Product Name

  • Name

    1,1'-Oxydi-2-propanol

  • EINECS 203-821-4
  • CAS No. 110-98-5
  • Article Data8
  • CAS DataBase
  • Density 1.034 g/cm3
  • Solubility MISCIBLE
  • Melting Point 46 - 48oC
  • Formula C6H14O3
  • Boiling Point 230.5 °C at 760 mmHg
  • Molecular Weight 134.175
  • Flash Point 137.8 °C
  • Transport Information
  • Appearance Colorless, slightly viscous liquid. Practically no odor.
  • Safety 24/25
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 110-98-5 (1,1'-Oxydi-2-propanol)
  • Hazard Symbols
  • Synonyms 2-Propanol,1,1'-oxydi- (6CI,7CI,8CI);1,1'-Dimethyldiethylene glycol;Bis(2-hydroxypropyl) ether;NSC 8688;
  • PSA 49.69000
  • LogP -0.23540

Synthetic route

propylene glycol
57-55-6

propylene glycol

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

methyloxirane

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

Conditions
ConditionsYield
at 117 - 118℃;
methyloxirane
75-56-9, 16033-71-9

methyloxirane

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

Conditions
ConditionsYield
With sodium hydroxide
methyloxirane
75-56-9, 16033-71-9

methyloxirane

inactive propylene glycol

inactive propylene glycol

A

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

B

'propylene glycol triether

'propylene glycol triether

Conditions
ConditionsYield
at 117 - 118℃;
dextrorotatory propylene oxide

dextrorotatory propylene oxide

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

Conditions
ConditionsYield
With potassium hydroxide at 117 - 119℃; levorotatory β.β'-dioxy-dipropyl ether;
With (-)-propane-1,2-diol at 117 - 119℃; levorotatory β.β'-dioxy-dipropyl ether;
(2R)-propane-1,2-diol
4254-14-2

(2R)-propane-1,2-diol

dextrorotatory propylene oxide

dextrorotatory propylene oxide

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

Conditions
ConditionsYield
ohne Kondensationsmittel;
inactive propylene oxide

inactive propylene oxide

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

Conditions
ConditionsYield
With (-)-propane-1,2-diol; sulfuric acid levorotatory β.β'-dioxy-dipropyl ether;
sulfuric acid
7664-93-9

sulfuric acid

(2R)-propane-1,2-diol
4254-14-2

(2R)-propane-1,2-diol

inactive propylene oxide

inactive propylene oxide

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

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

methyloxirane

sodium-compound of propane-1,2-diol

sodium-compound of propane-1,2-diol

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

Conditions
ConditionsYield
at 144℃;
propylene glycol
57-55-6

propylene glycol

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

Conditions
ConditionsYield
With amberlyst 36Dry at 130℃;13 %Chromat.
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

acrylic acid
79-10-7

acrylic acid

Conditions
ConditionsYield
With hydroquinone In cyclohexane; toluene at 160℃; for 3h; Temperature; Inert atmosphere;89%
Isopropenyl acetate
108-22-5

Isopropenyl acetate

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

(R,R)-bis(2-acetoxypropyl)ether
1017832-60-8

(R,R)-bis(2-acetoxypropyl)ether

Conditions
ConditionsYield
With Candida antarctica lipase B; catalyst 4; potassium tert-butylate; sodium carbonate In tetrahydrofuran; toluene at 50℃; for 46h; Inert atmosphere; optical yield given as %de;81%
Isopropenyl acetate
108-22-5

Isopropenyl acetate

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

C10H18O5

C10H18O5

Conditions
ConditionsYield
With Candida antarctica lipase B; dicarbonyl(chloro)(η5-pentaphenylcyclopentadienyl)ruthenium(II); potassium tert-butylate; sodium carbonate In toluene at 50℃; for 46h; Inert atmosphere; Enzymatic reaction; optical yield given as %ee;81%
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

n-Butyl chloride
109-69-3

n-Butyl chloride

dipropylene glycol dibutyl ether

dipropylene glycol dibutyl ether

Conditions
ConditionsYield
With tetrabutylammomium bromide; potassium hydroxide; sodium hydroxide at 120 - 160℃; for 20h;70%
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

1-Chloropropane
540-54-5

1-Chloropropane

dipropylene glycol dipropyl ether

dipropylene glycol dipropyl ether

Conditions
ConditionsYield
With tetrabutylammomium bromide; potassium hydroxide; sodium hydroxide at 55 - 65℃; for 10h;70%
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

2-methylallyl chloroformate
42068-70-2

2-methylallyl chloroformate

3,7-dimethyl-2,5,8-trioxa-nonanedioic acid dimethallyl ester

3,7-dimethyl-2,5,8-trioxa-nonanedioic acid dimethallyl ester

Conditions
ConditionsYield
With sodium hydroxide
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

2,2-Dichloropropionic acid
75-99-0

2,2-Dichloropropionic acid

1-[2-(2,2-dichloro-propionyloxy)-propoxy]-propan-2-ol

1-[2-(2,2-dichloro-propionyloxy)-propoxy]-propan-2-ol

Conditions
ConditionsYield
With ethylene glycol at 100℃;
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

2,6-Dimethyl-1,4-dioxene
3973-23-7

2,6-Dimethyl-1,4-dioxene

Conditions
ConditionsYield
With copper oxide-chromium oxide catalyst
With copper oxide-chromium oxide catalyst
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

bis-[2-(4-nitro-benzoyloxy)-propyl]-ether
95429-50-8

bis-[2-(4-nitro-benzoyloxy)-propyl]-ether

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

8-allyl-2-oxo-2H-chromene-3-carboxylic acid
82119-77-5

8-allyl-2-oxo-2H-chromene-3-carboxylic acid

mercury(II) diacetate
1600-27-7

mercury(II) diacetate

3-(3-carboxy-2-oxo-2H-chromen-8-yl)-2-[β-(2-hydroxy-propoxy)-isopropoxy]-propylmercury (1+); hydroxide

3-(3-carboxy-2-oxo-2H-chromen-8-yl)-2-[β-(2-hydroxy-propoxy)-isopropoxy]-propylmercury (1+); hydroxide

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

chloroformic acid ethyl ester
541-41-3

chloroformic acid ethyl ester

3,7-dimethyl-2,5,8-trioxa-nonanedioic acid diethyl ester

3,7-dimethyl-2,5,8-trioxa-nonanedioic acid diethyl ester

Conditions
ConditionsYield
With pyridine
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

trityl chloride
76-83-5

trityl chloride

bis-(2-trityloxy-propyl)-ether
96972-39-3

bis-(2-trityloxy-propyl)-ether

Conditions
ConditionsYield
With pyridine
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

allyl bromide
106-95-6

allyl bromide

bis-(2-allyloxy-propyl)-ether

bis-(2-allyloxy-propyl)-ether

Conditions
ConditionsYield
With sodium hydroxide at 70 - 75℃;
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

acrylonitrile
107-13-1

acrylonitrile

5,9-dimethyl-4,7,10-trioxa-tridecanedinitrile
55831-50-0

5,9-dimethyl-4,7,10-trioxa-tridecanedinitrile

Conditions
ConditionsYield
With sodium methylate at 25 - 45℃;
-butyl vinyl ether
111-34-2

-butyl vinyl ether

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

bis-(2-vinyloxy-propyl) ether
3891-40-5

bis-(2-vinyloxy-propyl) ether

Conditions
ConditionsYield
With mercury(II) diacetate
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

A

propylene glycol
57-55-6

propylene glycol

B

4-oxaheptandiol-2,6-monoformate

4-oxaheptandiol-2,6-monoformate

C

4-oxaheptandiol-2,6-monoacetate

4-oxaheptandiol-2,6-monoacetate

Conditions
ConditionsYield
With oxygen at 90℃; Mechanism; atmospheric pressure,;
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

copper oxide-chromium oxide

copper oxide-chromium oxide

2,6-Dimethyl-1,4-dioxene
3973-23-7

2,6-Dimethyl-1,4-dioxene

1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

sulfuric acid
7664-93-9

sulfuric acid

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

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

Conditions
ConditionsYield
at 80 - 115℃; bei der Destillation;
1,1'-oxydipropan-2-ol
110-98-5

1,1'-oxydipropan-2-ol

Diethylstilbestrol dimethyl ether
130-79-0

Diethylstilbestrol dimethyl ether

KOH

KOH

diethylstilbestrol
56-53-1

diethylstilbestrol

Conditions
ConditionsYield
at 215 - 235℃;

1,1'-Oxydi-2-propanol Consensus Reports

Reported in EPA TSCA Inventory.

1,1'-Oxydi-2-propanol Specification

The 1,1'-Oxydi-2-propanol is an organic compound with the formula C6H14O3. The IUPAC name of this chemical is 1-(2-hydroxypropoxy)propan-2-ol. With the CAS registry number 110-98-5, it is also named as Di(propylene glycol) . The product's classification code is Skin / Eye Irritant. Besides, it should be stored in a cool and well-ventilated place.

The other characteristics of this product can be summarized as: (1)ACD/LogP: -0.82; (2)ACD/LogD (pH 5.5): -0.82; (3)ACD/LogD (pH 7.4): -0.82; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 8.55; (7)ACD/KOC (pH 7.4): 8.55; (8)#H bond acceptors: 3; (9)#H bond donors: 2; (10)#Freely Rotating Bonds: 6; (11)Polar Surface Area: 27.69 Å2; (12)Index of Refraction: 1.445; (13)Molar Refractivity: 34.57 cm3; (14)Molar Volume: 129.7 cm3; (15)Polarizability: 13.7×10-24cm3; (16)Surface Tension: 36.4 dyne/cm; (17)Density: 1.034 g/cm3; (18)Flash Point: 137.8 °C; (19)Enthalpy of Vaporization: 54.3 kJ/mol; (20)Boiling Point: 230.5 °C at 760 mmHg; (21)Vapour Pressure: 0.0125 mmHg at 25 °C.

Preparation and Uses of 1,1'-Oxydi-2-propanol: this chemical can be prepared by 1,2 - propanediol and propylene oxide. The reaction temperature is 229 - 233 °C. Morteover, it is used for the manufacture of polyester resins. It is also used as a solvent of cellulose nitrate. And it is an intermediate used in organic synthesis.

When you are using this chemical, please be cautious about it as the following:
This chemical is irritating to eyes, respiratory system and skin. When you are using it, please avoid contact with skin and eyes.

You can still convert the following datas into molecular structure:
(1)SMILES: OC(C)COCC(O)C
(2)InChI: InChI=1/C6H14O3/c1-5(7)3-9-4-6(2)8/h5-8H,3-4H2,1-2H3
(3)InChIKey: AZUXKVXMJOIAOF-UHFFFAOYAB
(4)Std. InChI: InChI=1S/C6H14O3/c1-5(7)3-9-4-6(2)8/h5-8H,3-4H2,1-2H3
(5)Std. InChIKey: AZUXKVXMJOIAOF-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LD50 intravenous 11500mg/kg (11500mg/kg) BEHAVIORAL: ANTIPSYCHOTIC Food and Cosmetics Toxicology. Vol. 16, Pg. 729, 1978.
guinea pig LD50 oral 17600uL/kg (17.6mL/kg)   German Offenlegungsschrift Patent Document. Vol. #2703360,
mouse LD50 intraperitoneal 4494mg/kg (4494mg/kg) KIDNEY, URETER, AND BLADDER: "CHANGES IN TUBULES (INCLUDING ACUTE RENAL FAILURE, ACUTE TUBULAR NECROSIS)" Federation Proceedings, Federation of American Societies for Experimental Biology. Vol. 6, Pg. 342, 1947.
rabbit LD50 skin > 20mL/kg (20mL/kg)   Union Carbide Data Sheet. Vol. 12/17/1971,
rat LD50 intraperitoneal 10gm/kg (10000mg/kg)   Food and Cosmetics Toxicology. Vol. 16, Pg. 729, 1978.
rat LD50 intravenous 5800mg/kg (5800mg/kg) BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)

BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: TREMOR
AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 3, Pg. 448, 1951.
rat LD50 oral 14850mg/kg (14850mg/kg)   "Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 731, 1969.

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