Bromoform Property

Melting point:

8 °C

Boiling point:

150 °C

Density 

2.89 g/mL at 25 °C(lit.)

vapor density 

8.7 (vs air)

vapor pressure 

5 mm Hg ( 20 °C)

refractive index 

n20/D 1.595(lit.)

Flash point:

148-150°C

storage temp. 

Store at +15°C to +25°C.

solubility 

water: soluble800 part(lit.)

pka

13.7(at 25℃)

form 

Liquid

color 

White to off-white

Odor

Chloroform-like odor

Water Solubility 

slightly soluble, 0.301 g/100 mL

Sensitive 

Light Sensitive

Merck 

14,1420

BRN 

1731048

Henry's Law Constant

3.36 at 20.0 °C, 7.09 at 35.0 °C, 20.5 at 50.0 °C (equilibrium static cell, Wright et al., 1992)

Exposure limits

NIOSH REL: TWA 0.5 ppm (5 mg/m³), IDLH 85e respiratory irritation (Patnaik, 1992).

Dielectric constant

4.4（20℃）

Stability:

Stability May be an explosion hazard, especially when heated. Stable, but light-sensitive. Non-flammable. Incompatible with chemically active metals, strong bases. May contain ca 1% ethanol or 1-pentene (amylene) as a stabilizer.

InChIKey

DIKBFYAXUHHXCS-UHFFFAOYSA-N

LogP

2.400

CAS DataBase Reference

75-25-2(CAS DataBase Reference)

NIST Chemistry Reference

Methane, tribromo-(75-25-2)

IARC

3 (Vol. 52, 71) 1999

EPA Substance Registry System

Tribromomethane (75-25-2)

Safety

Hazard Codes 

T,N,F

Risk Statements 

23-36/38-51/53-22-39/23/24/25-23/24/25-11

Safety Statements 

28-45-61-28A-36/37-16-7-26-63

OEB

B

OEL

TWA: 0.5 ppm (5 mg/m3) [skin]

RIDADR 

UN 2515 6.1/PG 3

WGK Germany 

3

RTECS 

PB5600000

F 

8-10

TSCA 

Yes

HS Code 

2903 39 19

HazardClass 

6.1

PackingGroup 

III

Hazardous Substances Data

75-25-2(Hazardous Substances Data)

Toxicity

LD50 s.c. in mice: 7.2 mmol/kg (Kutob, Plaa)

IDLA

850 ppm

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H226Flammable liquid and vapour

H302Harmful if swallowed

H314Causes severe skin burns and eye damage

H331Toxic if inhaled

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Bromoform Chemical Properties,Usage,Production

Description

Bromoform is a colorless (turns yellow onexposure to air) with a sweet-smelling, chloroform-likeodor. Odor threshold=0.447 ppm. Molecular weight =252.8; Specific gravity (H2O:1)=2.9; Boiling point =149.5 ℃; Freezing/Melting point=8.3 ℃ (to hexagonalcrystals); Vapor pressure=5 mmHg at 20 ℃. HazardIdentification (based on NFPA-704 M Rating System):Health 2, Flammability 0, Reactivity 0. Soluble in water;solubility=0.1% at 20 ℃.

Chemical Properties

Bromoform is a colorless to pale yellow liquid with a high refractive index, very high density, and sweetish odor is similar to that of chloroform. It is slightly soluble in water and is nonflammable. Bromoform can form in drinking water as a by-product from the reaction of chlorine with dissolved organic matter and bromide ions.

Physical properties

Clear, colorless to yellow liquid with a chloroform-like odor. Odor threshold concentration in water is 0.3 mg/kg (Verschueren, 1982).

Uses

Bromoform is a colorless to yellow liquid with a density about three times that of water. It has an odor and sweetish taste similar to chloroform and is not combustible. It has been used as a degreasing solvent, in chemical synthesis, and in fire extinguishers, and is no longer used as a sedative for children with whooping cough. Currently, bromoform is produced only in small amounts for use in laboratories and in geological and electronics testing.

Definition

ChEBI: Bromoform is a member of bromomethanes and a bromohydrocarbon.

Application

In separating mixtures of minerals. Bromoform is used as a fluid for mineral ore separation in geological tests, as a laboratory reagent, and in the electronics industry in quality assurance programs.
Bromoform was formerly used as a solvent for waxes, greases, and oils, as an ingredient in fire-resistant chemicals and in fluid gauges. It was also used in the early part of this century as a medicine to help children with whooping cough get to sleep. Currently, bromoform is only produced in small amounts for use in laboratories and in geological and electronics testing.

Preparation

Bromoform can be prepared by reacting chloroform (see IAC, 1987) with aluminium tribromide at less th an or equal to 60°C; by reacting ethanol with sodium hypobromite; or by the redistribution reaction between chloroform and ethyl bromide (Harlow & Ross, 1932; Soroos & Hinkamp, 1945; Sherman & Kavasmaneck, 1980).

General Description

Bromoform appears as a colorless liquid with a chloroform-like odor. Denser than water (density: 2.9 g / cm3 ) and slightly soluble in water. Hence sinks in water. Nonflammable. Toxic by ingestion, inhalation and skin absorption. A lachrymator. Used as a solvent and to make pharmaceuticals. Often stabilized with 1 to 3% ethanol.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

Heating Bromoform to decomposition produces highly toxic fumes of carbon oxybromide (carbonyl bromide) and hydrogen bromide [Sax, 9th ed., 1996, p. 519]. Reaction with powdered potassium or sodium hydroxide, Li or Na/K alloys, is violently exothermic [Weizmann, C. et al., J. Am Chem. Soc., 1948, 70, p. 1189]. Explosive reaction with crown ethers in the presence of potassium hydroxide [Le Goaller, R. et al., Synth. Comm., 1982, 12, p. 1163].

Hazard

A questionable carcinogen. By ingestion, inhalation, and skin absorption. Liver damage, eye and upper respiratory tract irritant.

Health Hazard

Probable routes of human exposure to bromoform are inhalation, ingestion, and dermal contact.
Harmful if inhaled, swallowed, contacts skin or eyes or is absorbed through skin. It is a lachrymator, respiratory irritant, a narcotic and an hepatotoxin. Prolonged exposure may cause dermatitis. Inhalation causes irritation of nose and throat; provokes the flow of tears and saliva and reddening of the face. Ingestion may cause dizziness, disorientation and slurred speech, unconsciousness and death.
Non-Cancer: Bromoform is a central nervous system depressant, and its vapors are highly irritating to the eyes and respiratory tract. Limited observations in humans and animal studies indicate that acute inhalation or oral exposure to high levels of bromoform may cause liver and kidney injury. Chronic effects of bromoform exposure in humans have not been studied, although animal studies indicate adverse effects on the liver, kidney, and central nervous system (U.S. EPA, 1994a).

Fire Hazard

Behavior in Fire: May decompose to produce toxic gases and vapor such as hydrogen bromide and bromine.

Safety Profile

Suspected carcinogen with experimental neoplastigenic data. A human poison by ingestion. Moderately toxic by intraperitoneal and subcutaneous routes. Human mutation data reported. A lachrymator. It can damage the liver to a serious degree and cause death. It has anesthetic properties simdar to those of chloroform, but is not sufficiently volatile for inhalation purposes and is far too toxic for human use. As a sedative and antitussive its medicinal application has resulted in numerous poisonings. Inhalation of small amounts causes irritation, provoking the flow of tears and saliva, and reddening of the face. Abuse can lead to adhction and serious consequences. Explosive reaction with crown ethers or potassium hydroxide. Violent reaction with acetone or bases. Incompatible with Li or NaK alloys. When heated to decomposition it emits hghly toxic fumes of Br-. See also BROMIDES.

Potential Exposure

Tumorigen,Drug, Mutagen; Reproductive Effector; Human Data.
Bromoform is used in pharmaceutical manufacturing; as aningredient in fire-resistant chemicals and gauge fluids; andas a solvent for waxes, greases, and oils.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.

Environmental Fate

Biological. Bromoform showed significant degradation with gradual adaptation in a staticculture flask-screening test (settled domestic wastewater inoculum) conducted at 25 °C. At concentrations of 5 and 10 mg/L, percent losses after 4 wk of incubation were 48 and 35, respectively (Tabak et al., 1981).
Surface Water. Kaczmar et al. (1984) estimated the volatilization half-life of bromoform from rivers and streams to be 65.6 d.
Chemical/Physical. The estimated hydrolysis half-life in water at 25 °C and pH 7 is 686 yr (Mabey and Mill, 1978). Products of hydrolysis include carbon monoxide and hydrobromic acid (Kollig, 1993). When an aqueous solution containing bromoform was purged with hydrogen for 24 h, only 5% of the bromoform reacted to form methane and minor traces of ethane. In the presence of colloidal platinum catalyst, the reaction proceeded at a much faster rate forming the same end products (Wang et al., 1988). In an earlier study, water containing 2,000 ng/μL of bromoform and colloidal platinum catalyst was irradiated with UV light. After 20 h, about 50% of the bromoform had reacted. A duplicate experiment was performed but the concentration of bromoform was increased to 3,000 ng/μL and 0.1 g zinc was added. After 14 h, only 0.1 ng/μL bromoform remained. Anticipated transformation products include methane and bromide ions (Wang and Tan, 1988).
At influent concentrations of 1.0, 0.1, 0.01, and 0.001 mg/L, the adsorption capacities of the GAC used were 19.6, 5.9, 1.8, and 0.52 mg/g, respectively (Dobbs and Cohen, 1980).

storage

Color Code—Green: General storage may be used.Prior to working with this chemical you should be trainedon its proper handling and storage. Bromoform must bestored to avoid contact with incompatible materials listedabove. Store in tightly closed containers in a cool well-ventilated area away from heat and light.

Shipping

Bromoform requires a label of “POISONOUS/TOXIC MATERIALS.” It falls in Hazard Class 6.1 andPacking Group III.

Purification Methods

The storage and stability of bromoform and chloroform are similar. Ethanol, added as a stabilizer, is removed by washing with H2O or with saturated CaCl2 solution, and the CHBr3, after drying with CaCl2 or K2CO3, is fractionally distilled. Prior to distillation, CHBr3 has also been washed with conc H2SO4 until the acid layer is no longer coloured, then dilute NaOH or NaHCO3, and H2O. A further purification step is fractional crystallisation by partial freezing. [Beilstein 1 IV 82.]

Toxicity evaluation

Bromoform is not found as a liquid in the environment because it is expected to volatilize from dry soil surfaces due to its vapor pressure of 5.40mmHg at 25 °C. It is also expected to volatilize from moist or wet surfaces because Henry’s law constant is 5.4×10^-4 atmm3 mol^-1. Bromoform is expected to have high mobility in soil due to its Koc value of ～120. This low Koc value implies that bromoform will have only a little tendency to adsorb to soil or sediment from water sources. Bromoform does not hydrolyze in water. Bromoform undergoes limited biodegradation under aerobic conditions but is readily biodegraded in the presence of methane-producing bacteria under anaerobic conditions. Bromoform exhibits a low bioconcentration factor of 14, and little bioconcentration in aquatic organisms is expected.

Incompatibilities

Heat causes bromoform to decomposeforming toxic and corrosive hydrogen bromide and bromine.Bromoform is a weak acid. Reacts violently with oxidants,bases in powdered form. Reacts with chemicallyactive metals (alkaline metals), powdered aluminum, potassium, sodium, zinc, and magnesium and acetone under basicconditions, causing fire and explosion hazard. Attacks someforms of plastic, rubber, and coating. Corrosive to mostmetals.