Chemistry:Bromal
From HandWiki
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| Names | |
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| Other names
Tribromoacetaldehyde
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C2HBr3O | |
| Molar mass | 280.741 g·mol−1 |
| Appearance | Oily liquid |
| Melting point | −57.5 °C (−71.5 °F; 215.7 K) |
| Boiling point | 174 °C (345 °F; 447 K) |
| Reacts to form bromal hydrate | |
| Hazards | |
| Main hazards | Toxic |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H301, H310, H314 | |
| P260, P262, P264, P270, P280, P301+316Script error: No such module "Preview warning".Category:GHS errors, P301+330+331, P302+352, P302+361+354Script error: No such module "Preview warning".Category:GHS errors, P304+340, P305+354+338Script error: No such module "Preview warning".Category:GHS errors, P316Script error: No such module "Preview warning".Category:GHS errors, P321, P330, P361+364Script error: No such module "Preview warning".Category:GHS errors, P363, P405, P501 | |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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100 mg/kg (rat, oral)[1] 25 mg/kg (mice, oral)[1] |
| Related compounds | |
Related compounds
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Fluoral, Chloral, Iodal |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Bromal (tribromoacetaldehyde) is a brominated aldehyde. It reacts with water to form bromal hydrate.[3]
See also
References
- ↑ 1.0 1.1 "Initial Submission: Acute Toxicity Studies of Tribromoacetaldehyde with Cover Letter dated 09/21/92.". Environmental Protection Agency, Washington, DC. Office of Toxic. 1992. https://ntrl.ntis.gov/NTRL/dashboard/searchResults/titleDetail/OTS0555937.xhtml.
- ↑ "Tribromoacetaldehyde" (in en). https://pubchem.ncbi.nlm.nih.gov/compound/8256#section=Safety-and-Hazards.
- ↑ Novak, A.; Whalley, E. (January 1960). "Infrared spectra of fluoral, chloral and bromal hydrates". Spectrochimica Acta 16 (5): 521–527. doi:10.1016/0371-1951(60)80008-2. Bibcode: 1960AcSpe..16..521N.
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