1,2-butanediol structure 
             | 
        Common Name | 1,2-butanediol | ||
|---|---|---|---|---|
| CAS Number | 584-03-2 | Molecular Weight | 90.121 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 190.3±8.0 °C at 760 mmHg | |
| Molecular Formula | C4H10O2 | Melting Point | -50 °C | |
| MSDS | Chinese USA | Flash Point | 93.3±0.0 °C | |
| Name | butane-1,2-diol | 
|---|---|
| Synonym | More Synonyms | 
| Density | 1.0±0.1 g/cm3 | 
|---|---|
| Boiling Point | 190.3±8.0 °C at 760 mmHg | 
| Melting Point | -50 °C | 
| Molecular Formula | C4H10O2 | 
| Molecular Weight | 90.121 | 
| Flash Point | 93.3±0.0 °C | 
| Exact Mass | 90.068077 | 
| PSA | 40.46000 | 
| LogP | -0.81 | 
| Vapour Pressure | 0.1±0.8 mmHg at 25°C | 
| Index of Refraction | 1.438 | 
                                    CHEMICAL IDENTIFICATION
 
 
 
 
 
 
 
 
 HEALTH HAZARD DATAACUTE TOXICITY DATA
 
 
 
 
 
 
 
 
 
 
 
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| Precursor 10 | |
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| DownStream 10 | |
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                                    Analysis of eight glycols in serum using LC-ESI-MS-MS.
                                    
                                    
                                     J. Anal. Toxicol. 38(9) , 676-80, (2014) A liquid chromatography coupled with electrospray tandem mass spectrometry method was developed for the analysis of ethylene glycol, diethylene glycol, triethylene glycol, 1,4-butanediol, 1,2-butanedi...  | 
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                                    Efficient conversion of 1,2-butanediol to (R)-2-hydroxybutyric acid using whole cells of Gluconobacter oxydans.
                                    
                                    
                                     Bioresour. Technol. 115 , 75-8, (2012) (R)-2-Hydroxybutyric acid ((R)-2-HBA) is an important building block for azinothricin family of antitumour antibiotics and biodegradable poly(2-hydroxybutyric acid). However, optically active (R)-2-HB...  | 
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                                    Simultaneous extraction of flavonoids from Chamaecyparis obtusa using deep eutectic solvents as additives of conventional extractions solvents.
                                    
                                    
                                     J. Chromatogr. Sci. 53 , 836-40, (2015) Three flavones (quercetin, myricetin and amentoflavone) were extracted from Chamaecyparis obtusa leaves using deep eutectic solvents (DESs) as additives to conventional extractions solvents. Sixteen D...  | 
                                
| 1,2-Dihydroxybutane | 
| EINECS 209-527-2 | 
| Butanediol, 1,2- | 
| 1,2-(Dihydroxy)butane | 
| MFCD00004570 | 
| ±-1,2-Butanediol | 
| 1,2-butanediol | 
| 1,2-butylene glycol | 
| 1,2-Butanediol, (±)- | 
| butane-1,2-diol | 
| methylpropyldiol | 
| UNII:RUN0H01QEU |