Provenance

Reference data from EU CLP Annex VI and published regulations — verify against your supplier's SDS before use.

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Substance profile

1,3-Butadiene

1,3-Butadiene is a colorless gas with a mIldly aromatic odor.

CAS 106-99-0 Danger

01 · Identification

What 1,3-Butadiene is

1,3-Butadiene is a colorless gas with a mIldly aromatic odor. It boils at -4.5 °C, melts at -109 °C.

Under the GHS it carries the signal word Danger. It is classed as hazardous Air Pollutants (HAPs).

CAS number106-99-0
EC number203-450-8
Index number601-013-00-X
Chemical class Hazardous Air Pollutants (HAPs)

Other names for 1,3-Butadiene

  • buta-1,3-diene

02 · GHS classification

Hazards and label elements

Harmonised classification under CLP Annex VI. This is the legally binding classification in the EU; other jurisdictions may differ.

Signal wordDanger
Hazard statements assigned to 1,3-Butadiene
CodeHazard statement
H220 Extremely flammable gas.
H350 May cause cancer <state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard>.
H340 May cause genetic defects <state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard>.

Precautionary statements: P201, P210, P233, P280, P308, P313, P403

03 · Physical and chemical properties

1,3-Butadiene properties

Every value is shown with the conditions it was measured under and the source it came from. Where sources disagree, all values are listed rather than one being picked — the difference is usually a different form of the substance, not an error.

Property Value Conditions Source
Boiling point -4.5 °C (23.9 °F) HSDB
-4.44 °C (24 °F) NIOSH
-4.39 °C (24.1 °F) at 760 mmHg CAMEO
Melting point -108.97 °C (-164.1 °F) HSDB
-108.89 °C (-164 °F) NIOSH
Density 0.6 g/cm³ ICSC
0.621 g/cm³ at 20 °C CAMEO
0.6149 g/cm³ at 25 °C HSDB
Solubility Slightly soluble in methanol, ethanol; soluble in organic solvents such as carbon tetrachloride; alcohol dissolves about 40 vols at room temp. HSDB
Soluble in ethanol, ether, benzene; very soluble in acetone HSDB
In water, 735 mg/L at 20 °C at 20 °C HSDB
Vapor pressure 1824 mmHg NIOSH
1840 mmHg at 21.11 °C CAMEO
2052 mmHg at 25 °C HSDB
Flash point -76.11 °C (-105 °F) NIOSH
-76 °C (-104.8 °F) ICSC
Autoignition temperature 420 °C (788 °F) HSDB
414 °C (777.2 °F) ICSC
Lower explosive limit (LEL) 1.4 % by volume HSDB
2 % by volume HSDB
Upper explosive limit (UEL) 16.3 % by volume HSDB
12 % by volume HSDB
Vapor density 1.87 (air = 1) HSDB
1.9 (air = 1) ICSC
Odor threshold 4 MG/CU M HSDB
Detection: 4.50x10-1 ppm, purity not specified. HSDB
0.35 mg/cu m (odor low) 2.86 mg/cu m (odor high) HSDB
Critical temperature and pressure 161.8 °C (323.2 °F) HSDB
Corrosivity Non-corrosive HSDB

Values compiled from PubChem Laboratory Chemical Safety Summary. Temperatures converted to Fahrenheit for reference.

04 · Handling and storage

Storing and handling 1,3-Butadiene

Storage conditions

Outside or detached storage is preferred. Store in a cool, dry, well-ventilated location. Isolate from oxidizing materials.

Source: Hazardous Substances Data Bank (HSDB)

Incompatible materials

Solid butadiene at below -113 °C will absorb enough oxygen at subatmospheric pressure to explode violently when allowed to melt.

Source: Hazardous Substances Data Bank (HSDB)

Reactivity

A colorless gas, it can react with oxidizing reagents. Upon long exposure to air it forms explosive peroxides. They are sensitive to heat or shock; sudden polymerization may occur [Scott, D. A., Chem. Eng. News, 1940, 18, p.404]. Butadiene polyperoxides are insoluble in liquefied butadiene (m. p. -113 °C, b. p. -2.6 °C) and progressively separate leading to local concentration build up. Self-heating from a spontaneous decomposition will lead to explosion [Hendry, D. G. et al., Ind. Eng. Chem., 1968, 7, p. 136, 1145]. Explodes on contact with aluminum tetrahydroborate, potentially explosive reaction with chlorine dioxide (peroxide) and crotonaldehyde (above 180 °C). Reaction with sodium nitrite forms a spontaneously flammable product [Sax, 9th ed., 1996, p. 539].

Source: CAMEO Chemicals

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