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Merck
CN

45419

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:
533-74-4
Molecular Weight:
162.28
Beilstein:
116039
EC Number:
208-576-7
MDL number:
MFCD00023809
UNSPSC Code:
41116107
PubChem Substance ID:
329756716
NACRES:
NA.24

Key Documents

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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

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
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H319,H410

Hazard Classifications

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

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

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCBX4077

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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
R E Staub et al.
Chemical research in toxicology, 8(8), 1063-1069 (1995-12-01)
S-Methylation is a new bioactivation mechanism for metam and metabolites of methyl isothiocyanate and dazomet in mice. These soil fumigants are converted to S-methyl metam [MeNHC(S)SMe] which reaches peak levels in liver, kidney, brain, and blood 10-20 min after intraperitoneal
Dongmei Wu et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 22(9), 1245-1248 (2006-09-13)
A chelating resin coupling Amberlite XAD-2 functionalized with dithizone is synthesized and characterized. Dissolved cadmium is field-preconcentrated using a minicolumn packed with the synthesized resin and determined by flame atomic absorption spectrometry. Five experimental variables are evaluated. The enrichment factor
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
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