Chemistry:Dibromochloromethane
Names | |
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Preferred IUPAC name
Dibromo(chloro)methane | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Infobox references | |
|Section1=! colspan=2 style="background: #f8eaba; text-align: center;" |Identifiers
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|-
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|
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| Abbreviations | CDBM[citation needed] |-
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| 1731046 |-
| ChEMBL
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|- | ChemSpider
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|-
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- 204-704-0
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| KEGG
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|- | MeSH | chlorodibromomethane |-
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|- | RTECS number
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- PA6360000
|- | UNII
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|-
| colspan="2" |
- InChI=1S/CHBr2Cl/c2-1(3)4/h1HKey: GATVIKZLVQHOMN-UHFFFAOYSA-N
|-
| colspan="2" |
- ClC(Br)Br
|- |Section2=! colspan=2 style="background: #f8eaba; text-align: center;" |Properties
|-
|
| CHBr2Cl
|- | Molar mass
| 208.28 g·mol−1
|- | Appearance | Colorless liquid |-
| Density | 2.451 g mL−1 |- | Melting point | −22 °C (−8 °F; 251 K)
|- | Boiling point | 119 to 120 °C (246 to 248 °F; 392 to 393 K) at 99.7 kPa
|-
| log P | 2.206 |-
|
constant (kH)
| 8.6 μmol Pa−1 kg−1 |-
|
| -75.1·10−6 cm3/mol |-
|
| 1.547 |- |Section3=! colspan=2 style="background: #f8eaba; text-align: center;" |Hazards
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| GHS pictograms
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| GHS Signal word
|WARNING
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| H302 |-
| colspan=2 style="text-align:left; background-color:#f1f1f1;" | Lethal dose or concentration (LD, LC): |-
|- style="background:#f4f4f4;"
| style="padding-left:1em;" |
| 370 mg kg−1 (oral, rat)
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|- |Section4=! colspan=2 style="background: #f8eaba; text-align: center;" |Related compounds
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| 2-Chloroethanol |- }}
Dibromochloromethane is a colorless to yellow, heavy and nonflammable compound with formula CHBr2Cl.[1][2] It is a trihalomethane. The substance has a sweet odour.[3] Small quantities of dibromochloromethane are produced in ocean by algae.[citation needed]
Applications
Dibromochloromethane was formerly used as a flame retardant and as an intermediate in chemicals manufacturing. Today it is used only as a laboratory reagent. Dibromochloromethane is also a disinfection byproduct, formed by the reaction of chlorine with natural organic matter and bromide ions in the raw water supply. As a result, it is commonly found in chlorinated drinking water. Also, it is able to reduce methane production in ruminants by 79 %[4]
See also
References
- ↑ "Dibromochloromethane". sigmaaldrich.com. http://www.sigmaaldrich.com/catalog/product/aldrich/206326?lang=en®ion=RU. Retrieved 7 June 2017.
- ↑ "Public Health Statement for Bromoform and Dibromochloromethane". atsdr.cdc.gov. https://www.atsdr.cdc.gov/phs/phs.asp?id=711&tid=128. Retrieved 7 June 2017.
- ↑ "BROMOFORM AND DIBROMOCHLOROMETHANE". atsdr.cdc.gov. https://www.atsdr.cdc.gov/toxfaqs/tfacts130.pdf. Retrieved 7 June 2017.
- ↑ Identification of bioactives from the red seaweed Asparagopsis taxiformis that promote antimethanogenic activity in vitro
External links
- Dibromochlormethane in greenfacts.org glossary
- Dibromochloromethane toxicological review
- ToxFAQ for bromoform at ATSDR
Original source: https://en.wikipedia.org/wiki/Dibromochloromethane.
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