5-Bromovanillin structure 
             | 
        Common Name | 5-Bromovanillin | ||
|---|---|---|---|---|
| CAS Number | 2973-76-4 | Molecular Weight | 231.043 | |
| Density | 1.7±0.1 g/cm3 | Boiling Point | 289.5±35.0 °C at 760 mmHg | |
| Molecular Formula | C8H7BrO3 | Melting Point | 164-166 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 128.9±25.9 °C | |
| Symbol | 
             
            
            GHS07  | 
        Signal Word | Warning | |
| Name | 5-Bromovanillin | 
|---|---|
| Synonym | More Synonyms | 
| Density | 1.7±0.1 g/cm3 | 
|---|---|
| Boiling Point | 289.5±35.0 °C at 760 mmHg | 
| Melting Point | 164-166 °C(lit.) | 
| Molecular Formula | C8H7BrO3 | 
| Molecular Weight | 231.043 | 
| Flash Point | 128.9±25.9 °C | 
| Exact Mass | 229.957855 | 
| PSA | 46.53000 | 
| LogP | 2.40 | 
| Vapour Pressure | 0.0±0.6 mmHg at 25°C | 
| Index of Refraction | 1.623 | 
| Symbol | 
                                    
                                     
                                    
                                    GHS07  | 
                            
|---|---|
| Signal Word | Warning | 
| Hazard Statements | H315-H319-H335 | 
| Precautionary Statements | P261-P305 + P351 + P338 | 
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves | 
| Hazard Codes | Xi:Irritant; | 
| Risk Phrases | R36/37/38 | 
| Safety Phrases | S26-S37/39-S36/37/39-S22-S24/25-S20/21 | 
| RIDADR | NONH for all modes of transport | 
| WGK Germany | 3 | 
| HS Code | 2913000090 | 
| Precursor 9 | |
|---|---|
| DownStream 10 | |
| HS Code | 2913000090 | 
|---|---|
| Summary | HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0% | 
| 
                                    
                                    Dechlorination of chlorocatechols by stable enrichment cultures of anaerobic bacteria.
                                    
                                    
                                     Appl. Environ. Microbiol. 57(1) , 77-84, (1991) Metabolically stable anaerobic cultures obtained by enrichment with 5-bromovanillin, 5-chlorovanillin, catechin, and phloroglucinol were used to study dechlorination of chlorocatechols. A high degree ...  | 
                                |
| 
                                    
                                    Enzymatic release of halogens or methanol from some substituted protocatechuic acids.
                                    
                                    
                                     J. Bacteriol. 162(2) , 693-7, (1985) Four strains of gram-negative bacteria capable of growing at the expense of 5-chlorovanillate were isolated from soil, and the metabolism of one strain was studied in particular detail. In the presenc...  | 
                                |
| 
                                    
                                    Hydroxylation reaction catalyzed by the Burkholderia cepacia AC1100 bacterial strain. Involvement of the chlorophenol-4-monooxygenase.
                                    
                                    
                                     Eur. J. Biochem. 261(2) , 533-9, (1999) The Burkholderia cepacia AC1100 strain, known to degrade the herbicide, 2,4,5-Trichlorophenoxyacetic acid (2,4,5-T), is able to metabolize 4-hydroxyarylaldehyde, not only into the corresponding acid, ...  | 
                                
| 5-Bromo-4-Hydroxy-3-Methoxybenzaldehyde | 
| 3-methoxy-4-hydroxy-5-bromo-benzaldehyde | 
| EINECS 221-016-6 | 
| 3-Bromo-4-hydroxy-5-methoxybenzaldehyde | 
| 3-bromo4-hydroxy-5-methoxy-benzaldehyde | 
| 5-Bromovanillin | 
| 5-bromovanilin | 
| VHR DQ CE EO1 | 
| 3-BROMO-4-HYDROXY-5-METHOXY-BENZALDEHYDE | 
| 4-Hydroxy-3-methoxy bromobenzaldehyde | 
| Benzaldehyde, 3-bromo-4-hydroxy-5-methoxy- | 
| Bromovanillin | 
| Vanillin, 5-bromo- | 
| MFCD00006940 |