To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

Bromochloromethane

From Wikipedia, the free encyclopedia

Bromochloromethane
Stereo, skeletal formula of bromochloromethane with all explicit hydrogens added
Spacefill model of bromochloromethane
Names
Preferred IUPAC name
Bromo(chloro)methane
Other names
  • Bromochloromethane
  • Borothene[citation needed]
  • Chloromethyl bromide
  • Halon 1011[1]
  • Methylene bromochloride
  • Methyl chlorobromide[1]
  • Monochloromonobromomethane
  • Chlorobromomethane[1]
  • Fluorocarbon 1011[1]
Identifiers
3D model (JSmol)
3DMet
Abbreviations
1730801
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.752 Edit this at Wikidata
EC Number
  • 200-826-3
25577
KEGG
MeSH bromochloromethane
RTECS number
  • PA5250000
UNII
UN number 1887
  • InChI=1S/CH2BrCl/c2-1-3/h1H2 checkY
    Key: JPOXNPPZZKNXOV-UHFFFAOYSA-N checkY
  • ClCBr
Properties
CH2BrCl
Molar mass 129.38 g·mol−1
Appearance Colorless liquid
Odor Chloroform-like[1]
Density 1.991 g·mL−1
Melting point −88.0 °C; −126.3 °F; 185.2 K
Boiling point 68 °C; 154 °F; 341 K
16.7 g·L−1
log P 1.55
Vapor pressure 15.60 kPa (at 20.0 °C)
−86.88·10−6·cm3/mol
1.482
Hazards
GHS labelling:
GHS05: Corrosive
GHS07: Exclamation mark
Danger
H315, H318, H332, H335
P261, P280, P305+P351+P338
Flash point Non-combustible[1]
Lethal dose or concentration (LD, LC):
  • 5 g·mol−1 (oral, rat)
  • 20 g·kg−1 (dermal, rabbit)
  • 4300 mg·kg−1 (oral, mouse)[2]
3000 ppm (mouse, 7 hr)[2]
  • 28,800 ppm (rat, 15 min)
  • 29,000 ppm (rat, 15 min)
  • 27,000 ppm (mouse, 15 min)[2]
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 200 ppm (1050 mg/m3)[1]
REL (Recommended)
TWA 200 ppm (1050 mg/m3)[1]
IDLH (Immediate danger)
2000 ppm[1]
Related compounds
Related alkanes
Related compounds
2-Chloroethanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Bromochloromethane or methylene bromochloride and Halon 1011 is a mixed halomethane. It is a heavy low-viscosity liquid with refractive index 1.4808.

Halon 1011 was invented for use in fire extinguishers in Germany during the mid-1940s, in an attempt to create a less toxic, more effective alternative to carbon tetrachloride. This was a concern in aircraft and tanks as carbon tetrachloride produced highly toxic by-products when discharged onto a fire. It was slightly less toxic, and used up until the late 1960s, being officially banned by the NFPA for use in fire extinguishers in 1969, as safer and more effective agents such as halon 1211 and 1301 were developed. Due to its ozone depletion potential its production was banned from January 1, 2002, at the Eleventh Meeting of the Parties for the Montreal Protocol on Substances that Deplete the Ozone Layer.

A 1950s US CBM fire extinguisher.
Pyrene 1qt. pump-type chlorobromomethane (CB or CBM), 1960s, UK

Bromochloromethane's biodegradation is catalyzed by the hydrolase enzyme alkylhalidase:

CH2BrCl + H2O → CH2O + HBr + HCl

YouTube Encyclopedic

  • 1/5
    Views:
    226 271
    865 308
    391 406
    24 580
    313
  • Stereochemistry - R S Configuration & Fischer Projections
  • Sulfur Nitride, My Arch Nemesis - Ex&F
  • Super trick to determine R and S configuration in any optical active compound: Optical Iosmerism
  • Point Groups|Group Theory for CSIR NET|Point Group Symmetry Inorganic Chemistry
  • A Level Chemistry - 9701 Nov 18 - Paper 41 - Step-by-step tutorial - Q1

Transcription

Preparation

Bromochloromethane is prepared commercially from dichloromethane:

6 CH2Cl2 + 3 Br2 + 2 Al → 6 CH2BrCl + 2 AlCl3
CH2Cl2 + HBr → CH2BrCl + HCl

The latter route requires aluminium trichloride as a catalyst. The bromochloromethane is often used as a precursor to methylene bromide.[3]

References

  1. ^ a b c d e f g h i j NIOSH Pocket Guide to Chemical Hazards. "#0123". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ a b c "Chlorobromomethane". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  3. ^ Dagani, M. J.; Barda, H. J.; Benya, T. J.; Sanders, D. C. "Bromine Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a04_405.

External links

This page was last edited on 17 September 2023, at 22:13
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.