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1569-01-3 Usage

Chemical Properties

Clear colorless liquid

Flammability and Explosibility

Flammable

Check Digit Verification of cas no

The CAS Registry Mumber 1569-01-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1569-01:
(6*1)+(5*5)+(4*6)+(3*9)+(2*0)+(1*1)=83
83 % 10 = 3
So 1569-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O.C3H6.C2H6O2/c1-3-5-7-6-4-2;1-3-2;3-1-2-4/h3-6H2,1-2H3;3H,1H2,2H3;3-4H,1-2H2

1569-01-3 Well-known Company Product Price

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  • Aldrich

  • (424927)  Propyleneglycolpropylether  99%

  • 1569-01-3

  • 424927-1L

  • 534.69CNY

  • Detail
  • Aldrich

  • (424927)  Propyleneglycolpropylether  99%

  • 1569-01-3

  • 424927-4L

  • 1,347.84CNY

  • Detail
  • Aldrich

  • (424927)  Propyleneglycolpropylether  99%

  • 1569-01-3

  • 424927-18L

  • 3,724.11CNY

  • Detail
  • Aldrich

  • (484326)  Propyleneglycolpropylether  ≥98.5%

  • 1569-01-3

  • 484326-1L

  • 493.74CNY

  • Detail
  • Aldrich

  • (484326)  Propyleneglycolpropylether  ≥98.5%

  • 1569-01-3

  • 484326-4L

  • 1,491.75CNY

  • Detail

1569-01-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Propoxy-2-propanol (contains 2-Isopropoxy-1-propanol)

1.2 Other means of identification

Product number -
Other names 1-propoxypropan-2-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Solvents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1569-01-3 SDS

1569-01-3Synthetic route

propan-1-ol
71-23-8

propan-1-ol

methyloxirane
75-56-9, 16033-71-9

methyloxirane

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

Conditions
ConditionsYield
With Al2O3/MgO composite at 120℃; Inert atmosphere;34.4%
With KAcMIMOH at 60℃; for 4h;
With hematite at 160℃; for 8h; Autoclave;
propan-1-ol
71-23-8

propan-1-ol

methyloxirane
75-56-9, 16033-71-9

methyloxirane

A

2-propoxy-1-propanol
10215-30-2

2-propoxy-1-propanol

B

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

Conditions
ConditionsYield
at 100 - 200℃;
at 180 - 205℃;
With sulfuric acid Yield given. Yields of byproduct given;
sodium n-propoxide
6819-41-6

sodium n-propoxide

methyloxirane
75-56-9, 16033-71-9

methyloxirane

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

Allyl glycidyl ether
106-92-3

Allyl glycidyl ether

A

3-Propoxy-1,2-epoxypropan
3126-95-2

3-Propoxy-1,2-epoxypropan

B

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

Conditions
ConditionsYield
With hydrogen; 5percent Pd/C(en) In tetrahydrofuran at 20℃; for 2.5h; Catalytic hydrogenation; Title compound not separated from byproducts.;
propylene glycol
57-55-6

propylene glycol

A

propan-1-ol
71-23-8

propan-1-ol

B

Dipropyl ether
111-43-3

Dipropyl ether

C

2-propoxy-1-propanol
10215-30-2

2-propoxy-1-propanol

D

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

Conditions
ConditionsYield
With trifluorormethanesulfonic acid; hydrogen; [{CpRu(CO)2}2(μ-H)](+)*OTf(-); cyclopenta-1,3-diene In sulfolane at 110℃; under 39003.1 Torr; for 30h; Product distribution;A 54 % Chromat.
B 15 % Chromat.
C n/a
D n/a
propylene glycol
57-55-6

propylene glycol

A

propan-1-ol
71-23-8

propan-1-ol

B

2-ethyl-4-methyl-1,3-dioxolane
4359-46-0

2-ethyl-4-methyl-1,3-dioxolane

C

Dipropyl ether
111-43-3

Dipropyl ether

D

2-propoxy-1-propanol
10215-30-2

2-propoxy-1-propanol

E

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

F

propionaldehyde
123-38-6

propionaldehyde

Conditions
ConditionsYield
With bis(dicarbonyl)(μ-hydrido)(pentamethylcyclopentadiene)ruthenium trifluoromethanesulfonate; trifluorormethanesulfonic acid; hydrogen In sulfolane at 110℃; under 38787.1 Torr; for 30h; Mechanism; Kinetics; Solvent; Pressure; Concentration; Temperature; Time; regioselective reaction;A 54 %Chromat.
B n/a
C n/a
D n/a
E n/a
F n/a
propylene glycol
57-55-6

propylene glycol

A

propan-1-ol
71-23-8

propan-1-ol

B

propyl propionate
106-36-5

propyl propionate

C

propane
74-98-6

propane

D

2-propoxy-1-propanol
10215-30-2

2-propoxy-1-propanol

E

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

F

propionic acid
802294-64-0

propionic acid

G

1,3,5-trimethyl-benzene
108-67-8

1,3,5-trimethyl-benzene

Conditions
ConditionsYield
With [C6H3-2,6-(OP(tBu)2)2]IrH2; trifluorormethanesulfonic acid; hydrogen In 1,4-dioxane at 125℃; under 5171.62 Torr; Autoclave;
1-propoxy-2-propanyl formate

1-propoxy-2-propanyl formate

A

formic acid
64-18-6

formic acid

B

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

Conditions
ConditionsYield
With water at 80℃; for 24h; Equilibrium constant; Sealed tube;
1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

N’-(5-bromo-6-hydroxy-2-methyl-3-pyridyl)-N-ethyl-N-methyl-formamidine
1056233-21-6

N’-(5-bromo-6-hydroxy-2-methyl-3-pyridyl)-N-ethyl-N-methyl-formamidine

N’-[5-bromo-2-methyl-6-[1-methyl-2-propoxy-ethoxy]-3-pyridyl]-N-ethyl-N-methyl-formamidine

N’-[5-bromo-2-methyl-6-[1-methyl-2-propoxy-ethoxy]-3-pyridyl]-N-ethyl-N-methyl-formamidine

Conditions
ConditionsYield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20 - 40℃; for 1.66667h; Inert atmosphere;95%
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 1.5h; Inert atmosphere;95%
methanol
67-56-1

methanol

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

1-propoxy-2-propanyl formate

1-propoxy-2-propanyl formate

Conditions
ConditionsYield
With [bis({2‐[bis(propan‐2‐yl)phosphanyl]ethyl})amine](borohydride)(carbonyl)(hydride)iron(II); methacrylic acid methyl ester In toluene at 140℃; under 13689.1 Torr; for 4h; Autoclave; Inert atmosphere;71%
3-bromo-6-methyl-5-nitro-pyridin-2-ol
874493-25-1

3-bromo-6-methyl-5-nitro-pyridin-2-ol

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

5-bromo-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-nitro-pyridine

5-bromo-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-nitro-pyridine

Conditions
ConditionsYield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 40 - 65℃; for 12h; Inert atmosphere;60%
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 65℃; for 12h; Inert atmosphere;60%
1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

N’-(5-chloro-6-hydroxy-2-methyl-3-pyridyl)-N-ethyl-N-methyl-formamidine

N’-(5-chloro-6-hydroxy-2-methyl-3-pyridyl)-N-ethyl-N-methyl-formamidine

N’-[5-chloro-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-pyridyl]-N-ethyl-N-methyl-formamidine

N’-[5-chloro-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-pyridyl]-N-ethyl-N-methyl-formamidine

Conditions
ConditionsYield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 40 - 60℃; for 25h; Inert atmosphere;53%
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 60℃; for 25h; Inert atmosphere;53%
1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

1-propoxy-propan-2-one
68058-77-5

1-propoxy-propan-2-one

Conditions
ConditionsYield
With sodium dichromate; sulfuric acid at 4 - 5℃;
1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

water
7732-18-5

water

Na2Cr2O7

Na2Cr2O7

1-propoxy-propan-2-one
68058-77-5

1-propoxy-propan-2-one

Conditions
ConditionsYield
at 4 - 5℃;
1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

propoxy-acetone-phenylhydrazone

propoxy-acetone-phenylhydrazone

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: Na2Cr2O7; diluted H2SO4 / 4 - 5 °C
View Scheme
1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

A

propylpropylene glycol(2) methyl ether
4188-67-4

propylpropylene glycol(2) methyl ether

B

C8H16O4
1220964-45-3

C8H16O4

Conditions
ConditionsYield
With sodium methylate at 90℃; under 750.075 Torr; for 20h; Inert atmosphere;A 9 %Chromat.
B 91 %Chromat.
1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

5-bromo-2-methyl-6-(1-methyl-2-propoxy-ethoxy)pyridin-3-amine

5-bromo-2-methyl-6-(1-methyl-2-propoxy-ethoxy)pyridin-3-amine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 12 h / 40 - 65 °C / Inert atmosphere
2: ammonium chloride; iron / ethanol; water / 14 h / 85 °C
View Scheme
Multi-step reaction with 2 steps
1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 12 h / 65 °C / Inert atmosphere
2: ammonium chloride; iron / ethanol; water / 14 h / 85 °C
View Scheme
1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

N’-[5-bromo-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-pyridyl]-N-ethyl-formamidine

N’-[5-bromo-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-pyridyl]-N-ethyl-formamidine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 12 h / 40 - 65 °C / Inert atmosphere
2.1: ammonium chloride; iron / ethanol; water / 14 h / 85 °C
3.1: trichlorophosphate / dichloromethane / 1 h / 20 °C
3.2: 2 h / 20 °C
View Scheme
Multi-step reaction with 3 steps
1.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 12 h / 65 °C / Inert atmosphere
2.1: ammonium chloride; iron / ethanol; water / 14 h / 85 °C
3.1: trichlorophosphate / dichloromethane / 1 h / 20 °C
3.2: 2 h / 20 °C
View Scheme
1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

N’-[5-bromo-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-pyridyl]-N-isopropyl-N-methylformamidine

N’-[5-bromo-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-pyridyl]-N-isopropyl-N-methylformamidine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 12 h / 40 - 65 °C / Inert atmosphere
2.1: ammonium chloride; iron / ethanol; water / 14 h / 85 °C
3.1: trichlorophosphate / dichloromethane / 1 h / 20 °C
3.2: 2 h / 20 °C
View Scheme
1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

N’-(5-bromo-6-hydroxy-2-methyl-3-pyridyl)-N-ethyl-N-methyl-formamidine
1056233-21-6

N’-(5-bromo-6-hydroxy-2-methyl-3-pyridyl)-N-ethyl-N-methyl-formamidine

N’-[5-cyano-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-pyridyl]-N-ethyl-N-methyl-formamidine

N’-[5-cyano-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-pyridyl]-N-ethyl-N-methyl-formamidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 1.67 h / 20 - 40 °C / Inert atmosphere
2: tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 18 h / 120 °C / Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 1.5 h / 20 °C / Inert atmosphere
2: tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 18 h / 120 °C / Inert atmosphere
View Scheme
formic acid
64-18-6

formic acid

1-(1-propyloxy)propan-2-ol
1569-01-3

1-(1-propyloxy)propan-2-ol

1-propoxy-2-propanyl formate

1-propoxy-2-propanyl formate

Conditions
ConditionsYield
at 80℃; for 24h; Equilibrium constant; Sealed tube;

1569-01-3Downstream Products

1569-01-3Relevant articles and documents

MBA-cross-linked poly(N-vinyl-2-pyrrolidone)/ferric chloride macromolecular coordination complex as a novel and recyclable Lewis acid catalyst: Synthesis, characterization, and performance toward for regioselective ring-opening alcoholysis of epoxides

Rahmatpour, Ali,Zamani, Maryam

, (2021/09/30)

A novel macromolecular-metal coordination complex, MBA-cross-linked PNVP/FeCl3 material was fabricated by immobilization of water intolerant ferric chloride onto the porous cross-linked poly(N-vinyl-2-pyrrolidone) carrier beads as a macromolecular ligand or carrier which was prepared by suspension free-radical copolymerization of N-vinyl-2-pyrrolidone (NVP) and N,N′-methylene bis-acrylamide (MBA) as a crosslinking agent in water. The obtained PNVP/FeCl3 was characterized by UV/vis and FT-IR spectroscopies, TGA, FE-SEM, EDX, and ICP techniques. This heterogenized version of ferric chloride is a convenient and safe alternative to highly water intolerant ferric chloride. The catalytic performance of (PNVP/FeCl3) as an efficient and recyclable polymeric Lewis acid catalyst was appropriately probed in the regio-and stereoselective nucleophilic ring opening of various epoxides with various alcohols in excellent yields with TOF up to 182.48 h?1 without generating any waste. The activity data indicate that this heterogeneous catalyst is very active and could be easily recovered, and reused at least six times without appreciable loss of activity indicating its stability under experimental conditions.

PROCESS FOR MAKING FORMIC ACID UTILIZING LOWER-BOILING FORMATE ESTERS

-

Paragraph 00177; 00178, (2019/02/15)

Disclosed is a process for recovering formic acid from a formate ester of a C3 to C4 alcohol. Disclosed is also a process for producing formic acid by carbonylating a C3 to C4 alcohol, hydrolyzing the formate ester of the alcohol, and recovering a formic acid product. The alcohol may be dried and returned to the reactor. The process enables a more energy efficient production of formic acid than the carbonylation of methanol to produce methyl formate.

METHODS OF CONVERTING POLYOLS

-

Paragraph 0091-0092, (2015/01/06)

Methods for converting polyols are provided. The methods provided can include using a metal pincer catalyst (e.g., an iridium pincer catalyst) to remove at least one alcohol group from a polyol. The methods provided can include converting glycerol to 1,3-propanediol.

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