Bromal

Bromal
Names
	Other names Tribromoacetaldehyde
Identifiers
CAS Number	115-17-3 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL3189061;
ChemSpider	21106514;
ECHA InfoCard	100.003.698
EC Number	204-067-9;
PubChem CID	8256;
UNII	W2WDI7648E;
CompTox Dashboard (EPA)	DTXSID1021667 ;
	InChI InChI=1S/C2HBr3O/c3-2(4,5)1-6/h1H Key: YTGSYRVSBPFKMQ-UHFFFAOYSA-N;
	SMILES C(=O)C(Br)(Br)Br;
Properties
Chemical formula	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)
Solubility in water	Reacts to form bromal hydrate
Hazards
	Occupational safety and health (OHS/OSH):
Main hazards	Toxic
	GHS labelling:[1]
Pictograms
Signal word	Danger
Hazard statements	H301, H310, H314
Precautionary statements	P260, P262, P264, P270, P280, P301+P316, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P330, P361+P364, P363, P405, P501
	Lethal dose or concentration (LD, LC):
LD50 (median dose)	100 mg/kg (rat, oral)[2]; 25 mg/kg (mice, oral)[2]
Related compounds
Related compounds	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]

References

"Tribromoacetaldehyde". pubchem.ncbi.nlm.nih.gov.
"Initial Submission: Acute Toxicity Studies of Tribromoacetaldehyde with Cover Letter dated 09/21/92". Environmental Protection Agency, Washington, DC. Office of Toxic. 1992.
Novak, A.; Whalley, E. (January 1960). "Infrared spectra of fluoral, chloral and bromal hydrates". Spectrochimica Acta. 16 (5): 521–527. Bibcode:1960AcSpe..16..521N. doi:10.1016/0371-1951(60)80008-2.

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