Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2,4,6,8-Tetraoxanonane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13353-03-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 13353-03-2 Structure
  • Basic information

    1. Product Name: 2,4,6,8-Tetraoxanonane
    2. Synonyms: 2,4,6,8-Tetraoxanonane;2,4,6,8-Tetraoxanone
    3. CAS NO:13353-03-2
    4. Molecular Formula: C5H12O4
    5. Molecular Weight: 136.14638
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13353-03-2.mol
  • Chemical Properties

    1. Melting Point: -42--40.5 °C
    2. Boiling Point: 158-159℃
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.0242 g/cm3(Temp: 25 °C)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,4,6,8-Tetraoxanonane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4,6,8-Tetraoxanonane(13353-03-2)
    11. EPA Substance Registry System: 2,4,6,8-Tetraoxanonane(13353-03-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 13353-03-2(Hazardous Substances Data)

13353-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13353-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,5 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13353-03:
(7*1)+(6*3)+(5*3)+(4*5)+(3*3)+(2*0)+(1*3)=72
72 % 10 = 2
So 13353-03-2 is a valid CAS Registry Number.

13353-03-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methoxy(methoxymethoxymethoxy)methane

1.2 Other means of identification

Product number -
Other names bis-methoxymethoxy-methane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:13353-03-2 SDS

13353-03-2Synthetic route

formaldehyd
50-00-0

formaldehyd

methoxymethanol
4461-52-3

methoxymethanol

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

Conditions
ConditionsYield
With acetic acid Reflux;96.2%
formaldehyd
50-00-0

formaldehyd

Dimethoxymethane
109-87-5

Dimethoxymethane

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

Conditions
ConditionsYield
With sulfuric acid at 109.99℃; under 7500.75 Torr;A n/a
B 26%
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

C

POMM4
13352-75-5

POMM4

Conditions
ConditionsYield
With ZrO2#dotLa2O3 at 130℃; under 6000.6 Torr; for 4h; Pressure; Reagent/catalyst;A 23%
B 23.3%
C 14.9%
formaldehyd
50-00-0

formaldehyd

Dimethoxymethane
109-87-5

Dimethoxymethane

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

C

POMM4
13352-75-5

POMM4

Conditions
ConditionsYield
With La2O3 doped titania at 130℃; under 4500.45 Torr; for 4h; Reagent/catalyst; Pressure; Autoclave;A 22.4%
B 17.5%
C 8.4%
With macroporous strong acidic styrene type cation exchange resin catalyst at 100℃; under 15001.5 Torr; for 10h; Temperature; Time; Overall yield = 51.66 %;
With Cl -/TiO2-La2O3/SBA-15 (Si/Al=38) at 130℃; under 4500.45 Torr; for 4h; Reagent/catalyst; Temperature; Pressure;
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

Conditions
ConditionsYield
With ZrO2#dotLa2O3 at 130℃; under 5250.53 Torr; for 4h;A 8.3%
B 16.7%
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

Dimethoxymethane
109-87-5

Dimethoxymethane

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

Conditions
ConditionsYield
With sulfuric acid
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

Dimethoxymethane
109-87-5

Dimethoxymethane

sulfuric acid
7664-93-9

sulfuric acid

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

C

POMM4
13352-75-5

POMM4

1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

1,1-dimethoxyethane
534-15-6

1,1-dimethoxyethane

A

C11H24O10

C11H24O10

B

C13H28O12

C13H28O12

C

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

D

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

E

POMM4
13352-75-5

POMM4

F

CH3-(OCH2)8-OCH3
13352-78-8

CH3-(OCH2)8-OCH3

G

Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane
54261-86-8

Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane

H

POMM5
13352-76-6

POMM5

I

CH3-(OCH2)7-OCH3
13353-04-3

CH3-(OCH2)7-OCH3

J

CH3-(OCH2)6-OCH3
13352-77-7

CH3-(OCH2)6-OCH3

Conditions
ConditionsYield
Amberlite IR 120 at 100℃; for 24h; Product distribution / selectivity;
trifluorormethanesulfonic acid at 100℃; for 40h; Product distribution / selectivity;
sulfuric acid In water at 100℃; for 12h; Product distribution / selectivity;
1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

1,1-dimethoxyethane
534-15-6

1,1-dimethoxyethane

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

C

POMM4
13352-75-5

POMM4

Conditions
ConditionsYield
sulfuric acid In water at 100℃; for 16h; Product distribution / selectivity;
1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

1,1-dimethoxyethane
534-15-6

1,1-dimethoxyethane

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

A

C11H24O10

C11H24O10

B

C13H28O12

C13H28O12

C

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

D

POMM4
13352-75-5

POMM4

E

CH3-(OCH2)8-OCH3
13352-78-8

CH3-(OCH2)8-OCH3

F

Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane
54261-86-8

Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane

G

POMM5
13352-76-6

POMM5

H

CH3-(OCH2)7-OCH3
13353-04-3

CH3-(OCH2)7-OCH3

I

CH3-(OCH2)6-OCH3
13352-77-7

CH3-(OCH2)6-OCH3

Conditions
ConditionsYield
sulfuric acid In water at 100℃; for 12h; Product distribution / selectivity;
1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

A

C11H24O10

C11H24O10

B

C13H28O12

C13H28O12

C

1,1-dimethoxyethane
534-15-6

1,1-dimethoxyethane

D

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

E

POMM4
13352-75-5

POMM4

F

CH3-(OCH2)8-OCH3
13352-78-8

CH3-(OCH2)8-OCH3

G

Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane
54261-86-8

Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane

H

POMM5
13352-76-6

POMM5

I

CH3-(OCH2)7-OCH3
13353-04-3

CH3-(OCH2)7-OCH3

J

CH3-(OCH2)6-OCH3
13352-77-7

CH3-(OCH2)6-OCH3

Conditions
ConditionsYield
sulfuric acid In water at 100℃; for 12h; Product distribution / selectivity;
formaldehyd
50-00-0

formaldehyd

1,1-dimethoxyethane
534-15-6

1,1-dimethoxyethane

A

C11H24O10

C11H24O10

B

C13H28O12

C13H28O12

C

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

D

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

E

POMM4
13352-75-5

POMM4

F

CH3-(OCH2)8-OCH3
13352-78-8

CH3-(OCH2)8-OCH3

G

Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane
54261-86-8

Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane

H

POMM5
13352-76-6

POMM5

I

CH3-(OCH2)7-OCH3
13353-04-3

CH3-(OCH2)7-OCH3

J

CH3-(OCH2)6-OCH3
13352-77-7

CH3-(OCH2)6-OCH3

Conditions
ConditionsYield
Amberlite IR 120 at 100℃; for 8h; Product distribution / selectivity;
formaldehyd
50-00-0

formaldehyd

Dimethoxymethane
109-87-5

Dimethoxymethane

A

1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

B

C11H24O10

C11H24O10

C

C13H28O12

C13H28O12

D

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

E

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

F

POMM4
13352-75-5

POMM4

G

CH3-(OCH2)8-OCH3
13352-78-8

CH3-(OCH2)8-OCH3

H

Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane
54261-86-8

Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane

I

CH3-(OCH2)7-OCH3
13353-04-3

CH3-(OCH2)7-OCH3

J

C14H30O13

C14H30O13

K

C15H32O14

C15H32O14

L

CH3-(OCH2)6-OCH3
13352-77-7

CH3-(OCH2)6-OCH3

Conditions
ConditionsYield
With sulfuric acid at 55 - 115℃; Inert atmosphere;
1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

formaldehyd
50-00-0

formaldehyd

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

Conditions
ConditionsYield
With strong acidic styrene type cation exchange resin catalyst at 100℃; under 15001.5 Torr; for 3h; Temperature; Time; Overall yield = 43.26 %;
1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

formaldehyd
50-00-0

formaldehyd

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

C

POMM4
13352-75-5

POMM4

Conditions
ConditionsYield
With strong acidic styrene type cation exchange resin catalyst at 80 - 100℃; under 15001.5 Torr; for 3h; Temperature; Time; Overall yield = 47.55 %;
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

A

Dimethoxymethane
109-87-5

Dimethoxymethane

B

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

C

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

Conditions
ConditionsYield
With C16H36NO3S(1+)*CH3O4S(1-) at 125 - 130℃; under 26252.6 - 30003 Torr; Reagent/catalyst; Inert atmosphere;
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

A

Dimethoxymethane
109-87-5

Dimethoxymethane

B

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

C

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

D

POMM4
13352-75-5

POMM4

Conditions
ConditionsYield
With C16H36NO3S(1+)*CH3O4S(1-) at 125 - 130℃; under 26252.6 - 30003 Torr; Reagent/catalyst; Inert atmosphere;
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

POMM4
13352-75-5

POMM4

C

POMM5
13352-76-6

POMM5

Conditions
ConditionsYield
With C16H36NO3S(1+)*CH3O4S(1-) at 125 - 130℃; under 26252.6 - 30003 Torr; Reagent/catalyst; Inert atmosphere;
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

A

Dimethoxymethane
109-87-5

Dimethoxymethane

B

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

C

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

D

POMM4
13352-75-5

POMM4

E

POMM5
13352-76-6

POMM5

Conditions
ConditionsYield
With C16H36NO3S(1+)*CH3O4S(1-) In water at 125 - 130℃; under 26252.6 - 30003 Torr; Reagent/catalyst;
1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

Dimethoxymethane
109-87-5

Dimethoxymethane

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

Conditions
ConditionsYield
With C13H25N2O3S(1+)*HO4S(1-) at 150℃; for 10h; Autoclave;
1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

Dimethoxymethane
109-87-5

Dimethoxymethane

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

C

POMM4
13352-75-5

POMM4

D

POMM5
13352-76-6

POMM5

Conditions
ConditionsYield
With C10-AS-50 at 105℃; under 9750.98 Torr; for 2h; Catalytic behavior; Inert atmosphere;
formaldehyd
50-00-0

formaldehyd

Dimethoxymethane
109-87-5

Dimethoxymethane

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

C

POMM4
13352-75-5

POMM4

D

CH3-(OCH2)8-OCH3
13352-78-8

CH3-(OCH2)8-OCH3

E

POMM5
13352-76-6

POMM5

F

CH3-(OCH2)7-OCH3
13353-04-3

CH3-(OCH2)7-OCH3

G

CH3-(OCH2)6-OCH3
13352-77-7

CH3-(OCH2)6-OCH3

Conditions
ConditionsYield
With lanthanum(III) sulfate at 130℃; under 3750.38 Torr; for 6h; Reagent/catalyst; Concentration; Time; Temperature; Pressure; Overall yield = 75.5 %;A 20.74 %Chromat.
B 25.87 %Chromat.
C 13.77 %Chromat.
D 1.11 %Chromat.
E 8.14 %Chromat.
F 2.37 %Chromat.
G 4.23 %Chromat.
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

Dimethoxymethane
109-87-5

Dimethoxymethane

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

Conditions
ConditionsYield
With SO42-/ZrO2-La2O3/SBA-15 (Si/Al=50) at 90℃; for 4h;
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

Dimethoxymethane
109-87-5

Dimethoxymethane

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

C

POMM4
13352-75-5

POMM4

Conditions
ConditionsYield
With SO42-/ZrO2-La2O3/SBA-15 (Si/Al=25) at 130℃; under 6000.6 Torr; for 4h; Reagent/catalyst; Temperature;
formaldehyd
50-00-0

formaldehyd

Dimethoxymethane
109-87-5

Dimethoxymethane

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

Dimethyl ether
115-10-6

Dimethyl ether

C

Methyl formate
107-31-3

Methyl formate

Conditions
ConditionsYield
With C16AlF36O4(1-)*C3H9O(1+) at 25 - 30℃; Schlenk technique; Inert atmosphere;
1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

Dimethoxymethane
109-87-5

Dimethoxymethane

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

bis(methoxymethyl)ether
628-90-0

bis(methoxymethyl)ether

C

POMM4
13352-75-5

POMM4

Conditions
ConditionsYield
With Amberlyst A15 resin at 50℃; for 1h;A 33 %Chromat.
B 48 %Chromat.
C 12 %Chromat.
1,3,5-Trioxan
110-88-3

1,3,5-Trioxan

Dimethoxymethane
109-87-5

Dimethoxymethane

A

bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

B

POMM4
13352-75-5

POMM4

C

POMM5
13352-76-6

POMM5

Conditions
ConditionsYield
With Amberlyst A15 resin at 50℃; for 1h;A 42 %Chromat.
B 29 %Chromat.
C 14 %Chromat.
bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

6-ethyl-o-toluidine

6-ethyl-o-toluidine

2-methyl-6-ethyl-N-(methoxymethoxymethyl)aniline

2-methyl-6-ethyl-N-(methoxymethoxymethyl)aniline

Conditions
ConditionsYield
In benzene at 75 - 80℃; for 18h;97.2%
bis-methoxymethoxy-methane
13353-03-2

bis-methoxymethoxy-methane

phenol
108-95-2

phenol

A

Bis(2-hydroxyphenyl)methane
2467-02-9

Bis(2-hydroxyphenyl)methane

B

2-[(4-hydroxyphenyl)methyl]phenol
2467-03-0

2-[(4-hydroxyphenyl)methyl]phenol

C

bis-(4-hydroxyphenyl)methane
620-92-8

bis-(4-hydroxyphenyl)methane

Conditions
ConditionsYield
With phosphoric acid In water at 80℃; for 4h; Overall yield = 87.7 %;

13353-03-2Relevant articles and documents

AQUEOUS COMPOSITION BASED ON POLYOXYMETHYLENE DIALKYL ETHERS (POM) AND THEIR USE FOR THE PRESERVATION AND/OR EMBALMING OF THE HUMAN OR ANIMAL BODY

-

Paragraph 0060-0061, (2020/11/24)

The invention relates to a composition comprising: a) a mixture of polyoxymethylene dialkyl ethers (POM) having a restricted specific molecular distributionb) at least one biocidal agentc) at least one pro-penetrating agentd) at least one dyee) optionally, another additiveand water as diluent. It also relates to a non-therapeutic method of preserving and/or embalming a dead human or animal body using the composition, such as the use of this composition for anatomopathological purposes.

Novel synthesis method of alkoxymethylamine compound

-

Paragraph 0059; 0060, (2019/10/01)

The invention relates to a novel synthesis method of an alkoxymethylamine compound. The novel synthesis method comprises the steps: (1) dehydrating formaldehyde HCHO and alcohol R1OH by carrying out an aldolization under the action of an acid catalyst to obtain dialkoxymethane; and (2) carrying out a hydrocarbylation reaction on dialkoxymethane obtained in step (1) and substituted amine R2-NH2 toremove alcohol to obtain an alkoxymethyl substituent amine compound N-R1 oxymethyl-N-R2 amine. The synthesis method disclosed by the invention is simple in operation and high in yield reaching 92% orabove; and compared with the prior art, the novel synthesis method has the advantages that no acid wastewater, waste salts and chloromethyl alkyl ether serving as a cancerogen are greatly generated, the environment protection cost is favorably reduced, and the industrial prospect is higher.

Towards a Sustainable Synthesis of Oxymethylene Dimethyl Ether by Homogeneous Catalysis and Uptake of Molecular Formaldehyde

Peter, Andreas,Fehr, Samuel M.,Dybbert, Valentin,Himmel, Daniel,Lindner, Ines,Jacob, Eberhard,Ouda, Mohamed,Schaadt, Achim,White, Robin J.,Scherer, Harald,Krossing, Ingo

supporting information, p. 9461 - 9464 (2018/07/25)

Oxymethylene dimethyl ethers (OMEn; CH3(-OCH2-)nO-CH3, n=3–5) are a novel class of sustainable synthetic fuels, which are of increasing interest due to their soot-free combustion. Herein a novel anhyd

Three Binary Azeotropic Systems for 1-(Methoxymethoxy)-propane, 1-(Ethoxymethoxy)-propane, and Methoxy(methoxymethoxy)methane with Three Alcohols at 101.33 kPa: Experimental Data, Correlation, and Purification

Song, Yu-He,Hou, Xing-Ming,Song, Juan,Zhang, Yue,Wang, Jie,Wei, Ping-He,Li, Cun-Fu

, p. 138 - 146 (2018/01/18)

The isobaric vapor-liquid equilibrium (VLE) data for three binary systems of 1-(methoxymethoxy)-propane and ethanol, 1-(ethoxymethoxy)-propane and 1-butanol, methoxy(methoxymethoxy)methane and 1-propanol at 101.33 kPa were measured using an improved Rose still. Three minimum boiling azeotropes were found for three binary systems containing ethanol, 1-butanol, and 1-propanol for which the azeotropic temperature and composition are 349.35 K and 70.95 mol % (ethanol), 384.02 K and 36.02 mol % (1-butanol), 368.68 K and 69.26 mol % (1-propanol), at 101.33 kPa, respectively. The VLE measurements were correlated by the Van Laar, Wilson, and nonrandom two-liquid models, and the results showed that the measurements had a good correlation by using thethree models for the three binary systems, respectively. The measurements of these three binary systems were thermodynamic as checked by the Herington semiempirical method.

By poly-formaldehyde systems poly formaldehyde method of dimethyl ether

-

Paragraph 0019-0020, (2017/02/09)

The invention relates to a method for preparing polyoxymethylene dimethyl ether from paraformaldehyde, and mainly solves the problem in the prior art that the cost is relative high when triformol is adopted as a raw material to synthesize polyoxymethylene dimethyl ether. According to the invention, methanol, dimethoxymethane, and paraformaldehyde are adopted as raw materials, wherein the mass ratio of methanol : dimethoxymethane : paraformaldehyde is (0-10) : (0-10) : 1, wherein the quantities of methanol and dimethoxymethane cannot both be 0; the catalyst is chosen from at least one component of the following tombarthite modified solid superacid: SO4/ZrO2-La2O3, SO4/ZrO2-Ce2O3, Cl/TiO2-La2O3, Cl/TiO2-Ce2O3, Cl/Fe2O3-Ce2O3, SO4/Al2O3-La2O3 or S2O8/ZrO2-La2O3. The technical scheme excellently solves the problem, and can be applied to the industrial production of polyoxymethylene dimethyl ether.

Polyoxymethylene to dimethyl ether synthesis method of polyoxymethylene

-

Paragraph 0019; 0020; 0035; 0036, (2017/03/21)

The invention relates to a method for synthesizing polyoxymethylene dimethyl ether by using polyoxymethylene, and the method is mainly used for solving the problems of low reaction efficiency of the traditional catalyst and relatively high cost caused by taking trioxymethylene as a raw material. The problems are better solved according to the technical scheme that methanol, dimethoxymethane and polyoxymethylene are used as raw materials, wherein the mass ratio of methanol to dimethoxymethane to polyoxymethylene is (0-10):(0-10):1, the dosages of methanol and dimethoxymethane cannot be simultaneously equal to zero, the raw materials are in contact with a catalyst to react to generate polyoxymethylene dimethyl ether under the conditions that the reaction temperature is 70-200 DEG C and the reaction pressure is 0.2-6MPa, the dosage of the catalyst accounts for 0.05-10% of the weight of the raw materials, and the adopted catalyst comprises the following components in parts by weight: 30-80 parts of molecular sieve carriers (a) and 20-70 parts of rare earth modified solid super acid (b). The method can be used for industrial production of polyoxymethylene dimethyl ether.

Reaction system and process for preparing polymethoxy dimethyl ether

-

Paragraph 0082; 0083, (2015/04/15)

The invention relates to a reaction system and process for continuously preparing polymethoxy dimethyl ether (DMM3-8) by a continuous acetalization reaction between an aqueous formaldehyde solution or paraformaldehyde and methanol in the presence of a functionalized acidic ionic liquid as a catalyst. The reaction system of the invention preferably comprises a formaldehyde-concentrating unit, a vacuum-drying unit, an acetalization reaction unit, a product-separating unit and a catalyst-regenerating unit. The process of the invention uses aqueous formaldehyde solution as an initial raw material, which is concentrated in the formaldehyde-concentrating unit to a concentrated formaldehyde of 50~80 wt.%, and vacuum-dried to paraformaldehyde, or uses paraformaldehyde as raw material directly, then obtains DMM3-8 by an acetalization reaction. The raw materials of the reaction used in the invention are cheap and available easily, and the utilization rate of formaldehyde is high; an efficient separation between the catalyst and product, as well as the reuse of the catalyst and raw materials, are realized by a separation mode of combining extraction and rectification together.

REACTION SYSTEM AND PROCESS FOR PREPARING POLYMETHOXY DIMETHYL ETHER

-

Paragraph 0105-0108, (2015/04/15)

The invention relates to a reaction system and process for continuously preparing polymethoxy dimethyl ether (DMM3-8) by a continuous acetalization reaction between an aqueous formaldehyde solution or paraformaldehyde and methanol in the presen

Synthesis of polyoxymethylene dimethyl ethers catalyzed by rare earth compounds

Shi, Gao-Feng,Miao, Jian,Wang, Guo-Ying,Su, Jin-Mei,Liu, Hai-Xiao

, p. 2149 - 2153 (2015/11/28)

Polyoxymethylene dimethyl ethers (PODMEn) have been synthesized in moderate yields by the reaction of methylal (PODME1) and paraformaldehyde catalyzed by rare earth compounds. The activities of catalyst in the reaction were investigated and the

Shape selectivity extending to ordered supermicroporous aluminosilicates

Fu, Wen Hua,Liang, Xiao Min,Zhang, Haidong,Wang, Yi Meng,He, Ming Yuan

supporting information, p. 1449 - 1452 (2015/08/03)

In the synthesis of polyoxymethylene dimethyl ethers (PODEn) catalyzed by ordered supermicroporous aluminosilicates, shape selectivity was observed and the high selectivity for target products (PODE3-8) was attributed to the particul

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 13353-03-2