Co.,Ltd

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Asia Pacific Gas Enterprise Company Limited

Formula NO Application NO is produced on a massive scale as an intermediate in the Ostwald process for the synthesis of nitric acid from ammonia. Ni…

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Chemical Co.Ltd

Nitrogen oxide (NO)Appearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damaging the packages. Protect them fr

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NovaChemistry

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Matheson Tri-Gas

NITRIC OXIDE

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Linde Korea

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Linde Bangladesh Limited

Nitrogen oxide (NO)

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Synthetic route

: 7632-00-0
sodium nitrite

: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
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;

: hydrogen

: 10102-44-0
Nitrogen dioxide

A: 3352-57-6
hydroxyl

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In neat (no solvent) introduction of NO2 into an rapid streaming mixture of H-He;; spectrometric determination of OH concentration;;	A 100% B n/a
In gaseous matrix Kinetics; in argon carrier under 0.7 torr; followed by infrared chemiluminescence spectroscopy;
In gas crossed molecular beam experiment; Laser fluorescence spectroscopy;

...Expand

: 7664-41-7
ammonia

: 80937-33-3
oxygen

A: 7727-37-9
nitrogen

B: 10102-43-9
nitrogen(II) oxide

C: 10024-97-2
dinitrogen monoxide

Conditions

Conditions	Yield
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%

...Expand

: C10H13NOS

: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
With cobaltocene In fluorobenzene for 5h; Inert atmosphere;	100%

: magnesium nitrite

: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
With water; nitric acid at 20℃; under 75.0075 Torr; for 2.77778E-05h;	99.99%
In water decompn. in concd. soln. already at cool;
In water decompn. in concd. soln. already at cool;

: 7758-09-0
potassium nitrite

: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
With sulfuric acid; water at 20℃; under 375.038 Torr; for 2.22222E-05h; Pressure; Reagent/catalyst; Temperature; Time;	99.98%
With sulfuric acid; potassium iodide In not given byproducts: H2O, I2; washing with NaOH soln.;
above 500 °C, based on spect. results;

: 7664-41-7
ammonia

A: 7727-37-9
nitrogen

B: 10102-43-9
nitrogen(II) oxide

C: 10024-97-2
dinitrogen monoxide

Conditions

Conditions	Yield
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

...Expand

: 7664-41-7
ammonia

: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
With oxygen; platinum react. with air adding O2;	99%
With oxygen; platinum optimal time of contact at very high temp.:some E-6 s;	97%
With oxygen; Pt(90),Rh(10) (X%) 8 atm,high temp.;	96%

: 624-91-9
methyl nitrite

: 201230-82-2
carbon monoxide

A: 553-90-2
Dimethyl oxalate

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
With 0.5% Pd/C at 100℃; under 375.038 Torr; for 0.000555556h; Pressure; Reagent/catalyst; Temperature; Time;	A 98.9% B n/a

...Expand

: 7664-41-7
ammonia

: 80937-33-3
oxygen

A: 7727-37-9
nitrogen

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
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%

...Expand

: 16649-19-7, 38586-93-5
chloro(N,N'-ethylenebis(salicylideneiminato))iron(III)

: bis(triphenylphosphoranylidene)ammonium nitrite

A: 18601-34-8
(μ-oxo)bis[(1,2-ethanediamino-N,N'-bis(salicylidene))iron(III)]

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In acetonitrile under vac., equimolar mixt.; chromy.;	A n/a B 98%
With water In acetonitrile under vac., equimolar mixt.; chromy.;	A n/a B 63%

...Expand

: ammonium nitrate

A: 7727-37-9
nitrogen

B: 10102-43-9
nitrogen(II) oxide

C: 10102-44-0
Nitrogen dioxide

D: 10024-97-2
dinitrogen monoxide

Conditions

Conditions	Yield
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%

...Expand

: 16921-91-8
nitrosyl hexafluorophosphate

: 12793-14-5
niobocene dichloride

A: (η5-C5H5)2niobium(V)(Cl2) hexafluoroantimonate

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In liquid sulphur dioxide Reaction of Cp2NbCl2 with NOSbF6 in 1/1 molar ratio at room temp. under Ar.; sepn. of solvent and NO under vac., recrystn. (SO2), elem. anal.;	A 98% B n/a

...Expand

: nitrosonium tetrafluoroborate

: 7440-05-3
palladium

: 75-05-8
acetonitrile

A: tetrakis(acetonitrile)palladium(II) bis(tetrafluoroborate)

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In acetonitrile Pd sponge (1.0 g) and NOBF4 (2.2 g) stirred in MeCN (50 mL) under vac. for 12 h with periodical removing of NO generated during the react.; filtration; anhydrous ether added to the filtrate; resulting ppt. washed (anhydrous ether) and dried (vac.); elem. anal.;	A 98% B n/a

...Expand

: 119030-00-1, 97337-05-8, 1228763-68-5
(N,N'-ethylenebis(salicylideneiminato))iron(III) nitrate

: bis(triphenylphosphoranylidene)ammonium nitrite

A: 18601-34-8
(μ-oxo)bis[(1,2-ethanediamino-N,N'-bis(salicylidene))iron(III)]

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In acetonitrile under vac., equimolar mixt.; chromy.;	A n/a B 97%

...Expand

: 3982-91-0
trichlorothiophosphine

: 10102-44-0
Nitrogen dioxide

A: OPSCl3(1+)

B: NO*PSCl3(1+)

C: 10102-43-9
nitrogen(II) oxide

D: oxygen

Conditions

Conditions	Yield
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. NO2; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube;	A 97% B 3% C n/a D n/a

...Expand

: 1012315-99-9
C49H66O5*NO(1+)

A: 518981-39-0
C49H64O5

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
With tert.-butylnitrite; trifluoroacetic acid In chloroform Inert atmosphere;	A 95% B 97%

: tetra-n-butylammonium tetramethylaurate(III)

A: 10102-43-9
nitrogen(II) oxide

B: 7440-57-5, 457905-15-6
gold

Conditions

Conditions	Yield
With [NO(1+),HMB]BF4(1-) In acetonitrile byproducts: CH4, C2H6;	A 96% B n/a

: 12793-14-5
niobocene dichloride

: nitrosonium tetrafluoroborate

A: (η5-C5H5)2niobium(V)(Cl2) tetrafluoroborate

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In liquid sulphur dioxide Reaction of Cp2NbCl2 with NOBF4 in 1/1 molar ratio at room temp. under Ar.; sepn. of solvent and NO under vac., recrystn. (SO2), elem. anal.;	A 96% B n/a

...Expand

: tetra-n-butylammonium tetramethylaurate(III)

: 603-35-0
triphenylphosphine

: trimethyl(triphenylphosphine)gold(III)

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
With [NO(1+),HMB]BF4(1-) In acetonitrile	A 94% B 96%

...Expand

: 7783-99-5
silver(I) nitrite

: 119030-00-1, 97337-05-8, 1228763-68-5
(N,N'-ethylenebis(salicylideneiminato))iron(III) nitrate

A: 18601-34-8
(μ-oxo)bis[(1,2-ethanediamino-N,N'-bis(salicylidene))iron(III)]

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In acetonitrile under vac., equimolar mixt.; chromy.;	A n/a B 95%

...Expand

: [Cu(bis(6-methyl-2-pyridylmethyl)amine)(NO2)]2[((C6H5)3P)2N](PF6)

: 76-05-1
trifluoroacetic acid

A: [Cu(bis(6-methyl-2-pyridylmethyl)amine)](CF3COO)2

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In dichloromethane Kinetics; CF3COOH soln. added; UV;	A n/a B 95%

...Expand

: (2,6-(Ph2P(o-C6H4)CH=N)2C5H3N)Cu(NO2)

: 64-19-7
acetic acid

A: (2,6-(Ph2P(o-C6H4)CH=N)2C5H3N)Cu(OAc)2

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In dichloromethane gas chromy.;	A n/a B 95%

...Expand

: 34301-54-7
1-Adamantanethiol

: [Cl2NNF6]Cu(κ2-O2N)*THF

A: [Cl2NNF6]Cu(AdS-SAd)

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In diethyl ether at 20℃; for 0.25h; Solvent;	A 95% B n/a

...Expand

: 1282-37-7
ferrocenium(III) tetrafluoroborate

: 3695-77-0
triphenylmethanethiol

: Fe4H2N8O8S2(2-)

A: Roussin’s black salt

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
With [PPN]2[S5Fe(μ-S)2FeS5] In tetrahydrofuran; acetonitrile at 20℃; for 12h; Inert atmosphere; Schlenk technique;	A 92% B n/a

...Expand

: 7440-62-2
vanadium

: 15969-55-8
dinitrogen tetroxide

A: 15053-24-4
vanadium nitrate

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In acetonitrile acceleration with acetonitrile at o°C;;	A 91% B n/a

...Expand

: 7697-37-2
nitric acid

: 7440-22-4
silver

: hydrogen cation

A: 14701-21-4
silver (I) ion

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In perchloric acid byproducts: H2O; nitric acid soln. addn. to Ag suspn. at 30-40°C, mixt. keeping at tis temp. for 15 min;	A n/a B 90%

...Expand

: 119030-00-1, 97337-05-8, 1228763-68-5
(N,N'-ethylenebis(salicylideneiminato))iron(III) nitrate

: 7632-00-0
sodium nitrite

A: 18601-34-8
(μ-oxo)bis[(1,2-ethanediamino-N,N'-bis(salicylidene))iron(III)]

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In acetonitrile under vac., equimolar mixt.; chromy.;	A n/a B 90%

...Expand

: 122744-29-0
bis{octakis(dodecyloxy)phthalocyaninato}lutetium

: nitrosonium tetrafluoroborate

A: 122873-81-8
2(C12H25O)8C32H8N8(2-)*Lu(5+)*BF4(1-)={(C12H25O)8C32H8N8}2LuBF4

B: 10102-43-9
nitrogen(II) oxide

Conditions

Conditions	Yield
In dichloromethane evapn., dissolved in heptane, filtered, recrystn. (ethyl acetate); elem. anal.;	A 90% B n/a

...Expand

: copper(II)-hyponitrite

A: 7727-37-9
nitrogen

B: 10102-43-9
nitrogen(II) oxide

C: copper(II) oxide

D: 10024-97-2
dinitrogen monoxide

Conditions

Conditions	Yield
In neat (no solvent) decompn. at 225-230°C;;	A 2-6 B 3-5 C n/a D 90%
In neat (no solvent) decompn. at 225-230°C;;	A 2-6 B 3-5 C n/a D 90%

...Expand

: 10102-43-9
nitrogen(II) oxide

: 7727-37-9
nitrogen

Conditions

Conditions	Yield
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%

: 201230-82-2
carbon monoxide

: 10102-43-9
nitrogen(II) oxide

: cobalt(II) iodide

: cobalt tricarbonyl nitrosyl

Conditions

Conditions	Yield
In neat (no solvent) 85 atm CO, 15 atm NO, 200°C;;	100%

...Expand

: 10102-43-9
nitrogen(II) oxide

: cobalt(II) iodide

: Co(1-)*I(1-)*2NO(1+)=[CoI(NO)2]

Conditions

Conditions	Yield
In neat (no solvent) 105°C, humidity as catalyst;; sublimation in N2-stream at 115°C;;	100%
In neat (no solvent) 105°C, humidity as catalyst;; sublimation in N2-stream at 115°C;;	100%
In ethanol
In ethanol

: 201230-82-2
carbon monoxide

: 10102-43-9
nitrogen(II) oxide

: cobalt(II) bromide

: cobalt tricarbonyl nitrosyl

Conditions

Conditions	Yield
In neat (no solvent) 85 atm CO, 15 atm NO, 200°C;;	100%

...Expand

: 10102-43-9
nitrogen(II) oxide

: barium(II) hydroxide

: barium nitrite monohydrate

Conditions

Conditions	Yield
1.5h, 250°C; at room temp. slowly;	100%
1.5h, 250°C; at room temp. slowly;	100%
With oxygen In water
With oxygen In water

: 10102-43-9
nitrogen(II) oxide

: cobalt(II) iodide

: dinitrosyl cobalt(-I) iodide

Conditions

Conditions	Yield
In neat (no solvent) 2g dried CoI2 at 105°C reacts with NO gas during 15-20 h;; sublimation in N2 stream at 115°C;;	100%
In neat (no solvent) byproducts: I2; 70-80°C;;
With copper In neat (no solvent) at 140°C;;	0%
With nickel In neat (no solvent)

: 70936-44-6
Fe(tetraphenylporphyrinate)C6H5

: 10102-43-9
nitrogen(II) oxide

: 89672-69-5
{(C20H8(C6H5)4N4)Fe(C6H5)(NO)}

Conditions

Conditions	Yield
reaction of a solid complex in NO atm. or a soln. of complex in toluenesaturated with NO at -28°C;	100%
In neat (no solvent) exposure of degassed solid ((C20H8(C6H5)4N4)Fe(C6H5)) to 1 atm of nitric oxide;; elem. anal.;;	>99

: (η5-indenyl)(η1-phenylacetylide)bis(triphenylphosphine)ruthenium

: 10102-43-9
nitrogen(II) oxide

A: ((η5-indenyl)(carbonyl)bis(triphenylphosphine)ruthenium) perchlorate * 0.5CH2Cl2

B: 100-47-0
benzonitrile

Conditions

Conditions	Yield
With NaClO4; CH2Cl2 In dichloromethane room temp., 15 min;	A 80% B 100%
With CH2Cl2 In dichloromethane room temp., 15 min;	A n/a B 73%

...Expand

: [UIII(2,6-Ad-4-Me-C6H2O)3]

: 10102-43-9
nitrogen(II) oxide

: [(2,6-Ad-4-Me-C6H2O)3UV(O)]

Conditions

Conditions	Yield
In neat (no solvent) under 760.051 Torr; for 0.166667h;	100%

: [Rh(C6H(CH3)2(CH2P(tert-butyl)2)2)(NO)]•

: 10102-43-9
nitrogen(II) oxide

: C26H47N2O3P2Rh

Conditions

Conditions	Yield
In benzene Inert atmosphere;	100%

: 277309-56-5
[(1,3-bis[(di-tert-butylphosphino)methyl)-4,6-dimethylbenzene(-1H))Rh(N2)]

: 10102-43-9
nitrogen(II) oxide

: C26H47N2O3P2Rh

Conditions

Conditions	Yield
In tetrahydrofuran Inert atmosphere;	100%

: 1333-74-0
hydrogen

: 10102-43-9
nitrogen(II) oxide

: 10102-44-0
Nitrogen dioxide

: 7664-41-7
ammonia

Conditions

Conditions	Yield
With catalyst: Ni(2+)Y zeolite In neat (no solvent) reduction of very dild. mixt. of NO/NO2 in gas mixt. of N2/H2 on zeolite catalyst (300°C reaction temp.); gas chromy. (dimethylsulfolane coated diatomite);	99%
With catalyst: industrial nickel methanation catalyst In neat (no solvent) reduction of very dild. mixt. of NO/NO2 in gas mixt. of N2/H2 on zeolite catalyst (300°C reaction temp.); gas chromy. (dimethylsulfolane coated diatomite);	99%
With catalyst: phthalocyanineNiY zeolite In neat (no solvent) reduction of very dild. mixt. of NO/NO2 in gas mixt. of N2/H2 on zeolite catalyst (230°C reaction temp.); gas chromy. (dimethylsulfolane coated diatomite);	94%
With catalyst: NiY zeolite In neat (no solvent) reduction of very dild. mixt. of NO/NO2 in gas mixt. of N2/H2 on zeolite catalyst (450°C reaction temp.); gas chromy. (dimethylsulfolane coated diatomite);	84%

...Expand

: [(1,1',2,2'-bisdiphenylphosphinoethylene)Pt(CF3)(OOH)]

: 10102-43-9
nitrogen(II) oxide

: 79299-90-4
[(1,1',2,2'-bisdiphenylphosphinoethylene)Pt(CF3)(NO2)]

Conditions

Conditions	Yield
In tetrahydrofuran byproducts: HNO2;	99%
In tetrahydrofuran; diethyl ether suspended in THF/Et2O mixture, evacuated and saturated with NO, stirredat 25°C for 1.5 h, N2 bubbled; filtered, washed with Et2O, dried, recrystd. from CH2Cl2/MeOH;

: aquapentacyanoferrate(III)

: 10102-43-9
nitrogen(II) oxide

: pentacyanonitrosylferrate(III)

Conditions

Conditions	Yield
With perchloric acid; sodium perchlorate In water Kinetics; byproducts: H2O; HClO4 was added to soln. of Fe complex in aq. NaClO4 to pH 3; soln. was deoxygenated with N2; NO was bubbled; UV monitoring;	99%
With perchloric acid; sodium perchlorate; sodium thiocyanide In perchloric acid; water Kinetics; deoxygenated soln. of NaSCN in aq. HClO4 was satd. with NO and mixed with deoxygenated soln. of Fe complex in aq. NaClO4 (pH 3) at 25°C; UV monitoring;
With 1,4-pyrazine; perchloric acid; sodium perchlorate In perchloric acid; water Kinetics; deoxygenated soln. of pyrazine in aq. HClO4 was satd. with NO and mixed with deoxygenated soln. of Fe complex in aq. NaClO4 (pH 3) at 25°C; UV monitoring;

: 114581-86-1
[CuI(tris(2-pyridylmethyl)amine)(CH3CN)]2+

: 10102-43-9
nitrogen(II) oxide

A: 133578-96-8
[Cu(tris(2-pyridylmethyl)amine)(H2O)](2+)

B: 10024-97-2
dinitrogen monoxide

Conditions

Conditions	Yield
In water room temp., pH = 7.0; reaction followed by gas chromy.;	A 99% B n/a

...Expand

: [(1,1',2,2'-bisdiphenylphosphinoethane)Pt(CF3)(OOH)]

: 10102-43-9
nitrogen(II) oxide

: [(1,1',2,2'-bisdiphenylphosphinoethane)Pt(CF3)(NO2)]

Conditions

Conditions	Yield
In tetrahydrofuran byproducts: HNO2;	99%

: 79355-45-6
trans-[(PPh2Me)2Pt(CF3)(OOH)]

: 10102-43-9
nitrogen(II) oxide

: ((C6H5)2PCH3)2Pt(CF3)NO2

Conditions

Conditions	Yield
In tetrahydrofuran byproducts: HNO2;	99%

: 10102-43-9
nitrogen(II) oxide

: Cr(diisopropylamido)3

: Cr(NO)(N(i)Pr2)3

Conditions

Conditions	Yield
In diethyl ether reaction at 25°C;	99%

: 205433-03-0
[(η(3)-cyclooctenyl)Co(Pr(i)2PCH2CH2PPr(i)2)](+)BF4(-)

: 10102-43-9
nitrogen(II) oxide

: 205446-13-5
[(η(3)-cyclooctenyl)Co(Pr(i)2PCH2CH2PPr(i)2)NO](+)BF4(-)

Conditions

Conditions	Yield
In acetone Ar-atmosphere; excess NO, 4 h; collection (filtration), washing (Et2O), drying (vac.); elem. anal.;	99%

: [Ru2(N,N′-diphenylformamidinate)4]

: 10102-43-9
nitrogen(II) oxide

: Ru2(N,N'-diphenylformamidinate)4(NO)2

Conditions

Conditions	Yield
In further solvent(s) NO passed for 30 min through a CH2Cl2/tetra-n-butylammonium perchlorate soln. of Ru complex; the soln. purged with N2 until dry, washed (acetone); elem. anal.;	99%

: Cr(N(C(C(2)H3)2CH3)(C6H3(CH3)2))3

: 10102-43-9
nitrogen(II) oxide

: Cr(N(C(C(2)H3)2CH3)(C6H3(CH3)2))3NO

Conditions

Conditions	Yield
In diethyl ether reaction at 25°C;	99%

: [Cr(N(C6H3FCH3)C(CH3)(C(2)H3)2)3]

: 10102-43-9
nitrogen(II) oxide

: Cr(N(C(C(2)H3)2CH3)(C6H3(CH3)F))3NO

Conditions

Conditions	Yield
In diethyl ether reaction at 25°C;	99%

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