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inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
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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
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inquiry1,1,1-Trifluoroethane Basic information Product Name: 1,1,1-Trifluoroethane Synonyms: 1,1,1-Trifluorethan;1,1,1-trifluoro-ethan;1,1,1-Trifluoroform;CFC143A;CFC-143A
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiryJ&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
1)quick response within 12 hours; 2)quality guarantee: all products are strictly tested by our qc, confirmed by qa and approved by third party lab in china, usa, canada, germany, uk, italy, france etc. 3) oem/odm available; 4) rea
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Best service,high quality and cheap price. Storage:Keep away from heat,sparks and flames. Package:25kg/50kg/200kg drum or Customer demand Application:Used as pharmaceutical intermediates Transportation:BY sea/air or by courier
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
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
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
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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inquiryAmoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
1,1,1-TrifluoroethaneAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
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inquiry1,1,1-Trifluoroethane Basic information Product Name: 1,1,1-Trifluoroethane Synonyms: 1,1,1-Trifluorethan;1,1,1-trifluoro-ethan;1,1,1-Trifluoroform;CFC143A;CFC-
BaiFuChem is a Professional chemical raw material supplier in China, our main products include Biochemical , Pharma Intermediate and Organic chemical etc. BaiFuChem have wealth of products,experience , expertise and state-of-the-art
Package:in a cool and dry place Application:As a medium and low temperature refrigerant widely used today, R-404A is often used in cold storage, food refrigeration equipment, marine refrigeration equipment, industrial low temperature refrige
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inquiryProduct: Mixed Refrigerant R404A Quality Standard Purity, % ≥99.8 Moisture, ppm
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inquiryR410a Classification …Appearance:colourless Storage:yes Package:13.6kg/cyl;22.7kg/cyl Application:refrigerantion;car air
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inquiryProduct: R404a Components R125 R143 R134a Property of chloride : Molecular Weight 97.6 Boiling Point, °C -46.5 Critical Temperature, °…
1.OEM is accepted 2.Purity ≥99.8% 3.SGS/ROSH/PONY/ISO9001/ISO14001/ISO16949 Appearance:colorless, transparent Package:neutral package Application:R507 is commercial refrigeration system replace R22 and R502 HFC kind of refrigerant. Can be us
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inquiryhigh quality;competitive price Storage:keep sealed and keep from direct light Package:Sample: 50g/ bottle 100g/ bottle 1000g/ bottle bulk: 25kg/drum 50kg/drum 443kg/drum Application:Scientific research Transportation:For small batches, they will
Do best quality products, erect the morality model Application:please email us, thanks
The company have effective management team, professional technical R & D personnel, the service spirit of customer oriented. We have long-term cooperation with famous domestic manufacturer, and excellent customer resources overseas. We are skilled in
Conditions | Yield |
---|---|
at 200℃; for 2h; Conversion of starting material; | 100% |
With hydrogen fluoride; chlorine; antimonypentachloride at 15 - 20℃; under 6750.68 Torr; | 97% |
With hydrogen fluoride; chromium(III) water-soluble salt; graphite; magnesium oxide; water; mixture of, dried at 150 C, hydrofluorinated at 200-350 C at 200℃; under 7500.75 Torr; Continious process; | |
With neodymium(III) oxide; hydrogen fluoride; antimony pentafluoride at 10℃; under 2250.23 Torr; Reagent/catalyst; Large scale; |
Conditions | Yield |
---|---|
With sulfur tetrafluoride at 20℃; for 12h; steel autoclave; | 98% |
1,1-dichlorotetrafluoroethane
A
2,2,2-trifluoroethanol
B
1,1,1,2-tetrafluoroethane
C
1,1,1,2-tetrafluoro-2-chloroethane
Conditions | Yield |
---|---|
With hydrogen; palladium/alumina at 140℃; Product distribution; Mechanism; var. temp.; other catalysts; | A 5.5% B 84.3% C 10.2% |
With hydrogen; palladium at 149.85℃; under 770 Torr; Rate constant; Product distribution; Thermodynamic data; E(a); other Pd catalysts; effect of HCl and sulfur; | |
With hydrogen; palladium/alumina at 199.85℃; for 15h; Product distribution; also fluorinated aluminas catalysts; other substrate; | |
With hydrogenchloride; hydrogen; 5percent Pd/C-H Kinetics; Activation energy; Further Variations:; Catalysts; Dehydrochlorination; |
Conditions | Yield |
---|---|
at 200℃; for 2h; Conversion of starting material; | 82% |
1,1-Dichloroethylene
A
2,2,2-trifluoroethanol
B
1-Chloro-1,1-difluoroethane
C
HCFC-141b
Conditions | Yield |
---|---|
With hydrogen fluoride; SbCl5 on Carbon at 100℃; under 760.051 Torr; for 0.00277778h; | A 80% B n/a C n/a |
(Z)-5,5,6,6-Tetrafluoro-4-hydroxy-hex-3-en-2-one
A
2,3,3,4,4-pentafluorobut-1-ene
B
2,2,2-trifluoroethanol
Conditions | Yield |
---|---|
With sulfur tetrafluoride at 80℃; for 20h; Autoclave; | A 58% B 7% |
Conditions | Yield |
---|---|
With manganese(IV) oxide; hydrogen fluoride at 125℃; | |
With chromium(III) oxide; hydrogen fluoride at 50℃; unter Druck; | |
With hydrogen fluoride; lead dioxide at 125℃; |
1-Chloro-1,1-difluoroethane
A
2,2,2-trifluoroethanol
B
1-chloro-1-fluoroethane
Conditions | Yield |
---|---|
With aluminum(III) fluoride at 325℃; | |
With aluminum(III) fluoride at 300 - 400℃; |
Conditions | Yield |
---|---|
With hydrogen fluoride at 210℃; under 268460 Torr; | |
With hydrogen fluoride; antimonypentachloride at 30 - 40℃; under 27949.3 Torr; | |
With aluminium fluoride oxide-cobalt halide; hydrogen fluoride at 290℃; |
1,1,1-trifluoro-2-chloroethane
A
2,2,2-trifluoroethanol
B
1,1,1,4,4,4-hexafluorobutane
C
1,1,1,4,4,4-hexafluoro-2,3-dichlorobutane
Conditions | Yield |
---|---|
mit UV-Licht.Irradiation; |
Conditions | Yield |
---|---|
With aluminum(III) fluoride; hydrogen fluoride |
1,1-Dichloroethylene
A
2,2,2-trifluoroethanol
B
1-Chloro-1,1-difluoroethane
Conditions | Yield |
---|---|
With hydrogen fluoride; diphenylamine at 180 - 195℃; unter Druck; |
Conditions | Yield |
---|---|
With dibutyl ether; platinum under 29420.3 - 36775.4 Torr; Hydrogenation; |
acetic acid
A
2,2,2-trifluoroethanol
B
α,α,α',α'-Tetrafluordiaethylaether
Conditions | Yield |
---|---|
With sulfur tetrafluoride at -10℃; for 48h; |
2,2,2-trifluorodiazoethane
cyclohexene
A
trans-1,1,1,4,4,4-hexafluoro-2-butene
B
2,2,2-trifluoroethanol
C
7-Trifluormethyl-norcaran
D
1,1,2-trifluoroethylene
Conditions | Yield |
---|---|
for 168h; Irradiation; |
benzoic acid methyl ester
trifluoromethanide
A
2,2,2-trifluoroethanol
B
benzoate
Conditions | Yield |
---|---|
In gas Thermodynamic data; ΔH0, nucleophilic reactions of F3C- at sp2 and sp3 carbon in the gas phase, competitive reactions; |
1,1,1-trichloroethane
A
2,2,2-trifluoroethanol
B
1-Chloro-1,1-difluoroethane
C
HCFC-141b
D
1,1-Dichloroethylene
Conditions | Yield |
---|---|
With fluorinated (with SF4) γ-alumina; hydrogen fluoride for 2h; Product distribution; Ambient temperature; | |
With hydrogen fluoride; antimonypentachloride at 60℃; under 7500.6 Torr; Mechanism; var. reaction partners and temp.; | |
With chromium(III) oxide; sulfur tetrafluoride; hydrogen fluoride at 20℃; for 2h; Product distribution; Further Variations:; Reagents; |
1,1-dichlorotetrafluoroethane
1,2-dichloro-1,1,2,2-tetrafluoroethane
A
2,2,2-trifluoroethanol
B
1,1,1,2-tetrafluoroethane
C
1,1,2,2-tetrafluoroethane
D
2-chloro-1,1,2,2-tetrafluoroethane
E
1,1,1,2-tetrafluoro-2-chloroethane
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal at 240℃; for 0.00611111h; Product distribution; Mechanism; other times, other temperatures; |
trifluoroacetic acid-methyl ester
trifluoromethanide
A
2,2,2-trifluoroethanol
B
trifluoroacetate
Conditions | Yield |
---|---|
In gas Rate constant; Thermodynamic data; ΔH0, nucleophilic reactions of F3C- at sp2 and sp3 carbon in the gas phase, competitive reactions; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
methyltrifluoromethyldioxirane
A
2,2,2-trifluoroethanol
B
acetic acid methyl ester
C
trifluoroacetic acid-methyl ester
D
carbon dioxide
E
trifluoromethyl acetate
F
trifluoroacetic acid
Conditions | Yield |
---|---|
In tetrachloromethane; chloroform-d1 at 20℃; for 0.166667h; Product distribution; Mechanism; Irradiation; thermal and photochemical dicomposition in gas, solution, and matrix phases; | A 1 % Spectr. B 14 % Spectr. C 18 % Spectr. D n/a E 53 % Spectr. F 14 % Spectr. |
1,1,2-trifluoroethylene
A
2,2,2-trifluoroethanol
B
1,1,2-Trifluoroethan
C
1,1,1,4,4,4-hexafluorobutane
D
1,2,2,3,3,4-hexafluoro-butane
Conditions | Yield |
---|---|
With hydrogen; mercury under 100 - 750 Torr; Product distribution; Ambient temperature; Irradiation; different H2 pressure; |
1,1,2-trifluoroethylene
A
2,2,2-trifluoroethanol
B
1,1,1,4,4,4-hexafluorobutane
C
1,2,2,3,3,4-hexafluoro-butane
Conditions | Yield |
---|---|
With hydrogen; mercury under 100 - 750 Torr; Product distribution; Ambient temperature; Irradiation; different H2 pressure; |
2,2-dimethylpropane
Hexafluoroacetone
A
methane
B
ethane
C
propane
D
ethene
E
trifluoromethan
F
2,2,2-trifluoroethanol
Conditions | Yield |
---|---|
at 300℃; for 2h; Product distribution; Mechanism; Irradiation; other temperature, UV lamp, reaction time, in packed and unpacked vessel; |
Hexafluoroacetone
acetone
A
ethane
B
2,2,2-trifluoroethanol
C
Hexafluoroethane
Conditions | Yield |
---|---|
In ethyl acetate for 0.5h; Product distribution; Irradiation; further temperature; |
trifluoromethanide
carbonic acid dimethyl ester
A
2,2,2-trifluoroethanol
B
methyl carbonate
Conditions | Yield |
---|---|
In gas nucleophilic reactions of F3C- at sp2 and sp3 carbon in the gas phase, competitive reactions; |
Conditions | Yield |
---|---|
With potassium fluoride; copper(l) iodide; cadmium(II) iodide In N,N,N,N,N,N-hexamethylphosphoric triamide at 120℃; for 8h; | 81 % Turnov. |
Conditions | Yield |
---|---|
With potassium fluoride; copper(l) iodide; cadmium(II) iodide In N,N,N,N,N,N-hexamethylphosphoric triamide at 90℃; for 8h; | 75 % Turnov. |
1,1,1-trichloroethane
A
2,2,2-trifluoroethanol
B
1-Chloro-1,1-difluoroethane
C
HCFC-141b
D
Vinylidene fluoride
Conditions | Yield |
---|---|
With fluorinated Fe3O4 for 2h; Ambient temperature; Yields of byproduct given. Title compound not separated from byproducts; |
1,1-Dichloroethylene
A
1,1,1-Trichloro-2,2,2-trifluoroethane
B
2,2,2-trifluoroethanol
C
1-Chloro-1,1-difluoroethane
D
HCFC-141b
Conditions | Yield |
---|---|
With fluorinated Co3O4 for 2h; Ambient temperature; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; |
2,2,2-trifluoroethanol
Conditions | Yield |
---|---|
In water at 20℃; | 90% |
polytetrafluoroethylene
2,2,2-trifluoroethanol
1,1,1,2,2,3,3-heptafluorobutane
Conditions | Yield |
---|---|
With antimony pentafluoride at 50℃; for 16h; | 89% |
perfluoropropylene
2,2,2-trifluoroethanol
1,1,1,2,3,3,5,5,5-Nonafluoropentan
Conditions | Yield |
---|---|
at 310℃; for 144h; | 71% |
2,2,2-trifluoroethanol
1,1,2-trifluoroethylene
A
1,1,1,2,3,3-hexafluorobutane
Conditions | Yield |
---|---|
With antimony pentafluoride at 20℃; for 8h; Title compound not separated from byproducts; | A 70% B 1% C 2% |
Conditions | Yield |
---|---|
Stage #1: 2,2,2-trifluoroethanol; thiourea In ethanol; water at 90℃; for 5h; Stage #2: With water; sodium hydroxide for 3h; pH=12 - Ca. 13; Reflux; | 65% |
Conditions | Yield |
---|---|
With copper(l) iodide; tetrabutylammoniun azide; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In acetonitrile at 20℃; Irradiation; | 65% |
cis-[Ru(PMe3)4(H)(NH2)]
2,2,2-trifluoroethanol
cis-[Ru(PMe3)4(H)(NH3)]F
Conditions | Yield |
---|---|
In benzene mixt. was stirred at room temp. for 48 h in closed vessel; soln. was evapd. to dryness, residue was dissolved in THF, layered with pentane, cooled to -35°C over 24 h; elem. anal.; | 59% |
Conditions | Yield |
---|---|
With antimony pentafluoride at 20℃; for 8h; | 45% |
Conditions | Yield |
---|---|
With antimony pentafluoride for 8h; | 16% |
Conditions | Yield |
---|---|
With bromine at 500℃; |
Conditions | Yield |
---|---|
With chlorine at 500℃; |
2,2,2-trifluoroethanol
A
Vinylidene fluoride
B
1,1,2,2-tetrafluorocyclobutane
Conditions | Yield |
---|---|
at 750 - 910℃; |
Conditions | Yield |
---|---|
With chlorine at 497℃; |
Conditions | Yield |
---|---|
With bromine at 500℃; |
Conditions | Yield |
---|---|
With bromine at 600℃; |
Conditions | Yield |
---|---|
at 820℃; |
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