Identification | Back Directory | [Name]
4,4'-DDE | [CAS]
72-55-9 | [Synonyms]
P,P'-DDE 4,4'-DDE NSC 1153 4,4'-DDEe DDE(p,p') NCI-C00555 PARAPARADDE 4,4'-dde solution p, p’-DDE Standard p, p'-DDE solution ddtdehydrochloride DDT dehydrochloride p,p'-DDE in Methanol P,P'-DDE, 100MG, NEAT 2,4'-DDE, 100MG, NEAT 4,4'-DDE, 1000MG, NEAT p,p'-DDE solution,10ppm p,p'-DDE Solution, 100ppm p,p'-DDE solution,1000ppm p.p'-DDE 100mg [72-55-9] DICHLORODIPHENYLDICHLOROETHENE 4,4'-DDE, 1X1ML, MEOH, 20UG/ML 4,4'-DDE, 1X10ML, ISO, 200UG/ML 4, 4′-DDE, 100 μg/μL in acetone 4,4' DDE, 1X1ML, MEOH, 5000UG/ML Dichlorodiphenyldichloroethylene DI(PARA-CHLOROPHENYL)DICHLOROETHENE 4,4'-DICHLORODIPHENYLDICHLOROETHYLENE p,p’-dichlorodiphenyldichloroethylene 2,2-bis(p-Chlorophenyl)-1-chloroethene BIS(4-CHLOROPHENYL)-1,1-DICHLOROETHENE p,p'-(Dichlorodiphenyl)dichloroethylene PARAPARADICHLORODIPHENYLDICHLOROETHYLENE 4,4'-DDE PESTANAL, 250 MG (2,2-BIS(4-CHL 2,2-bis(4-chlorophenyl)1,1-dichloroethene 2,2-Bis(4-chlorophenyl)-1,1-dichloroethene 1,1-Dichloro-2,2-bis(p-chlorophenyl)ethene 1,1-dichloro-2,2-bis(4-chlorophenyl)ethene 1,1-BIS(4-CHLOROPHENYL)-2,2-DICHLOROETHENE 1,1-DI(4-CHLOROPHENYL)-2,2-DICHLOROETHYLENE 1,1-dichloro-2,2-bis(4-chorophenyl)ethylene 1,1-Dichloro-2,2-di(p-chlorophenyl)ethylene bis(chloro-4phenyl)-2,2dichloro-1,1ethylene p,p'-(Dichlorodiphenyl)-2,2-dichloroethylene 2,2-BIS(4-CHLOROPHENYL)-1,1-DICHLOROETHYLENE 2,2-BIS(P-CHLOROPHENYL)-1,1-DICHLOROETHYLENE 1,1-dichloro-2,2-bis(p-chlorophenyl)-ethylen 1,1-Bis(p-chlorophenyl)-2,2-dichloroethylene 2,2-Dichloro-1,1-bis(4-chlorophenyl)ethylene 1,1’-(dichloroethylidene)bis(4-chlorobenzene) 1,1-DICHLORO-2,2-BIS(P-CHLOROPHENYL)-ETHYLENE 1,1’-dichloroethenylidene)bis(4-chlorobenzene) 1,1’-(dichloroethenylidene)bis(4-chloro-benzen 1,1-Dichloro-2,2-bis(4-chlorophenyl)ethene 99% 1,1’-(dichloroethenylidene)bis(4-chloro-Benzene 1,1’-(dichloroethenylidene)bis(4-chlorobenzene) 1,1'-(Dichloroethenylidene)bis(4-chlorobenzene) 1,1-dichloro-2,2-bis(para-chlorophenyl)ethylene Ethylene, 1,1-dichloro-2,2-bis(p-chlorophenyl)- p,p'-DDE [4,4'-Dichlorodiphenyldichloroethylene] 2,2-Bis(4-chlorophenyl)-1,1-dichloroethylene,99% dde(1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene) Benzene, 1,1'-(dichloroethenylidene)bis*4-chloro- Benzene, 1,1'-(dichloroethenylidene)bis[4-chloro- 1,1-Dichloro-2,2-bis(4-chlorophenyl)ethene
p,p'-DDE 1,1-dichloro-2,2-bis(4-chlorophenyl)ethene solution 1,1-Dichloro-2,2-bis(4-chlorophenyl)ethene, 4,4μ-DDE 2,2-BIS-(4-CHLOROPHENYL)-1,1-DICHLOROETHYLENE (4,4'-DDE) 1-Chloro-4-[2,2-dichloro-1-(4-chlorophenyl)vinyl]benzene 1,1-Dichloro-2,2-bis(4-chlorophenyl)ethene solution, 4,4μ-DDE solution | [EINECS(EC#)]
200-784-6 | [Molecular Formula]
C14H8Cl4 | [MDL Number]
MFCD00000837 | [MOL File]
72-55-9.mol | [Molecular Weight]
318.03 |
Chemical Properties | Back Directory | [Appearance]
white crystalline powder | [Melting point ]
88-90 °C(lit.)
| [Boiling point ]
403.45°C (rough estimate) | [density ]
1.3406 (rough estimate) | [vapor pressure ]
13 at 30 °C (Wescott et al., 1981) | [refractive index ]
1.6000 (estimate) | [Fp ]
11 °C | [storage temp. ]
APPROX 4°C
| [solubility ]
ethanol: soluble | [form ]
neat | [color ]
White, crystalline, odorless powder | [Stability:]
Stable, but light-sensitive. Incompatible with strong bases, strong oxidizing agents. | [Water Solubility ]
292mg/L(25 ºC) | [BRN ]
1913355 | [Henry's Law Constant]
0.33 at 25 °C (gas stripping-GC, Jantunen and Bidleman, 2006) | [EPA Substance Registry System]
|
Hazard Information | Back Directory | [Chemical Properties]
white crystalline powder | [Definition]
ChEBI: A chlorophenylethylene that is ethylene substituted by two 4-chlorophenyl groups at position 1 and two chlorine atoms at position 2. | [General Description]
White crystalline solid or white powder. | [Air & Water Reactions]
Insoluble in water. | [Reactivity Profile]
4,4'-DDE is sensitive to exposure to light. 4,4'-DDE is incompatible with strong oxidizing agents and strong bases. Oxidation is catalyzed by UV radiation. | [Fire Hazard]
Flash point data for 4,4'-DDE are not available. 4,4'-DDE is probably combustible. | [Uses]
1,1-Dichloro-2,2-bis(4-chlorophenyl)ethane(DDE) has been used to study the ability of Pseudomonas acidovorans M3GY to transform DDE and its unchlorinated analog, 1,1-diphenylethylene (DPE).It has been used to investigate the role of incubation time, solvent type, yeast inoculum growth stage and concentration on the results of yeast assay for estrogenic compounds. | [Uses]
Military product; chemical research. Degradation product of p,p′-DDT. | [Health Hazard]
A derivative of DDT; structurally and toxicproperties are similar to those of DDT;however, the acute effects are somewhatmilder; moderately toxic by ingestion; ateratogenic substance; adequate evidence ofcarcinogenicity in experimental animals LD50 oral (rat): 880 mg/kg LD50 oral (mouse): 700 mg/kg. | [Safety Profile]
Suspected carcinogen withexperimental carcinogenic and neoplastigenic data. Poisonby ingestion. Experimental reproductive effects. Mutationdata reported. An insecticide. When heated todecomposition it emits very toxic fumes of Cl-. | [Source]
Agricultural runoff degradation of p,p′-DDT (quoted, Verschueren, 1983). | [Environmental Fate]
Biological. In four successive 7-day incubation periods, p,p′-DDE (5 and 10 mg/L) was recalcitrant to degradation in a settled domestic wastewater inoculum (Tabak et al.,1981). Photolytic. When an aqueous solution of p,p′-DDE (0.004uM) in natural water samples
collected from California and Hawaii was irradiated (maximum λ= 240 nm) for 120
hours, 62% was photooxidized to p,p′-dichlorobenzophenone (Ross and Crosby, 1985). When p,p′-DDE in water was irradiated at 313 nm, a quantum yield of 0.3 was
achieved. A photolysis half-life of 0.9 days in summer and 6.1 days in winter by direct
sunlight at 40° latitude was observed. Photolysis products included DDMU (yield 20%),
o-chl When p,p′-DDE in a methanol solvent was photolyzed at 260 nm, a dichloro-benzophenone,
a dichlorobiphenyl, DDMU and 3,6-dichlorofluorenone (yield 10%) formed
as the major products (Plimmer et al., 1970).
Chemical/Physical. May degrade to bis(chlorophenyl)acetic acid (DDA) and hydrochloric
acid in water (Verschueren, 1983) or oxidize to p,p′-dichlorobenzophenone using
UV light as a catalyst (U.S. Department of Health and Human Services, 1989). | [Purification Methods]
Crystallise DDE from MeOH or EtOH and dry it in vacuo. The purity is checked by TLC. [G.tzi & Stammbach Helv Chim Acta 28 569 1946, Beilstein 5 H 639, 5 III1891.] POSSIBLE CARCINOGEN. |
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Energy Chemical
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Company Name: |
BioBioPha Co., Ltd.
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