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627-82-7

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627-82-7 Usage

Chemical Properties

colourless viscous liquid

Uses

Different sources of media describe the Uses of 627-82-7 differently. You can refer to the following data:
1. diglycerin can increase the water content in the top layers of the skin. Formulators may select this ingredient for its humectant properties, and also when needing a skin-conditioning agent or a solvent. It is synthetically manufactured.
2. Diglycerol was used in cosmetic deodorants. It is also a component in thickening and gelatation agents.

Check Digit Verification of cas no

The CAS Registry Mumber 627-82-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 627-82:
(5*6)+(4*2)+(3*7)+(2*8)+(1*2)=77
77 % 10 = 7
So 627-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O5/c7-1-5(9)3-11-4-6(10)2-8/h5-10H,1-4H2/t5-,6+

627-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,3-dihydroxypropoxy)propane-1,2-diol

1.2 Other means of identification

Product number -
Other names Diglycerine

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:627-82-7 SDS

627-82-7Synthetic route

4-[(2,3-dihydroxypropoxy)methyl]-1,3 dioxolan-2-one

4-[(2,3-dihydroxypropoxy)methyl]-1,3 dioxolan-2-one

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
With water; potassium carbonate In methanol for 2h; Reflux;99%
With water; potassium carbonate In methanol at 90℃; for 2h;81%
glycerol
56-81-5

glycerol

A

1,3-dioxolane-4-methanol
5464-28-8

1,3-dioxolane-4-methanol

B

glycerol formal
4740-78-7

glycerol formal

C

glycolic Acid
79-14-1

glycolic Acid

D

ethyl 2-hydroxyacetate
623-50-7

ethyl 2-hydroxyacetate

E

diglycerol
627-82-7

diglycerol

F

oxiranyl-methanol
556-52-5

oxiranyl-methanol

G

hydroxy-2-propanone
116-09-6

hydroxy-2-propanone

H

acrolein
107-02-8

acrolein

Conditions
ConditionsYield
With pretreated aluminium vanadium phosphate In water at 280℃; under 760.051 Torr; Catalytic behavior; Activation energy; Reagent/catalyst; Temperature;A n/a
B n/a
C n/a
D n/a
E n/a
F n/a
G n/a
H 62%
glycerol
56-81-5

glycerol

A

diglycerol
627-82-7

diglycerol

B

2,4-bis(hydroxymethyl)-3-oxapentane-1,5-diol
100450-00-8

2,4-bis(hydroxymethyl)-3-oxapentane-1,5-diol

C

5-hydroxymethyl-4-oxahexane-1,2,6-triol

5-hydroxymethyl-4-oxahexane-1,2,6-triol

Conditions
ConditionsYield
With lithium hydroxide In neat (no solvent) at 240℃; under 760.051 Torr; for 1.5h; Inert atmosphere; Overall yield = 40 %;A 45%
B n/a
C n/a
With 10 wtpercent Li-10 wtpercent Mg in SBA-15 support In neat (no solvent) at 240℃; under 760.051 Torr; for 14h; Time; Inert atmosphere;
With 10 wtpercent Li-10 wtpercent Mg in SBA-15 support In neat (no solvent) at 240℃; under 760.051 Torr; for 18h; Time; Inert atmosphere; Overall yield = 63 %;
glycerol
56-81-5

glycerol

A

triglycerin
20411-31-8

triglycerin

B

diglycerol
627-82-7

diglycerol

C

2,4-bis(hydroxymethyl)-3-oxapentane-1,5-diol
100450-00-8

2,4-bis(hydroxymethyl)-3-oxapentane-1,5-diol

D

5-hydroxymethyl-4-oxahexane-1,2,6-triol

5-hydroxymethyl-4-oxahexane-1,2,6-triol

Conditions
ConditionsYield
With 20% Ca1.6La0.6/MCM-41 at 250℃; under 760.051 Torr; for 2h; Dean-Stark; Inert atmosphere;A n/a
B 43%
C 16%
D 41%
With 20% Ca1.6La0.6/MCM-41 at 250℃; under 760.051 Torr; for 8h; Reagent/catalyst; Temperature; Time; Dean-Stark; Inert atmosphere;A 25%
B n/a
C n/a
D n/a
glycerol
56-81-5

glycerol

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
25%
With calcium oxide at 140℃; im Vakuum, Einleiten von CO2 in das wasserfreie Gemisch bei derselben Temperatur und Erhitzen des Reaktionsprodukts auf 200grad;
glycerol
56-81-5

glycerol

A

2,5-Bis(hydroxymethyl)-1,4-dioxane
14236-12-5

2,5-Bis(hydroxymethyl)-1,4-dioxane

B

2,6-bis(hydroxymethyl)-1,4-dioxane

2,6-bis(hydroxymethyl)-1,4-dioxane

C

triglycerin
20411-31-8

triglycerin

D

diglycerol
627-82-7

diglycerol

E

4,8,12-trioxapentadecane-1,2,6,10,14,15-hexaol
21872-45-7

4,8,12-trioxapentadecane-1,2,6,10,14,15-hexaol

Conditions
ConditionsYield
With dihydrogen peroxide at 250℃; for 6h; Reagent/catalyst; Time;A n/a
B n/a
C 5.95%
D 19.55%
E n/a
Allyl ether
557-40-4

Allyl ether

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
With Peroxyformic acid at 40℃;
With calcium hypochlorite; water und Verseifen des entstandenen Dichlorhydrins mit Natriumdicarbonat-Loesung bei 140 - 160grad unter Druck;
With potassium permanganate at 2 - 5℃;
With AD-mix (K2OsO2(OH)4, K3Fe(CN)6, (DHQ)2-AQN as ligand) for 96h;
oxiranyl-methanol
556-52-5

oxiranyl-methanol

glycerol
56-81-5

glycerol

diglycerol
627-82-7

diglycerol

3-monochloro-1,2-propanediol
96-24-2

3-monochloro-1,2-propanediol

glycerol
56-81-5

glycerol

A

diglycerol
627-82-7

diglycerol

B

oxiranyl-methanol
556-52-5

oxiranyl-methanol

Conditions
ConditionsYield
die Mononatriumverbindung reagiert;
sodium acetate
127-09-3

sodium acetate

glycerol
56-81-5

glycerol

diglycerol
627-82-7

diglycerol

glycerol
56-81-5

glycerol

A

3-Hydroxypropanal
2134-29-4

3-Hydroxypropanal

B

diglycerol
627-82-7

diglycerol

C

oxiranyl-methanol
556-52-5

oxiranyl-methanol

D

hydroxy-2-propanone
116-09-6

hydroxy-2-propanone

Conditions
ConditionsYield
at 170 - 250℃; Produkt 5: Acrylaldehyd;
Diglycidyl ether
2238-07-5

Diglycidyl ether

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
With water at 70℃; Rate constant; variation of pH;
1,2-O-allylidenediglycerol
85282-79-7

1,2-O-allylidenediglycerol

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
With phosphoric acid In water at 30℃; for 0.5h;
4-[(2,3-dihydroxypropoxy)methyl]-1,3 dioxolan-2-one

4-[(2,3-dihydroxypropoxy)methyl]-1,3 dioxolan-2-one

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
With water; potassium carbonate In methanol for 2h; Reflux;99%
With water; potassium carbonate In methanol at 90℃; for 2h;81%
glycerol
56-81-5

glycerol

A

1,3-dioxolane-4-methanol
5464-28-8

1,3-dioxolane-4-methanol

B

glycerol formal
4740-78-7

glycerol formal

C

glycolic Acid
79-14-1

glycolic Acid

D

ethyl 2-hydroxyacetate
623-50-7

ethyl 2-hydroxyacetate

E

diglycerol
627-82-7

diglycerol

F

oxiranyl-methanol
556-52-5

oxiranyl-methanol

G

hydroxy-2-propanone
116-09-6

hydroxy-2-propanone

H

acrolein
107-02-8

acrolein

Conditions
ConditionsYield
With pretreated aluminium vanadium phosphate In water at 280℃; under 760.051 Torr; Catalytic behavior; Activation energy; Reagent/catalyst; Temperature;A n/a
B n/a
C n/a
D n/a
E n/a
F n/a
G n/a
H 62%
glycerol
56-81-5

glycerol

A

diglycerol
627-82-7

diglycerol

B

2,4-bis(hydroxymethyl)-3-oxapentane-1,5-diol
100450-00-8

2,4-bis(hydroxymethyl)-3-oxapentane-1,5-diol

C

5-hydroxymethyl-4-oxahexane-1,2,6-triol

5-hydroxymethyl-4-oxahexane-1,2,6-triol

Conditions
ConditionsYield
With lithium hydroxide In neat (no solvent) at 240℃; under 760.051 Torr; for 1.5h; Inert atmosphere; Overall yield = 40 %;A 45%
B n/a
C n/a
With 10 wtpercent Li-10 wtpercent Mg in SBA-15 support In neat (no solvent) at 240℃; under 760.051 Torr; for 14h; Time; Inert atmosphere;
With 10 wtpercent Li-10 wtpercent Mg in SBA-15 support In neat (no solvent) at 240℃; under 760.051 Torr; for 18h; Time; Inert atmosphere; Overall yield = 63 %;
glycerol
56-81-5

glycerol

A

triglycerin
20411-31-8

triglycerin

B

diglycerol
627-82-7

diglycerol

C

2,4-bis(hydroxymethyl)-3-oxapentane-1,5-diol
100450-00-8

2,4-bis(hydroxymethyl)-3-oxapentane-1,5-diol

D

5-hydroxymethyl-4-oxahexane-1,2,6-triol

5-hydroxymethyl-4-oxahexane-1,2,6-triol

Conditions
ConditionsYield
With 20% Ca1.6La0.6/MCM-41 at 250℃; under 760.051 Torr; for 2h; Dean-Stark; Inert atmosphere;A n/a
B 43%
C 16%
D 41%
With 20% Ca1.6La0.6/MCM-41 at 250℃; under 760.051 Torr; for 8h; Reagent/catalyst; Temperature; Time; Dean-Stark; Inert atmosphere;A 25%
B n/a
C n/a
D n/a
glycerol
56-81-5

glycerol

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
25%
With calcium oxide at 140℃; im Vakuum, Einleiten von CO2 in das wasserfreie Gemisch bei derselben Temperatur und Erhitzen des Reaktionsprodukts auf 200grad;
glycerol
56-81-5

glycerol

A

2,5-Bis(hydroxymethyl)-1,4-dioxane
14236-12-5

2,5-Bis(hydroxymethyl)-1,4-dioxane

B

2,6-bis(hydroxymethyl)-1,4-dioxane

2,6-bis(hydroxymethyl)-1,4-dioxane

C

triglycerin
20411-31-8

triglycerin

D

diglycerol
627-82-7

diglycerol

E

4,8,12-trioxapentadecane-1,2,6,10,14,15-hexaol
21872-45-7

4,8,12-trioxapentadecane-1,2,6,10,14,15-hexaol

Conditions
ConditionsYield
With dihydrogen peroxide at 250℃; for 6h; Reagent/catalyst; Time;A n/a
B n/a
C 5.95%
D 19.55%
E n/a
Allyl ether
557-40-4

Allyl ether

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
With Peroxyformic acid at 40℃;
With calcium hypochlorite; water und Verseifen des entstandenen Dichlorhydrins mit Natriumdicarbonat-Loesung bei 140 - 160grad unter Druck;
With potassium permanganate at 2 - 5℃;
With AD-mix (K2OsO2(OH)4, K3Fe(CN)6, (DHQ)2-AQN as ligand) for 96h;
oxiranyl-methanol
556-52-5

oxiranyl-methanol

glycerol
56-81-5

glycerol

diglycerol
627-82-7

diglycerol

3-monochloro-1,2-propanediol
96-24-2

3-monochloro-1,2-propanediol

glycerol
56-81-5

glycerol

A

diglycerol
627-82-7

diglycerol

B

oxiranyl-methanol
556-52-5

oxiranyl-methanol

Conditions
ConditionsYield
die Mononatriumverbindung reagiert;
sodium acetate
127-09-3

sodium acetate

glycerol
56-81-5

glycerol

diglycerol
627-82-7

diglycerol

glycerol
56-81-5

glycerol

A

3-Hydroxypropanal
2134-29-4

3-Hydroxypropanal

B

diglycerol
627-82-7

diglycerol

C

oxiranyl-methanol
556-52-5

oxiranyl-methanol

D

hydroxy-2-propanone
116-09-6

hydroxy-2-propanone

Conditions
ConditionsYield
at 170 - 250℃; Produkt 5: Acrylaldehyd;
Diglycidyl ether
2238-07-5

Diglycidyl ether

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
With water at 70℃; Rate constant; variation of pH;
1,2-O-allylidenediglycerol
85282-79-7

1,2-O-allylidenediglycerol

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
With phosphoric acid In water at 30℃; for 0.5h;
glycerol
56-81-5

glycerol

A

triglycerin
20411-31-8

triglycerin

B

diglycerol
627-82-7

diglycerol

C

4,8,12-trioxapentadecane-1,2,6,10,14,15-hexaol
21872-45-7

4,8,12-trioxapentadecane-1,2,6,10,14,15-hexaol

Conditions
ConditionsYield
ion exchange resin A19 at 124℃; for 6h; Product distribution; also with ion exchange resin C264 as catalyst;A 8 % Chromat.
B 22 % Chromat.
C 3 % Chromat.
soap In methanol at 20 - 270℃; for 0.5h; Product distribution / selectivity; Microwave irradiation;
soap In methanol at 20 - 270℃; for 0.5h; Product distribution / selectivity; Microwave irradiation;
3-oxiranylmethoxy-propane-1,2-diol
40909-95-3

3-oxiranylmethoxy-propane-1,2-diol

sulfuric acid
7664-93-9

sulfuric acid

diglycerol
627-82-7

diglycerol

sulfuric acid
7664-93-9

sulfuric acid

1,2-diacetoxy-3-(2,3-epoxy-propoxy)-propane

1,2-diacetoxy-3-(2,3-epoxy-propoxy)-propane

diglycerol
627-82-7

diglycerol

iodine
7553-56-2

iodine

glycerol
56-81-5

glycerol

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
at 210℃;
glycerol
56-81-5

glycerol

hydrated waterglass

hydrated waterglass

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
at 220 - 240℃; im Rohr unter Ruehren und Durchleiten von Kohlendioxyd;
glycerol
56-81-5

glycerol

magnesium oxide

magnesium oxide

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
at 220 - 240℃; im Rohr unter Ruehren und Durchleiten von Kohlendioxyd;
glycerol
56-81-5

glycerol

Na2SiO3+9H2O

Na2SiO3+9H2O

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
at 220 - 240℃; im Rohr unter Ruehren und Durchleiten von Kohlendioxyd;
glycerol
56-81-5

glycerol

A

diglycerol
627-82-7

diglycerol

B

polyglycerol

polyglycerol

Conditions
ConditionsYield
at 290 - 295℃;
at 290 - 295℃;
tetrachloromethane
56-23-5

tetrachloromethane

glycerol
56-81-5

glycerol

NaOH-solution <45 percent >

NaOH-solution <45 percent >

A

diglycerol
627-82-7

diglycerol

B

triglycerol

triglycerol

Conditions
ConditionsYield
at 250℃;
glycerol
56-81-5

glycerol

water free Na2SO4

water free Na2SO4

nitrogen

nitrogen

A

diglycerol
627-82-7

diglycerol

B

triglycerol

triglycerol

Conditions
ConditionsYield
at 250℃;
sodium acetate
127-09-3

sodium acetate

glycerol
56-81-5

glycerol

A

2-(hydroxymethyl)-2-methylpropane-1,3-diol
77-85-0

2-(hydroxymethyl)-2-methylpropane-1,3-diol

B

diglycerol
627-82-7

diglycerol

C

triglycerol

triglycerol

D

tetraglycerol

tetraglycerol

Conditions
ConditionsYield
weitere Produkte: Hexaglycerin; Heptaglycerin; 2.5(oder 2.6)-Bis-oxymethyl-dioxan-(1.4);
formic acid
64-18-6

formic acid

Allyl ether
557-40-4

Allyl ether

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
at 40℃;
Allyl ether
557-40-4

Allyl ether

hypochloric acid
13898-47-0

hypochloric acid

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
und anschliessenden Verseifung mit Natriumdicarbonatloesung bei 140-160grad unter Druck;
diglycide ether

diglycide ether

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
With sulfuric acid
With water at 100℃;
Allyl ether
557-40-4

Allyl ether

water
7732-18-5

water

KMnO4

KMnO4

diglycerol
627-82-7

diglycerol

Conditions
ConditionsYield
at 2 - 5℃;
glycerol
56-81-5

glycerol

A

diglycerol
627-82-7

diglycerol

B

triglycerol

triglycerol

Conditions
ConditionsYield
With sodium hydroxide; xylene at 250℃; Trennung erfolgt durch Ueberfuehrung in die Isopropyliden-Derivate, fraktionierte Destillation und kurzes Erwaermen des Bis-<2.3-isopropylidendioxy-propyl>-aethers mit verd.HCl auf dem Wasserbad;
With sodium sulfate at 245℃;
diglycerol
627-82-7

diglycerol

isobutyraldehyde
78-84-2

isobutyraldehyde

4,4'-[oxydi(methylene)]-bis-2-diisopropyl-1,3-dioxolane

4,4'-[oxydi(methylene)]-bis-2-diisopropyl-1,3-dioxolane

Conditions
ConditionsYield
With sulfuric acid at 80℃;100%
formaldehyd
50-00-0

formaldehyd

diglycerol
627-82-7

diglycerol

4,4'-[oxydi(methylene)]-bis-1,3-dioxolane

4,4'-[oxydi(methylene)]-bis-1,3-dioxolane

Conditions
ConditionsYield
With sulfuric acid at 80℃;100%
Dodecanal
112-54-9

Dodecanal

diglycerol
627-82-7

diglycerol

C30H58O5

C30H58O5

Conditions
ConditionsYield
With para-dodecylbenzenesulfonic acid In water at 120℃; for 2h; Catalytic behavior; Reagent/catalyst; Temperature; Time; Inert atmosphere; Dean-Stark; Green chemistry;93.9%
With para-dodecylbenzenesulfonic acid In water at 120℃; for 4h; Catalytic behavior; Temperature; Inert atmosphere; Green chemistry;88.67%
diglycerol
627-82-7

diglycerol

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

4-[(2,3-di-hydroxy-propoxy)methyl]-1,3-dioxolan-2-one
1312715-72-2

4-[(2,3-di-hydroxy-propoxy)methyl]-1,3-dioxolan-2-one

Conditions
ConditionsYield
Stage #1: diglycerol; carbonic acid dimethyl ester With calcium oxide at 81.84℃; for 48h; Inert atmosphere;
Stage #2: at 499.84℃; for 3h; Kinetics; Catalytic behavior; Time; Calcination;
90%
nonan-1-al
124-19-6

nonan-1-al

diglycerol
627-82-7

diglycerol

C24H46O5

C24H46O5

Conditions
ConditionsYield
With para-dodecylbenzenesulfonic acid In water at 90℃; for 10h; Inert atmosphere; Green chemistry;88.12%
N-(4-(azidocarbonyl)phenyl)maleimide
58174-51-9

N-(4-(azidocarbonyl)phenyl)maleimide

diglycerol
627-82-7

diglycerol

1,2,6,7-tetra[N-(p-maleimidophenyl)carbamoyloxy]-4-oxaheptane

1,2,6,7-tetra[N-(p-maleimidophenyl)carbamoyloxy]-4-oxaheptane

Conditions
ConditionsYield
Stage #1: N-[4-(azidocarbonyl)phenyl]maleimide; diglycerol With 1,4-diaza-bicyclo[2.2.2]octane; cyclopentyl methyl ether; hydroquinone In N,N-dimethyl-formamide at 80℃; for 24h; Inert atmosphere;
Stage #2: In N,N-dimethyl-formamide; hexan-1-ol at 50℃; for 3h; Inert atmosphere;
88%
diglycerol
627-82-7

diglycerol

n-hexadecylaldehyde
629-80-1

n-hexadecylaldehyde

C38H74O5

C38H74O5

Conditions
ConditionsYield
With para-dodecylbenzenesulfonic acid In water at 150℃; for 6h; Inert atmosphere; Green chemistry;87.21%
caprinaldehyde
112-31-2

caprinaldehyde

diglycerol
627-82-7

diglycerol

C26H50O5

C26H50O5

Conditions
ConditionsYield
With p-ethylbenzenesulfonic acid In water at 100℃; for 12h; Inert atmosphere; Green chemistry;86.61%
diglycerol
627-82-7

diglycerol

hexanal
66-25-1

hexanal

C12H24O5

C12H24O5

Conditions
ConditionsYield
With magnesium chloride at 80℃; for 2h; Inert atmosphere;86.6%
diglycerol
627-82-7

diglycerol

undecylaldehyde
112-44-7

undecylaldehyde

C28H54O5

C28H54O5

Conditions
ConditionsYield
With p-octylbenzenesulfonic acid In water at 110℃; for 8h; Inert atmosphere; Green chemistry;86.38%
diglycerol
627-82-7

diglycerol

myristylaldehyde
124-25-4

myristylaldehyde

C34H66O5

C34H66O5

Conditions
ConditionsYield
With p-octylbenzenesulfonic acid In water at 80℃; for 18h; Inert atmosphere; Green chemistry;86.28%
n-pentadecanal
2765-11-9

n-pentadecanal

diglycerol
627-82-7

diglycerol

C36H70O5

C36H70O5

Conditions
ConditionsYield
With p-ethylbenzenesulfonic acid In water at 140℃; for 15h; Inert atmosphere; Green chemistry;86.08%
Octanal
124-13-0

Octanal

diglycerol
627-82-7

diglycerol

C22H42O5

C22H42O5

Conditions
ConditionsYield
With toluene-4-sulfonic acid In water at 70℃; for 24h; Inert atmosphere; Green chemistry;85.75%
diglycerol
627-82-7

diglycerol

trimethyl orthoformate
149-73-5

trimethyl orthoformate

2-methoxy-4-{[(2-methoxy-1,3-dioxolan-4-yl)methoxy]methyl}-1,3-dioxolane

2-methoxy-4-{[(2-methoxy-1,3-dioxolan-4-yl)methoxy]methyl}-1,3-dioxolane

Conditions
ConditionsYield
In acetonitrile at 20℃; Inert atmosphere;85.6%
With toluene-4-sulfonic acid In acetonitrile at 20℃; Inert atmosphere;62.87%
With toluene-4-sulfonic acid In acetonitrile
diglycerol
627-82-7

diglycerol

tridecanal
10486-19-8

tridecanal

C32H62O5

C32H62O5

Conditions
ConditionsYield
With toluene-4-sulfonic acid In water at 150℃; for 7h; Inert atmosphere; Green chemistry;85.36%
diglycerol
627-82-7

diglycerol

butyraldehyde
123-72-8

butyraldehyde

C10H20O5

C10H20O5

Conditions
ConditionsYield
With iron(II) chloride at 50℃; for 12h; Inert atmosphere;85.3%
diglycerol
627-82-7

diglycerol

dibromo-1,1-dimethoxyethane

dibromo-1,1-dimethoxyethane

4,4-dimethoxy-di-(2-bromomethyl-1,3-dioxolane)

4,4-dimethoxy-di-(2-bromomethyl-1,3-dioxolane)

Conditions
ConditionsYield
With toluene-4-sulfonic acid In diethylene glycol dimethyl ether at 110 - 150℃; for 3h;85.2%
methyl hexanoate
106-70-7

methyl hexanoate

diglycerol
627-82-7

diglycerol

3-(2,3-dihydroxypropoxy)-2-hydroxypropyl hexanoate
1026295-85-1

3-(2,3-dihydroxypropoxy)-2-hydroxypropyl hexanoate

Conditions
ConditionsYield
at 130℃; for 16h; Inert atmosphere;83%

627-82-7Relevant articles and documents

Identification of Cyclic Acetals in Polyols by Mass Spectrometry

Sanders, Robert A.

, p. 1194 - 1197 (1983)

-

Facile route to multigram synthesis of environmentally friendly non-isocyanate polyurethanes

Tryznowski, Mariusz,?widerska, Aleksandra,Zo?ek-Tryznowska, Zuzanna,Go?ofit, Tomasz,Parzuchowski, Pawe? G.

, p. 228 - 236 (2015)

Non-isocyanate poly(hydroxyurethanes) (NIPUs) are a fast growing class of polymers prepared by an environmentally friendly method without the use of toxic phosgene and isocyanates. In this work, we report a one-step procedure to synthesize bis(2,3-dihydroxypropyl)ether dicarbonate from a commercially available diglycerol. The product was characterized by 1H NMR, 13C NMR, and FTIR spectroscopies and for the first time by X-Ray diffraction measurements. Enantiomers RR and SS of the obtained monomer were observed in the single crystal structure. The bis(cyclic carbonate) monomer was used as a precursor for the synthesis of various NIPUs. The NIPUs were prepared in a non-solvent process. Spectral, thermal and rheological properties of the NIPUs formed from ten various diamines were compared.

Oligo-glycerol based non-ionic amphiphilic nanocarriers for lipase mediated controlled drug release

Aarti,Achazi, Katharina,Haag, Rainer,Mittal, Ayushi,Nie, Chuanxiong,Parmanand,Sharma, Sunil K.,Singh, Abhishek K.

, p. 37555 - 37563 (2020/10/28)

A new class of non-ionic amphiphiles is synthesized using a diaryl derivative of diglycerol as a central core and functionalizing it with long alkyl chains (C-12/C-15) and monomethoxy PEG moiety (Mn: 350/550) by following a chemo-enzymatic approach. The aggregation behavior of the amphiphiles in aqueous medium is studied by using dynamic light scattering (DLS) and fluorescence spectroscopy, whereas the size and morphology of the aggregates are studied by transmission electron microscopy (TEM). A hydrophobic dye, Nile red and a hydrophobic drug, nimodipine, are used to demonstrate the nano-carrier capability of these non-ionic amphiphilic systems and the results are compared with amphiphilic analogues obtained from the triaryl derivatives of triglycerol. Thein vitrocontrolled release of the encapsulated dye is successfully carried out in the presence of immobilizedCandida antarcticalipase (Novozym 435). Furthermore, cytotoxicity data is also collected which suggests that the amphiphiles are suitable for biomedical applications.

Catalytic behaviour of mesoporous metal phosphates in the gas-phase glycerol transformation

Lopez-Pedrajas,Estevez,Navarro,Luna,Bautista

, p. 92 - 101 (2016/06/09)

The catalytic behaviour of mesoporous simple (M = Al, Fe, Co, Mn) and binary (Al/M; M = Fe,V,Ca; molar ratio Al/Fe = 50; Al/V = 2; Al/Ca = 1) metal phosphates, synthesized by an economical gelation method, in the gas-phase glycerol reaction at temperatures between 220 °C and 280 °C, has been investigated. The morphology, textural properties and the acidity by pyridine TPD, of the phosphates were also determined. The activity of the phosphates in the formation of the main reaction product (acrolein) depended not only on their acidity (mainly acid sites of weak-medium strength) but also on the redox sites and morphology exhibited. Thus, the aluminium-vanadium phosphate showed the highest value of yield to acrolein, 62% (equivalent to a productivity of 0.88 gACRgcath) at 280 °C, whereas the amorphous FePO4 and AlPO4 were appreciably more active than the rest of the simple phosphates, exhibiting a high crystalline character. The apparent activation energy values obtained for the acrolein formation ranged between 18 and 91 kJ/mol. Based on the identified products in this study, some possible reactions involved in the glycerol transformation have been suggested.

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