ChemicalBook >> CAS DataBase List >>1,2-Dibromo-3-chloropropane

1,2-Dibromo-3-chloropropane

CAS No.
96-12-8
Chemical Name:
1,2-Dibromo-3-chloropropane
Synonyms
DBCP;bbcp;bbc12;sd1897;NEMAFU;BBC 12;os1897;DBCP(R);Fumagon;Nemagon
CBNumber:
CB1728552
Molecular Formula:
C3H5Br2Cl
Molecular Weight:
236.33
MDL Number:
MFCD00039365
MOL File:
96-12-8.mol
MSDS File:
SDS
Last updated:2024-03-14 15:18:25

1,2-Dibromo-3-chloropropane Properties

Melting point 6°C
Boiling point 195°C
Density 2.05
vapor pressure 0.8 at 21 °C (quoted, Verschueren, 1983)
refractive index n/D 1.5542
Flash point 77 °C
storage temp. Refrigerator
solubility Miscible with oils, dichloropropane, and isopropanol (Windholz et al., 1983)
form Dense Liquid
color Colorless to Light yellow
Water Solubility 0.123 g/100 mL
Merck 14,3020
BRN 1732077
Henry's Law Constant 2.49 x 10-4 atm?m3/mol at 20 °C (approximate - calculated from water solubility and vapor pressure)
Exposure limits OSHA PEL: TWA 1 ppb.
Stability Stable. Flammable. Incompatible with strong oxidizing agents, chemically active metals and their alloys. May attack some rubber-based materials.
EPA Primary Drinking Water Standard MCL:0.0002,MCLG:zero
FDA 21 CFR 165.116
CAS DataBase Reference 96-12-8(CAS DataBase Reference)
EWG's Food Scores 10
FDA UNII 96K0FD4803
Proposition 65 List 1,2-Dibromo-3-chloropropane (DBCP)
IARC 2B (Vol. 20, Sup 7, 71) 1999
NIST Chemistry Reference Propane, 1,2-dibromo-3-chloro-(96-12-8)
EPA Substance Registry System 1,2-Dibromo-3-chloropropane (96-12-8)
Pesticides Freedom of Information Act (FOIA) DBCP

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS08
Signal word  Danger
Hazard statements  H301-H340-H350-H360-H373-H412
Precautionary statements  P202-P260-P264-P270-P273-P301+P310
Hazard Codes  T,F
Risk Statements  45-46-60-25-48/20/22-52/53-39/23/24/25-23/24/25-11
Safety Statements  53-45-61-36/37-16-7
RIDADR  2872
WGK Germany  3
RTECS  TX8750000
Hazard Note  Toxic
TSCA  T
HazardClass  6.1(b)
PackingGroup  III
HS Code  2903793090
Toxicity LD50 in rats, mice (g/kg): 0.17, 0.26 orally (Torkelson)
NFPA 704
2
4 0

1,2-Dibromo-3-chloropropane price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 48338 1,2-Dibromo-3-chloropropane solution certified reference material, 200?μg/mL in methanol 96-12-8 1mL $28.3 2022-05-15 Buy
Sigma-Aldrich 31257 1,2-Dibromo-3-chloropropane PESTANAL , analytical standard 96-12-8 250mg $55.5 2022-05-15 Buy
TCI Chemical C0806 1,2-Dibromo-3-chloropropane >98.0%(GC) 96-12-8 25g $51 2024-03-01 Buy
Sigma-Aldrich 676713 1,2-Dibromo-3-chloropropane 97% 96-12-8 5g $36.24 2024-03-01 Buy
Sigma-Aldrich 676713 1,2-Dibromo-3-chloropropane 97% 96-12-8 25g $114 2024-03-01 Buy
Product number Packaging Price Buy
48338 1mL $28.3 Buy
31257 250mg $55.5 Buy
C0806 25g $51 Buy
676713 5g $36.24 Buy
676713 25g $114 Buy

1,2-Dibromo-3-chloropropane Chemical Properties,Uses,Production

Description

DBCP is an amber to brown liquid (a solidbelow 6℃/43°F) with a strong, pungent odor. It has an odorand taste threshold at 0.01 mg/L in water. Molecularweight = 236.35; Specific gravity (H2O:1): 2.1; Boilingpoint = 196℃ (decomposes); Freezing/Meltingpoint = 6.1℃; Vapor pressure 5=0.8 mmHg at 20℃; Flashpoint = 77℃. Hazard Identification (based on NFPA-704 MRating System): Health 2, Flammability 2, Reactivity 0.Slightly soluble in water; solubility = 0.1%.

Chemical Properties

colourless to slightly yellow liquid

Physical properties

Colorless when pure, however, technical grades are yellowish to dark brown. Pungent odor at high concentrations

Uses

Formerly as an agricultural nematocide (use banned in the US in 1977)

Uses

Soil fumigant, nematocide and pesticide

Uses

Soil fumigant; nematocide; intermediate in organic synthesis.

Definition

ChEBI: 1,2-Dibromo-3-chloropropane is an organochlorine compound.

Production Methods

DBCP is produced by liquid phase addition of bromine to allyl chloride. It was first produced commercially in the United States in 1955.

General Description

A colorless liquid. Denser than water. Flash point 170°F. Boiling point 195°F. Toxic by ingestion and inhalation. Used as a pesticide and fumigant.

Air & Water Reactions

Flammable. Soluble in water. Hydrolyzed in alkali.

Reactivity Profile

1,2-Dibromo-3-chloropropane reacts with chemically active metals such as aluminum, magnesium, tin and their alloys. 1,2-Dibromo-3-chloropropane will attack some rubber materials and coatings.

Health Hazard

Inhalation of vapors or dust is extremely irritating. May cause burning of eyes and flow of tears. May cause coughing, difficult breathing and nausea. Brief exposure effects last only a few minutes. Exposure in an enclosed area may be very harmful. Fire will produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may cause pollution.

Fire Hazard

Some of these materials may burn, but none ignite readily. Containers may explode when heated.

Agricultural Uses

Nematicide, Fumigant: DBCP has been used in agriculture as a nematicide since 1955, being supplied for such use in the forms of liquid concentrate, emulsifiable concentrate, powder, granules, and solid material. A rebuttable presumption against registration for pesticide uses was issued by U.S. EPA on September 22, 1977, on the basis of oncogenicity and reproductive effects. Then, as of November 3, 1977, EPA in a further action suspended all registrations of end-use products, subject to various specific restrictions. Not listed as registered in EU countries.

Trade name

BBC 12®; FUMAGONE®; FUMAZONE®[C]; MEMATOCIDE®; NEMABROM®; NEMAFUM®; NEMAGON®[C]; NEMAGON SOIL FUMIGANT®[C]; NEMANAX®; NEMAPAZ®; NEMASET®; NEMATOCIDE®[C]; NEMATOX®; NEMAZON®; OS 1897®; OXY BCP®[C]; SD 1897®

Safety Profile

Confirmed human carcinogen with experimental carcinogenic and teratogenic data. Poison by ingestion, inhalation, and subcutaneous routes. Moderately toxic by skin contact. An eye and severe skin irritant. Narcotic in high concentrations. Has been implicated in causing human sterihty in male factory workers. Human mutation data reported. A soil fumigant. Combustible. When heated to decomposition it emits toxic fumes of Cl and Br-. See also CHLORIDES and BROLVIDES.

Potential Exposure

AgriculturalChemical; Tumorigen, Mutagen; Reproductive Effector;Human Data; Primary Irritant. DBCP has been used in agriculture as a fumigant for control of nematodes since 1955,being supplied for such use in the forms of liquid concentrate, emulsifiable concentrate, powder, granules, and solidmaterial. A rebuttable presumption against registration forpesticide uses was issued by US EPA on September 22,1977, on the basis of oncogenicity and reproductive effects.Then, as of November 3, 1977, the EPA in a further action,suspended all registrations of end-use products, subject tovarious specific restrictions.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least2030 min, occasionally lifting upper and lower lids. Seekmedical 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. Contact local poison control center for adviceabout inducing vomiting. Medical observation is recommended for 2448 h after breathing overexposure, as pulmonary edema may be delayed. As first aid for pulmonaryedema, a doctor or authorized paramedic may consideradministering a corticosteroid spray.

Carcinogenicity

1,2-Dibromo-3-chloropropane is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity fromstudies in experimental animals.

Environmental Fate

Biological. Biodegradation is not expected to be significant in removing 1,2-dibromo- 3-chloropropane. In aerobic soil columns, no degradation was observed after 25 days (Wilson et al., 1981a).
Soil. Soil water cultures converted 1,2-dibromo-3-chloropropane to n-propanol, bromide and chloride ions. Precursors to the alcohol formation include allyl chloride and allyl alcohol (Castro and Belser, 1968). The reported half-life in soil is 6 months (Jury et al., 1987).
Groundwater. According to the U.S. EPA (1986) 1,2-dibromo-3-chloropropane has a high potential to leach to groundwater.
Chemical/Physical. 1,2-Dibromo-3-chloropropane is subject to both neutral and basemediate hydrolysis (Kollig, 1993). Under neutral conditions, the chlorine or bromine atoms may be displaced by hydroxyl ions. If nucleophilic attack occurs at the carbon-chlorine bond, 2,3-dibromopropanol is formed which reacts further to give 2,3-dihydroxybromopropane via the intermediate epibromohydrin. 2,3-Dihydroxybromopropane will undergo hydrolysis via the intermediate 1-hydroxy-2,3-propylene oxide which further reacts with water to give glycerol. If the nucleophilic attack occurs at the carbon-bromine bond, 2- bromo-3-chloropropanol is formed which further reacts forming the end product glycerol (Kollig, 1993). If hydrolysis of 1,2-dibromo-2-chloropropane occurs under basic conditions, the compound will undergo dehydrohalogenation to form 2-bromo-3-chloropropene and 2,3-dibromo-1-propene as intermediates. Both compounds are subject to further attack forming 2-bromo-3-hydroxypropene as the end product (Burlinson et al., 1982; Kollig, 1993). The hydrolysis half-life at pH 7 and 25°C was calculated to be 38 years (Burlinson et al., 1982; Ellington et al., 1986).
Emits toxic chloride and bromide fumes when heated to decomposition (Lewis, 1990).

storage

Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with DBCPyou should be trained on its proper handling and storage.Store in a refrigerator. Protect from alkalis and reactivemetals. Protection from light is recommended for long-termstorage. Where possible, automatically pump liquid fromdrums or other storage containers to process containers. Aregulated, marked area should be established where thischemical is handled, used, or stored in compliance withOSHA Standard 1910.1045.

Shipping

DBCP requires a “POISONOUS/TOXIC MATERIALS” label. It falls in Hazard Class 6.1 and Packing Group III.

Toxicity evaluation

DBCP in soil can volatilize from near-surface soil. Based on estimated Koc values of 149 in Lincoln fine sand and 128 in an unspecified soil, DBCP will be highly mobile in soil and has the capacity to leach into groundwater. It is estimated that the volatilization half-life for this chemical will vary between 0.6 days in dry soil with low soil organic content and 26.2 days in a wet soil containing high values of soil organic content. It is important to notice that fields treated with DBCP will present a significant retardation in the volatilization loss from the soil if plastic coverings are used.
DBCP will exist primarily in the vapor phase in the ambient atmosphere. It is expected that very small amounts of this chemical will be present in the particulate phase, and this could explain the fact that dry deposition to the earth’s surface will not result in a significant removal process. DBCP presents high water solubility, and then small amounts present in the air can be removed by wet deposition.
If found in water, DBCP will volatilize quite rapidly to the atmosphere; the estimated volatilization half-life from a pond is 8 days. Using again the estimated Koc values of 128–149, this chemical is not expected to adsorb significantly to sediment and suspended organic matter. Based on an estimated bioconcentration factor (BCF) of 11.2, it is not expected to bioconcentrate in fish and other aquatic organisms. There is no sufficient data to indicate that DBCP could be a potential risk in terms of biomagnifications in different aquatic or terrestrial food chains. However, some biodegradation of DBCP in groundwater might ensue under anaerobic conditions.

Incompatibilities

Reacts with oxidizers and chemicallyactive metals (i.e., aluminum, magnesium, and tin alloys).Attacks some rubber materials and coatings. Corrosive tometals.

107-05-1
96-12-8
37161-81-2
32753-90-5
32753-89-2
Synthesis of 1,2-Dibromo-3-chloropropane from Allyl chloride
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