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PROPANE Basic information Product Name: PROPANE Synonyms: PROPANE, NATURAL;A-108;C3H8;Freon 290;HC290;HC-290;Hydrocarbon propellant;hydrocarbonpropellanta-108 CAS:
Cas:74-98-6
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:74-98-6
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiry1)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
Cas:74-98-6
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryhigh 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
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:74-98-6
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
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
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Cas:74-98-6
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryPropaneisusedasbarbecues,portablestovesandmotorvehiclefuel.Propaneisusuallyusedtodrivetrains,buses,forklifts,andtaxis,butalsoretailliquefied&nAppearance:Colorless, no cloudy Storage:Cool shade Package:30LB*6.5KG Application:Steam cracker feed of the
PROPANE Basic information Product Name: PROPANE Synonyms: PROPANE,
1. Competitive price 2. Fast delivery 3. Good cooling performance 4. OEM Appearance:colorless, not muddy Storage:Keep in cool and dry place. Package:Refillable Steel Cylinders: 118L 400L 800L 926L. ISO TANK: 24m3 TANK CAR: 58m3 Application:H
Cas:74-98-6
Min.Order:0 Metric Ton
FOB Price: $1400.0 / 1600.0
Type:Trading Company
inquiry.Quality assured products .Competitive prices .Timely delivery .Ethical business dealings .Large clientele .Efficient team Appearance:Colorless and clear Package:Neutral Packing/OEM Application:Used as refrigerant,for central conditioning
Cas:74-98-6
Min.Order:6 Metric Ton
Negotiable
Type:Trading Company
inquiryHuBei ipure is a diversified product production and operation enterprise, with API, pharma intermediates, and other fine chemicals as well as R&D and pigments development and sales as one of the large enterprises, with more than 130 acres of pl
sub/micron to mesh powders (near/spheres, whiskers, flake, fiber, porous) and grain/ball, thin/ thick metal / alloys pieces / parts, thin and thick (particle) film materials /target, and custom-made crystals, substrates/parts. In the industries and a
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
Purity Grade 99.5% Formula C3H8 Application Propane is used as a feedstock for the production of base petrochemicals in steam cracking. P…
Product: R290 Property of chloride : Molecular Weight 44.097 Boiling Point, °C -42.07 Critical Temperature, °C 96.67 Critical Pressure, …Appearance:Colorless and Clear Storage:Mpa Package:Cylinder,Can,Iso-Tank Application:refrigeranting Transp
propane 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
Property of chloride : Molecular Weight 44.097 Boiling Point, °C -42.07 Critical Temperature, °C 96.67 Critical Pressure, Mpa …Appearance:Colorless, clear Package:Disposable cylinder 13.2lb/6kg,22lb/10kg, Recyclable cylinder 926L Ap
Supply top quality products with a reasonable price Application:api
CFTC?PharmaChem?is?a?service?based?company?in?China,?a?pharmachem?division?of?Changzhou?Foreign?Trade?Corp.,supplying?raw?materials,?intermediates,?APIs?and?fine?chemicals?for?the?pharmaceutical?and?specialty?chemical?industries?worldwide. Applicatio
propene
propane
Conditions | Yield |
---|---|
With para-hydrogen under 5414.51 Torr; Flow reactor; | 100% |
With hydrogen; nickel at 40℃; Thermodynamic data; Ea, various catalysts; | |
With hydrogen at 151.9 - 326.9℃; under 100 Torr; Kinetics; Ir(1.1.1)-surface; pc-C3H6 2.0 torr; kapp0, Eapp; |
carbon monoxide
A
methane
B
ethane
C
propane
D
carbon dioxide
Conditions | Yield |
---|---|
With hydrogen; nickel at 329.9℃; nickel powder, prepared by evaporation-condensation; Yields of byproduct given; | A 98% B n/a C n/a D n/a E n/a |
Conditions | Yield |
---|---|
With DIP-Co catalysts at 23℃; Reagent/catalyst; Inert atmosphere; Glovebox; | A n/a B 98% |
Conditions | Yield |
---|---|
In benzene-d6 Kinetics; thermolysis at 167 +/- 1°C; | A <2 B 97% |
In benzene Irradiation (UV/VIS); photolysis in a frozen benzene soln.; |
Conditions | Yield |
---|---|
In neat (no solvent) 150°C, 60 h; further products; | A 91% B 5% C 95% |
tetrachloromethane
oxygen
diisopropylmercury
A
propane
B
isopropyl chloride
C
chloroform
D
isopropylmercury(II) chloride
Conditions | Yield |
---|---|
In neat (no solvent) 20°C, 96 h; further products; | A 4% B 48% C 30% D 95% E 5% |
triethylsilane
2-butyl ethyl ether
A
propane
B
ethoxytriethylsilane
Conditions | Yield |
---|---|
nickel at 100 - 120℃; for 1h; | A n/a B 90% |
triethylsilane
butyl isopropyl ether
A
propane
B
n-butoxytriethylsilane
Conditions | Yield |
---|---|
nickel at 100 - 120℃; for 1h; | A n/a B 90% |
Conditions | Yield |
---|---|
With triethylamine In water at 20℃; for 2h; Inert atmosphere; Irradiation; | 90% |
Co(BF4)2(bipy)n Product distribution; Electrochemical reaction; |
water
A
methane
B
ethane
C
propane
D
ethene
E
acetylene
Conditions | Yield |
---|---|
In neat (no solvent) hydrolysis in water vapor (11.0E2 Nm**2); | A 0.24% B 6.77% C 0.14% D 2.54% E 89.5% |
Conditions | Yield |
---|---|
With hydrogen In further solvent(s) High Pressure; in perhydrocumol at 100 at;; | A 89% B n/a |
With H2 In further solvent(s) High Pressure; in perhydrocumol at 100 at;; | A 89% B n/a |
(PPh3)3CoH(N2)
phenyl butanoate
A
HCo(CO)(P(C6H5)3)3
B
phenoxotris(triphenylphosphine)cobalt(I)
C
propane
D
butyl butyrate
E
nitrogen
Conditions | Yield |
---|---|
In toluene byproducts: H2; n-PrCO2Ph added to CoH(N2)(PPh3)3 in toluene in vac., reacted for 1 day at room temp.; liquid phase analysed by GLC; hexane added, ppt. filtered, washed with hexane, dried in vac., recrystd. from C6H6-hexane; | A n/a B 60% C 12% D 38% E 89% |
methanol
A
propene
B
methane
C
ethane
D
propane
E
ethene
F
n-butane
Conditions | Yield |
---|---|
Ni-SAPO-34 at 450℃; under 760 Torr; for 1h; Product distribution; var. temp.; | A 5.26% B 1.5% C 1.02% D 0.15% E 88.04% F 0.03% |
molecular sieve In gas at 300℃; Product distribution; other temperatures; other products; | |
With hydrogen; proton-type ZSM-5 at 330℃; under 1050.11 Torr; Product distribution / selectivity; Gas phase; |
2,2-dimethylpropane
A
methane
B
ethane
C
propane
D
Isobutane
E
methylbutane
Conditions | Yield |
---|---|
With hydrogen; platinum at 243℃; Product distribution; further reaction temperatures, catalysts; | A 2.7% B 1.5% C 1.5% D 6.7% E 87.8% |
at 304℃; Product distribution; also from n-butane, other products,other temperatures, other catalysts; | A 7% B 1.7% C 2.4% D 15.6% E 73.3% |
With hydrogen; NaY-500; palladium at 216℃; Product distribution; Kinetics; Thermodynamic data; other catalysts, other temperatures; activation energies; | |
With hydrogen In neat (no solvent) at 275℃; under 1225.5 Torr; Reagent/catalyst; Inert atmosphere; |
Conditions | Yield |
---|---|
With hydrogen In 1,4-dioxane at 159.84℃; under 60006 Torr; for 24h; Autoclave; | A 87% B 9% |
With [Ru(OH2)3(4'-phenyl-2,2':6',2''-terpy)](OTf)2; hydrogen; ortho-tungstic acid In water at 250℃; under 41254.1 Torr; for 24h; | A 39 %Chromat. B 52 %Chromat. |
With hydrogen In water at 200℃; under 18751.9 Torr; for 16h; Autoclave; |
A
1-butylene
B
(Z)-2-Butene
C
trans-2-Butene
D
propane
E
ethene
Conditions | Yield |
---|---|
In toluene thermal decompn. at 60°C (15 h); further product: cyclobutane; | A 85.9% B 3.4% C 3.6% D 1% E 5.7% |
In toluene thermal decompn. at 95°C (15 h); further product: cyclobutane; | A 58.7% B 2.5% C 2.5% D 1% E 36.3% |
tetraisobutyl stannane
A
propane
B
Isobutane
C
isobutene
D
n-butane
Conditions | Yield |
---|---|
With hydrogen byproducts: C5 hydrocarbons, paraffin; 20 h, 300-310°C, 100 atm; | A 1.6% B 85.7% C 2.5% D 3.1% |
With H2 byproducts: C5 hydrocarbons, paraffin; 20 h, 300-310°C, 100 atm; | A 1.6% B 85.7% C 2.5% D 3.1% |
Conditions | Yield |
---|---|
With methanol; toluene-4-sulfonic acid at 25℃; for 12h; Time; Sealed tube; Inert atmosphere; UV-irradiation; | A 85% B 11% |
With methanol; 5% Pd/TiO2; toluene-4-sulfonic acid at 25℃; for 12h; Inert atmosphere; UV-irradiation; |
carbon monoxide
A
propene
B
methane
C
ethane
D
propane
Conditions | Yield |
---|---|
With hydrogen; nickel at 473℃; under 159.8 Torr; | A 8% B 84% C 4% D 4% |
With hydrogen; cobalt-manganese oxide at 190℃; under 4500.4 Torr; Further byproducts given. Yields of byproduct given; | |
With hydrogen; TiC Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; |
n-butane
A
propene
B
methane
C
ethane
D
propane
E
ethene
Conditions | Yield |
---|---|
at 570 - 630℃; Kinetics; | A 68% B 83% C 20% D 4% E 30% |
ferrerite zeolite at 650℃; |
butanoic acid anhydride
(PPh3)3CoH(N2)
A
Co(OCO-n-C3H7)
B
propane
C
butyl butyrate
D
nitrogen
E
hydrogen
Conditions | Yield |
---|---|
In toluene in toluene at room temp. for 1 day; | A n/a B 16% C 30% D 81% E 13% |
ethyl bromide
dimethylnickel{1,2-bis(diphenylphosphino)ethane}
A
dibromo[1,2-bis(diphenylphosphino)ethane]nickel(II)
B
methane
C
ethane
D
propane
E
ethene
Conditions | Yield |
---|---|
In toluene EtBr added into toluene soln. of Ni complex, stirred at 35°C for48 h; evapd. in vac., crystd. from Et2O-hexane; GLC anal.; | A 48% B 78% C 70% D 10% E 33% |
chloroform
ethylmagnesium chloride
A
propane
B
3-ethylpentane
C
pentane
Conditions | Yield |
---|---|
With C31H37ClN3NiO2(1-)*Li(1+) In tetrahydrofuran at 25℃; for 0.333333h; Inert atmosphere; Overall yield = 93.4 %; | A 6% B 9.4% C 78% |
With C31H37ClFeN3O2 In tetrahydrofuran at 25℃; for 0.0833333h; Inert atmosphere; |
butanoic acid anhydride
A
Co(OCO-n-C3H7)
B
propene
C
methane
D
propane
E
2-Pentanone
Conditions | Yield |
---|---|
In tetrahydrofuran in THF at -40-20°C; | A n/a B 7% C 6% D 2% E 76% |
Conditions | Yield |
---|---|
With hydrogen; Ni-B(P-1) at 473℃; under 159.8 Torr; | A 75% B 17% C 8% |
With hydrogen; technetium at 240℃; Product distribution; Thermodynamic data; E(a); other supporting materials of the technetium catalyst; var. temperatures; | A 81.0 % Chromat. B 17.9 % Chromat. C 1.1 % Chromat. |
With hydrogen at 210.3℃; under 3723.56 Torr; Product distribution / selectivity; |
Conditions | Yield |
---|---|
With sulfuric acid In not given acidolysis with H2SO4 (residue not identified); | A 74.5% B 16.3% C 21% D 72.3% |
Conditions | Yield |
---|---|
for 16h; Product distribution / selectivity; γ-Irradiation; 25 psig; | A 74% B n/a |
allyl iodid
ReH7*2P(C6H5)3=ReH7(P(C6H5)3)2
A
propane
B
2(C6H5)3PC3H5(1+)*ReI6(2-)=((C6H5)3PC3H5)2ReI6
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: H2, propene; under N2, allyl iodide was reacted with Re-complex with stirring in THFat room temp. for 3 h; filtered, washed with THF and Et2O, recrystd. from CH2Cl2-THF; elem. anal.; | A <1 B 74% |
Conditions | Yield |
---|---|
In solid thermolysis at 110°C to propane, n-butane and an unidentified residue; | A 22.3% B 72.2% |
trans-NiMe2(triethylphosphine)2
propyl bromide
trans-dibromobis(triethylphosphine)nickel(II)
B
propene
C
methane
D
ethane
E
propane
Conditions | Yield |
---|---|
In toluene propyl bromide added into toluene soln. of NiMe2(PEt3)2, stirred at room temp. for 12 h; evapd. in vac., crystd. from Et2O-hexane; GLC anal.; | A 71% B 127 % C 115 % D 46% E 35% |
Conditions | Yield |
---|---|
In gas byproducts: H2O; in gaseous phase; ion cyclotron resonance; | 100% |
Conditions | Yield |
---|---|
In gas reaction in a mass spectrometer; sample pressure 4E-7 Torr; | A 100% B 100% |
Conditions | Yield |
---|---|
In gas byproducts: H2O; in gaseous phase; ion cyclotron resonance; | 100% |
Conditions | Yield |
---|---|
In gas in gaseous phase; ion cyclotron resonance; | 100% |
propane
carbon monoxide
4-chlorophenyltrimethylsilane
1-(4-chlorophenyl)-2-methylpropan-1-one
Conditions | Yield |
---|---|
With aluminum tri-bromide; carbon tetrabromide In various solvent(s) at 0℃; for 0.5h; | 97% |
Conditions | Yield |
---|---|
With 2AlBr3*CBr4; bromine at -20℃; for 3h; | 96% |
With antimony pentafluoride; 1,2-dibromomethane 1.) -78 deg C, 2 h, 2.) RT, 24 h; | 64% |
With 2AlBr3*CBr4; bromine In various solvent(s) at -20℃; for 3h; | 48 % Turnov. |
Conditions | Yield |
---|---|
In 5,5-dimethyl-1,3-cyclohexadiene | 95% |
propane
[(η3-[2.1.1]-2,6-pyridinophane)Pt(IV)HMe2]B[3,5-(CF3)2C6H3]4
[Pt(η2-C3H6)H(η3-[2.1.1]-(2,6)-pyridinophane)] tetrakis[3,5-bis(trifluoromethyl)phenyl]borate
Conditions | Yield |
---|---|
In dichloromethane Kinetics; byproducts: CH4; by a react. of propane (3 M) with Pt-contg. compd. at room temp. in CH2Cl2 soln. for 8 h; NMR studies; two diastereomers; | 95% |
Conditions | Yield |
---|---|
With aluminum tri-bromide; carbon tetrabromide In various solvent(s) at 0℃; for 1.5h; | 94% |
With aluminum tri-bromide; carbon tetrabromide at 0℃; for 1.5h; Mechanism; |
Conditions | Yield |
---|---|
With chromium(III) oxide; carbon dioxide at 549.9℃; Product distribution; other supporting materials for Cr2O3; also in the absence of CO2; | A 91.3% B 6.4% C 0.7% D 1.6% |
at 500 - 600℃; Kinetics; | A 46% B 55% C 7% D 47% |
With hydrogen-permeable palladium module and chromia-alumina catalyst (9.0 wt % Cr) at 550℃; Temperature; | A 30% B n/a C n/a D n/a |
Conditions | Yield |
---|---|
In gas in gaseous phase; ion cyclotron resonance; | A 10% B 90% |
Conditions | Yield |
---|---|
With oxygen; multimetal oxide catalyst at 274 - 316℃; Gas phase; | 86.1% |
Conditions | Yield |
---|---|
With oxygen; multimetal oxide catalyst at 274 - 316℃; Gas phase; | 86.1% |
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