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Supelco

Dichlofluanid

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H11Cl2FN2O2S2
CAS Number:
1085-98-9
Molecular Weight:
333.23
Beilstein:
2947992
EC Number:
214-118-7
MDL number:
MFCD00078639
UNSPSC Code:
41116107
PubChem Substance ID:
329756729
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)c1ccccc1

InChI

1S/C9H11Cl2FN2O2S2/c1-13(2)18(15,16)14(17-9(10,11)12)8-6-4-3-5-7-8/h3-7H,1-2H3

InChI key

WURGXGVFSMYFCG-UHFFFAOYSA-N

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General description

Dichlofluanid is a fungicide widely used to control many fungal diseases in plants. It is also added as an antifouling agent to copper-based boat paints.

Application

Dichlofluanid may be used as a reference standard for the determination of the analyte:
  • In must and wines by gas chromatographic method.
  • In estuarine water samples as an antifouling paint booster biocide by analytical procedures.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H317,H319,H332,H400

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Acute 1 - Eye Irrit. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM3301
BCCF7286
BCBZ7563
SZBF140XV
SZBC240XV

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Analytical methods for the determination of 9 antifouling paint booster biocides in estuarine water samples.
Voulvoulis N, et al.
Chemosphere, 38(15), 3503- 3516 (1999)
Photocatalyzed degradation of the biocides chlorothalonil and dichlofluanid over aqueous TiO2 suspensions.
Sakkas VA and Albanis TA
Applied Catalysis. B, Environmental, 46(1), 175- 188 (2003)
Martina Orosová et al.
Acta biologica Hungarica, 61(4), 411-422 (2010-11-30)
The effect of the fungicide Euparen Multi (containing 50% tolylfluanid) was investigated on the induction of chromosomal aberrations (CA) in cultured bovine peripheral lymphocytes. Cultures from two healthy donors were treated with tolylfluanid-based fungicide at concentrations ranging from 1.7 to
T A Albanis et al.
Chemosphere, 48(5), 475-485 (2002-07-31)
Organic booster biocides were recently introduced as alternatives to organotin compounds in antifouling products, after restrictions imposed on the use of tributyltin in 1987. In this study, the concentrations of three biocides commonly used as antifoulants, Irgarol 1051 (2-methylthio-4-tertiary-butylamino-6-cyclopropylamino-s-triazine), dichlofluanid
Dimitra A Lambropoulou et al.
Journal of chromatography. A, 1010(1), 1-8 (2003-09-25)
Solid-phase microextraction (SPME) coupled to gas chromatography-mass spectrometry was applied to determine the antifouling biocides chlorothalonil, dichlofluanid, sea nine 211 and irgarol 1051 in marine sediments. Two experimental approaches were selected before the submission of the aqueous extracts to SPME
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