ChemicalBook >> CAS DataBase List >>Glycidol

Glycidol

CAS No.
556-52-5
Chemical Name:
Glycidol
Synonyms
Oxiranemethanol;2,3-EPOXY-1-PROPANOL;GLYCEROLGLYCIDE;2,3-Epoxypropanol;oxiranyl-methanol;GLYCEROGLYCIDE;Glycidyl alcohol;OXYRANYL METHANOL;3-HYDROXY-1,2-EPOXYPROPANE;Levodropropizine EP Impurity C
CBNumber:
CB5338946
Molecular Formula:
C3H6O2
Molecular Weight:
74.08
MDL Number:
MFCD00005147
MOL File:
556-52-5.mol
MSDS File:
SDS
Last updated:2024-04-03 17:07:09

Glycidol 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)
EWG's Food Scores 6
FDA UNII S54CF1DV9A
NIST Chemistry Reference Glycidol(556-52-5)
Proposition 65 List Glycidol
IARC 2A (Vol. 77) 2000
EPA Substance Registry System Glycidol (556-52-5)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS08
Signal word  Danger
Hazard statements  H302+H312-H315-H319-H330-H335-H341-H350-H360F
Precautionary statements  P202-P280-P301+P312-P302+P352+P312-P304+P340+P310-P305+P351+P338
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
10-21
Autoignition Temperature 780 °F
Hazard Note  Toxic
HazardClass  6.1(b)
PackingGroup  III
HS Code  29109000
Toxicity Acute oral LD50 for mice 431 mg/kg, rats 420 mg/kg (quoted, RTECS, 1985).
IDLA 150 ppm

Glycidol price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich G5809 Glycidol 96% 556-52-5 2.5kg $760 2024-03-01 Buy
Sigma-Aldrich 74595 (±)-Glycidol analytical standard 556-52-5 100mg $72.7 2024-03-01 Buy
Sigma-Aldrich G5809 Glycidol 96% 556-52-5 5g $45 2024-03-01 Buy
Sigma-Aldrich G5809 Glycidol 96% 556-52-5 100g $64.9 2024-03-01 Buy
Sigma-Aldrich Y0001048 Levodropropizine impurity C European Pharmacopoeia (EP) Reference Standard 556-52-5 y0001048 $153 2024-03-01 Buy
Product number Packaging Price Buy
G5809 2.5kg $760 Buy
74595 100mg $72.7 Buy
G5809 5g $45 Buy
G5809 100g $64.9 Buy
Y0001048 y0001048 $153 Buy

Glycidol Chemical Properties,Uses,Production

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

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

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.

Global( 289)Suppliers
Supplier Tel Email Country ProdList Advantage
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Hebei Yanxi Chemical Co., Ltd.
+8617531190177 peter@yan-xi.com China 5993 58
Hebei Guanlang Biotechnology Co,.LTD
+8619930503252 daisy@crovellbio.com China 5964 58
Hebei Saisier Technology Co., LTD
+86-18400010335 +86-13102810335 admin@hbsaisier.cn China 366 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21695 55
Shanghai Time Chemicals CO., Ltd.
+86-021-57951555 +8617317452075 jack.li@time-chemicals.com China 1807 55
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070 product@chemlin.com.cn CHINA 3012 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58

View Lastest Price from Glycidol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Glycidol pictures 2024-04-12 Glycidol
556-52-5
US $6.00 / KG 1KG More than 99% 2000KG/Month Hebei Saisier Technology Co., LTD
Glycidol pictures 2024-04-12 Glycidol
556-52-5
US $6.00 / KG 1KG More than 99% 2000KG/Month Hebei Saisier Technology Co., LTD
Glycidol pictures 2024-01-04 Glycidol
556-52-5
US $0.00 / kg 1kg 99% 1000000 Hebei Jingbo New Material Technology Co., Ltd
  • Glycidol pictures
  • Glycidol
    556-52-5
  • US $6.00 / KG
  • More than 99%
  • Hebei Saisier Technology Co., LTD
  • Glycidol pictures
  • Glycidol
    556-52-5
  • US $6.00 / KG
  • More than 99%
  • Hebei Saisier Technology Co., LTD
  • Glycidol pictures
  • Glycidol
    556-52-5
  • US $0.00 / kg
  • 99%
  • Hebei Jingbo New Material Technology Co., Ltd
(+/-)-GLYCIDOL GLYCIDOL 3-HYDROXYPROPYLENE OXIDE 2,3-EPOXYPROPAN-1-OL 2,3-EPOXYPROPANOL-1 (+/-)-OXIRANE-2-METHANOL (±)-Oxiranyl-methanol 2-hydroxymethyloxiran 2-Oxiranylmethanol (RS)-Glycidol ±-Oxiranyl-methanol 1,2-Epoxy-3-hydroxypropane 1-Hydroxy-2,3-epoxypropane 1-Propanol, 2,3-epoxy- 1-Propanol,2,3-epoxy- 2-(Hydroxymethyl)oxirane 2,3-epoxy-1-propano 2,3-Epoxyproqanol rac-(R*)-Oxirane-2-methanol rac-Oxirane-2α*-methanol Glycidol ,97% 3-Hydroxy-1,2-propenoxide lycidol Glycidol, 2,3-Epoxypropan-1-ol, 2-(Hydroxymethyl)oxirane, Epihydrin alcohol Glycidol, 96% 100ML Glycidol, 96% 500ML 3-Hydroxy-1,2-Propenoxide/Glycidol [3-(hydroxyMethyl)oxiran-2-yl](oxiran-2-yl)Methanol Glycidol 96% Glycidol, 2,3-Epoxypropan-1-ol, Epihydrin alcohol, 3-Hydroxy-1,2-propenoxide 3-Hydroxypropenoxid Allyl alcohol oxide allylalcoholoxide dl-Glycidol Epihydrin alcohol epihydrinalcohol EpiolOH Epoxypropyl alcohol epoxypropylalcohol Glyceringlycid Glycide glycidylalcohol Hydroxymethyl ethylene oxide hydroxymethylethyleneoxide Hydroxymethyloxiran Hydroxymethyloxirane Methanol, oxiranyl- Monoepoxide glycidol NCI-C55549 Oxiranemethanol,(±)- Oxiranmethanol oxiranyl-methano Oxiranylmethanol Racemicglycidol 2,3-Epoxy-1-propanol (Glycidol) 2 3-EPOXY-1-PROPANOL 97% (GC) Glycidol96% (2S)-Oxirane-2-methanol