Dayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities
Cas:928-45-0
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
high qualityAppearance:white crystalline powder Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Cas:928-45-0
Min.Order:0
Negotiable
Type:Manufacturers
inquiryAnsciep 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
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:928-45-0
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryYinghao Pharm products include: leader molecule, heterocyclic compounds,chiral compounds, photoelectric materials, biochemical reagents etc. For example:benzene, pyrimidine, boricacid,pyridine, pyrazole, imidazole, pyrrole, fluorine and other derivat
Best quality & Attractive price & Professional service; Trial & Pilot & CommercialHenan Fine Chemicals Co., LTD. is a diversified technology - oriented integrated company, which mainly concentrates on fine chemicals. Our company is committed to becom
Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
Conditions | Yield |
---|---|
With N-nitro-2,4,6-trimethylpyridinium tetrafluoroborate In acetonitrile at 0℃; for 2h; | 100% |
With carbon dioxide; dinitrogen pentoxide at 0℃; under 45004.5 - 60006 Torr; for 0.5h; Autoclave; | 94% |
With nitric acid; urea; europium(III) trifluoromethanesulfonate In cyclohexane at 80℃; for 10h; Schlenk technique; | 90% |
N-Butyl-2,4,6-triphenylpyridinium nitrate
butyl nitrate
Conditions | Yield |
---|---|
at 250℃; under 760 Torr; for 3h; | 50% |
Conditions | Yield |
---|---|
With silver nitrate; acetonitrile | |
With silver nitrate In acetonitrile |
Conditions | Yield |
---|---|
With silver nitrate; acetonitrile | |
With nitric acid at -10℃; |
Conditions | Yield |
---|---|
With nitric acid Electrolysis.an Platinanoden; |
Conditions | Yield |
---|---|
With dichloromethane; dinitrogen tetraoxide; butan-1-ol at -80℃; |
butyl-nitro-amine; ammonium salt
butyl nitrate
Conditions | Yield |
---|---|
With nitrylfluoride In acetonitrile |
Conditions | Yield |
---|---|
With dinitrogen pentoxide In dichloromethane at 0 - 10℃; |
n-butane
A
n-Butyl nitrite
B
butyl nitrate
C
sec-butyl nitrite
D
2-nitrobutane
E
2-butyl nitrate
F
1-nitrobutane
Conditions | Yield |
---|---|
With dihydrogen peroxide; Nitrogen dioxide at 24.9℃; under 300.02 Torr; Rate constant; Product distribution; Mechanism; boric-acid-coated surface; various pressure and carrier-gas composition; | A 6 % Chromat. B 0.3 % Chromat. C 31 % Chromat. D 51 % Chromat. E 3 % Chromat. F 7 % Chromat. |
Conditions | Yield |
---|---|
With methyl nitrite; ultra-zero air; nitrogen(II) oxide at 25.9℃; for 0.333333h; Product distribution; Rate constant; Irradiation; other alkyl peroxy radical generator (Cl2); |
n-butane
A
butyl nitrate
B
sec-butyl nitrite
C
2-nitrobutane
D
2-butyl nitrate
E
butyraldehyde
F
butanone
Conditions | Yield |
---|---|
With dihydrogen peroxide; oxygen; Nitrogen dioxide at 24.9℃; under 300.02 Torr; Rate constant; Product distribution; Mechanism; boric-acid-coated surface; various O2 concn.; |
pentanal
A
butyl nitrate
B
peroxyacetyl nitrate
D
n-pentanoyl peroxynitrate
Conditions | Yield |
---|---|
With air; nitrogen(II) oxide Nitration; sunlight; Further byproducts given. Title compound not separated from byproducts; |
peroxypentanoic acid
A
methyl nitrate
B
butyl nitrate
C
peroxyacetyl nitrate
D
n-pentanoyl peroxynitrate
Conditions | Yield |
---|---|
With nitric acid In dodecane Nitration; Title compound not separated from byproducts; |
acetic acid
N-butylamine
A
butyl nitrate
B
sec-Butyl acetate
C
acetic acid butyl ester
Conditions | Yield |
---|---|
Mechanism; |
n-butane
A
ethyl nitrate
B
butyl nitrate
C
2-butyl nitrate
D
peroxyacetyl nitrate
F
butanone
Conditions | Yield |
---|---|
With air; Nitrogen dioxide at 25℃; for 6h; Product distribution; Mechanism; Kinetics; Irradiation; also addition of NO; | A 1.3 % Chromat. B 1.3 % Chromat. C 16 % Chromat. D 23 % Chromat. E 1.3 % Chromat. F 37 % Chromat. G n/a |
Conditions | Yield |
---|---|
Reaktion des Natriumsalzes; Produkt 5: Octan; Produkt 6: Octandioldinitrat.Electrolysis; |
Conditions | Yield |
---|---|
With sodium nitrate; water Electrolysis; |
ethene
nitric acid
A
ethyl nitrate
B
butyl nitrate
C
1,2-ethyl dinitrate
D
diethylene glycol dinitrate
Conditions | Yield |
---|---|
Electrolysis; |
ethene
nitric acid
acetic acid
A
ethyl nitrate
B
butyl nitrate
C
1,2-ethyl dinitrate
D
diethylene glycol dinitrate
Conditions | Yield |
---|---|
Electrolysis; |
ethene
acetone
A
ethyl nitrate
B
butyl nitrate
C
1,2-ethyl dinitrate
D
diethylene glycol dinitrate
Conditions | Yield |
---|---|
Electrolysis; |
ethene
acetic acid
A
ethyl nitrate
B
butyl nitrate
C
1,2-ethyl dinitrate
D
diethylene glycol dinitrate
Conditions | Yield |
---|---|
Electrolysis; |
ethene
water
acetone
A
ethyl nitrate
B
butyl nitrate
C
1,2-ethyl dinitrate
D
diethylene glycol dinitrate
Conditions | Yield |
---|---|
Electrolysis; |
sodium proprionate
A
ethyl nitrate
B
butyl nitrate
C
1,2-ethyl dinitrate
D
1,4-butanediol dinitrate
Conditions | Yield |
---|---|
Elektrolyse an Platinanode.Electrolysis; |
sodium proprionate
A
ethyl nitrate
B
butyl nitrate
C
1,2-ethyl dinitrate
D
1,4-butanediol dinitrate
Conditions | Yield |
---|---|
Produkt5:Aethylpropionat ;Elektrolyse an Platinanode.Electrolysis; |
sodium proprionate
A
ethyl nitrate
B
butyl nitrate
C
1,2-ethyl dinitrate
D
1,4-butanediol dinitrate
Conditions | Yield |
---|---|
Elektrolyse an Platinanode.Electrolysis; |
1-methyl-1H-imidazole
butyl nitrate
1-butyl-3-methylimidazolium nitrate
Conditions | Yield |
---|---|
at 120℃; for 0.5h; Microwave irradiation; | 96% |
In ethyl acetate for 24h; Reflux; | 89% |
Conditions | Yield |
---|---|
Mehrtaegiges Stehenlassen.; |
Conditions | Yield |
---|---|
zersetzt sich beim Erhitzen explosionsartig; |
butyl nitrate
p-toluidine
A
N-butyl-4-methylaniline
B
para-methyl anilinium nitrate
Conditions | Yield |
---|---|
at 100℃; |
Conditions | Yield |
---|---|
at 100℃; |
Conditions | Yield |
---|---|
at 100℃; |
butyl nitrate
toluene
A
1-methyl-4-nitrobenzene
B
1-methyl-2-nitrobenzene
Conditions | Yield |
---|---|
With sulfuric acid at 40 - 60℃; |
Conditions | Yield |
---|---|
at 100℃; |
cycloactanone
butyl nitrate
A
2-nitrocyclooctanone
B
butyl 8-nitrooctanoate
Conditions | Yield |
---|---|
With dihexylamine at 60℃; Rate constant; |
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