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Captan

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Captan
Captan
Captan-from-xtal-1981-CM-3D-balls.png
Names
IUPAC name
(3aR,7aS)-2-[(Trichloromethyl)sulfanyl]-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.004.626
KEGG
PubChem CID
UNII
  • InChI=1S/C9H8Cl3NO2S/c10-9(11,12)16-13-7(14)5-3-1-2-4-6(5)8(13)15/h1-2,5-6H,3-4H2 checkY
    Key: LDVVMCZRFWMZSG-UHFFFAOYSA-N checkY
  • InChI=1/C17H19ClN2O3/c18-13-7-3-4-8-14(13)19-15(21)9-10-20-16(22)11-5-1-2-6-12(11)17(20)23/h3-4,7-8,11-12H,1-2,5-6,9-10H2,(H,19,21)/t11-,12-/m1/s1
    Key: PIBUBEBGJVBNLY-VXGBXAGGBJ
  • InChI=1/C9H8Cl3NO2S/c10-9(11,12)16-13-7(14)5-3-1-2-4-6(5)8(13)15/h1-2,5-6H,3-4H2
    Key: LDVVMCZRFWMZSG-UHFFFAOYAB
  • C1C=CC[C@H]2[C@@H]1C(=O)N(C2=O)SC(Cl)(Cl)Cl
  • ClC(Cl)(Cl)SN1C(=O)C2C/C=C\CC2C1=O
Properties
C9H8Cl3NO2S
Molar mass 300.58 g·mol−1
Appearance white solid; yellow powder (commercial)
Density 1.74 g/cm3
Melting point 178 °C (352 °F; 451 K) (decomposes)
Boiling point N/A
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
combustible, potential occupational carcinogen
NIOSH (US health exposure limits):
PEL (Permissible)
none
REL (Recommended)
Ca TWA 5 mg/m3
IDLH (Immediate danger)
N.D.
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Captan is a general use pesticide (GUP) that belongs to the phthalimide class of fungicides. It is a white solid, although commercial samples appear yellow or brownish.

Applications

Although it can be applied on its own, Captan is often added as a component of other pesticide mixtures. It is used to control diseases on a number of fruits and vegetables as well as ornamental plants. It also improves the outward appearance of many fruits, making them brighter and healthier-looking. Captan is utilized by both home and agricultural growers and is often applied during apple production. It is also active against certain oomycetes, such as Pythium, making it useful for controlling damping off.

Biodegradation

The compound biodegrades with halflife of less than 1 day in soil.

Potential health effects

Captan was previously cited as Group B2, a probable human carcinogen by the US Environmental Protection Agency (EPA), but was reclassified in 2004. Since the mode of action has been established as a proliferative response (in mice only) after intestinal villi are disrupted, captan has been deemed not likely to cause tumors at doses that do not irritate the intestine. The EPA now states, "The new cancer classification considers captan to be a potential carcinogen at prolonged high doses that cause cytotoxicity and regenerative cell hyperplasia. These high doses of captan are many orders of magnitude above those likely to be consumed in the diet, or encountered by individuals in occupational or residential settings. Therefore, captan is not likely to be a human carcinogen nor pose cancer risks of concern when used in accordance with approved product labels. A similar reclassification has been made for folpet, a structurally related fungicide, which shares a common mechanism of toxicity. A key finding for captan (and folpet) is these fungicides are not mutagenic in the animal (in vivo).

Production

It is the product of the reaction trichloromethylsulfenyl chloride with sodium salt of tetrahydrophthalamide.

External links


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