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Glycidaldehyde

HCID 13002
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
765-34-4
Standard SMILES
O=CC1CO1
InChIKey
IWYRWIUNAVNFPE-UHFFFAOYSA-N
Molecular formula
C3H4O2
Average molar mass
72.06 g/mol
Monoisotopic mass
72.02112937

Overview

Glycidaldehyde can cause cancer according to an independent committee of scientific and health experts.

Names & identifiers

Preferred name
Glycidaldehyde
IUPAC
oxirane-2-carbaldehyde
English name
GLYCIDALDEHYDE
Molecular formula
C3H4O2
Molecular weight
72.06

Names & synonyms

GLYCIDALDEHYDE765-34-4OxiranecarboxaldehydeGlycidalGlycidylaldehyde2,3-EpoxypropanalEpihydrinaldehydeEpihydrine aldehydeEpoxypropanal2-Oxiranecarboxaldehyde2,3-EpoxypropionaldehydeFormyloxiran
Show more names
epihydrinealdehyde(R)-GLYCIDALDEHYDErcrawastenumberu126
Glycinaldehyde2,3-Epoxy-1-propanalOxirane-carboxaldehydePropionaldehyde, 2,3-epoxy-KYS59R58SKFORMYLOXIRANENSC-521506DTXSID9020665

Database identifiers

CAS
765-34-4
PubChem CID
13002
DTXSID
DTXSID9020665
ChEBI
CHEBI:82332
UNII
KYS59R58SK
EC Number
212-143-8
Nikkaji
J3.323E

Properties

Computed structural properties

XLogP
-0.6
Topological polar surface area
29.6 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
2
Rotatable bonds
1
Heavy atoms
5
Formal charge
0
Complexity
50.9

Experimental & physicochemical properties

Chemical Classes · 2 items

Other Classes -> Other Organic Compounds

Carcinogens

PesticidesPesticide -> EPA IRIS
Odor · 2 items

Pungent

PRONOUNCED ALDEHYDE-LIKE

Density · 2 items

SPECIFIC GRAVITY: 1.1403 @ 20 °C/4 °C

1.1403 @ 20°C

Color/FormCOLORLESS LIQUID
SolubilityMISCIBLE WITH WATER & ALL COMMON SOLVENTS; IMMISCIBLE WITH PETROLEUM ETHER.
Flash Point88 °F (OPEN CUP)
Boiling Point · 2 items

112.5 °C

112.5 °C @760 [mm Hg]

DecompositionWhen heated to decomposition it emits acrid smoke and irritating fumes.
Melting Point · 2 items

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 6 items

Danger

H350: May cause cancer [Danger Carcinogenicity]

P203, P280, P318, P405, and P501 (click each P-code to see the statement)

Danger

H225: Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501 (click each P-code to see the statement)

Hazard information

Regulatory Information · 2 items

Hazard Traits - Carcinogenicity

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

DOT LabelFlammable Liquid Poison
Fire Hazards · 2 items

Excerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:

· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.

Fire PotentialFlammable when exposed to heat, flame, or oxidizing materials.
Health Hazards · 2 items

Excerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:

· TOXIC; may be fatal if inhaled, ingested or absorbed through skin.

Hazards Summary · 2 items

A strong skin irritant; A moderate skin and respiratory tract irritant; May cause CNS stimulation followed by CNS depression after inhalation of high concentrations; [HSDB] Glycidaldehyde (UN2622) has warning of explosive polymerization; [ERG 2016]

The major hazards encountered in the use and handling of glycidaldehyde stem from its toxicologic properties and flammability. Toxic by all routes (ie, inhalation, ingestion, dermal absorption), exposure to this pungent-smelling, colorless liquid may occur from its use as a cross-linking agent for finishing of wool, for oil tanning and fat-liquoring of leather and surgical sutures, for protein insolubilization, and as a research chemical. Effects from exposure may include irritation or contact burns to the skin and eyes, and stimulatory/depressive effects on the central nervous system. Also, the International Agency for Research on Cancer (IARC) has designated glycidaldehyde as a Group 2B carcinogen, ie, "The agent is possibly carcinogenic to humans." Mechanical exhaust ventilation with a high-efficiency particulate arrestor (HEPA) or charcoal filter should be used to minimize airborne levels of this substance. In activities and situations where over-exposure may occur, wear a positive pressure self-contained breathing apparatus and chemical protective clothing which is specifically recommended by the shipper or manufacturer. If contact should occur, irrigate exposed eyes with copious amounts of tepid water for at least 15 minutes, and wash exposed skin thoroughly with soap and water. Contaminated clothing and shoes should be removed at the site. Glycidaldehyde may be ignited by heat, sparks, or flames (flash point: 88 °F, open cup). Its heavier-than-air vapor may travel to a source of ignition and flash back, or accumulate to explosive concentrations in enclosed spaces such as sewers. Also, containers of this substance may explode in the heat of a fire. For fires involving glycidaldehyde, extinguish with dry chemical, CO2, water spray, fog, or alcohol-resistant foam. Dike fire-control water, and isolate for 1/2 mile in all directions if a tank, rail car or tank truck is involved. Small spills of this substance should be taken up with sand or other noncombustible absorbent and placed into containers for later disposal. Large spills should be diked far ahead of the spill for later disposal.

Chemistry & industry

Pharmacology

Absorption, Distribution and ExcretionAbsorbed through skin.

Uses & manufacturing

Uses · 5 items

Used as a cross-linking agent for wool finishing; for the tanning and fat liquoring of leather; in surgical sutures; as a research chemical; to inactivate foot-and-mouth virus; and to make the immune serum to protect animals against that disease; [HSDB] Used to make other chemicals; [CAMEO]

Leather Tanning and Processing [Category: Industry]

As a crosslinking agent for the finishing of wool, for the tanning and fat liquoring of leather; surgical sutures.

RESEARCH CHEMICAL

MEDICATION (VET)

U.S. Production · 2 items

(1978) NOT PRODUCED COMMERCIALLY IN USA

(1982) NOT PRODUCED COMMERCIALLY IN USA

General Manufacturing InformationLiquid phase oxidation of the double bond of acrolein, eg, with hydrogen peroxide, gives either glycidaldehyde or glyceraldehyde.
Applications · 3 items

UsesGlycidaldehyde is prepared from the hydrogen peroxide epoxidation of acrolein. It is suggested as a bifunctional chemical intermediate and as a cross-linking agent for textile treatment, leather tanning, and protein insolubilization.

UsesButylene oxide is used as a cross-linkingagent in wool finishing, for tanning andfat liquoring of leather, and to insolubilizeprotein.

General DescriptionA colorless liquid. Slightly denser than water and insoluble in water. Flash point near 100°F. May irritate skin and eyes. Toxic by ingestion and inhalation. Used to make other chemicals.

Upstream & downstream products

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes

-62 °C

-62 °C

Vapor Density2.58 (AIR= 1)
Vapor Pressure45.3 [mmHg]

Physicochemical properties

Melting point
-62 °C · -62°C
Boiling point
86.43 °C · 86.43°C (rough estimate)
Density
1.417 · 1.4170
refractive index
1.602 · 1.6020 (estimate)
solubility
soluble in Chloroform, Ethyl Acetate
form
Oil
color
Cleat Colorless
Henry's Law Constant
1.9 · 1.9×101 mol/(m3Pa) at 25℃, HSDB (2015)
Exposure limits
1 ppm · No exposure limit is set. It is recommended that human exposure to glycidaldehyde in the work environment should not exceed 1 ppm (3 mg/m3 ) concentration in air.
EWG's Food Scores
2 · 2
FDA UNII
59 R58SK · KYS59R58SK
Proposition 65 List
Glycidaldehyde
IARC
2 B · 2B (Vol. 11, Sup 7, 71) 1999
EPA Substance Registry System
Glycidylaldehyde (765-34-4)
Risk Statements
11 · 11
Safety Statements
9 · 9-16-33
RIDADR
2622 · UN 2622
HazardClass
3 · 3
PackingGroup
II
Hazardous Substances Data
765 · 765-34-4(Hazardous Substances Data)
DOT ID and Guide2622 131P
Reactive GroupAldehydes
Special Reports · 2 items

Beauchamp RO et al; A Critical Review of the Literature on Acrolein Toxicity CRC Crit Rev Toxicol 14: 309-380 (1985).

Van Duuren BL; Direct-Acting Alkylating and Acylating Agents. DNA Adduct Formation, Structure-Activity, and Carcinogenesis Ann NY Acad Sc 534: 620-34 (1988).

RCRA Requirements · 1 item

U126; As stipulated in 40 CFR 261.33, when glycidaldehyde, as a commercial chemical product or manufacturing chemical intermediate or an off-specification commercial chemical product or a manufacturing chemical intermediate, becomes a waste, it must be managed according to Federal and/or State hazardous waste regulations. Also defined as a hazardous waste is any residue, contaminated soil, water, or other debris resulting from the cleanup of a spill, into water or on dry land, of this waste. Generators of small quantities of this waste may qualify for partial exclusion from hazardous waste regulations (40 CFR 261.5).

Reactivity AlertsHighly Flammable
Reactivity Profile · 1 item

GLYCIDALDEHYDE is an epoxide and an aldehyde. Aldehydes are frequently involved in self-condensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation. Epoxides are highly reactive. They polymerize in the presence of catalysts or when heated. These polymerization reactions can be violent. Compounds in this group react with acids, bases, and oxidizing and reducing agents. They react, possibly violently with water in the presence of acid and other catalysts.

Safety & protection

Fire FightingExcerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:
Accidental Release Measures · 2 items

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.

First Aid · 2 items

Excerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:

General First Aid:

Exposure Control and Personal Protection· Wear positive pressure self-contained breathing apparatus (SCBA).
Storage Conditions · 1 item

PRECAUTIONS FOR "CARCINOGENS": Storage site should be as close as practical to lab in which carcinogens are to be used, so that only small quantities required for ... expt need to be carried. Carcinogens should be kept in only one section of cupboard, an explosion-proof refrigerator or freezer (depending on chemicophysical properties ...) that bears appropriate label. An inventory ... should be kept, showing quantity of carcinogen & date it was acquired ... Facilities for dispensing ... should be contiguous to storage area. /Chemical Carcinogens/

Cleanup Methods · 1 item

PRECAUTIONS FOR "CARCINOGENS": A high-efficiency particulate arrestor (HEPA) or charcoal filters can be used to minimize amt of carcinogen in exhausted air ventilated safety cabinets, lab hoods, glove boxes or animal rooms ... Filter housing that is designed so that used filters can be transferred into plastic bag without contaminating maintenance staff is avail commercially. Filters should be placed in plastic bags immediately after removal ... The plastic bag should be sealed immediately ... The sealed bag should be labelled properly ... Waste liquids ... should be placed or collected in proper containers for disposal. The lid should be secured & the bottles properly labelled. Once filled, bottles should be placed in plastic bag, so that outer surface ... is not contaminated ... The plastic bag should also be sealed & labelled. ... Broken glassware ... should be decontaminated by solvent extraction, by chemical destruction, or in specially designed incinerators. /Chemical Carcinogens/

Nonfire Spill ResponseExcerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:
Disposal Methods · 5 items

Generators of waste (equal to or greater than 100 kg/mo) containing this contaminant, EPA hazardous waste number U126, must conform with USEPA regulations in storage, transportation, treatment and disposal of waste.

A good candidate for liquid injection incineration at a temperature range of 650 to 1,600 °C and a residence time of 0.1 to 2 seconds. A good candidate for rotary kiln incineration at a temperature range of 820 to 1,600 °C and residence times of seconds for liquids and gases, and hours for solids. A good candidate for fluidized bed incineration at a temperature range of 450 to 980 °C and residence times of seconds for liquids and gases, and longer for solids.

PRECAUTIONS FOR "CARCINOGENS": There is no universal method of disposal that has been proved satisfactory for all carcinogenic compounds & specific methods of chem destruction ... published have not been tested on all kinds of carcinogen-containing waste. ... summary of avail methods & recommendations ... /given/ must be treated as guide only. /Chemical Carcinogens/

PRECAUTIONS FOR "CARCINOGENS": ... Incineration may be only feasible method for disposal of contaminated laboratory waste from biological expt. However, not all incinerators are suitable for this purpose. The most efficient type ... is probably the gas-fired type, in which a first-stage combustion with a less than stoichiometric air:fuel ratio is followed by a second stage with excess air. Some ... are designed to accept ... aqueous & organic-solvent solutions, otherwise it is necessary ... to absorb soln onto suitable combustible material, such as sawdust. Alternatively, chem destruction may be used, esp when small quantities ... are to be destroyed in laboratory. /Chemical Carcinogens/

For more Disposal Methods (Complete) data for GLYCIDALDEHYDE (7 total), please visit the HSDB record page.

Preventive Measures · 5 items

SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.

PRECAUTIONS FOR "CARCINOGENS": Smoking, drinking, eating, storage of food or of food & beverage containers or utensils, & the application of cosmetics should be prohibited in any laboratory. All personnel should remove gloves, if worn, after completion of procedures in which carcinogens have been used. They should ... wash ... hands, preferably using dispensers of liq detergent, & rinse ... thoroughly. Consideration should be given to appropriate methods for cleaning the skin, depending on nature of the contaminant. No standard procedure can be recommended, but the use of organic solvents should be avoided. Safety pipettes should be used for all pipetting. /Chemical Carcinogens/

PRECAUTIONS FOR "CARCINOGENS": In animal laboratory, personnel should remove their outdoor clothes & wear protective suits (preferably disposable, one-piece & close-fitting at ankles & wrists), gloves, hair covering & overshoes. ... clothing should be changed daily but ... discarded immediately if obvious contamination occurs ... /also,/ workers should shower immediately. In chemical laboratory, gloves & gowns should always be worn ... however, gloves should not be assumed to provide full protection. Carefully fitted masks or respirators may be necessary when working with particulates or gases, & disposable plastic aprons might provide addnl protection. If gowns are of distinctive color, this is a reminder that they should not be worn outside of lab. /Chemical Carcinogens/

PRECAUTIONS FOR "CARCINOGENS": ... Operations connected with synth & purification ... should be carried out under well-ventilated hood. Analytical procedures ... should be carried out with care & vapors evolved during ... procedures should be removed. ... Expert advice should be obtained before existing fume cupboards are used ... & when new fume cupboards are installed. It is desirable that there be means for decreasing the rate of air extraction, so that carcinogenic powders can be handled without ... powder being blown around the hood. Glove boxes should be kept under negative air pressure. Air changes should be adequate, so that concn of vapors of volatile carcinogens will not occur. /Chemical Carcinogens/

For more Preventive Measures (Complete) data for GLYCIDALDEHYDE (10 total), please visit the HSDB record page.

Isolation and Evacuation · 2 items

Excerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:

Immediate precautionary measure

Protective Action Criteria (PAC) · 3 items

0.17 [ppm]

1.8 [ppm]

11 [ppm]

Personal Protective Equipment (PPE) · 3 items

Excerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:

Preferred respirators incl gas masks with organic vapor cannisters and high-efficiency particulate filters or supplied-air respirators. All body surfaces should be protected against contact with epoxy cmpd through the use of gloves, aprons, face shields, goggles and other protective equipment and clothing as necessary. /Epoxy cmpd/

PRECAUTIONS FOR "CARCINOGENS": ... Dispensers of liq detergent /should be available./ ... Safety pipettes should be used for all pipetting. ... In animal laboratory, personnel should ... wear protective suits (preferably disposable, one-piece & close-fitting at ankles & wrists), gloves, hair covering & overshoes. ... In chemical laboratory, gloves & gowns should always be worn ... however, gloves should not be assumed to provide full protection. Carefully fitted masks or respirators may be necessary when working with particulates or gases, & disposable plastic aprons might provide addnl protection. ... gowns ... /should be/ of distinctive color, this is a reminder that they are not to be worn outside the laboratory. /Chemical Carcinogens/

Toxicology

Target OrgansEndocrine
Environmental Fate · 3 items

TERRESTRIAL FATE: Glycidaldehyde is expected to hydrolyze rapidly in moist soil based data for a structurally similar compound, glycidol, which has a chemical hydrolysis half-life of 12 days(1). Based on a classification scheme(2), an estimated Koc value of 1(SRC), determined from a structure estimation method(3), indicates that glycidaldehyde is expected to have very high mobility in soil(SRC). Volatilization of glycidaldehyde from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 5.1X10-7 atm-cu m/mole(SRC), using a fragment constant estimation method(4). Epoxides, such as glycidaldehyde, are expected to react with organic matter in soils and sediment(SRC). The potential for volatilization of glycidaldehyde from dry soil surfaces may exist(SRC) based upon an estimated vapor pressure of 45 mm Hg(SRC), determined from a fragment constant method(5). Glycidaldehyde is expected to biodegrade rapidly based on the biodegradation of a structurally similar compound, glycidol(SRC). Ring-opening of glycidol to glycerol occurs spontaneously in aqueous solutions but is accelerated through microbial activity(1). Under aerobic and anaerobic conditions, levels of glycidol (initial concn = 100 ppm) were below the detection limit of 0.6 ppm after about 10 days in inoculated nutrient broth cultures(1).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 1(SRC), determined from a structure estimation method(2), indicates that glycidaldehyde is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 5.1X10-7 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Epoxides, such as glycidaldehyde, are expected to react with organic matter in water(SRC). According to a classification scheme(5), an estimated BCF of 3(SRC), from an estimated log Kow and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Glycidaldehyde is expected to biodegrade rapidly based on the biodegradation of a structurally similar compound, glycidol(SRC). Ring-opening of glycidol to glycerol occurs spontaneously in aqueous solutions but is accelerated through microbial activity(7). Under aerobic and anaerobic conditions, levels of glycidol (initial concn = 100 ppm) were below the detection limit of 0.6 ppm after about 10 days in inoculated nutrient broth cultures(7).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), glycidaldehyde, which has an estimated vapor pressure of 45 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere(SRC). Vapor-phase glycidaldehyde is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 22.8 hrs(SRC), calculated from its rate constant of 1.7X10-11 cu cm/molecule-sec at 25 °C(3).

Food Survey Values · 1 item

Glycidylaldehyde occurs in sunflower oil, and its concentration increases with that of peroxides during storage, causing deterioration of the flavor. To maintain high quality of the oil, peroxides should not exceed 0.25% and glycidylaldehyde not more than 0.46%(1). Glycidylaldehyde has been detected in rancid samples of commercial lard(1).

Adverse EffectsNeurotoxin - Other CNS neurotoxin
EPA IRIS Information · 3 items

Glycidaldehyde

Endocrine

4 x 10 ^-4 mg/kg-day

Medical Surveillance · 1 item

PRECAUTIONS FOR "CARCINOGENS": Whenever medical surveillance is indicated, in particular when exposure to a carcinogen has occurred, ad hoc decisions should be taken concerning ... /cytogenetic and/or other/ tests that might become useful or mandatory. /Chemical Carcinogens/

Soil Adsorption/Mobility · 1 item

Using a structure estimation method based on molecular connectivity indices(1), the Koc for glycidaldehyde can be estimated to be 1(SRC). According to a classification scheme(2), this estimated Koc value suggests that glycidaldehyde is expected to have very high mobility in soil(SRC).

Human Toxicity Excerpts · 4 items

Glycidaldehyde will produce marked skin irritation and sensitization, but effective hygiene practices should prevent exposure.

Glycidaldehyde is moderately toxic following dermal exposure, and is extremely irritating to the skin. It is a moderate eye and respiratory tract irritant. It is mutagenic in vitro in nonmammalian assays, and is a skin carcinogen in rodents.

Can cause stimulation of CNS followed by depression.

Human systemic effects by inhalation: changes in CNS electrical activity, olfactory changes, and excitement.

Artificial Pollution Sources · 1 item

Glycidaldehyde's former production and use as a crosslinking agent for the finishing of wool; and for the tanning and fat liquoring of leather and surgical sutures(1) may result in its release to the environment through various waste streams(SRC).

Environmental Biodegradation · 1 item

Glycidaldehyde is expected to biodegrade rapidly based on the biodegradation of a structurally similar compound, glycidol(SRC). Ring-opening of glycidol to glycerol occurs spontaneously in aqueous solutions but is accelerated through microbial activity(1). Under aerobic and anaerobic conditions, levels of glycidol (initial concn = 100 ppm) were below the detection limit (i.e., 0.6 ppm) after about 10 days in inoculated nutrient broth cultures(1).

Carcinogen Classification · 5 items

Glycidaldehyde

Group 2B: Possibly carcinogenic to humans

Volume 11: (1976) Cadmium, Nickel, Some Epoxides, Miscellaneous Industrial Chemicals and General Considerations on Volatile Anaesthetics

1999

1998

Environmental Bioconcentration · 1 item

An estimated BCF of 3 was calculated for glycidaldehyde(SRC), using an estimated log Kow of -0.12(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).

Regulatory information

RCRA Requirements · 1 item

U126; As stipulated in 40 CFR 261.33, when glycidaldehyde, as a commercial chemical product or manufacturing chemical intermediate or an off-specification commercial chemical product or a manufacturing chemical intermediate, becomes a waste, it must be managed according to Federal and/or State hazardous waste regulations. Also defined as a hazardous waste is any residue, contaminated soil, water, or other debris resulting from the cleanup of a spill, into water or on dry land, of this waste. Generators of small quantities of this waste may qualify for partial exclusion from hazardous waste regulations (40 CFR 261.5).

CERCLA Reportable Quantities · 1 item

Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 10 lb or 4.54 kg. The toll free number of the NRC is (800) 424-8802; In the Washington D.C. metropolitan area (202) 426-2675. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).

Safety data

ridadr
UN 2622
risk_code
11
safety_code
9-16-33
hazard_class
3
packing_group
II
Hazardous Substances Data
765-34-4(Hazardous Substances Data)

Upstream raw materials

3,4-epoxybutane-1,2-diolepoxypropionic acid3-Hydroxypropionic acidAcroleinGlycidol

Suppliers9 total

Career Henan Chemica Co+86-0371-86658258 +86-13203830695 · [email protected]
安耐吉化学&3A(安徽泽升科技有限公司)021-58432009 400-005-6266 · [email protected]
南通合润生物科技有限公司18362409333 · [email protected]
昆山中莱特贸易有限公司0512-55170668 13913095008;13770601296 · [email protected]
艾吉析科技(上海)有限公司17717235263 17717235263 · [email protected]
陕西缔都医药化工有限公司+86-29-81139210 +86-17392587031 · [email protected]
厦门盈融达化工有限公司+86-0592-6210733 · [email protected]
上海宝杨宝欣生物科技有限公司021-56698539 19921169802 · [email protected]
DAYANG CHEM (HANGZHOU) CO.,LTD+86-88938639 +86-17705817739 · [email protected]

Additional notes

DefinitionChEBI: Glycidaldehyde is an epoxide.