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inquiryItems Standard Result Appearance Colorless clarity liquid Colorless clarity liquid Purity
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inquiryProduct Description Product website: http://www.finerchem.com Product Name Isopropanol CAS No. 67-63-0 Appe
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Isopropanol CAS No.:67-63-0 Name: Isopropanol Synonyms: 2-Propanol; Isopropyl alcohol; IPA Molecular Structure Molecular Formula: C3H8O Molecular Weight: 60.09 CAS Registry Number: 6
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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
Isopropyl alcohol alias: Dimethyl methanol, 2-propanol, the industry known as IPA CAS: 67-63-0 Molecular formula: C3H8O
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inquiryProduct Name Isopropyl alcohol CAS No. 67-63-0 EINECS No. 200-661-7 Molecular Formula C3H8O Molecular Weight 60.1g·mol-1
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inquiryMethanesulfonic acid is a raw material for medicine and pesticide. It can also be used as dehydrating agent, curing accelerator for coating, treating agent for fiber, solvent, catalysis, and esterification as well as polymerization reaction. It c
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inquiryProduct Name: Isopropyl alcohol Synonyms: LABOTEST-BB LT02090809;2-PROPANOL, HISTOLOGICAL GRADE;2-PROPANOL PESTANAL CAS: 67-63-0 MF: C3H8O MW: 60.1 EINECS: 200-661-7 Mol File: 67-63-0.mol Chemical Properties colourless liquid with sl
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Low price, high quality ,with a high praise from international customers Appearance:Colorless clarity liquid、No odour Package:800KG/IBC DRUM,16MT/FCL;160KG/DRUM,12.8MT/FCL;18-18.5MT/ISO TANK; or Bulk ship Application:Isopropyl alcohol is an imp
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inquirySuperior quality, moderate price & quick delivery. Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:160kg/drum;18MT/ISO Tank Application:When compared to ethanol, 50% less is re
Product name: Isopropanol CAS No.: 67-63-0 Molecule Formula:C3H8O Molecule Weight:60.10 Purity: 99.0% Package: 200kg/drum Description:Colorless liquid Manufacture Standards:Enterprise Standard TESTING ITEMS
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Conditions | Yield |
---|---|
With hydrogen; mer-Os(PPh3)3HBr(CO) In toluene at 150℃; under 51680 Torr; for 3h; | 100% |
With hydrogen; sodium methylate; chromium(0) hexacarbonyl In methanol at 120℃; under 75006 Torr; for 3h; | 100% |
With hydrogen; Ru((R,R)-cyP2N2)HCl In benzene-d6 at 20℃; under 2280.15 Torr; for 12h; Product distribution / selectivity; Alkaline conditions; Cooling with liquid nitrogen; | 100% |
methanol
Isopropyl acetate
A
acetic acid methyl ester
B
isopropyl alcohol
Conditions | Yield |
---|---|
With triethylamine at 20℃; under 8250660 Torr; for 2h; Product distribution; | A 100% B n/a |
methanol
isopropyl benzoate
A
benzoic acid methyl ester
B
isopropyl alcohol
Conditions | Yield |
---|---|
With triethylamine at 20℃; under 8250660 Torr; for 2h; Product distribution; | A 100% B n/a |
Conditions | Yield |
---|---|
In gas byproducts: CH3CHCH2; decomposition at a pressure of ca. 0.01 mm of Hg at 700°C; org. compounds collected in a liquid-N2 trap; NMR; GC; mass spectra; | A n/a B 100% |
hexakis[μ-(2-propanolato)]hexakis(2-propanolato)tetraaluminum
3-mercaptopropionic acid
B
isopropyl alcohol
Conditions | Yield |
---|---|
In benzene exclusion of moisture, addn. of 3-mercaptopropionic acid in benzene to Al(OiPr)3 in benzene (molar ratio 2:1), refluxing; elem. anal.; | A 100% B n/a |
piperazine
titanium(IV) isopropylate
dibenzo[b,f][1,4]thiazepin-11-one
A
11-(1-piperazinyl)dibenzo[b,f][1,4]thiazepine
B
isopropyl alcohol
Conditions | Yield |
---|---|
at 170℃; for 5h; Heating / reflux; | A 99% B n/a |
hexakis[μ-(2-propanolato)]hexakis(2-propanolato)tetraaluminum
3-mercaptopropionic acid
B
isopropyl alcohol
Conditions | Yield |
---|---|
In benzene exclusion of moisture, addn. of 3-mercaptopropionic acid in benzene to Al(OiPr)3 in benzene (molar ratio 1:1), refluxing; elem. anal.; | A 99% B n/a |
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
2-((phenylamino)methyl)phenol
B
isopropyl alcohol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; for 4 - 5h; Heating; | A 98.7% B n/a |
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
B
isopropyl alcohol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; for 4 - 5h; Heating; | A 98.6% B n/a |
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
2-((4-chlorophenylamino)methyl)phenol
B
isopropyl alcohol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; for 4 - 5h; Heating; | A 98.6% B n/a |
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
N-(2-hydroxybenzyl)-p-anisidine
B
isopropyl alcohol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; for 4 - 5h; Heating; | A 98.4% B n/a |
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
4-bromo-2-(((4-bromophenyl)amino)methyl)phenol
B
isopropyl alcohol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; for 4 - 5h; Heating; | A 98.3% B n/a |
4-bromo-2-(((4-methoxyphenyl)amino)methyl)phenol
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
B
isopropyl alcohol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; for 4 - 5h; Heating; | A 98.2% B n/a |
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
2-(2-chloro-anilinomethyl)-phenol
B
isopropyl alcohol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; for 4 - 5h; Heating; | A 98.2% B n/a |
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
2-((p-toluidino)methyl)phenol
B
isopropyl alcohol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; for 4 - 5h; Heating; | A 98.1% B n/a |
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
N-phenyl-N-2-hydroxy-5-bromobenzylamine
B
isopropyl alcohol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; for 4 - 5h; Heating; | A 98.1% B n/a |
pyridine
A
isopropyl chloride
B
cis-Cl(py)Pt(COMe)[C(OiPr)(Me)]
C
isopropyl alcohol
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 at 55℃; for 21h; | A n/a B 98% C n/a |
Conditions | Yield |
---|---|
With methanol; boron trichloride In neat (no solvent) at 20℃; for 0.05h; Green chemistry; | 98% |
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
4-bromo-2-(((2-bromophenyl)amino)methyl)phenol
B
isopropyl alcohol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; for 4 - 5h; Heating; | A 97.8% B n/a |
hexakis[μ-(2-propanolato)]hexakis(2-propanolato)tetraaluminum
mercaptoacetic acid
B
isopropyl alcohol
Conditions | Yield |
---|---|
In benzene exclusion of moisture, addn. of 2-mercaptoacetic acid in benzene to Al(OiPr)3 in benzene (molar ratio 3:1), refluxing; elem. anal.; | A 96% B n/a |
titanium(IV) isopropylate
3,4-dimercaptotoluene
A
C13H20O2S2Ti
B
isopropyl alcohol
Conditions | Yield |
---|---|
In benzene N2-atmosphere; azeotropic distn. of i-PrOH, evapn. (reduced pressure), repeated dissoln. in petroleum, evapn. (reduced pressure); | A 95% B n/a |
propene
acetic acid
A
di-isopropyl ether
B
Isopropyl acetate
C
isopropyl alcohol
Conditions | Yield |
---|---|
With water; cesium nitrate; tungstophosphoric acid; water; mixture of, dried, tabletted at 105.6 - 165℃; under 6750.68 Torr; Product distribution / selectivity; Gas phase; | A 2.3% B 94.7% C 2.8% |
hexakis[μ-(2-propanolato)]hexakis(2-propanolato)tetraaluminum
mercaptoacetic acid
B
isopropyl alcohol
Conditions | Yield |
---|---|
In benzene exclusion of moisture, addn. of 2-mercaptoacetic acid in benzene to Al(OiPr)3 in benzene (molar ratio 1:1), refluxing (100°C bath temp.); slow evapn. (3 h), ppt. is filtered and dried under reduced pressure, elem. anal.; | A 94% B n/a |
hexakis[μ-(2-propanolato)]hexakis(2-propanolato)tetraaluminum
mercaptoacetic acid
B
isopropyl alcohol
Conditions | Yield |
---|---|
In benzene exclusion of moisture, addn. of 2-mercaptoacetic acid in benzene to Al(OiPr)3 in benzene (molar ratio 2:1), refluxing; elem. anal.; | A 93% B n/a |
1,3-dimethylbarbituric acid
acetone
A
di-isopropyl ether
B
1,3-dimethyl-5-isopropylbarbituric acid
C
isopropyl alcohol
Conditions | Yield |
---|---|
Stage #1: 1,3-dimethylbarbituric acid; acetone Stage #2: With sulfuric acid; hydrogen; platinum on activated charcoal In water under 3878.61 Torr; for 48h; | A n/a B 92% C n/a |
benzaldehyde
isopropylamine
acetophenone
A
2,4,6-triphenylpyridine
B
isopropyl alcohol
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate at 120℃; for 5h; Neat (no solvent); regioselective reaction; | A 92% B 90 %Chromat. |
Conditions | Yield |
---|---|
With hydrogen at 180℃; under 37503.8 Torr; Catalytic behavior; chemoselective reaction; | A 91.2% B 7.8% |
With hydrogen In water at 179.84℃; under 22502.3 Torr; for 10h; Autoclave; | A 76% B 9% |
With hydrogen In water at 130℃; under 30003 Torr; for 24h; |
1-(2-hydroxyethyl)piperazine
titanium(IV) isopropylate
dibenzo[b,f][1,4]thiazepin-11-one
A
O-Dealkyl Quetiapine
B
isopropyl alcohol
Conditions | Yield |
---|---|
at 170℃; for 5.5h; Heating / reflux; | A 91% B n/a |
Conditions | Yield |
---|---|
at 90℃; for 6h; | 100% |
for 6h; Reflux; | 99% |
With 1-hydro-3-(3-sulfopropyl)-imidazolium 4-methyl-benzenesulfonate at 60℃; Heating; | 92% |
Conditions | Yield |
---|---|
Stage #1: 4-amino-benzoic acid; isopropyl alcohol With thionyl chloride at 20℃; for 90h; Reflux; Stage #2: With sodium hydrogencarbonate In water; isopropyl alcohol | 100% |
With thionyl chloride; sodium carbonate for 2h; Heating; | 89% |
With hydrogenchloride |
isopropyl alcohol
3,5-dinitrobenoyl chloride
3,5-dinitro-benzoic acid isopropyl ester
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran for 0.333333h; Heating; | 100% |
With diethyl ether | |
With pyridine; benzene |
isopropyl alcohol
propene
Conditions | Yield |
---|---|
1 percent alumina-modified MCM-41 at 250℃; Product distribution; Further Variations:; Catalysts; Temperatures; Dehydration; | 100% |
With mesoporous silica MCM-4l/Al at 246.84℃; for 50h; | 100% |
With hydrogen at 174.84℃; for 6h; Catalytic behavior; | 99.5% |
Conditions | Yield |
---|---|
With indium(III) chloride; dimethylmonochlorosilane; benzil In dichloromethane at 20℃; for 6h; | 100% |
With priphenylchlorophosphonium phosphorodichloridate at 20℃; Arbuzov reaction; | 84% |
With hydrogenchloride at 120℃; under 7500.75 Torr; Flow reactor; | 54% |
Conditions | Yield |
---|---|
With trans-4L1(O)2>ClO4 In acetonitrile at 25℃; for 7h; stoicheiometric oxidation ( electrochemical oxidation in a non-aqueous medium (acetonitrile), an Ag-AgNO3 reference electrode; | 100% |
With C19H20N3O2Ru(2+)*2F6P(1-) In aq. buffer at 24.84℃; for 1h; pH=1.8; Thermodynamic data; Activation energy; Reagent/catalyst; | 100% |
With tert-butylethylene; C32H52ClIrP2; sodium t-butanolate at 200℃; for 2h; Catalytic behavior; Reagent/catalyst; Inert atmosphere; Glovebox; | 100% |
Conditions | Yield |
---|---|
With erbium(III) triflate at 25℃; for 1.5h; | 100% |
With ytterbium(III) triflate at 20℃; for 12h; | 98% |
With tin(IV)tetraphenylporphyrinato trifluoromethanesulfonate for 0.0833333h; Heating; | 98% |
Conditions | Yield |
---|---|
Stage #1: isopropyl alcohol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; Inert atmosphere; Stage #2: benzyl bromide In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 5h; Inert atmosphere; | 100% |
With iron(II) sulfate at 75℃; for 12h; | 92% |
With silver(II) oxide Heating; | 90% |
With potassium hydroxide; tetrafluoroboric acid; mercury(II) oxide In dichloromethane 1.) room temp., 1 h; | 60% |
(i) Ag2O, (ii) Py, PhCOCl; Multistep reaction; |
Conditions | Yield |
---|---|
With silver hexafluoroantimonate; C29H33AuClN3O2 In chloroform-d1 at 20℃; | 100% |
dirhodium tetraacetate In dichloromethane for 0.1h; Ambient temperature; | 92% |
p-Tolylisocyanate
isopropyl alcohol
carbamic acid, (4-methylphenyl)-, 1-methylethyl ester
Conditions | Yield |
---|---|
Ambient temperature; | 100% |
In dichloromethane at 20℃; for 4.5h; Inert atmosphere; | 13 mg |
ethyl 5-oxo-2-phenyl-2,5-dihydroisoxazole-4-carboxaldehyde
isopropyl alcohol
(Z)-2-Isopropoxy-3-phenylamino-acrylic acid ethyl ester
Conditions | Yield |
---|---|
Irradiation; pyrex filter; | 100% |
Conditions | Yield |
---|---|
at 20 - 30℃; for 1.5h; Inert atmosphere; | 100% |
With water for 1h; Ambient temperature; | 85.5% |
at 25 - 30℃; for 49h; |
ethyl 2-hydroxypyrrolidine-1-carboxylate
isopropyl alcohol
2-isopropoxy-pyrrolidine-1-carboxylic acid ethyl ester
Conditions | Yield |
---|---|
With acetic acid | 100% |
2,6-Difluorobenzyl bromide
isopropyl alcohol
Conditions | Yield |
---|---|
With silver(II) oxide for 1h; Heating; | 100% |
3-(2-vinyloxyethoxy)-1,2-propylene carbonate
isopropyl alcohol
4-[2-(1-Isopropoxy-ethoxy)-ethoxymethyl]-[1,3]dioxolan-2-one
Conditions | Yield |
---|---|
With heptafluorobutyric Acid at 20 - 45℃; for 3h; | 100% |
2,3-di-O-benzoyl-L-(+)-tartaric anhydride
isopropyl alcohol
isopropyl hydrogen 2,3-di-O-benzoyl-L-(+)-tartrate
Conditions | Yield |
---|---|
In chloroform at 60℃; for 3h; | 100% |
Conditions | Yield |
---|---|
In diethyl ether for 1h; | 100% |
isopropyl alcohol
exo-cis-7-oxabicyclo<2.2.1>hept-5-ene-2,3-dimethanol carbonate
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid for 8h; Heating; | 100% |
Conditions | Yield |
---|---|
With C13H20N2O*Ir(1+); hydrogen at 80℃; under 3000.3 Torr; for 23h; Reagent/catalyst; Autoclave; Green chemistry; | 100% |
With nickel at 20℃; for 26h; | 70% |
Pt on TiO2 for 10h; Ambient temperature; Irradiation; | 36.32% |
2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl trichloroacetimidate
isopropyl alcohol
isopropyl 2,3,4,6-tetra-O-benzyl-D-glucopyranoside
Conditions | Yield |
---|---|
With trimethylsilyl trifluoromethanesulfonate; 1-ethyl-3-methylimidazolium triflate at 20℃; for 0.333333h; | 100% |
With 1-ethyl-3-methylimidazolium triflate at 20℃; | 100% |
With molecular sieve; lithium perchlorate In dichloromethane at 25℃; | 96% |
chlorosulfonylacetyl chloride
isopropyl alcohol
isopropyl (chlorosulfonyl)acetate
Conditions | Yield |
---|---|
In diethyl ether at 0℃; Esterification; | 100% |
In tetrahydrofuran at 0℃; for 0.333333h; | 100% |
In dichloromethane | |
In diethyl ether | |
In tetrahydrofuran at 0 - 20℃; for 2.33333h; Inert atmosphere; |
isopropyl alcohol
isopropyl hypophosphite
Conditions | Yield |
---|---|
With triethylammonium phosphinate In dichloromethane at 20℃; for 0.166667h; | 100% |
With hypophosphorous acid In benzene for 15h; Dean-Stark; Inert atmosphere; Reflux; | 100% |
With pyrophosphorous acid In benzene Heating; | 100 % Spectr. |
(R)-5-oxo-5,6-dihydro-2H-pyran-2-yl acetate
isopropyl alcohol
Conditions | Yield |
---|---|
With palladium diacetate; triphenylphosphine at 20℃; for 1h; | 100% |
isopropyl alcohol
trans 4-(bromomethyl)-2-methoxy-1,3-dioxolane
trans 4-(bromomethyl)-2-isopropoxy-1,3-dioxolane
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene at 90℃; | 100% |
cycl-isopropylidene malonate
isopropyl alcohol
i-propyl malonic half ester
Conditions | Yield |
---|---|
In acetonitrile for 22h; Heating; | 100% |
Reflux; | 76% |
In toluene for 5h; Heating; |
Conditions | Yield |
---|---|
With thionyl chloride at -20℃; for 4h; Heating / reflux; | 100% |
With thionyl chloride for 16h; Heating; |
isopropyl alcohol
3-phenylsulfanyl-butyric acid 4-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl)-benzyl ester
Conditions | Yield |
---|---|
With titanium(IV) isopropylate for 6h; Heating; | 100% |
isopropyl alcohol
3-(4-tert-butyl-phenylsulfanyl)-hexanoic acid 4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-decyl)-benzyl ester
Conditions | Yield |
---|---|
With titanium(IV) isopropylate for 6h; Heating; | 100% |
isopropyl alcohol
4-(2-perfluorodecyl)ethylbenzyl 2-methyl-3-phenylthiopropanoate
Conditions | Yield |
---|---|
With titanium(IV) isopropylate for 6h; Heating; | 100% |
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