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Names | |
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Preferred IUPAC name
Butane-1,2-diol | |
Other names
1,2-Dihydroxybutane
α-Butylene glycol | |
Identifiers | |
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3D model (
JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.008.663 |
EC Number |
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PubChem
CID
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RTECS number |
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UNII | |
CompTox Dashboard (
EPA)
|
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Properties [1] | |
C4H10O2 | |
Molar mass | 90.121 g/mol |
Density | 1.0023 g/cm3 (20 °C) |
Melting point | −50 °C (−58 °F; 223 K) [note 1] |
Boiling point | 195 to 196.9 °C (383.0 to 386.4 °F; 468.1 to 470.0 K) (96.5 °C at 10 mmHg) |
miscible | |
Solubility | soluble in ethanol, acetone; sparingly soluble in esters and ethers; insoluble in hydrocarbons |
Refractive index (nD)
|
1.4378 (20 °C) |
Viscosity | 7.3 mPa·s (20 °C) |
Thermochemistry | |
Std enthalpy of
formation (ΔfH⦵298) |
−532.8 kJ/mol [2] |
Std enthalpy of
combustion (ΔcH⦵298) |
−2479 kJ/mol |
Hazards [3] | |
Flash point | 90 °C (194 °F; 363 K) |
Safety data sheet (SDS) | ICSC 0395 |
Related compounds | |
Related
butanediols
|
1,3-Butanediol 1,4-Butanediol 2,3-Butanediol |
Related compounds
|
Ethylene glycol Propylene glycol 2-Hydroxybutyraldehyde 2-Hydroxybutyric acid α-Ketobutyric acid |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
1,2-Butanediol is the organic compound with the formula HOCH2(HO)CHCH2CH3. It is classified as a vic-diol ( glycol). It is chiral, although typically it is encountered as the racemic mixture. It is a colorless liquid.
This diol was first described by Charles-Adolphe Wurtz in 1859. [4]
It is produced industrially by hydration of 1,2-epoxybutane. [5] [6]
This process requires a ten- to twenty-fold excess of water to suppress the formation of polyethers. Depending on the amount of excess water, the selectivity varies from 70 to 92%. [7] Sulfuric acid or strongly acidic ion exchange resins may be used as catalysts, which allows the reaction to occur under 160 °C and at slightly above atmospheric pressure.
1,2-Butanediol is a byproduct of the production of 1,4-butanediol from butadiene. [8] It is also a byproduct of the catalytic hydrocracking of starches and sugars such as sorbitol to ethylene glycol and propylene glycol. [9]
It can also be obtained from the dihydroxylation of but-1-ene by OsO4.
It has been patented for the production of polyester resins and plasticizers. [6] [8] It is a potential feedstock for the industrial production of α-ketobutyric acid, a precursor to some amino acids. [10]
The LD50 (rats, oral) is 16g/kg. [5]
![]() | |
![]() | |
Names | |
---|---|
Preferred IUPAC name
Butane-1,2-diol | |
Other names
1,2-Dihydroxybutane
α-Butylene glycol | |
Identifiers | |
| |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.008.663 |
EC Number |
|
PubChem
CID
|
|
RTECS number |
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties [1] | |
C4H10O2 | |
Molar mass | 90.121 g/mol |
Density | 1.0023 g/cm3 (20 °C) |
Melting point | −50 °C (−58 °F; 223 K) [note 1] |
Boiling point | 195 to 196.9 °C (383.0 to 386.4 °F; 468.1 to 470.0 K) (96.5 °C at 10 mmHg) |
miscible | |
Solubility | soluble in ethanol, acetone; sparingly soluble in esters and ethers; insoluble in hydrocarbons |
Refractive index (nD)
|
1.4378 (20 °C) |
Viscosity | 7.3 mPa·s (20 °C) |
Thermochemistry | |
Std enthalpy of
formation (ΔfH⦵298) |
−532.8 kJ/mol [2] |
Std enthalpy of
combustion (ΔcH⦵298) |
−2479 kJ/mol |
Hazards [3] | |
Flash point | 90 °C (194 °F; 363 K) |
Safety data sheet (SDS) | ICSC 0395 |
Related compounds | |
Related
butanediols
|
1,3-Butanediol 1,4-Butanediol 2,3-Butanediol |
Related compounds
|
Ethylene glycol Propylene glycol 2-Hydroxybutyraldehyde 2-Hydroxybutyric acid α-Ketobutyric acid |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
1,2-Butanediol is the organic compound with the formula HOCH2(HO)CHCH2CH3. It is classified as a vic-diol ( glycol). It is chiral, although typically it is encountered as the racemic mixture. It is a colorless liquid.
This diol was first described by Charles-Adolphe Wurtz in 1859. [4]
It is produced industrially by hydration of 1,2-epoxybutane. [5] [6]
This process requires a ten- to twenty-fold excess of water to suppress the formation of polyethers. Depending on the amount of excess water, the selectivity varies from 70 to 92%. [7] Sulfuric acid or strongly acidic ion exchange resins may be used as catalysts, which allows the reaction to occur under 160 °C and at slightly above atmospheric pressure.
1,2-Butanediol is a byproduct of the production of 1,4-butanediol from butadiene. [8] It is also a byproduct of the catalytic hydrocracking of starches and sugars such as sorbitol to ethylene glycol and propylene glycol. [9]
It can also be obtained from the dihydroxylation of but-1-ene by OsO4.
It has been patented for the production of polyester resins and plasticizers. [6] [8] It is a potential feedstock for the industrial production of α-ketobutyric acid, a precursor to some amino acids. [10]
The LD50 (rats, oral) is 16g/kg. [5]