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115-77-5

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115-77-5 Usage

Physical and chemical properties

Pentaerythritol is also called 2, 2-double (hydroxymethyl)-1, 3-propanediol, four hydroxymethyl methane, MetabAuxil, Penetek. White crystal powder. It was first found in 1882 by Tollens, and is colorless tetragonal crystal double tetrahedral crystal precipitated from dilute hydrochloric acid. The relative molecular mass is 136.15. Relative density is 1.399. Melting point is 262 oC (industrial products containing 10%~15% Dipentaerythritol, melting point is 180~225 oC). The boiling point is 276 oC (4.00 x 103 pa). The refractive index is 1.54~1.56. Can sublimate. Slowly soluble in cold water, soluble in hot water, insoluble in carbon tetrachloride, ethyl ether, benzene, petroleum ether, ethanol, acetone, solubility at 25 oC (g/100 g) in water, methanol, ethanol, butylamine, dimethyl sulfoxide, ethanolamine are 0.75, 7.23, 0.33, 16, 16.5 4.5, respectively. 1 g of dipentaerythritol can soluble in 18 ml of water at 15 oC. Pentaerythritol will polymerize when heated to above melting point, and generates a shrinkage second shrinkage e four season three pentaerythritol, etc. Stability in the air. The hydroxyl groups of Pentaerythritol can form complex with many kinds of metal; Can directly react with nitric acid trough nitration; Under the effect of catalyst, the hydroxy can be oxidized to acid; Can react with chlorine to generate the chloride; In acid medium, the product react with carbonyl compounds, generate cyclic acetal and ketal; Like other alcohols, can esterify with an acid or anhydride to generate four ester; The halides can dehalogenate to generate cyclic ether in the role of alkali. The addition reaction intermediate of 3-hydroxy aldehyde can react with formaldehyde through Cannizzaro reaction to generate season four amyl alcohol and formic acid. In 1938, it was first generated by United States with acetaldehyde and five times the amount of formaldehyde in the reaction of calcium hydroxide solution system. It is the only production method used in the industrial. Main purpose is to make explosives and synthetic resin (mainly used for various coatings).

The main purpose and effect

As quaternary alcohol, pentaerythritol is easily generated by esterification acid and ester, so most of the classes used in alkyd resin coatings raw materials, mainly used for architectural coatings and automotive primer. Pentaerythritol is used to esterification with nitric acid to generate pentaerythritol tetranitrate (also known as PETN) in 5~15 oC in industrial, which is a kind of high explosives and bigger than TNT explosive, most as a booster, or mix with TNT. A lot of PETN have been used in the second world war. PETN has the effect of diastolic blood vessels, is a long-term vasodilator and can treat angina pectoris. Pentaerythritol reaction with rosin acid can produce rosin pentaerythritol ester, which can be mixed with drying oil and is a kind of coating with better hardness, water resistance and weather resistance, can be used in ink of varnish, floor, etc. By esterification condensation pentaerythritol or glycerol with phthalic anhydride, fatty acid can make an alkyd resin coating. Use of different kinds and different amount of fatty acid can improve the properties of alkyd resin, making it a suitable coating of various kinds in need. It is widely used as a coating on the surface of the metal, wood, as a bridge, railway, derrick, building and other aspects of commonly used industrial paint and architectural paint. Because of the price is low, alkyd resin of reactants, easy modification, strong adaptability, good comprehensive, it has become the backbone of the coating industry since 1927. Pentaerythritol is often used in coating industry, is of alkyd coating raw material for the production of highly cross linked coatin using four hydroxyls, the coating has good hardness and color, can improve the hardness, luster and durability of the coating film. Used as varnish, paint and ink production of rosin ester raw material, and can be used as flame retardants, drying oil, aviation lubricating oil. Pentaerythritol fatty acid ester is polyvinyl chloride (PVC), plasticizer and stabilizer is also used in medicine, pesticide, lube oil manufacture. Pentaerythritol acrylic ester generated by Pentaerythritol and acrylic acid has a fast drying property, it is widely used in radiation-curing coatings and quick drying of printing ink, water soluble alkyd resin, the polymer can be used as adhesive. The C6~C10 fatty acid ester of Pentaerythritol are mainly used as advanced lubricant for steam turbine, automobile engine etc. The ester produced by this product with C10~C12 fatty acid, can be used as a plastic plasticizer, which has low volatility and high ageing resistance; Reaction with epoxy compound, and its product can be used as a surface active agent, widely used in detergent and cosmetics and perfume raw materials; This product is used as the material of explosives, medicine, pesticides, organic intermediates, etc. The above information is edited by the lookchem of Duan Yalan.

Chemical additives

Pentaerythritol can be used as a stabilizing agent, and has synergistic effect with zinc salt stabilizers, can replace allyl chloride to stabilize PVC. General dosage is half serving. But the compatibility with the resin of this product is small, easy to bloom, and soluble in water, easy sublimation, easy deposit on processing equipment and interfere with the processing in the process of sublimation.

Harmful effects and symptoms of poisoning

Pentaerythritol has low toxicity, from rat infected through the mouth to the dose of 40 g/kg body weight, no obvious toxic symptoms. The US Food and Drug Administration permits it for food packaging materials (FDA121.2566), the highest dosage is 0.4%. Someone reports and food studies showed that 85% of pentaerythritol were discharged from the urine after oral within 30 h. Generally speaking, according to the usual route of exposure even under abnormal use concentration, no significant effect to health.

Uses

Different sources of media describe the Uses of 115-77-5 differently. You can refer to the following data:
1. It is mainly used in alkyd resin production, also used for manufacturing ink, lubricants, plasticizer, surface active agent, explosives and drugs raw materials. Used as a resin and synthetic fiber antistatic agent, solvent conditioner, oil, etc. Pentaerythritol is mainly used in the coating industry, is the source of alkyd resin coating, can make the coating film hardness, gloss, with improved durability, it is used as varnish, color paint and printing ink of pine resin needed raw materials, and with smoldering sex coating, drying oil and matter could be empty lubricating oil and so on. Pentaerythritol tetranitrate is a kind of high explosives (taian); The fatty acid ester is an efficient lubricant and PVC plasticizer; The epoxide production is the raw material from the raw surface active agent, pentaerythritol easy forms authority complex with metal, also as hard water softener used in detergent formulation, in addition, it can also be used in medicine, pesticide and other production. Gas chromatographic stationary liquid [highest use temperature 150 ℃, the solvent of chloroform + butyl alcohol (1:1)], separation and analysis of low boiling point oxygen-containing compounds, amine compounds, nitrogen or oxygen heterocyclic compounds. Organic synthesis, preparation, resin synthesized polyols.
2. In the manufacture of pentaerythritol tetranitrate; alkyd resins in surface-coating compositions; pentaerythritol triacrylate and protective coatings; insecticides; pharmaceuticals
3. Pentaerythritol is a compound most commonly used in cosmetics (in its rosinate form). It is used as a skin conditioning agent (used as part of a cream base in lotions), and is also used to increase viscosity of cosmetic formulations.
4. Pentaerythritol is a versatile starting material to synthesize various dendrimers and star-shaped polymers. It is widely used in the preparation of flame-retardant epoxy resins and polymer composites. It is also used in the synthesis of the vasodilator, pentaerythritol tetranitrate (PETN).

Production method

It is produced using formaldehyde and acetaldehyde as raw materials, in the presence of alkaline condensation agent reaction. When using sodium hydroxide as condensing agent, it is called sodium method. The molar ratio of raw materials for acetaldehyde: formaldehyde: alkali is 1.5: 6: 1.1-1.3. Adding sodium hydroxide solution to 37% formaldehyde solution, join the acetaldehyde under stirring at 25-32 oC and react for 6 to 7 h. By the neutralization filter to obtain pentaerythritol. Raw material consumption quota: formaldehyde (37%) 2880 kg/t, acetaldehyde 350 kg/t. When using calcium hydroxide as a condensing agent, it is called calcium method. The molar ratio of raw materials for acetaldehyde: formaldehyde: lime is 1: 4.7: 0.7-0.8. Add the formaldehyde solution, 20% acetaldehyde solution and 25% lime milk to reaction pot, react at 60 oC, condensate until liquid color turned to blue from gray. Gradually cooled to 45 oC in the acidification of pan. Acidificate the condensed liquid with 60-70% of the sulfuric acid to the pH of 2-2.5, then use filter airland to calcium sulfate. Filtrate through ion exchange column to remove residual calcium ion, stress concentration, keep gas temperature under 70 oC, vacuum at 77.3 kPa. Began to crystallize, transfer concentrate in the crystallizer, mixing the cooling crystallization, centrifugal separation, washed with water to the pH of 3, drying by the airflow then obtain products. The consumption of Calcium method is high, and also has the problem of "three wastes". Raw material consumption quota: formaldehyde (36.5%) 4700 kg/t, acetaldehyde 550 kg/t.

Category

Flammable fluid.

Toxicity grading

Poisoning

Acute toxicity

Oral-LD50 in rats: 12600 mg/kg. Oral LD50 in mice: 4097 mg/kg.

Stimulus data

Skin-rabbit 500 mg/24 hours light; Eyes-rabbit 126 mg light.

Flammability hazard characteristics

Flammable. Combustion produces stimulation of smoke.

Storage Characteristics

Warehouse ventilation, dry at low temperature.

Extinguishing agent

Dry powder, foam, sandy soil, and water.

Occupational standards

The TLV-TWA 10 mg/cubic meter.

Chemical Properties

Pentaerythritol is a white crystalline solid. Odorless.

Definition

pentaerythritol: white crystallinecompound, C(CH2OH)4; m.p.260°C; b.p. 276°C (30 mmHg). It isused in making the explosive pentaerythritoltrinitrate and in producingresins and other organicproducts.

General Description

Odorless white solid. Sinks and mixes slowly with water.

Air & Water Reactions

Water soluble.

Reactivity Profile

Pentaerythritol is an alcohol. Pentaerythritol is incompatible with the following: Organic acids, oxidizers [Note: Explosive compound is formed when a mixture of PE & thiophosphoryl chloride is heated.] .

Health Hazard

Non-toxic; no symptoms likely

Flammability and Explosibility

Notclassified

Safety Profile

Mildly toxic by ingestion. A nuisance dust. Flammable from heat or flame or oxidizers. Wxtures with thiophosphoryl chloride react when heated to form a product that ignites and then explodes on contact with air. Used in coatings, stabdizers, explosives, P.E.T.N resins, drugs, insecticides, and lubricants When heated to decomposition it emits acrid smoke and irritating fumes

Potential Exposure

Pentaerythritol is used in coatings and stabilizers; in the formation of alkyd resins and varnishes. It is used as an intermediate in the manufacture of plasticizers, explosives (PETN),and pharmaceuticals.

Shipping

UN1987 Alcohols, n.o.s., Hazard Class: 3; Labels: 3-Flammable liquid.

Purification Methods

Reflux pentaerythritol with an equal volume of MeOH, then cool, and the precipitate is collected and dried at 90o. It can also be crystallised from dilute aqueous HCl. After sublimation under high vacuum at 200o it has m 265.5o. Its solubility in H2O is 10%. [Beilstein 18 III 2361, 1 IV 2812.]

Incompatibilities

Dust may form explosive mixture with air. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong acids, organic acids, strong bases. Aquesous solution is acidic. Explosive compound is formed when a mixture of Pentaerythritol and thiophosphoryl chloride (CAS 3892-91-0) is heated.

Check Digit Verification of cas no

The CAS Registry Mumber 115-77-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 115-77:
(5*1)+(4*1)+(3*5)+(2*7)+(1*7)=45
45 % 10 = 5
So 115-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H12O4/c6-1-5(2-7,3-8)4-9/h6-9H,1-4H2

115-77-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Pentaerythritol

1.2 Other means of identification

Product number -
Other names 1,3-Propanediol, 2,2-bis(hydroxymethyl)-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adhesives and sealant chemicals,Flame retardants,Functional fluids (closed systems),Intermediates,Lubricants and lubricant additives,Paint additives and coating additives not described by other categories
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:115-77-5 SDS

115-77-5Synthetic route

formaldehyd
50-00-0

formaldehyd

formic acid
64-18-6

formic acid

acetaldehyde
75-07-0

acetaldehyde

A

Pentaerythritol
115-77-5

Pentaerythritol

B

Dipentaerythritol
126-58-9

Dipentaerythritol

C

sodium formate
141-53-7

sodium formate

Conditions
ConditionsYield
Stage #1: formaldehyd; acetaldehyde With sodium hydroxide at 45 - 65℃; under 1500.15 Torr; for 1.38333h; Inert atmosphere;
Stage #2: formic acid pH=6; Product distribution / selectivity;
A 87.4%
B 5%
C 99.7%
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
Stage #1: formaldehyd; acetaldehyde With sodium hydroxide In water
Stage #2: With formic acid In water pH=5.7; Product distribution / selectivity;
90%
With ortho-tungstic acid; calcium hydroxide In water at 30 - 48℃; for 1.16667h; Reagent/catalyst;7.7%
With sodium hydroxide at 10℃; for 4.16667h; Product distribution; pH=12.7; different reaction times;
Formaldehyd-bis(pentaerythrityl)acetal
6228-26-8

Formaldehyd-bis(pentaerythrityl)acetal

A

5,5-bis-hydroxymethyl-[1,3]dioxane
6228-25-7

5,5-bis-hydroxymethyl-[1,3]dioxane

B

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
With hydrogenchloride at 80℃; for 2h; Title compound not separated from byproducts;A 33.8 % Chromat.
B 65%
With hydrogenchloride at 80℃; for 0.166667h; Title compound not separated from byproducts;A 9.3 % Chromat.
B 88.6 % Chromat.
With hydrogenchloride at 60℃; for 2h; Product distribution; further temperatures: 23, 40, 80 deg C; different times: 10, 20, 30, 60, 120 min;A 21.9 % Chromat.
B 76.8 % Chromat.
formaldehyd
50-00-0

formaldehyd

2-hydroxy-propionitrile
78-97-7

2-hydroxy-propionitrile

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
With sodium hydroxide; water
formaldehyd
50-00-0

formaldehyd

acetaldol
107-89-1

acetaldol

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
With lead(II) hydroxide on calcium carbonate; water
With calcium hydroxide; water
formaldehyd
50-00-0

formaldehyd

3-Hydroxypropanal
2134-29-4

3-Hydroxypropanal

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
With sodium hydroxide; water in mehreren Stufen;
pentaerythritol bisacetate
5419-74-9

pentaerythritol bisacetate

A

Pentaerythritol
115-77-5

Pentaerythritol

B

pentaerythritol triacetate
13051-30-4

pentaerythritol triacetate

C

pentaerythritol tetracetate
597-71-7

pentaerythritol tetracetate

Conditions
ConditionsYield
beim Aufbewahren;
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

A

Pentaerythritol
115-77-5

Pentaerythritol

B

Formaldehyd-bis(pentaerythrityl)acetal
6228-26-8

Formaldehyd-bis(pentaerythrityl)acetal

Conditions
ConditionsYield
With methyllithium Title compound not separated from byproducts;
With methyllithium; ethyl acetate 2) 1 h, reflux; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
als Nebenprodukt bei der Darstellung von Pentaerythrit; Isolierung aus technischen Pentaerytrit;
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

A

Pentaerythritol
115-77-5

Pentaerythritol

B

Dipentaerythritol
126-58-9

Dipentaerythritol

Conditions
ConditionsYield
With alkali Trennung ueber die Salpersaeureester;
With alkali Trennung von Pentaerythrit ueber die Salpetersaeureester;
With calcium hydroxide; water at 20℃;
formaldehyd
50-00-0

formaldehyd

acrolein
107-02-8

acrolein

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
With calcium hydroxide; water
formaldehyd
50-00-0

formaldehyd

crotonaldehyde
123-73-9

crotonaldehyde

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
With calcium hydroxide; water
formaldehyd
50-00-0

formaldehyd

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
2-(Diethylamino)ethanol In water at 100℃; for 20h; Product distribution;
2-(Diethylamino)ethanol In water at 100℃; for 20h;
With sodium hydroxide In water at 25℃; for 3h; Irradiation;
With potassium carbonate 1.) H2O, 20 deg C, 10 h, irradiation, 2.) 25 deg C, 7-14 d; Yield given. Multistep reaction;
formaldehyd
50-00-0

formaldehyd

A

formic acid
64-18-6

formic acid

B

Pentaerythritol
115-77-5

Pentaerythritol

C

ethylene glycol
107-21-1

ethylene glycol

Conditions
ConditionsYield
calcium hydroxide In water at 25℃; Irradiation;
calcium hydroxide In water at 25℃; Product distribution; Irradiation; various inorganic catalysts;
formaldehyd
50-00-0

formaldehyd

A

glycolic Acid
79-14-1

glycolic Acid

B

Pentaerythritol
115-77-5

Pentaerythritol

C

meso-erythritol
909878-64-4

meso-erythritol

D

glyceric acid
473-81-4

glyceric acid

E

ethylene glycol
107-21-1

ethylene glycol

F

glycerol
56-81-5

glycerol

Conditions
ConditionsYield
With zeolite of type X under 1 Torr; for 144h; Product distribution; Irradiation; other objects of study: dependence of product distribution on time of irradiation, thermal pretreatment of zeolite, and water content of zeolite;
Formaldehyd-bis(pentaerythrityl)acetal
6228-26-8

Formaldehyd-bis(pentaerythrityl)acetal

A

5,5-bis-hydroxymethyl-[1,3]dioxane
6228-25-7

5,5-bis-hydroxymethyl-[1,3]dioxane

B

formaldehyd
50-00-0

formaldehyd

C

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
Heating; heating more than 149 deg C;
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

A

2,2-di(hydroxymethyl)-acetic acid
68516-39-2

2,2-di(hydroxymethyl)-acetic acid

B

Pentaerythritol
115-77-5

Pentaerythritol

C

2-hydroxymethyl-1,3-propanediol
4704-94-3

2-hydroxymethyl-1,3-propanediol

D

α,α,α-tris(hydroxymethyl)acetic acid
2831-90-5

α,α,α-tris(hydroxymethyl)acetic acid

E

2-Hydroxymethyl-2-(methoxymethoxymethyl)-1,3-propandiol
68658-38-8

2-Hydroxymethyl-2-(methoxymethoxymethyl)-1,3-propandiol

F

trimethyleneglycol
504-63-2

trimethyleneglycol

Conditions
ConditionsYield
With calcium hydroxide Mechanism;
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

A

Pentaerythritol
115-77-5

Pentaerythritol

B

tri(hydroxymethyl)acetaldehyde
3818-32-4

tri(hydroxymethyl)acetaldehyde

C

Dipentaerythritol
126-58-9

Dipentaerythritol

D

tripentaerythritol
78-24-0

tripentaerythritol

E

3-(3-Hydroxy-2,2-bis-hydroxymethyl-propoxy)-2,2-bis-hydroxymethyl-propionaldehyde

3-(3-Hydroxy-2,2-bis-hydroxymethyl-propoxy)-2,2-bis-hydroxymethyl-propionaldehyde

F

3-[3-(3-Hydroxy-2,2-bis-hydroxymethyl-propoxy)-2,2-bis-hydroxymethyl-propoxy]-2,2-bis-hydroxymethyl-propionaldehyde

3-[3-(3-Hydroxy-2,2-bis-hydroxymethyl-propoxy)-2,2-bis-hydroxymethyl-propoxy]-2,2-bis-hydroxymethyl-propionaldehyde

Conditions
ConditionsYield
With sodium hydroxide at 30℃; Product distribution; Mechanism; pH=12.5; different initial acetaldehyde concentrations;
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

A

Pentaerythritol
115-77-5

Pentaerythritol

B

acetaldol
107-89-1

acetaldol

C

Dipentaerythritol
126-58-9

Dipentaerythritol

Conditions
ConditionsYield
With sodium hydroxide at 10℃; for 5h; Product distribution; Mechanism; different initial aldehyde concentrations and reaction times; effect of additional pentaerythritol;
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

A

Pentaerythritol
115-77-5

Pentaerythritol

B

3-Hydroxypropanal
2134-29-4

3-Hydroxypropanal

C

bis-(hydroxymethyl)-acetaldehyde
40364-80-5

bis-(hydroxymethyl)-acetaldehyde

Conditions
ConditionsYield
With sodium hydrogencarbonate at 30℃; for 2.5h; Product distribution;
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

A

Pentaerythritol
115-77-5

Pentaerythritol

B

Tetrapentaerythrit 2,2,6,6,10,10,14,14-Octakis(hydroxymethyl)-4,8,12-trioxapentadecan-1,15-diol
4376-78-7

Tetrapentaerythrit 2,2,6,6,10,10,14,14-Octakis(hydroxymethyl)-4,8,12-trioxapentadecan-1,15-diol

Conditions
ConditionsYield
With methyllithium Yield given. Title compound not separated from byproducts;
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

A

Pentaerythritol
115-77-5

Pentaerythritol

B

2-methyl-1.3-propanediol
2163-42-0

2-methyl-1.3-propanediol

C

2-hydroxymethyl-1,3-propanediol
4704-94-3

2-hydroxymethyl-1,3-propanediol

D

trimethyleneglycol
504-63-2

trimethyleneglycol

Conditions
ConditionsYield
With sodium hydroxide; sulfuric acid; hydrogen; 5% activated charcoal-supported ruthenium catalyst 1.) 25 deg C, 30 min, 2.) 50 psi, 25 deg C, 4 h; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
With sodium hydroxide; sulfuric acid; hydrogen; Ru-carbon 1.) 25 deg C, 30 min, 2.) 50 psi, 25 deg C 4 h; Yield given. Multistep reaction. Yields of byproduct given;
formaldehyd
50-00-0

formaldehyd

water
7732-18-5

water

acrolein
107-02-8

acrolein

Ca(OH)2

Ca(OH)2

Pentaerythritol
115-77-5

Pentaerythritol

formaldehyd
50-00-0

formaldehyd

water
7732-18-5

water

crotonaldehyde
123-73-9

crotonaldehyde

Ca(OH)2

Ca(OH)2

Pentaerythritol
115-77-5

Pentaerythritol

formaldehyd
50-00-0

formaldehyd

water
7732-18-5

water

acetaldehyde
75-07-0

acetaldehyde

lime/chalk/

lime/chalk/

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
bei monatelangem Stehen;
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

Ca(OH)2

Ca(OH)2

A

Pentaerythritol
115-77-5

Pentaerythritol

B

Dipentaerythritol
126-58-9

Dipentaerythritol

Conditions
ConditionsYield
je nach Bedingungen wechselnden Mengen;
formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

aqueous NaOH-solution

aqueous NaOH-solution

Pentaerythritol
115-77-5

Pentaerythritol

Conditions
ConditionsYield
at 0 - 40℃; Kinetics;
formaldehyd
50-00-0

formaldehyd

acrolein
107-02-8

acrolein

calcium hydroxide

calcium hydroxide

Pentaerythritol
115-77-5

Pentaerythritol

formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

lime milk

lime milk

A

Pentaerythritol
115-77-5

Pentaerythritol

B

Dipentaerythritol
126-58-9

Dipentaerythritol

methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

A

Pentaerythritol
115-77-5

Pentaerythritol

B

monomethyl ether of pentaerythritol

monomethyl ether of pentaerythritol

C

dimethyl ether of pentaerythritol

dimethyl ether of pentaerythritol

formaldehyd
50-00-0

formaldehyd

acetaldehyde
75-07-0

acetaldehyde

A

Pentaerythritol
115-77-5

Pentaerythritol

B

Formaldehyd-bis(pentaerythrityl)acetal
6228-26-8

Formaldehyd-bis(pentaerythrityl)acetal

C

Dipentaerythritol
126-58-9

Dipentaerythritol

D

various other products

various other products

Conditions
ConditionsYield
In water at 10℃; Rate constant; Mechanism; Product distribution; and equilibrium constants;
Pentaerythritol
115-77-5

Pentaerythritol

cyclohexanone
108-94-1

cyclohexanone

7,11,18,21-tetraoxa-trispiro[5.2.2.5.2.2]heneicosane
183-10-8

7,11,18,21-tetraoxa-trispiro[5.2.2.5.2.2]heneicosane

Conditions
ConditionsYield
With sulfuric acid at 80℃;100%
With pyrographite In toluene for 8h; Heating;94%
peroxodisulfate ion; zirconium(IV) oxide In toluene for 4h; Heating;94%
Pentaerythritol
115-77-5

Pentaerythritol

isobutyraldehyde
78-84-2

isobutyraldehyde

3,9-diisopropyl-2,4,8,10-tetraoxaspiro<5.5>undecane
69695-04-1

3,9-diisopropyl-2,4,8,10-tetraoxaspiro<5.5>undecane

Conditions
ConditionsYield
With sulfuric acid at 80℃;100%
With indium(III) chloride at 120℃; for 3h;89%
With hydrogenchloride
Pentaerythritol
115-77-5

Pentaerythritol

acrylonitrile
107-13-1

acrylonitrile

tetrakis-[(2-cyanoethoxy)methyl]methane
2465-91-0

tetrakis-[(2-cyanoethoxy)methyl]methane

Conditions
ConditionsYield
In diethyl ether; dichloromethane; tetramethyl ammoniumhydroxide; water100%
tetramethyl ammoniumhydroxide In water at 20℃; for 20h; Cooling with ice;100%
With sodium hydroxide Ambient temperature;99%
Pentaerythritol
115-77-5

Pentaerythritol

[2,2-bis(trifluoromethyl)-5-oxo-1,3-oxathiolan-4-yl]-acetyl chloride
170996-99-3

[2,2-bis(trifluoromethyl)-5-oxo-1,3-oxathiolan-4-yl]-acetyl chloride

Conditions
ConditionsYield
In toluene for 72h; Heating;100%
Pentaerythritol
115-77-5

Pentaerythritol

phenyl isocyanate
103-71-9

phenyl isocyanate

tetrakis[(N-phenylcarbamoyloxy)methyl]methane
125614-20-2

tetrakis[(N-phenylcarbamoyloxy)methyl]methane

Conditions
ConditionsYield
With MoCl2O2(dmf)2 In N,N-dimethyl-formamide at 60℃; for 0.333333h; Inert atmosphere;100%
Pentaerythritol
115-77-5

Pentaerythritol

di(n-butyl)tin oxide
818-08-6

di(n-butyl)tin oxide

C13H28O4Sn
111190-92-2

C13H28O4Sn

Conditions
ConditionsYield
In methanol for 4h; Reflux;100%
In methanol for 4h; Reflux;
In methanol for 4h; Reflux;
Pentaerythritol
115-77-5

Pentaerythritol

ortho-nitrofluorobenzene
1493-27-2

ortho-nitrofluorobenzene

C29H24N4O12
121564-67-8

C29H24N4O12

Conditions
ConditionsYield
With tetrabutylammomium bromide; potassium hydroxide In toluene at 70℃; for 18h;99.6%
Pentaerythritol
115-77-5

Pentaerythritol

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

pentaerythritol tetratosylate
1522-89-0

pentaerythritol tetratosylate

Conditions
ConditionsYield
With pyridine at 0 - 20℃; for 48h;99.5%
With pyridine at 0 - 20℃; for 48h;99.5%
With pyridine at 20℃; for 16h;89%
Pentaerythritol
115-77-5

Pentaerythritol

benzaldehyde
100-52-7

benzaldehyde

3,9-diphenyl-2,4,8,10-tetraoxa-spiro[5,5]undecane
2064-95-1

3,9-diphenyl-2,4,8,10-tetraoxa-spiro[5,5]undecane

Conditions
ConditionsYield
With pyrographite In benzene for 1.5h; Heating;99%
With toluene-4-sulfonic acid In benzene for 4h; Condensation; acetalization; Heating;99%
With montmorillonite K-10 In benzene for 0.6h; Heating;98%
Pentaerythritol
115-77-5

Pentaerythritol

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

3,9-di(4-methoxyphenyl)-2,4,8,10-tetraoxaspiro<5,5>undecane
1130782-84-1, 1130782-85-2

3,9-di(4-methoxyphenyl)-2,4,8,10-tetraoxaspiro<5,5>undecane

Conditions
ConditionsYield
With Sulfate; zirconium(IV) oxide In toluene for 0.8h; Heating;99%
With pyrographite In benzene for 1.8h; Heating;96%
With tetrachlorosilane In acetonitrile at 20℃;95%
Pentaerythritol
115-77-5

Pentaerythritol

acetylene
74-86-2

acetylene

tetrakis(vinyloxymethyl)methane
757-46-0

tetrakis(vinyloxymethyl)methane

Conditions
ConditionsYield
With potassium hydroxide In dimethyl sulfoxide at 120℃; for 5h;99%
(i) /BRN= 906677/, aq. KOH, (ii) /BRN= 906677/, KOEt, EtOH; Multistep reaction;
With potassium hydroxide In dimethyl sulfoxide at 100℃; under 759.8 Torr;
With potassium hydroxide In dimethyl sulfoxide
Pentaerythritol
115-77-5

Pentaerythritol

phosphonic acid diethyl ester
762-04-9

phosphonic acid diethyl ester

pentaerythritol tris(diethyl phosphate)

pentaerythritol tris(diethyl phosphate)

Conditions
ConditionsYield
With triethylamine In tetrachloromethane for 16h; Ambient temperature;99%
Pentaerythritol
115-77-5

Pentaerythritol

2-methyl-benzyl alcohol
89-95-2

2-methyl-benzyl alcohol

C19H20O6

C19H20O6

Conditions
ConditionsYield
With Sulfate; zirconium(IV) oxide In toluene for 1.5h; Heating;99%
Pentaerythritol
115-77-5

Pentaerythritol

C6H5CH2OCH2CH2CH2CB10H10CCH2CH2COOH
865835-76-3

C6H5CH2OCH2CH2CH2CB10H10CCH2CH2COOH

(C6H5CH2OCH2CH2CH2CB10H10CCH2CH2COOCH2)4C

(C6H5CH2OCH2CH2CH2CB10H10CCH2CH2COOCH2)4C

Conditions
ConditionsYield
With N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; 4-(dimethylamino)pyridinium tosylate In pyridine; dichloromethane CH2Cl2-pyridine 3:2, room temp., > 12 h; column chromy.;99%
isocyanate de chlorosulfonyle
1189-71-5

isocyanate de chlorosulfonyle

Pentaerythritol
115-77-5

Pentaerythritol

pentaerythritol tetracarbamate
24794-44-3

pentaerythritol tetracarbamate

Conditions
ConditionsYield
Stage #1: isocyanate de chlorosulfonyle; Pentaerythritol In acetonitrile at 0 - 20℃; for 1h;
Stage #2: With water In acetonitrile Cooling with ice;
99%
Stage #1: isocyanate de chlorosulfonyle; Pentaerythritol In acetonitrile at 25℃; for 2h; Cooling with ice;
Stage #2: With water In acetonitrile at 20℃; for 1h; Cooling with ice;
Pentaerythritol
115-77-5

Pentaerythritol

butanedioic acid, monoethyl ester
1070-34-4

butanedioic acid, monoethyl ester

cis-Octadecenoic acid
112-80-1

cis-Octadecenoic acid

C65H116O10

C65H116O10

Conditions
ConditionsYield
Stage #1: Pentaerythritol; cis-Octadecenoic acid In water at 130 - 135℃; Inert atmosphere;
Stage #2: butanedioic acid, monoethyl ester In water at 130 - 135℃; for 2h; Inert atmosphere;
99%
Pentaerythritol
115-77-5

Pentaerythritol

methyl hydrogen succinate
3878-55-5

methyl hydrogen succinate

cis-Octadecenoic acid
112-80-1

cis-Octadecenoic acid

C64H114O10

C64H114O10

Conditions
ConditionsYield
Stage #1: Pentaerythritol; cis-Octadecenoic acid In water at 130 - 135℃; Inert atmosphere;
Stage #2: methyl hydrogen succinate In water at 130 - 135℃; for 2h; Inert atmosphere;
99%
Pentaerythritol
115-77-5

Pentaerythritol

2-nitro-benzaldehyde
552-89-6

2-nitro-benzaldehyde

3,9-bis-(2-nitro-phenyl)-2,4,8,10-tetraoxa-spiro[5.5]undecane
102174-89-0

3,9-bis-(2-nitro-phenyl)-2,4,8,10-tetraoxa-spiro[5.5]undecane

Conditions
ConditionsYield
With copper(II) chloride dihydrate In N,N-dimethyl-formamide at 70℃; for 1.33333h;98.8%
With toluene-4-sulfonic acid In toluene at 140℃; for 3h;98.8%
With toluene-4-sulfonic acid for 0.0666667h; microwave irradiation at 600 W power;97.5%
Pentaerythritol
115-77-5

Pentaerythritol

dimethyldibromosilane
4095-10-7

dimethyldibromosilane

3,3,9,9,-tetramethyl-3,9-disila-2,4,8,10-tetraoxaspiro<5,5>undecane
14896-25-4

3,3,9,9,-tetramethyl-3,9-disila-2,4,8,10-tetraoxaspiro<5,5>undecane

Conditions
ConditionsYield
In diethylene glycol dimethyl ether at 50 - 130℃; for 6h; Solvent; Temperature;98.6%
Pentaerythritol
115-77-5

Pentaerythritol

stearic acid
57-11-4

stearic acid

pentaerythritol monostearate
78-23-9

pentaerythritol monostearate

Conditions
ConditionsYield
With zinc/copper couple at 160℃; under 600.06 Torr; for 2.33333h; Temperature; Pressure; Reagent/catalyst;98.3%
at 240℃;
With phenol at 180 - 230℃;
1-octadecanol
112-92-5

1-octadecanol

Pentaerythritol
115-77-5

Pentaerythritol

dioctadecyl pentaerythritol diphosphite
3806-34-6

dioctadecyl pentaerythritol diphosphite

Conditions
ConditionsYield
With lithium hydroxide; triethyl phosphite at 130 - 160℃; for 2h; Temperature; Reagent/catalyst; Time;98.2%
Pentaerythritol
115-77-5

Pentaerythritol

3-(n-dodecylthio)-propanoic acid,methyl ester
19759-75-2

3-(n-dodecylthio)-propanoic acid,methyl ester

pentaerythritol tetrakis(β-dodecylmercapto)propionate
29598-76-3

pentaerythritol tetrakis(β-dodecylmercapto)propionate

Conditions
ConditionsYield
With [BCl2(1-methylimidazole)][Al2Cl7] at 120℃; for 3h; Reagent/catalyst; Temperature; Large scale;98.2%
Pentaerythritol
115-77-5

Pentaerythritol

acetic anhydride
108-24-7

acetic anhydride

pentaerythritol tetracetate
597-71-7

pentaerythritol tetracetate

Conditions
ConditionsYield
With methanesulfonic acid at 25℃; for 2h; Inert atmosphere;98%
With aluminum triflate at 20℃; for 0.00833333h;95%
aluminium dodecatungsten phosphate at 20℃; for 0.583333h;94%
Pentaerythritol
115-77-5

Pentaerythritol

4-methyl-benzaldehyde
104-87-0

4-methyl-benzaldehyde

3,9-di-p-tolyl-2,4,8,10-tetraoxa-spiro[5.5]undecane
53731-74-1

3,9-di-p-tolyl-2,4,8,10-tetraoxa-spiro[5.5]undecane

Conditions
ConditionsYield
With Sulfate; zirconium(IV) oxide In toluene for 1h; Heating;98%
With pyrographite In benzene for 1.5h; Heating;97%
With tetrachlorosilane In acetonitrile at 20℃;96%
Pentaerythritol
115-77-5

Pentaerythritol

methanesulfonyl chloride
124-63-0

methanesulfonyl chloride

2,2-bis(((methylsulfonyl)oxy)methyl)propane-1,3-diyl dimethanesulfonate
7511-62-8

2,2-bis(((methylsulfonyl)oxy)methyl)propane-1,3-diyl dimethanesulfonate

Conditions
ConditionsYield
With pyridine Cooling with ice; Inert atmosphere;98%
Stage #1: Pentaerythritol With triethylamine In dichloromethane at 0℃; for 0.166667h;
Stage #2: methanesulfonyl chloride In dichloromethane at 20℃; for 12h;
87.3%
With pyridine
With pyridine Inert atmosphere; Schlenk technique;
With triethylamine In toluene at 0 - 20℃; Dean-Stark;
Pentaerythritol
115-77-5

Pentaerythritol

hexanoic acid
142-62-1

hexanoic acid

pentaerythritol tetracaproate
7445-47-8

pentaerythritol tetracaproate

Conditions
ConditionsYield
With pyridine; <(chlorosulfinyloxy)methylene>dimethylammonium chloride In dichloromethane at 20℃; for 6h;98%
With sulfuric acid; toluene-4-sulfonic acid at 105℃; for 0.15h; Neat (no solvent); Microwave irradiation;96%
at 180℃;
In toluene at 158℃; for 10h; Catalytic behavior; Reagent/catalyst; Green chemistry;98 %Spectr.
With (cetyltrimethylammonium)1/3[Cu46(C9H3O6)24(OH)12](PW12O40)3·xH2O (COK-15b) In toluene at 155℃; for 6h; Green chemistry;94 %Spectr.
trichloroethylene epoxide
16967-79-6

trichloroethylene epoxide

Pentaerythritol
115-77-5

Pentaerythritol

tetra(dichloroacetato)pentaerythritol
33216-80-7

tetra(dichloroacetato)pentaerythritol

Conditions
ConditionsYield
With magnesium sulfate for 6h; Heating;98%
Pentaerythritol
115-77-5

Pentaerythritol

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

3,9-di(m-chlorophenyl)-2,4,8,10-tetraoxaspiro[5.5]undecane
35583-09-6

3,9-di(m-chlorophenyl)-2,4,8,10-tetraoxaspiro[5.5]undecane

Conditions
ConditionsYield
peroxodisulfate ion; zirconium(IV) oxide In toluene for 0.5h; Heating;98%
silica sulfate In benzene for 0.5h; microwave irradiation;98%
With pyrographite In toluene for 0.8h; Heating;97%
Pentaerythritol
115-77-5

Pentaerythritol

2-Ethylhexanoic acid
149-57-5

2-Ethylhexanoic acid

pentaerythritol tetra(2-ethylhexanoate)
7299-99-2

pentaerythritol tetra(2-ethylhexanoate)

Conditions
ConditionsYield
With pyridine; <(chlorosulfinyloxy)methylene>dimethylammonium chloride In dichloromethane at 20℃; for 6h;98%
With sulfuric acid82%
Stage #1: Pentaerythritol; 2-Ethylhexanoic acid at 170 - 250℃; for 6h;
Stage #2: With 2-ethylhexanoic acid anhydride at 150 - 170℃; for 0.5h; Reagent/catalyst;

115-77-5Related news

Measurement and correlation for phase equilibrium of HFO1234yf with three Pentaerythritol (cas 115-77-5) esters from 293.15 K to 348.15 K08/29/2019

2,3,3,3-Tetrafluoroprop-1-ene (HFO1234yf) is recently recognized as a new generation refrigerant to replace R134a in automotive air-conditioning system and other refrigeration applications. The knowledge of phase equilibrium property for refrigerant with lubricant oil is therefore interested in ...detailed

Absorption of isobutane in three linear chained Pentaerythritol (cas 115-77-5) esters between 293.15 and 348.15 KAbsorption d'isobutane dans trois esters de pentaérythritol en chaîne linéaire entre 293,15 et 348,15 K08/28/2019

Isobutane (R600a) is widely used in small capacity refrigeration equipment, especially domestic refrigerator. Knowledge of refrigerant absorption in lubricant oil is one of the essential factors for designing refrigeration system and choosing suitable oil. In this work, the liquid mole fractions...detailed

Experimental investigation for the solubility of R1234ze(E) in Pentaerythritol (cas 115-77-5) tetrahexanoate and Pentaerythritol (cas 115-77-5) tetraoctanoate08/27/2019

The phase behavior of refrigerant with lubricant oil is an important issue for designing the refrigeration system. R1234ze(E) was proposed as a possible replacement for R134a recently. In this work, the p–T–x data of R1234ze(E) with pentaerythritol tetrahexanoate (PEC6) and pentaerythritol tet...detailed

Solubility of dimethyl ether in Pentaerythritol (cas 115-77-5) tetrabutyrate and in Pentaerythritol (cas 115-77-5) tetrapentanoate. Comparison with other Pentaerythritol (cas 115-77-5) tetraalkyl esters08/25/2019

The solubilities of dimethyl ether (DME) in pentaerythritol tetrabutyrate (PEC4) and in pentaerythritol tetrapentanoate (PEC5) between T = (283.15 and 353.15) K have been measured by isochoric saturation method. The experimental solubility data were correlated by the Peng–Robinson equation of s...detailed

Experimental thermal degradation analysis of Pentaerythritol (cas 115-77-5) with alumina nano additives for thermal energy storage application08/24/2019

The present work investigates the effect of addition of Al2O3 nanoparticles on thermal degradation kinetics of pentaerythritol (PE), a solid-solid phase change material, using a Thermogravimetry analyzer. For this TGA experiments were conducted using PE added 0.1% and 1% weight fractions of Al2O...detailed

Production of Pentaerythritol (cas 115-77-5) Monoricinoleate (PEMR) by immobilized Candida antarctica lipase B08/23/2019

In the present study, green synthesis of pentaerythritol monoricinoleate (PEMR) was carried out using Candida antarctica lipase B immobilized on hydrophobic adsorbent via interfacial activation. Various reaction parameters such as reaction time, organic solvent, molar ratio, the enzyme load, and...detailed

Energy storage performance of Pentaerythritol (cas 115-77-5) blended with indium in exhaust heat recovery application08/22/2019

This paper presents the effect of adding indium, a low melting metal on thermal energy storage performance of pentaerythritol in IC engine exhaust gas heat recovery application. Charging and discharging experiments were conducted using pentaerythritol added with 0.1, 0.5 and 1.0 wt. % of indium ...detailed

115-77-5Relevant articles and documents

SELECTIVE FORMOSE REACTION CATALYZED BY DIETHYLAMINOETHANOL

Matsumoto, Toshihiko,Komiyama, Makoto,Inoue, Shohei

, p. 839 - 842 (1980)

Selective formose reactions were achieved by diethylaminoethanol as catalyst at 100 deg C in the presence and the absence of D-fructose as co-catalyst.The reaction in the presence of the co-catalyst gave 2-hydroxymethylglycerol and other three main products in high yields, whereas in its absence pentaerythritol was the sole product.

Shigemasa et al.

, p. 222,223-225 (1977)

SELECTIVE FORMOSE REACTION INITIATED BY PHOTO- AND γ-IRRADIATION

IRIE, Setsuko

, p. 2153 - 2156 (1984)

A selective formose synthesis was achieved by photo- and γ-irradiation of formaldehyde in the presence of base.Photoirradiation of aqueous formaldehyde solution gave pentaerythritol as a single product, while γ-irradiation resulted in the formation of glycolaldehyde as the main product.These results suggest that the formose reaction under photo- and γ-irradiation is considerably different from the thermal formose reaction.

A redox-metric study of the formation of coloring substances in the synthesis of pentaerythritol

Demchenko,Belkin

, p. 1398 - 1403 (2011)

The redox potentials of the reaction mixtures in the course of pentaerythritol synthesis and of transformations of formaldehyde and glucose in a NaOH solution without catalyst and in the presence of copper prepared by reduction of CuO were measured. Pleiades Publishing, Ltd., 2011.

A new type of pH-sensitive phospholipid

Zhan, Li,Chang, Shuyuan,Liu, Ting,Yu, Shanbao,Li, Hui,Lu, Minjie,Zhu, Yong,Luo, Yu,Yu, Jiahui,Yang, Fan,Tang, Jie

supporting information, p. 4724 - 4727 (2017/11/17)

We describe the synthesis and characterization of a type of pH-sensitive pentaerythritol phospholipids, using a trialkoxybenzylidene acetal as the acid-labile moiety. This lipid was prepared by an eight-step synthesis via a latentiation strategy. Liposomes were prepared via the thin film extrusion method. The changes of liposomal sizes were measured by dynamic light scattering. Content release rates of the liposomes as a function of pH were monitored by using a calcein fluorescence dequenching assay. These results indicated that this new liposomal system was capable of releasing its contents under mildly acidic conditions. At last, in vitro cytotoxicity was assayed against three cell lines, suggesting this type of phospholipids was low toxic.

Formaldehyde fifth heavenly stem four mellow Shan Suo double-quarter of the six-ester

-

Paragraph 0127-0128, (2017/03/21)

wherein the carboxylic acids comprise C9 branched aliphatic monocarboxylic acid, and any one of carboxylic acids selected from C4 to C8 aliphatic monocarboxylic acids. The hexaester is used as one component of a refrigerant oil composition, and gives excellent characteristics, such as oxidation stability, lubricity, and low temperature properties, to a refrigerant oil composition.