Appearance..........................................................................................................................................................Colourless and Transparent Liquid. Color (APHA)......................................
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Cas:126-71-6
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inquiryAbout Product Details Triisobutyl phosphate Basic information Product Name: Triisobutyl
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inquiryProduct name Triisobutyl phosphate CAS NO. 126-71-6 Molecular formula C12H27O4P Molecular weight 266.31 Physicochemica
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Cas:126-71-6
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inquiryPhosphoric acid CAS:126-71-6 Specification Product Name Triisobutyl phosphate CAS No. 126-71-6 Appearance Colorless clear liquid Assay
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inquirySuperior quality, moderate price & quick delivery. Appearance:Colorless transparent liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Thi
Product name: Tri-Isobutyl Phosphate CAS No.: 126-71-6 Molecule Formula:C12H27O4P Molecule Weight:266.31 Purity: 99.0% Package: 200kg/drum Description:Colorless transparent liquid Manufacture Standards:Enterprise Standard TESTING
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inquiry2-methyl-propan-1-ol
A
triisobutyl phosphate
B
diphosphoric acid tetraisobutyl ester
Conditions | Yield |
---|---|
With phosphorous; tetraethylammonium iodide In water at 50℃; Electrolysis; | A 4% B 81% |
2-methyl-propan-1-ol
A
diisobutyl phosphite
B
diisobutyl phosphoric acid
C
triisobutyl phosphate
Conditions | Yield |
---|---|
With sodium hypophosphite; copper dichloride at 24.9℃; for 148h; | A 5.6% B 66.6% C 27.8% |
Conditions | Yield |
---|---|
With pyridine; trichlorophosphate; benzene | |
With argon; phosphan; copper(l) chloride; copper dichloride In acetonitrile | |
With argon; phosphan; copper(l) chloride; copper dichloride In acetonitrile at 24.9℃; Rate constant; Thermodynamic data; Product distribution; E(excit.), ΔS(excit.); |
sodium isobutoxide
triisobutyl phosphate
Conditions | Yield |
---|---|
With diethyl ether; trichlorophosphate | |
With phosphorus trichloride |
Conditions | Yield |
---|---|
With 2-methyl-propan-1-ol; chlorine |
triisobutyl phosphite
A
triisobutyl phosphate
B
diphosphoric acid tetraisobutyl ester
Conditions | Yield |
---|---|
With iodoacetophenone; silver perchlorate In benzene for 0.316667h; Title compound not separated from byproducts; |
phosphorochloridic acid diisobutyl ester
2-methyl-propan-1-ol
triisobutyl phosphate
Conditions | Yield |
---|---|
at 60℃; Rate constant; Thermodynamic data; activation energy, activation enthalpy, other temperature (40, 50, 70, 80 deg C); |
Conditions | Yield |
---|---|
With phosphan; copper dichloride In N,N-dimethyl-formamide at 59.9℃; |
Conditions | Yield |
---|---|
With phosphan; chlorine at 20℃; Rate constant; Thermodynamic data; Ea, ΔS(excit.); var. temp.; also in the presence of pyridine; |
phosphonic acid diisobutyl ester
A
triisobutyl phosphate
B
diphosphorus (IV)-oic acid tetraisobutyl ester
C
diphosphoric acid tetraisobutyl ester
Conditions | Yield |
---|---|
With sodium perchlorate In acetonitrile electrochemical oxidation, 2.4 A h; Pt anode, Ni cathode; Ag/AgNO3 reference electrode; Title compound not separated from byproducts; |
hydrogenchloride
2-methyl-propan-1-ol
oxygen
A
diisobutyl phosphoric acid
B
triisobutyl phosphate
C
isobutyryl chloride
D
zinc(II) chloride
Conditions | Yield |
---|---|
copper dichloride In further solvent(s) Kinetics; |
Conditions | Yield |
---|---|
With O2; CuCl2 In neat (no solvent) Kinetics; byproducts: H2O, HCl; the alcohol was loaded together with CuCl2 into the reactor and purged with an Ar-O2 mixture; then Cu3P was added and the mixt. reacted at 293 K, 323 K or 343 K;; |
n-butyllithium
triisobutyl phosphate
diisobutyl butylphosphonate
Conditions | Yield |
---|---|
In tetrahydrofuran; hexane at -78 - 0℃; | 93% |
triisobutyl phosphate
Conditions | Yield |
---|---|
In acetonitrile (N2 or Ar); ligand added to a soln. of U salt; crystd. overnight at room temp.; elem. anal.; | 87% |
triisobutyl phosphate
Conditions | Yield |
---|---|
In methanol addn. of phosphorus compd. to a soln. of thorium compd. in methanol; centrifugation, sepn., washing ppt. with methanol, centrifugation, sepn., evapn. of supernatant, drying in vac., dissolving in methanol, filtration, keeping at 4°C for 3 d; elem. anal.; | 75% |
triisobutyl phosphate
Conditions | Yield |
---|---|
In ethanol soln. of P ligand (2 equiv.) in EtOH was added dropwise to soln. of U compd. in EtOH; evapd.; crystd. (hexane, away from direct sunlight); filtered; dried in air; elem. anal.; | A n/a B 70% |
chloral hydrate
triisobutyl phosphate
(2,2,2-trichloro-1-hydroxy-ethyl)-phosphonic acid diisobutyl ester
Conditions | Yield |
---|---|
In hexane Heating; | 60% |
Conditions | Yield |
---|---|
In ethanol; water To an aqueous soln. of EuCl3*6H2O was added an ethanolic soln. of pyromellitic acid and triisobutyl phosphate, neutralization with NH3 to pH 6 and warming to 30°C for 30-40 min.; Elem. anal.; | 55% |
triisobutyl phosphate
Conditions | Yield |
---|---|
In ethanol Irradiation (UV/VIS); allowed to evap. slowly in direct sunlight; decanted; elem. anal.; | 35% |
triisobutyl phosphate
1-amino-naphthalene
diisobutyl-[1]naphthyl-amine
triisobutyl phosphate
naphthalen-2-ylamine
diisobutyl-[2]naphthyl-amine
Conditions | Yield |
---|---|
Multistep reaction; |
Conditions | Yield |
---|---|
In diethyl ether at 0℃; Yield given; | |
In tetrahydrofuran; hexane at -78 - 0℃; |
triisobutyl phosphate
tris(2-methyl-1-propyl) phosphate radical
Conditions | Yield |
---|---|
In water at 18.9℃; pulse radiolysis, pH 4.5-5; fast hydrolysis of alkyl radicals radiolytically formed; |
triisobutyl phosphate
A
Phosphorsaeure-sec.-butylester
B
diisobutyl phosphoric acid
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 100℃; for 2h; Title compound not separated from byproducts.; |
triisobutyl phosphate
diisobutyl (1-methylbutyl)phosphonate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: tetrahydrofuran; hexane / -78 - 0 °C 2: 89 percent / tetrahydrofuran; hexane / -78 - -20 °C View Scheme | |
Multi-step reaction with 2 steps 1: diethyl ether / 0 °C 2: 83 percent View Scheme |
triisobutyl phosphate
diisobutyl butylphosphonate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: diethyl ether / 0 °C 2: 73 percent / H3O(1+) View Scheme |
4-chloro-1H-isoindole-1,3(2H)-dione
3-chlorophthalic anhydride
triisobutyl phosphate
aminosulfonic acid
A
5-Chloroisatoic anhydride
B
8-chloro-2H-benzo[d][1,3]oxazine-2,4(1H)-dione
Conditions | Yield |
---|---|
In water; formamide |
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