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GLYCEROGLYCIDE

Glycidol

CAS: 556-52-5

Molecular Formula: C3H6O2

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GLYCEROGLYCIDE - Names and Identifiers

Name Glycidol
Synonyms Glycidol
GLYCIDOL
GLYCEROGLYCIDE
GLYCEROLGLYCIDE
oxiran-2-ylmethanol
2,3-EPOXY-1-PROPANOL
2,3-Epoxy-1-propanol
2,3-EPOXYPROPAN-1-OL
(2R)-oxiran-2-ylmethanol
3-HYDROXYPROPYLENE OXIDE
(2S)-oxiran-2-ylmethanol
3-Hydroxy-1,2-epoxypropane
3-HYDROXY-1,2-EPOXYPROPANE
CAS 556-52-5
EINECS 209-128-3
InChI InChI=1/C2H4O.CH4O/c1-2-3-1;1-2/h1-2H2;2H,1H3
InChIKey CTKINSOISVBQLD-UHFFFAOYSA-N

GLYCEROGLYCIDE - Physico-chemical Properties

Molecular FormulaC3H6O2
Molar Mass74.08
Density1.117 g/mL at 25 °C (lit.)
Melting Point-54 °C
Boling Point61-62 °C/15 mmHg (lit.)
Flash Point178°F
Water Solubilitysoluble
Solubility Soluble in acetone, alcohol, benzene, chloroform, and ether (Weast, 1986)
Vapor Presure0.9 mm Hg ( 25 °C)
Vapor Density2.15 (vs air)
AppearancePowder, Crystals or Chunks
ColorWhite to light yellow-beige
Exposure LimitTLV-TWA 75 mg/m3(25 ppm) (ACGIH);150 mg/m3(50 ppm) (OSHA); IDLH500 ppm (NIOSH).
Merck13,4503
BRN383562
pKa14.62±0.10(Predicted)
Storage Condition-20°C
StabilityStability Stable, but may explode on contact with strong acids, strong bases, heavy metals, heavy metal salts. May decompose on exposure to water or moist air.
Refractive Indexn20/D 1.433(lit.)
Physical and Chemical PropertiesColorless and nearly odorless liquid.
UseIt is used as a stabilizer for natural oil and vinyl polymer, demulsifier, dyeing layering agent, for surface coating, chemical synthesis, bactericide, etc

GLYCEROGLYCIDE - Risk and Safety

Hazard SymbolsT - Toxic
Toxic
Risk CodesR45 - May cause cancer
R60 - May impair fertility
R21/22 - Harmful in contact with skin and if swallowed.
R23 - Toxic by inhalation
R36/37/38 - Irritating to eyes, respiratory system and skin.
R68 - Possible risk of irreversible effects
Safety DescriptionS53 - Avoid exposure - obtain special instructions before use.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S36/37 - Wear suitable protective clothing and gloves.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
UN IDsUN 2810 6.1/PG 3
WGK Germany3
RTECSUB4375000
FLUKA BRAND F CODES10-21
HS Code29109000
Hazard NoteToxic
Hazard Class6.1(b)
Packing GroupIII
ToxicityAcute oral LD50 for mice 431 mg/kg, rats 420 mg/kg (quoted, RTECS, 1985).

GLYCEROGLYCIDE - Nature

Open Data Verified Data

A colorless and nearly odorless liquid. Boiling point 16 2~163 degrees C (decomposition). Melting Point -53 °c. Flash point 71.5 °c. Ignition point: 415 ℃. The relative density was 1. 115. Refractive index (nDo) 4311. Viscosity (20 °c) 4.OOrnPa.s. Surface tension 45.3mN/m (22 °c). Water, low carbon alcohol, ether, benzene, toluene, chloroform and other miscible, partially soluble in xylene, tetrachloroethylene, 1,1,1 trichloroethane, almost insoluble in aliphatic and cycloaliphatic hydrocarbons.

Last Update:2024-01-02 23:10:35

GLYCEROGLYCIDE - Preparation Method

Open Data Verified Data
  1. glycerol chlorohydrin method this method was the main synthesis method of glycidol before the 50s of the 20th century.
  2. allyl alcohol method allyl alcohol and hydrogen peroxide in the catalyst (such as NaHW04) in aqueous solution reaction (temperature 40~45 ℃,pH 4~5), the by-produced acrolein and unreacted allyl alcohol were separated, and then the glycidol was obtained by vacuum distillation.
Last Update:2022-01-01 10:15:29

GLYCEROGLYCIDE - Use

Open Data Verified Data

It is mainly used as epoxy resin diluent, plastic and fiber modifier, halogenated hydrocarbon stabilizer, food preservation agent, bactericide, refrigeration system desiccant and aromatic extractant. Glycidol derivatives are resins, plastics, pharmaceuticals, pesticides and additives and other industrial raw materials.

Last Update:2022-01-01 10:15:30

GLYCEROGLYCIDE - Safety

Open Data Verified Data
  • can be inhaled through the skin of the human body. Contact with it can cause skin, eyes, respiratory tract, gastrointestinal mucosa corrosion. Long-term contact will cause skin necrosis and serious harm to the cornea. Safety glasses, protective gloves and related protective equipment must be worn when handling and handling glycidol.
  • the storage container must be clean to prevent rearrangement and polymerization. In order to prevent the occurrence of the polymerization reaction, it is often stored in an inert solvent such as benzene, toluene, ketone, Ester, ether, secondary alcohol or tertiary alcohol.
Last Update:2022-01-01 10:15:30

GLYCEROGLYCIDE - Reference Information

LogP-0.95 at 25℃
NIST chemical information Information provided by: webbook.nist.gov (external link)
(IARC) carcinogen classification 2A (Vol. 77) 2000
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
packaging and storage storage containers for glycidyl must be cleaned to prevent rearrangement and polymerization. In order to prevent polymerization, it is often stored in inert solvents, such as benzene, toluene, ketones, and ethers.
introduction
epoxy propanol is also called glycidyl, which is used as a stabilizer for natural oil and vinyl polymer, demulsifier and dyeing layering agent, and is used for surface coating, chemical synthesis, fungicide, etc. Part of the oil is hydrolyzed in the human gastrointestinal tract after high-temperature refining, and eventually epoxy propanol is formed.
use mainly used as epoxy resin diluent, plastic and fiber modifier, halogenated hydrocarbon stabilizer, food preservation agent, fungicide, refrigeration system desiccant and aromatic hydrocarbon extractant, etc. Derivatives of glycidyl are raw materials for resins, plastics, medicines, pesticides and additives.
An important fine chemical raw material, used as a stabilizer for natural oil and vinyl polymers, demulsifiers, dyeing layering agents, and also used to synthesize glycerol, glycidyl ether (amine, etc.) intermediates. Can be used for surface coatings, chemical synthesis, medicine, pharmaceutical chemicals, fungicides and solid fuel gels.
Production method 1. The glycerol chloride method is obtained by reacting chloropropanediol in the presence of alkali. The reaction is carried out at about 0 ℃, and the reaction products are separated from the salts and refined by distillation under reduced pressure to obtain pure glycidyl. 2. Glycidyl can be obtained by epoxidation of allyl alcohol with hydrogen peroxide or peracetic acid by alcohol propylene method. When peracetic acid is used as a cyclic oxidant, the reaction speed is faster, and the glycidyl in the product is very easy to react with acetic acid to form glycidyl acetate, which makes distillation and separation difficult, and the mixture of glycidyl and acetic acid can occur at room temperature Strong exothermic reaction causes explosion, so this method is very difficult to apply in industry. When hydrogen peroxide is used as cyclic oxidant, hexavalent tungstic acid is used as catalyst, the reaction temperature is 40-45 ℃, the molar ratio of raw materials is water: allyl alcohol: hydrogen peroxide = 33.5:1.5:1.0, the amount of catalyst is 1.5-2.0g/mol hydrogen peroxide, the pH value of the reaction mixture is 4-5, and the reaction residence time is 2.5-3h.
category toxic substances
toxicity classification highly toxic
acute toxicity oral-rat LD50: 420 mg/kg; Oral-mouse LD50: 431 mg/kg
stimulation data skin-rabbit 100 mg/24 hours moderate; Eye-rabbit 2 mg/24 hours severe
explosive hazard characteristics high temperature mixed with air can explode
flammability hazard characteristics combustible, spicy and irritating smoke from the fire site
storage and transportation characteristics warehouse is low temperature, ventilated and dry; Fire prevention; Store separately from oxidant and food raw materials
fire extinguishing agent water, carbon dioxide, dry powder
occupational standard TWA 75 mg/m3; STEL 113 mg/m3
auto-ignition temperature 780 °F
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
immediate life-threatening and health concentration 150 ppm
Last Update:2024-04-09 21:11:58
GLYCEROGLYCIDE
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View History
GLYCEROGLYCIDE
1-二苯甲基-2-吖啶甲醇
氯化甲氧基甲基三苯基磷盐
盐酸氯丙咪嗪
1260169-39-8
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