Glycidol Chemical Properties

Melting point:

-54 °C

Boiling point:

61-62 °C/15 mmHg (lit.)

Density 

1.117 g/mL at 25 °C (lit.)

vapor density 

2.15 (vs air)

vapor pressure 

0.9 mm Hg ( 25 °C)

refractive index 

n20/D 1.433(lit.)

Flash point:

178 °F

storage temp. 

-20°C

solubility 

Soluble in acetone, alcohol, benzene, chloroform, and ether (Weast, 1986)

pka

14.62±0.10(Predicted)

form 

Powder, Crystals or Chunks

color 

White to light yellow-beige

Water Solubility 

soluble

Merck 

13,4503

BRN 

383562

Exposure limits

TLV-TWA 75 mg/m³ (25 ppm) (ACGIH); 150 mg/m³ (50 ppm) (OSHA); IDLH 500 ppm (NIOSH).

Stability:

Stability 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.

InChIKey

CTKINSOISVBQLD-UHFFFAOYSA-N

LogP

-0.95 at 25℃

CAS DataBase Reference

556-52-5(CAS DataBase Reference)

NIST Chemistry Reference

Glycidol(556-52-5)

IARC

2A (Vol. 77) 2000

EPA Substance Registry System

Glycidol (556-52-5)

Safety Information

Hazard Codes 

T

Risk Statements 

45-60-21/22-23-36/37/38-68

Safety Statements 

53-45-36/37-26

RIDADR 

UN 2810 6.1/PG 3

WGK Germany 

3

RTECS 

UB4375000

F 

10-21

Autoignition Temperature

780 °F

Hazard Note 

Toxic

HazardClass 

6.1(b)

PackingGroup 

III

HS Code 

29109000

Hazardous Substances Data

556-52-5(Hazardous Substances Data)

Toxicity

Acute oral LD50 for mice 431 mg/kg, rats 420 mg/kg (quoted, RTECS, 1985).

IDLA

150 ppm

MSDS

• Language:English Provider:ACROS
• Language:English Provider:SigmaAldrich

Glycidol Usage And Synthesis

Description

Glycidol is a chiral molecule with epoxide and primary alcohol functional groups. It is racemic mixture and exists in the dextrorotatory and the levorotatory enantiomeric forms. Several synthetic methods are available for preparation of glycidol. However, it is commercially prepared from the epoxidation of allyl alcohol with hydrogen peroxide and a catalyst (tungsten or vanadium), or from the reaction of epichlorohydrin with caustic. Glycidol has been used in the industrial synthesis of pharmaceutical products since the 1970s. However, its use for research purposes has been reported since 1956. Available information indicates that glycidol is manufactured by several companies in Japan, Germany, and the United States.

Chemical Properties

colourless liquid

Chemical Properties

Glycidol is a colorless liquid.

Uses

Glycidol is used as a stabilizer for natural oilsand vinyl polymers, as a demulsifier, and asa leveling agent for dyes.

Uses

Stabilizer in manufacturing of vinyl polymers; intermediate in synthesis of glycerol, glycidyl ethers, and amines; additive for oil and synthetic hydraulic fluids; epoxy resin diluent.

Uses

Glycidol is a Stabilizer in the manufacture of vinyl polymers; chemical intermediate in preparation of glycerol, glycidyl ethers, esters, and amines; in pharmaceuticals; in sanitary chemicals.

Definition

an epoxide

General Description

Odorless clear colorless liquid.

Air & Water Reactions

Sensitive to moisture.

Reactivity Profile

Glycidol is sensitive to moisture. Glycidol is also sensitive to light. Glycidol may polymerize if heated above room temperature. Glycidol may darken on storage. Stability studies of Glycidol stored for two week protected from light indicated definite decomposition at 140° F, and strongly indicated instability at 77° F. A solution of Glycidol in water was found to be unstable when stored at room temperature, even after one day in the dark. Glycidol is incompatible with strong oxidizers. Glycidol will undergo explosive decomposition in the presence of strong acids or bases, salts (such as aluminum chloride, iron(III)chloride or tin(IV) chloride) or metals (such as copper and zinc). Glycidol is also incompatible with nitrates. Glycidol will attack some forms of plastics, rubber and coatings.

Hazard

Toxic material. Probable carcinogen.

Health Hazard

Glycidol is an eye, lung, and skin irri-tant. The pure compound caused severebut reversible corneal injury in rabbit eyes(ACGIH 1986). Exposure to its vapor causedirritation of lung in mice, resulting in pneu-monitis. There is no evidence of any cumula-tive toxicity. From the limited toxicity data,it appears that the health hazard to humansfrom its exposure is, primarily, respiratoryirritation, stimulation of the central nervoussystem, and depression.
Glycidol is mutagenic, testing positive inthe histidine reversion–Ames test. There isno report of its carcinogenic action. Oraland intraperitoneal administration of gly-cidol in rats showed harmful effects onfertility.

Fire Hazard

Glycidol is combustible.

Flammability and Explosibility

Non flammable

Safety Profile

Confirmed carcinogen with carcinogenic data reported. Poison by intraperitoneal route. Moderately toxic by ingestion, inhalation, and sh contact. Experimental teratogenic and reproductive effects. A skin irritant. Human mutation data reported. Animal experiments suggest somewhat lower toxicity than for related epoxy compounds. Readdy absorbed through the skin. Causes nervous excitation followed by depression. Explodes when heated or in the presence of strong acids,bases, metals (e.g., copper, zinc), and metal salts (e.g., aluminum chloride, iron(II1) chloride, tin(Iy chloride). When heated to decomposition it emits acrid smoke and fumes. See also DIGLYCIDYL ETHER.

Potential Exposure

Glycidol is used as an intermediate in the synthesis of glycerol, glycidyl ethers, esters, and amines.

Carcinogenicity

Glycidol is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.

Environmental Fate

Chemical/Physical. May hydrolyze in water forming glycerin (Lyman et al., 1982).

Shipping

UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Purification Methods

[S(-)-isomer, § also available on polymer support, has b 49-50o/7mm, 66-67o/19mm, [ ] D -1 5o(neat)], [R(+)-isomer has b 56 -5 6 . 5o/11mm, d 4 1.117, n D 1.429, [ ] D +15o (neat)]. Purify glycidol by fractional distillation.

Toxicity evaluation

Glycidol is a small molecule possessing a chemically reactive epoxide group. Therefore, it acts as a direct alkylating agent. Nucleophilic bioactive compounds such as glutathione react readily with glycidol. Glycidol decreases glutathione content in rat liver by direct binding to the glutathione. In vitro experiments revealed that glycidol reacts with purified DNA to form the DNA adducts. This is likely to be responsible for the genotoxic activity of the compound without a requirement for metabolic activation.

Incompatibilities

May form explosive mixture with air. Violent reaction with strong oxidizers, nitrates. Decomposes on contact (especially in the presence of heat) with strong acids, strong bases, water, metal salts, e.g., alu minum chloride, ferric chloride, and tin chloride), or metals (copper and zinc), causing fire and explosion hazard. Contact with barium, lithium, sodium, magnesium, and tita nium may cause polymerization. Attacks some plastics, rubber, and coatings.

Waste Disposal

Concentrated waste contain ing no peroxides: discharge liquid at a controlled rate near a pilot flame. Concentrated waste containing peroxides: perforation of a container of the waste from a safe distance followed by open burning.

Glycidol(556-52-5)Related Product Information

• Allyl glycidyl ether
• Propylene oxide
• Phenolic epoxy resin
• 1-Propanol
• Isopropyl alcohol
• GLYCIDAMIDE
• Epichlorohydrin
• ETHYLENE OXIDE
• CHLOROPHOSPHONAZO III
• Titanium tetraisopropanolate
• Titanium ethoxide
• TETRAETHYL METHYLENEDIPHOSPHONATE
• Tetrabutylammonium Difluorotriphenylsilicate
• Glycidyl acrylate
• Glycidic acid methyl ester
• Glycidol methacrylate
• 1,3-Butadiene diepoxide
• Glycidol phenyl ether