Reciprocal Net Site sponsor
   Site Info    |    Search
Common molecules sample 50771 - Reciprocal Net Log in
You will need to download and install a Java plug-in in order to view this applet. Download Sun's Java plug-in from here.

Switch to another visualization applet:

> miniJaMM open in new window...
- JaMM1
- JaMM2
Empirical formula: C9H8Cl3NO2S
a: 10.744 Å
b: 10.898 Å
c: 9.978 Å
α (alpha): 90.00 °
β (beta): 90.00 °
γ (gamma): 90.00 °
Volume: 1168.31 Å3
Space group: Pmcn
Calculated density: 1.709 g/cm3
Z: 4
Temperature: 22.0 °C
Formula weight: 300.592 g/mole
R(F): 0.0340
CSD refcode: BARDUT
Short description: Captan is a General Use Pesticide (GUP).
Keyword: Agrox
Keyword: Pesticide
Keyword: Vancide 89
Common name: Captan
Citation of a publication: Reference:Cryst.Struct.Commun., 10,(1981)p 1545 Authors:L.E.Moss, R.A.Jacobson
IUPAC name: N-(Trichloromethylthio)-3a,4,7,7a-tetrahydrophthalimide
Layman's explanation: Captan was introduced in the 1950s and is used to control fungal growth on fruit, ornamental, and vegetable crops. It inhibits mycelial growth from germinating fungus spores and is very commonly used in apple orchards. Captan is generally nontoxic, as classified by toxicity class IV, but can cause skin and eye irritation in concentrated forms. It is a nonsystemic phthalimide fungicide. Captan is white in its commercial use and a clear crystal in pure form. It has a pungent smell in its commercial form. Captan for the most part has not been used on food crops since 1989.
Lab name: Common molecules
Sample provider: Obtained courtesy of the Cambridge Structural Database
Status: Complete, visible to public
Repository Files:
50771.cif 50771.crt 50771.gif 50771.GIF 50771.pdb
50771.sdt

Reciprocal Net site software 0.9.1-50, copyright (c) 2002-2009, The Trustees of Indiana University
Files and data presented via this software are property of their respective owners.
Reciprocal Net is funded by the U.S. National Science Foundation as part of the National Science Digital Library project. NSDL