4,4'-DDT
Synonym(s):1,1,1-Trichloro-2,2-bis(4-chlorophenyl)ethane;1,1,1-Trichloro-2,2-bis(4-chlorophenyl)ethane solution;1,1-Bis(4-chlorophenyl)-2,2,2-trichloroethane;4,4′-DDT solution
- CAS NO.:50-29-3
- Empirical Formula: C14H9Cl5
- Molecular Weight: 354.49
- MDL number: MFCD00000802
- EINECS: 200-024-3
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-03-14 15:18:26
What is 4,4'-DDT?
Description
DDT is a polychlorinated persistent chemical that exists as a solid under normal conditions.Even though DDT seemed to be a cheap and effective pesticide, enough was known in its early development to raise concerns. DDT is a persistent chemical that lasts a long time in the environment. DDT is fat-soluble and not readily metabolized by higher organisms. Th is meant that DDT accumulated in the fat tissues of higher organisms.
Description
Dichlorodiphenyltrichloroethane (DDT) is a notorious insecticide that was considered to be a great scientific breakthrough. It goes by many other names, including the more formal 1,1’-(2,2,2-trichloroethylidene)bis(4-chlorobenzene) and 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane.
DDT has been known since 1874, when Austrian chemist Othmar Zeidler synthesized it from chloral (trichloroacetaldehyde) and chlorobenzene. But it was not found to be a potent insecticide until 65 years later.
Swiss chemist Paul Hermann Müller, working at J. R. Geigy (Basel; now part of Novartis International), studied how insects absorb chemicals. Based on this research, he synthesized molecules that he thought would be taken up by insects and kill them. In 1939, after 4 years of research, the 350th compound Müller tested, DDT, killed a fly. For this breakthrough and subsequent work, he received the 1948 Nobel Prize in Physiology or Medicine.
DDT was an instant success against insects that carried disease and destroyed crops. It was used extensively during World War II and for three decades afterward to control insects that bore the pathogens for malaria and yellow fever. It is credited with saving the lives of millions of people who would likely have died from these diseases and others.
Soon after DDT was introduced, however, researchers found that it has a dark side. For humans and many other animal species, it acts as an acute and chronic toxin. It is an endocrine disruptor that can impair reproduction and harm the embryo or fetus. It is also a probable carcinogen. To make matters worse, it is not biodegradable and thus can build up in animal tissues with high lipid contents. Rachel Carson called attention to the dangers of DDT in her widely read 1962 book Silent Spring.
Carson’s work and subsequent findings led to the restricted use of DDT and, in 1972, an outright ban on its agricultural use in the United States. Under the Stockholm Convention on Persistent Organic Pollutants, it was banned worldwide in 2004; but it is still used, somewhat controversially, in emergencies against malaria outbreaks.
The ban on DDT is recognized as a major factor in preventing the extinction of the bald eagle and peregrine falcon in the United States. On January 10, Save the Eagles Day, you can celebrate the 2007 removal of the bald eagle from the endangered species list.
The Uses of 4,4'-DDT
4,4'-Dichlorodiphenyltrichloroethane is a synthetic organochlorine insecticide. 4,4'-Dichlorodiphenyltrichloroethane functions by opening sodium ion channels in the insects’neurons, causing them to f ire spontaneously which in turn leads to death. 4,4'-Dichlorodiphenyltrichloroethane is banned for agricultural use in North America, it is still commonly used in some countries and particularly as a means of malaria control.
What are the applications of Application
4,4′-DDT is a pesticide and DDT derivative
Properties of 4,4'-DDT
Melting point: | 107-110 °C(lit.) |
Boiling point: | 440.74°C (rough estimate) |
Density | 1.556 g/cm3 |
Flash point: | 72 °C |
storage temp. | APPROX 4°C
|
solubility | 25 μg/l |
form | neat |
Water Solubility | Practically insoluble in water |
appearance | white crystals or powder |
Safety information for 4,4'-DDT
Signal word | Danger |
Pictogram(s) |
Skull and Crossbones Acute Toxicity GHS06 Health Hazard GHS08 Environment GHS09 |
GHS Hazard Statements |
H351:Carcinogenicity H372:Specific target organ toxicity, repeated exposure H410:Hazardous to the aquatic environment, long-term hazard |
Precautionary Statement Codes |
P202:Do not handle until all safety precautions have been read and understood. P260:Do not breathe dust/fume/gas/mist/vapours/spray. P273:Avoid release to the environment. P280:Wear protective gloves/protective clothing/eye protection/face protection. P301+P310:IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. |
Computed Descriptors for 4,4'-DDT
New Products
3-N-BOC-(S)-AMINO BUTYRONITRILE 4-Piperidinopiperidine 2-Methyl-4-nitrobenzoic acid 2-(4-bromophenyl)-2-methylpropanoic acid 4-Acetyl-2-methylbenzoicacid Acetyl-meldrum's acid Ethyl-4-Pyrazole carboxylate 2,6 Di acetylpyridine 2,6-Pyridinedimethanol 5,7-Dichloro-3H-Imidazo[4,5-B]Pyridine 5-Bromo-2-Methoxy-4-Methyl-3-Nitropyridine 2-Fluoro-5-Iodopyridine 2-Fluoro-5-Methylpyridine 2-Chloro-3-Bromo-5-Amiopyridine METHYL-4-(BUTYRYLAMINO)3-METHYL-5-NITROBENZOATE TRANS-CYCLOBUTANE-1,2- DICARBOXYLIC ACID 5-Nitro indazole R-(-)-5-(2-AMINO-PROPYL)-2-METHOXY-BENZENESULFONAMIDE 1,3-cyclohexanedione 4-Aminophenaethylalchol (S)-(+)-4-BENZYL-2-OXAZOLIDINONE 3-NITRO-5-ACETYL IMINODIBENZYL 4-FLUORO PHENYL MAGNESIUM BROMIDE 1.0 M IN THF 1-HYDROXY-4-METHYL6-(2,4,4-TRI METHYL PHENYL)-2-PYRIDONE MONO ETHANOL AMINE(PIROCTONE OLAMINE)Related products of tetrahydrofuran
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