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1085-98-9

1085-98-9 structural image
Product Name: DICHLOFLUANID
Formula: C9H11Cl2FN2O2S2
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CHEMICAL AND PHYSICAL PROPERTIES

Physical Description White solid; Sensitive to light; [Merck Index] Colorless solid; [MSDSonline]
Color/Form WHITE POWDER
Melting Point 105-105.6 °C
Solubility INSOL IN WATER; 1.5% IN METHANOL; 7% IN XYLENE
Vapor Pressure 0.00000011 [mmHg]
Stability/Shelf Life LIGHT-SENSITIVE BUT DISCOLORATION DOES NOT AFFECT ITS BIOLOGICAL ACTIVITY
Decomposition Decomposed by alkaline media; DT50 (22 °C) >15 days (pH = 4), >18 hours (pH = 7), < 10 minutes (pH = 9), and by polysulfides. Light sensitive.
Ionization Efficiency Positive
Kovats Retention Index 1921 1943 1930.8 1929.6 1916.5 1946.5
Chemical Classes Pesticides -> Fungicides

SAFETY INFORMATION

Signal word Warning
Pictogram(s)

Exclamation Mark
Irritant
GHS07

Environment
GHS09
GHS Hazard Statements H317:Sensitisation, Skin
H319:Serious eye damage/eye irritation
H332:Acute toxicity,inhalation
H400:Hazardous to the aquatic environment, acute hazard
Precautionary Statement Codes P261:Avoid breathing dust/fume/gas/mist/vapours/spray.
P273:Avoid release to the environment.
P280:Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

COMPUTED DESCRIPTORS

Molecular Weight 333.2 g/mol
XLogP3 3.6
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 6
Rotatable Bond Count 5
Exact Mass 331.9623035 g/mol
Monoisotopic Mass 331.9623035 g/mol
Topological Polar Surface Area 74.3 Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 367
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

PRODUCT INTRODUCTION

description

Dichlofluanid is a member of the class of sulfamides that is sulfamide in which the hydrogens attached to one of the nitrogens are replaced by methyl groups, while those attached to the other nitrogen are replaced by a phenyl and a [dichloro(fluoro)methyl]sulfanediyl group. A fungicide introduced in 1965 and used in the cultivation of fruit and vegetables, as well as in wood preservatives, it is no longer approved for use in the European Union. It has a role as an acaricide and an antifungal agrochemical. It is a member of sulfamides, an organofluorine compound, an organochlorine compound and a phenylsulfamide fungicide. It is functionally related to a sulfamide.