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45419

Supelco

Dazomet

PESTANAL®, analytical standard

Synonym(s):

3,5-Dimethyltetrahydro-1,3,5-thiadiazine-2-thione, Thiadiazine

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About This Item

Empirical Formula (Hill Notation):
C5H10N2S2
CAS Number:
Molecular Weight:
162.28
Beilstein/REAXYS Number:
116039
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

CN1CSC(=S)N(C)C1

InChI

1S/C5H10N2S2/c1-6-3-7(2)5(8)9-4-6/h3-4H2,1-2H3

InChI key

QAYICIQNSGETAS-UHFFFAOYSA-N

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Application

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

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Caroline Eberlein et al.
Frontiers in plant science, 11, 812-812 (2020-07-09)
Productivity of sugar beet and brassica vegetable crops is constrained by the nematode Heterodera schachtii worldwide. In sugar beet cropping areas of Central Europe and North America, H. schachtii is managed by crop rotation, and cultivation of resistant brassica cover
M Peluso et al.
Environmental and molecular mutagenesis, 32(2), 179-184 (1998-10-17)
Dazomet is a soil fumigant effective against germinating weed seeds, nematodes, soil fungi, and soil insects. Dazomet is primarily used for preplanting control in tobacco and forest nursery crops and is now marketed for a wider range of open field
Ioannis O Giannakou et al.
Pest management science, 58(3), 290-296 (2002-04-27)
The complete phase-out of methyl bromide from use in developed countries by 1 January 2005 will cause many problems in agricultural industries that are now heavily reliant on its use. Three field experiments were established to compare management tactics on
E Van Wambeke
Communications in agricultural and applied biological sciences, 72(2), 61-70 (2008-04-11)
Almost no single commercially available or registered compound is able to replace the broad spectrum activity of methyl bromide. However, combinations of for long known fumigants or their generators, showing good activity in the control of specific groups of soil
Ronald Kluger et al.
Bioorganic chemistry, 34(6), 337-344 (2006-09-26)
Benzoylformate decarboxylase (BFD) enhances the rate of decarboxylation of its key intermediate compared to the nonenzymic reaction by a factor of about 10(6). It has been proposed that desolvation into a hydrophobic environment will lower the reaction barrier in TDP-dependent

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