A
Isobutane
C
deuterium
Conditions | Yield |
---|---|
With water In water byproducts: H2, HD; acid hydrolysis with 20% DCl (84%); quantities of the products determined; | A n/a B 100% C n/a D n/a |
Conditions | Yield |
---|---|
With water In water acid hydrolysis with 20% HCl; quantities of the products determined; | A n/a B 100% C n/a D n/a |
Conditions | Yield |
---|---|
With triisopropylborane; trifluorormethanesulfonic acid In 1,1,2-Trichloro-1,2,2-trifluoroethane 1.) -30 deg C, 30 min 2.) room temp., 6 h; | A 99.9% B 0.1% |
Conditions | Yield |
---|---|
With tris-(trimethylsilyl)silane; 2,2'-azobis(isobutyronitrile) In toluene at 80℃; for 0.5h; | 98% |
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In 1,1,2-Trichloro-1,2,2-trifluoroethane 1.) -30 deg C 2.) room temp.; | A 92.5% B 7.5% |
Conditions | Yield |
---|---|
In hexane room temp.; further products:t-butylcyclopentadiene, tetramethylbutane, 2-methyl-4,4-dimethyl-1-pentene; GCL; | A 92% B n/a C n/a D n/a |
Conditions | Yield |
---|---|
With aluminium trichloride; polyethoxysilane (silicone GKZh-94) In nitromethane Product distribution; | A 6% B 91% |
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; |
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% |
{bis(triphenylphosphine)nitrogen}{HW(CO)5}
t-butyl bromide
A
bromopentacarbonyl tungstate(0)(1-)
B
Isobutane
Conditions | Yield |
---|---|
In tetrahydrofuran Kinetics; 26.0°C, 20-fold excess of alkyl halide; second-order rate const. is given; anal. of the reaction mixt. by gas chromy.; | A n/a B 81% |
Isobutane
Conditions | Yield |
---|---|
With hydrogen | 79.5% |
With H2 | 79.5% |
With hydrogen | 79.5% |
Conditions | Yield |
---|---|
With aluminium trichloride; polyethoxysilane (silicone GKZh-94) In nitromethane Product distribution; | A 4% B 78% |
2,4,6-tri-t-butylphenyl-fluoro-(ethylamino)borane
A
2,4,6-tri-t-butylphenyl-(ethylimino)borane
B
Isobutane
Conditions | Yield |
---|---|
With tert.-butyl lithium In hexane byproducts: LiF; dropping a soln. of t-butyl lithium in n-hexane to a soln. of 2,4,6-tri-t-butylphenyl-fluoro-(ethylamino)borane in n-hexane under N2 at -50°C and allowing to stand overnight; removal of the solvent under reduced pressure and subliming the iminoborane from the residue in an oil pump vacuum, elem. anal.; | A 78% B n/a |
adamantylamino-2,4,6-tri-t-butylphenyl fluoroborane
A
(adamantylimino)-2,4,6-tri-t-butylphenyl-borane
B
Isobutane
Conditions | Yield |
---|---|
With tert.-butyl lithium In hexane byproducts: LiF; dropping a soln. of t-butyl lithium in n-hexane to a soln. of adamantylamino-2,4,6-tri-t-butylphenyl-fluoroborane in n-hexane under N2 at -50°C, allowing to stand overnight and refluxing for 12 h; removal of the solvent under reduced pressure and subliming the iminoborane from the residue in an oil pump vacuum, elem. anal.; | A 73% B n/a |
diethyl(2,2'-bipyridyl)nickel(II)
tertiary butyl chloride
A
dichloro(2,2'-bipyridine)nickel(II)
B
ethane
C
Isobutane
D
isobutene
E
n-butane
Conditions | Yield |
---|---|
In neat (no solvent) t-BuCl added by trap-to-trap distn. to NiEt2(bpy), stirred at room temp. for 3 d; evapd. in vac.; GLC anal.; | A 70% B 2% C 4% D 50% E 64% |
Conditions | Yield |
---|---|
With aluminum oxide; silica gel; boron trichloride at 59.85℃; Product distribution; | A 1.8% B 68.8% |
2-Methylpentane
A
2-Methylhexane
B
methane
C
ethane
D
propane
E
Isobutane
F
methylbutane
Conditions | Yield |
---|---|
With hydrogen; tungsten film at 223.9℃; Product distribution; various temperature; | A 0.2% B n/a C n/a D 1.5% E 1.4% F 65.8% |
(η5-pentamethylcyclopentadienyl)2(zirconium)(H)(iosbutyl)2
A
Cp'2Zr(H)Ph
B
Isobutane
Conditions | Yield |
---|---|
With benzene In benzene Irradiation (UV/VIS); (C5Me5)2Zr(H)CH2CH(CH3) in benzene is degassed and photolyzed with a blacklight for 10 days (vac.).; Evapn., addn. of petroleum ether at -78°C, stirring for several hours, cold filtn. of yellow solid, washing (cold petroleum ether), recrystn. (-78°C, petroleum ether), elem. anal.; | A 65.6% B n/a |
Conditions | Yield |
---|---|
With aluminium trichloride; polyethoxysilane (silicone GKZh-94) In nitromethane Product distribution; | A 64% B 26% |
Conditions | Yield |
---|---|
With aluminum oxide; silica gel; boron trichloride at 59.85℃; Product distribution; Further Variations:; Reagents; | A 8% B 64% |
Sulfate; tin(IV) oxide at 249.9℃; Product distribution; pulse reactor; catalyst activity studied, prep. of catalyst varied; | A 7.5% B 3% |
aluminum oxide; boron trifluoride at 19.9℃; under 201.02 Torr; Rate constant; different catalytic systems, different BF3-pressure; |
Conditions | Yield |
---|---|
phosphotungstic acid; Al2O3-F; platinum at 310℃; Product distribution; Further Variations:; Catalysts; Temperatures; | A 0.6% B 62.1% C 0.6% |
With tertiary butyl chloride; C9H20N(1+)*Al2Cl7(1-) at 95℃; under 13446.2 Torr; for 4.4h; Time; Reagent/catalyst; Inert atmosphere; | A 30.79% B 21.33% C 8.72% |
aluminum tri-bromide; copper dichloride at 28℃; for 2h; Yield given; |
Conditions | Yield |
---|---|
With hydrogen at 380℃; under 2250.23 Torr; Temperature; | 62% |
With hydrogen; Pt-η-Al2O3-Cl at 200℃; under 15001.2 - 22501.8 Torr; Product distribution; test chlorinated catalysts for the isomerization of C4-C6 alkanes; also other alkanes (n-pentane, hexane fraction and their mixtures); | 53.83% |
With Ga(3+)-modified sulfated zirconia at 190℃; under 760.051 Torr; Reagent/catalyst; Flow reactor; | 30% |
chloroform
butyl magnesium bromide
A
2,4-dimethylpentane
B
Isobutane
Conditions | Yield |
---|---|
With C31H37ClN3NiO2(1-)*Li(1+) In tetrahydrofuran at 25℃; for 0.333333h; Inert atmosphere; Overall yield = 96.3 %; | A 62% B 34.3% |
Conditions | Yield |
---|---|
silica/alumina-supp. -O-W[(C-tBu)(-CH2-tBu)2] at 150℃; under 600 Torr; for 120h; Product distribution; Further Variations:; Catalysts; | A 61.7% B 3.4% C 25.7% D 5.5% |
Isobutane
Conditions | Yield |
---|---|
With water | 61% |
Isobutane
Conditions | Yield |
---|---|
With hydrogen In benzene-d6 at 24.84℃; under 760.051 Torr; Kinetics; Mechanism; Pressure; | 60% |
1-butylene
carbon monoxide
A
methane
B
propane
C
Isobutane
D
n-butane
Conditions | Yield |
---|---|
With hydrogen; dodecacarbonyltetrairidium In various solvent(s) at 175℃; under 760 Torr; Further byproducts given; | A 0.5% B 16% C 59% D 11% |
propene
carbon monoxide
A
methane
B
propane
C
Isobutane
D
n-butane
Conditions | Yield |
---|---|
With hydrogen; dodecacarbonyltetrairidium In various solvent(s) at 175℃; under 760 Torr; Further byproducts given; | A 1% B 17% C 56% D 11% |
n-heptane
A
2-Methylhexane
B
3-methyl-hexane
C
Isobutane
D
methylbutane
Conditions | Yield |
---|---|
With aluminum oxide; silica gel; boron trichloride at 59.85℃; Product distribution; | A n/a B n/a C 13% D 55% |
2,4,6-tri-t-butylphenyl-fluoro-(phenylamino)borane
A
2,4,6-tri-t-butylphenyl-(phenylimino)borane
B
Isobutane
Conditions | Yield |
---|---|
With tert.-butyl lithium In hexane byproducts: LiF; dropping a soln. of t-butyl lithium in n-hexane to a soln. of 2,4,6-tri-t-butylphenyl-fluoro-(phenylamino)borane in n-hexane under N2 at -20°C and allowing to stand overnight; removal of the solvent under reduced pressure and subliming the iminoborane from the residue in an oil pump vacuum, elem. anal.; | A 54% B n/a |
Conditions | Yield |
---|---|
With N-hydroxyphthalimide; air; cobalt acetylacetonate In benzonitrile at 100℃; under 7600 Torr; for 8h; Oxidation; | A 13% B 84% |
With oxygen; azido(tetraphenylporphyrinato) complex of Cr(III) In benzene at 80℃; under 5171.5 Torr; for 6h; | A 0.8 mmol B 6.3 mmol |
Conditions | Yield |
---|---|
With copper(l) iodide; caesium carbonate; ethylenediamine In toluene Reflux; | 83% |
Conditions | Yield |
---|---|
With oxygen Rate constant; Product distribution; var. oxygen pressure; time dependence; | A 20% B 80% |
Isobutane
methyl-d3-propane-1,1,1,3,3,3-d6
Conditions | Yield |
---|---|
With DUSY zeolite at 200℃; Substitution; | 80% |
perfluoropropylene
Isobutane
A
4,4-Dimethyl-1,1,1,2,3,3-hexafluoropentane
Conditions | Yield |
---|---|
With di-tert-butyl peroxide at 140℃; for 24h; Product distribution; Further Variations:; Reagents; Temperatures; time; irradiation; Addition; | A 80% B 3% |
Conditions | Yield |
---|---|
With dichloromethane; antimony pentafluoride 1.) -78 deg C, 2 h, 2.) RT, 24 h; | 76% |
at -15℃; Photochlorierung; | |
at 54℃; bei der photochemischen Chlorierung; | |
at 450 - 500℃; bei der thermischen Chlorierung; |
Conditions | Yield |
---|---|
With tetrakis(tetrabutylammonium)decatungstate(VI) In water; acetonitrile at 20℃; under 7500.75 Torr; for 4h; UV-irradiation; Flow reactor; | 76% |
Conditions | Yield |
---|---|
With antimony pentafluoride; 1,2-dibromomethane 1.) -78 deg C, 2 h, 2.) RT, 24 h; | 75% |
With bromine | |
With bromine | |
With bromine |
Conditions | Yield |
---|---|
oxyhydrogen flame; ratio of i-C4H10/NH3 = 1.07; | 71.8% |
Conditions | Yield |
---|---|
With tetrakis(tetrabutylammonium)decatungstate(VI) In water; acetonitrile at 20℃; under 7500.75 Torr; for 4h; UV-irradiation; Flow reactor; | 71% |
Conditions | Yield |
---|---|
In dichloromethane Product distribution; 1.) -30 deg C, 2.) 17-19 deg C; other alkanes and cycloalkanes and aprotic superacids, also bromobenzene, var. temp. and time; | A 68% B 35% |
.
The Isobutane , with the register number75-28-5, has other names as 1,1-Dimethylethane;2-Methylpropan ; 2-methyl-propan ; a31(hydrocarbon) ; i-Butane ; Isobutan ; Isobutane mixtures ; isobutane(dot) .
The physical properties of this chemcial are as followings: (1)ACD/LogP: 2.70 ; (2)ACD/LogD (pH 5.5): 2.7 ; (3)ACD/LogD (pH 7.4): 2.7 ; (4)ACD/BCF (pH 5.5): 66.02 ; (5)ACD/BCF (pH 7.4): 66.02 ; (6)ACD/KOC (pH 5.5): 698.43 ; (7)ACD/KOC (pH 7.4): 698.43 ; (8)Index of Refraction: 1.352 ; (9)Molar Refractivity: 20.53 cm3 ; (10)Molar Volume: 94.9 cm3 ; (11)Polarizability: 8.14 ×10-24 cm3 ; (12)Surface Tension: 15.5 dyne/cm ; (13)Density: 0.612 g/cm3 ; (14)Enthalpy of Vaporization: 21.3 kJ/mol ; (15)Vapour Pressure: 2580 mmHg at 25°C.
This is a kind of air with no odour and no color but is flammable and combustible. This is stable. And this is widely used in many ways. It could be used as the aerosol and the aerating agent. Besides, it could also be applied in Standard gas for the Petrochemical Corporation analysis and detecting instrument. What's more, it can be used in making the isooctane, and being the improver & refrigerant for the gasoline octane number.
Its product categories are including refrigerants;Organics;Refrigerant;Gas Cylinders;Hydrocarbons (Low Boiling point);Synthetic Organic Chemistry. Besides, its raw materials are in the following: Liquefied petroleum ges, C4 Fraction while its preparation products are the below: Propylene oxide, ISOBUTYLENE, Methacrylic acid, (1R-cis)-3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropane carboxylic acid, N-BUTANE, 1-BUTENE, 1R-cis crysanthemic acid, ETHOPERMETHRIN,95%, 2,2,4-Trimethylpentane, etc.
Being a kind of extremely flammable chemical, it has an extremely low flash point and boiling point, and gases that catch fire in contact with air. So while dealing with it, you should be very cautious.
Keep container in a well-ventilated place and keep away from sources of ignition - No smoking
Additionally, you could convert the following data information into the molecular structure:
SMILES:CC(C)C
InChI:InChI=1/C4H10/c1-4(2)3/h4H,1-3H3
InChIKey:NNPPMTNAJDCUHE-UHFFFAOYAY
Below are the toxicity information of this chemical:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LCLo | inhalation | 1041gm/m3/2H (1041000mg/m3) | BEHAVIORAL: EXCITEMENT | Journal of Pharmacology and Experimental Therapeutics. Vol. 58, Pg. 74, 1936. |
rat | LC50 | inhalation | 57pph/15M (570000ppm) | BEHAVIORAL: TREMOR BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION | Human Toxicology. Vol. 1, Pg. 239, 1982. |
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