1,3-Butadiene diepoxide Chemical Properties

Melting point:

2-4 °C(lit.)

Boiling point:

56-58 °C25 mm Hg(lit.)

alpha 

0°(neat)

Density 

1.113 g/mL at 25 °C(lit.)

vapor pressure 

25 mm Hg ( 56 °C)

refractive index 

n20/D 1.434(lit.)

Flash point:

114 °F

storage temp. 

0-6°C

Specific Gravity

1.1

color 

Colorless liquid

Water Solubility 

Soluble in water (1000 g/L).

Merck 

14,3676

BRN 

79831

CAS DataBase Reference

1464-53-5(CAS DataBase Reference)

IARC

(Vol. 11, Sup 7) 1987

EPA Substance Registry System

Diepoxybutane (1464-53-5)

Safety Information

Hazard Codes 

T+

Risk Statements 

45-46-24/25-26-34-10

Safety Statements 

53-45-36/37/39-28-26

RIDADR 

UN 3384 6.1/PG 1

WGK Germany 

1

RTECS 

EJ8225000

F 

8-10-18

TSCA 

Yes

HazardClass 

6.1

PackingGroup 

II

HS Code 

29109000

Hazardous Substances Data

1464-53-5(Hazardous Substances Data)

Toxicity

LD50 orl-rat: 78 mg/kg AMIHBC 10,61,54

MSDS

• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

1,3-Butadiene diepoxide Usage And Synthesis

Description

Diepoxybutane is a flammable, colorless liquid. Molecular weight=86.09; Boiling point=57℃ at25℃; Freezing/Melting point=19℃; also reported at2-4℃; Flash point=44.8℃. Hazard Identification (basedon NFPA-704 M Rating System): Health 3, Flammability 0,Reactivity 0. Mixes with water.

Chemical Properties

clear colorless to very slightly yellow liquid

Uses

Diepoxybutane has been used as a research chemical, as a chemical intermediate, as a curing agent for polymers, as a cross-linking agent for textile fabrics, and to prevent microbial spoilage (IARC 1976, HSDB 2009). It has also been used to synthesize erythritol and pharmaceuticals (HSDB 2009). Because of its cross-linking properties, diepoxybutane is used as a test agent in the diagnosis of Fanconi anemia, which is characterized by chromosomal instability (Auerbach et al. 1989).

Uses

Curing of polymers; cross-linking of textile fibers; prevention of microbial spoilage

Uses

Butadiene diepoxide is used as a research chemical, as a chemical intermediate, as a curing agent for polymers, as a cross-linking agent for textile fabrics, and to prevent microbial spoilage. It is also been used to synthesize erythritol and pharmaceuticals.

Uses

1,3-Butadiene Diepoxide is used as a substance in the evaluation of anti-diabetic and anti-ulcer potential of selected fresh fruits samples and their GC/MS analysis. Also in the inhibitory potency of 4-carbon alkanes and alkenes towards CYD2E1 activity.

Definition

ChEBI: Diepoxybutane is an epoxide. It has a role as a mutagen.

Production Methods

Diepoxybutane is prepared by chlorination of butadiene followed by epoxidation with peracetic acid, with subsequent hydrolysis of the epoxide group and final reepoxidation with caustic.

General Description

Colorless liquid. Used in curing polymers; crosslinking textile fibers and to prevent spoilage.

Air & Water Reactions

Highly Flammable

Reactivity Profile

Epoxides, such as 1,3-BUTADIENE DIEPOXIDE, 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.

Hazard

Probable carcinogen; neoplastigen; tumorigenic; poison; mutagen.

Health Hazard

Severe skin and eye irritant. Accidental minor exposure caused swelling of the eyelids, upper respiratory tract irritation and painful eye irritation 6 hours after exposure.NOTE: The dl- and meso-forms (CAS Registry Numbers 298-18-0 and 564-00-1, respectively) as well as the L(-) form (CAS Registry Number 30031-64-2) have all been determined to be positive animal carcinogens.

Fire Hazard

When heated to decomposition 1,3-BUTADIENE DIEPOXIDE emits acrid smoke and irritating fumes.

Safety Profile

Confirmed carcinogen withexperimental tumorigenic data. Poison by ingestion,inhalation, skin contact, and intraperitoneal routes.Human mutation data reported. A severe skin and eyeirritant. When heated to decomposition it emits acridsmoke and irritat

Potential Exposure

DEB is primarily used in researchand experimental work; as a curing agent for polymers; asa crosskicking agent for textile fabrics; and in preventingmicrobial spoilage in substances. DEB is also used commercially as mixed stereoisomers and as individual isomers in the preparation of erythritol and otherpharmaceuticals.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.

Carcinogenicity

Diepoxybutane is reasonably anticipated to be a human carcinogenbased on sufficient evidence of carcinogenicity from studies in experimental animals.

storage

Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with diepoxybutane you should be trained on its proper handling andstorage. Store in tightly closed containers in a cool, wellventilated area. A regulated, marked area should be established where this chemical is handled, used, or stored incompliance with OSHA Standard 1910.1045.

Shipping

Toxic liquids, flammable, organic, n.o.s. requirea shipping label of “POISONOUS/TOXIC MATERIALS,FLAMMABLE LIQUID.” It falls in Hazard Class 6.1 andPacking Group I.

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