1,2-Dichloropropane
- CAS No.
- 78-87-5
- Chemical Name:
- 1,2-Dichloropropane
- Synonyms
- Dichloropropane;PROPYLENE DICHLORIDE;1,2-Dichlorpropan;1,2-DCP;Dichloropropanes;R270da;ent15,406;ENT 15,406;NCI-C55141;CH3CHClCH2Cl
- CBNumber:
- CB0472531
- Molecular Formula:
- C3H6Cl2
- Molecular Weight:
- 112.99
- MDL Number:
- MFCD00000868
- MOL File:
- 78-87-5.mol
- MSDS File:
- SDS
Melting point | −100 °C(lit.) |
---|---|
Boiling point | 95-96 °C(lit.) |
Density | 1.156 g/mL at 25 °C(lit.) |
vapor density | 3.89 (vs air) |
vapor pressure | 40 mm Hg ( 19.4 °C) |
refractive index |
n |
Flash point | 40 °F |
storage temp. | Refrigerator |
solubility | Miscible with organic solvents (U.S. EPA, 1985). |
form | Liquid |
color | Clear colorless to light yellow |
Odor | Sweet. |
explosive limit | 14.5% |
Viscosity | 0.757mm2/s |
Water Solubility | 3 g/L (20 ºC) |
Merck | 14,7854 |
BRN | 1718880 |
Henry's Law Constant | 0.81, 1.06, 1.32, 2.01, and 2.74 at 2.0, 6.0, 10.0, 18.0, and 25.0 °C, respectively (EPICS-SPME, Dewulf et al., 1999) |
Exposure limits | Potential occupational carcinogen. NIOSH REL: IDLH 400 ppm; OSHA PEL: TWA 75 ppm (350 mg/m3); ACGIH TLV: TWA 75 ppm, STEL 110 ppm (adopted). |
Dielectric constant | 9.0(Ambient) |
Stability | Stale. Highly flammable. Incompatible with strong oxidizing agents. |
InChIKey | KNKRKFALVUDBJE-UHFFFAOYSA-N |
EPA Primary Drinking Water Standard | MCL:0.005,MCLG:zero |
LogP | 2-2.25 at 20-25℃ |
CAS DataBase Reference | 78-87-5(CAS DataBase Reference) |
EWG's Food Scores | 6 |
FDA UNII | RRZ023OFWL |
Proposition 65 List | 1,2-Dichloropropane |
IARC | 1 (Vol. 41, Sup 7, 71, 110) 2017 |
NIST Chemistry Reference | Propane, 1,2-dichloro-(78-87-5) |
EPA Substance Registry System | 1,2-Dichloropropane (78-87-5) |
Pesticides Freedom of Information Act (FOIA) | 1,2-Dichloropropane |
SAFETY
Risk and Safety Statements
Symbol(GHS) | ![]() ![]() ![]() GHS02,GHS06,GHS08 |
|||||||||
---|---|---|---|---|---|---|---|---|---|---|
Signal word | Danger | |||||||||
Hazard statements | H225-H302-H331-H350 | |||||||||
Precautionary statements | P201-P210-P301+P312+P330-P304+P340+P311-P308+P313 | |||||||||
Hazard Codes | F,Xn,T | |||||||||
Risk Statements | 11-20/22-39/23/24/25-23/24/25-23/25 | |||||||||
Safety Statements | 16-24-45-36/37-7 | |||||||||
RIDADR | UN 1279 3/PG 2 | |||||||||
WGK Germany | 3 | |||||||||
RTECS | TX9625000 | |||||||||
Autoignition Temperature | 1035 °F | |||||||||
TSCA | Yes | |||||||||
HazardClass | 3 | |||||||||
PackingGroup | II | |||||||||
HS Code | 29031990 | |||||||||
Toxicity | LD50 orally in rats: 1.19 ml/kg (Smyth) | |||||||||
IDLA | 400 ppm | |||||||||
NFPA 704 |
|
1,2-Dichloropropane price More Price(22)
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
Sigma-Aldrich | 02577 | 1,2-Dichloropropane analytical standard | 78-87-5 | 1ml | $27 | 2024-03-01 | Buy |
TCI Chemical | D0398 | 1,2-Dichloropropane >98.0%(GC) | 78-87-5 | 25g | $24 | 2024-03-01 | Buy |
TCI Chemical | D0398 | 1,2-Dichloropropane >98.0%(GC) | 78-87-5 | 500g | $105 | 2024-03-01 | Buy |
Alfa Aesar | L03083 | 1,2-Dichloropropane, 98% | 78-87-5 | 25g | $18.65 | 2024-03-01 | Buy |
Alfa Aesar | L03083 | 1,2-Dichloropropane, 98% | 78-87-5 | 100g | $49.65 | 2024-03-01 | Buy |
1,2-Dichloropropane Chemical Properties,Uses,Production
Description
Dichloropropane is a colorless stable liquid.Sweet, chloroform-like odor. The odor threshold in air is0.25 ppm. Molecular weight=112.99; Specific gravity(H2O:1)=1.16; Boiling point=96℃; Freezing/Meltingpoint=-100℃; Vapor pressure=40 mmHg at 20℃;Flash point=16℃ (cc); Autoignition temperature=557℃.Explosive limits: LEL=3.4%; UEL=14.5%. HazardIdentification (based on NFPA-704 M Rating System):Health 2, Flammability 3, Reactivity 0. Very slightly soluble in water; solubility=0.3% at 20℃.
Chemical Properties
colourless liquid
Chemical Properties
Dichloropropane is a colorless stable liquid. Sweet, chloroform-like odor. The odor threshold in air is 0.25 ppm.
Physical properties
Clear, colorless liquid with a sweet, chloroform-like odor. The average least detectable odor threshold concentration in water at 60 °C was 0.10 mg/L (Alexander et al., 1982). Experimentally determined detection and recognition odor threshold concentrations were 1.2 mg/m3 (260 ppbv) and 2.4 mg/m3 (520 ppbv), respectively (Hellman and Small, 1974).
Uses
Soil fumigant for nematodes.
Uses
1,2-Dichloropropane is used as a soil fumigant, often as a mixture with 1,3-dichloropropene to control nematodes and soil pests.
Uses
1,2-Dichloropropane is a byproduct in the production of epichlorohydrin (E582310), an important industrial chemical, is a bifunctional alkylating agent with the potential to form DNA cross-links.
Uses
Solvent for oils, fats, resins, waxes, rubber; in ion exchange manufacture; in photographic film production; paper coating; petroleum catalyst regeneration. Has been used as a soil fumigant.
Definition
ChEBI: Rac-1,2-dichloropropane is a racemate comprising equimolar amounts of (R)- and (S)-1,2-dichloropropane. It is used as a fumigant to control nematodes in soil and insects in stored grain. It has a role as a fumigant insecticide, an agrochemical, a carcinogenic agent and a polar aprotic solvent. It contains a (R)-1,2-dichloropropane and a (S)-1,2-dichloropropane.
General Description
Colorless watery liquid with a sweet odor. Sinks in water. Produces an irritating vapor.
Air & Water Reactions
Highly flammable. Insoluble in water.
Reactivity Profile
1,2-Dichloropropane reacts with strong oxidizers and strong acids. 1,2-Dichloropropane also reacts with aluminum. When confined, this reaction can lead to an explosion. 1,2-Dichloropropane is incompatible with bases and aluminum alloys. 1,2-Dichloropropane will attack some forms of plastics, rubber and coatings.
Hazard
Flammable, dangerous fire risk, explosive limits in air 3.4–14.5%. Toxic by ingestion and inhalation. Upper respiratory tract irritant and body weight effects. Questionable carcinogen.
Health Hazard
Contact with skin or eyes may cause irriation.
Fire Hazard
Special Hazards of Combustion Products: Toxic and irritating gases may be generated.
Flammability and Explosibility
Highly flammable
Chemical Reactivity
Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.
Safety Profile
Suspected carcinogen with experimental carcinogenic data. Moderately toxic by inhalation and ingestion. Mddly toxic by skin contact. An eye irritant. Mutation data reported. Can cause liver, kidney, and heart damage. Can cause dermatitis. One of the more toxic chlorinated hydrocarbons. A suggested order of increasing toxicity is dichloromethane, trichloroethylene, carbon tetrachloride, dichloropropane, dichloroethane. Animals exposed to hgh concentrations often showed marked visceral congestion, fatty degeneration of the liver, kidney, and, less frequently, of the heart. They also showed areas of coagulation and necrosis of the liver. There was found to be a heavy mortality among mice exposed to 400 ppm concentrations. A flammable liquid and very dangerous fire hazard when exposed to heat or flame. Reacts with aluminum to form aluminum chloride. This reaction, when confined, can lead to explosion. Can react vigorously with oxidizing materials. To fight fire, use water, foam, CO2, dry chemical. When heated to decomposition it emits toxic fumes of Cl-. See also CHLORINATED HYDROCARBONS , ALIPH AT1 C
Potential Exposure
Dichloropropane is used as a chemical intermediate in perchloroethylene and carbon tetrachloride synthesis, and as a lead scavenger for antiknock fluids. It is also used as a solvent for fats, oils, waxes, gums and resins; and in solvent mixtures for cellulose esters and ethers. Other applications include the use of dichloropropane; as a fumigant, alone and in combination with dichloropropane, as a scouring compound; and a metal degreasing agent. It is also used as an insecticidal fumigant
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.
Carcinogenicity
The EPA states, “This substance
has not undergone a complete evaluation and determination
under US EPA’s IRIS program for evidence of
human carcinogenicity potential.”
An epidemiological study of 71 Italian florists, who
were found to have used an average of 162 kg/year of 1,2-
dichloropropane, showed that the mean frequency of peripheral
lymphocyte micronuclei for the florists was higher than the mean for 75 controls, but these findings are questionable.
An oral cancer bioassay conducted in rats and mice by
NTP, concluded that there was “some evidence of
carcinogenicity in both male and female mice based on
incidences of liver tumors (primarily adenomas, equivocal
evidence of carcinogenicity in female rats based on mammary
gland adenocarcinomas and no evidence of carcinogenicity
in male rats.” Additional detail is provided below.
Propylene dichloride was fed by gavage to rats and mice,
5 days/week for 103 weeks. Dosageswere 0 (corn oil controls),
125, and 250 mg/kg for mice and 0, 62, and 125 mg/kg for
rats. Survival was reduced in high-dose female rats and
mice (possibly due to infection in female mice). Body weight
was reduced in high-dose rats of both sexes, and clear-cell
changes and necrosis of the livers were found in high-dose
female rats. The investigators concluded that dose-related
increases were observed for adenomas of the liver in both
male (control, 7/50; low dose, 10/50; high dose, 17/50) and
female mice. The increase in the frequency
of liver carcinomas supported the evidence that there was a
neoplastic response in the mouse liver for both sexes (males:
11/50, 17/50, 16/50; females: 1/50, 3/50, 4/50). Hepatocytomegaly
and hepatic necrosis were increased in male mice,
but not in female mice.
Environmental Fate
Biological. 1,2-Dichloropropane showed significant degradation with gradual adaptation
in a static-culture flask-screening test (settled domestic wastewater inoculum) conducted
at 25°C. At concentrations of 5 and 10 mg/L, percent losses after 4 weeks of
incubation were 89 and 81, respectively. The amount lost due to volatilization was only
0–3% (Tabak et al., 1981).
Soil. Boesten et al. (1992) investigated the transformation of 14C-labeled 1,2-dichloropropane
under laboratory conditions of three sub-soils collected from the Netherlands
(Wassenaar low-humic sand, Kibbelveen peat, Noord-Sleen humic sand podsol). The
groundwater saturated soils were incubated in the dark at 9.5–10.5°C. In the Wassenaar
soil, no transformation of 1,2-dichloropropane was observed after 156 days of incubation.
After 608 and 712 days, however, >90% degraded to nonhalogenated volatile compounds
which were detected in the headspace above the soil. These investigators postulated these
compounds could be propylene and n-propane in a ratio of 8:1. Degradation of 1,2-
dichloropropane in the Kibbelveen peat and Noord-Sleen humic sand podsoil was not
observed possibly because the soil redox potentials in both soils (50–180 and 650–670
mV, respectively) were higher than the redox potential in the Wassenaar soil (10–20 mV).
Groundwater. According to the U.S. EPA (1986) 1,2-dichloropropane has a high
potential to leach to groundwater.
Photolytic. Distilled water irradiated with UV light (λ= 290 nm) yielded the following
photolysis products: 2-chloro-1-propanol, allyl chloride, allyl alcohol and acetone. The
half-lives in distilled water and distilled water containing hydrogen peroxide were 50 and
30 minutes, respectively (Milano et al., 1988).
Chemical/Physical. Hydrolysis of 1,2-dichloropropane in distilled water at 25°C produced
1-chloro-2-propanol and hydrochloric acid (Milano et al., 1988). The calculated
hydrolysis half-life at 25°C and pH 7 is 15.8 years (Ellington et al., 1988). Ozonolysis
yielded carbon dioxide at low ozone concentrations (Medley and Stover, 1983).
Emits toxic chloride fumes when heated to decomposition (Lewis, 1990).
Metabolic pathway
1,2-Dichloropropane is quite stable to hydrolytic and microbial degradation in soils. It is metabolised rapidly and extensively in animals via a combination of gluthathione conjugation, reductive dechlorination, hydrolytic displacement of the halogen and oxidation and hydroxylation reactions (Scheme 1).
storage
Color Code—Red: Flammability Hazard: Store ina flammable liquid storage area or approved cabinet awayfrom ignition sources and corrosive and reactive materials.Prior to working with 1,2-dichloropropane you should betrained on its proper handling and storage. Before enteringconfined space where this chemical may be present, checkto make sure that an explosive concentration does not exist.1,2-dichloropropane must be stored to avoid contact withaluminum since violent reactions occur. Store in tightlyclosed containers in a cool, well-ventilated area away fromstrong oxidizers (such as chlorine, bromine, and fluorine),strong acids (such as hydrochloric, sulfuric, and nitric), odichlorobenzene, and 1,2-dichloroethane. Sources of ignition, such as smoking and open flames, are prohibited where1,2-dichloropropane, is handled, used, or stored. Metal containers involving the transfer of=gallons or more of 1,2-dichloropropane should be grounded and bonded. Drumsmust be equipped with self-closing valves, pressure vacuumbungs, and flame arresters. Use only nonsparking tools andequipment, especially when opening and closing containersof 1,2-dichloropropane. Wherever 1,2-dichloropropane isused, handled, manufactured, or stored, use explosion-proofelectrical equipment and fittings. A regulated, marked areashould be established where this chemical is handled, used,or stored in compliance with OSHA Standard 1910.1045.
Shipping
UN1279 1,2-Dichloropropane, Hazard Class: 3; Labels: 3-Flammable liquid.
Purification Methods
Distil the propane from CaH2. It has a limited shelf life. [Beilstein 1 IV 195.]
Degradation
1,2-Dichloropropane (1) is stable to hydrolytic degradation with a DT50
of 15.8 years (est.) at pH 7 and 25 °C (Ellington et aE., 1988). Milano et al.
(1988) reported that the dechlorination of 1,2-dichloropropane in distilled
water (25 °C) yielded 1-chloro-2-propanol(2) and HCl(3).
1,2-Dichloropropane was degraded rapidly in distilled water (DT50 50
min) after irradiation under UV light (290 nm) to yield 2, allyl chloride (4),
allyl alcohol (5) and acetone (6) (Milano et al., 1988).
Incompatibilities
May form explosive mixture with air. May accumulate static electrical charges, and may cause ignition of its vapors. Contact with strong oxidizers, powdered aluminum may cause fire and explosion hazard. Strong acids can cause decomposition and the formation of hydrogen chloride vapors. Reacts with strong bases; o-dichlorobenzene, 1,2-dichloroethane. Corrosive to aluminum and its alloys. Attacks some plastics, rubber, and coatings.
Waste Disposal
Incineration, preferably after mixing with another combustible fuel. Care must be exercised to assure complete combustion to prevent the formation of phosgene. An acid scrubber is necessary to remove the halo acids produced. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≧100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.
1,2-Dichloropropane Preparation Products And Raw materials
Raw materials
Preparation Products
Supplier | Tel | Country | ProdList | Advantage | |
---|---|---|---|---|---|
Henan Bao Enluo International TradeCo.,LTD | +86-17331933971 +86-17331933971 | deasea125996@gmail.com | China | 2503 | 58 |
Shanghai Daken Advanced Materials Co.,Ltd | +86-371-66670886 | info@dakenam.com | China | 16914 | 58 |
Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 | info@tianfuchem.com | China | 21668 | 55 |
Hangzhou FandaChem Co.,Ltd. | 008657128800458; +8615858145714 | fandachem@gmail.com | China | 9332 | 55 |
career henan chemical co | +86-0371-86658258 +8613203830695 | sales@coreychem.com | China | 29894 | 58 |
Hubei Jusheng Technology Co.,Ltd. | 18871490254 | linda@hubeijusheng.com | CHINA | 28180 | 58 |
Xi'an Kono chem co., Ltd., | 029-86107037 13289246953 | info@konochemical.com | China | 2995 | 58 |
Hubei xin bonus chemical co. LTD | 86-13657291602 | linda@hubeijusheng.com | CHINA | 22968 | 58 |
Shanghai Longyu Biotechnology Co., Ltd. | +8619521488211 | info@longyupharma.com | China | 2534 | 58 |
Chongqing Chemdad Co., Ltd | +86-023-6139-8061 +86-86-13650506873 | sales@chemdad.com | China | 39916 | 58 |
View Lastest Price from 1,2-Dichloropropane manufacturers
Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
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2023-12-26 | 1,2-Dichloropropane
78-87-5
|
US $100.00-1.00 / KG | 1KG | 99% | g-kg-tons, free sample is available | Henan Fengda Chemical Co., Ltd | |
![]() |
2023-08-04 | 1,2-Dichloropropane
78-87-5
|
US $10.00 / kg | 1kg | 99% | 500t/month | Henan Bao Enluo International TradeCo.,LTD | |
![]() |
2023-07-27 | 1,2-Dichloropropane
78-87-5
|
US $1.10 / g | 1g | 99.0% Min | 100 Tons | Shaanxi Didu New Materials Co. Ltd |
-
- 1,2-Dichloropropane
78-87-5
- US $100.00-1.00 / KG
- 99%
- Henan Fengda Chemical Co., Ltd
-
- 1,2-Dichloropropane
78-87-5
- US $10.00 / kg
- 99%
- Henan Bao Enluo International TradeCo.,LTD
-
- 1,2-Dichloropropane
78-87-5
- US $1.10 / g
- 99.0% Min
- Shaanxi Didu New Materials Co. Ltd