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Chemical substance record

Dazomet

533-74-4C5H10N2S2162.283 g/mol

A dithiocarbamic ester that is 1,3,5-thiadiazinane with a thione moiety at position 2 and in which the hydrogens attached to the nitrogens are replaced by methyl groups. A fungicide, herbicide and nematicide, it is used prior to sowing or planting for the control of soil fungi, nematodes, bacteria and germinating weeds, and as fumigant for poultry litter and eggs to control Salmonella. It is a non-ozone-depleting alternative to methyl bromide. — ChEBI

Safety references

Safety documents & references

1 indexed references
JP · NITE

Government GHS classification

R02-B-102-MHLW, MOE · FY2020

View classification

Find a product-specific SDS

Safety guides and government classification records are not a manufacturer’s SDS. Match supplier, product number, concentration, physical form, region and revision before using a document.

Identity & molecular properties

Source-linked values
CAS number533-74-4ChEBI ↗
Molecular formulaC5H10N2S2ChEBI ↗
Molar mass162.283 g/molChEBI ↗
Monoisotopic mass162.02854 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:75212ChEBI ↗

Cross-source molecular data

PubChem
Molar mass162.3 g/molPubChem ↗
Exact mass162.02854067 DaPubChem ↗
Computed XLogP1.3PubChem ↗
Topological polar surface area (Ų)63.9PubChem ↗
H-bond donors0PubChem ↗
H-bond acceptors3PubChem ↗
Rotatable bonds0PubChem ↗

PubChem computed values are shown separately from the ChEBI record. An exact InChIKey match was used to connect the records. Molecular descriptors do not describe a supplied product’s purity, particle size or performance.

Names & structural identifiers

Copy any identifier
dazomet
3,5-dimethyl-1,3,5-thiadiazinane-2-thione
QAYICIQNSGETAS-UHFFFAOYSA-N
CN1CSC(=S)N(C)C1
InChI=1S/C5H10N2S2/c1-6-3-7(2)5(8)9-4-6/h3-4H2,1-2H3

Names & synonyms

3,5-dimethyl-1,3,5-thiadiazinane-2-thioneBasamidCrag 974DazobergMylone

Names are supplied by ChEBI. Trade names and related synonyms may describe a broader product context.

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

herbicidenematicideantibacterial agentantifungal agrochemical

Database role annotations describe reported biological or chemical roles; they are not product approvals or recommendations for use.

Safety classification · Japan

NITE / Japanese government
Japan · FY2020 source classification
2-Thioxo-3,5-dimethyltetrahydro-2H-1,3,5-thiadiazine; Dazomet · R02-B-102-MHLW, MOE
EndpointReported classification
Acute toxicity (Oral)Category 4
Reproductive toxicityCategory 1B
Specific target organ toxicity - Single exposureCategory 2 (nervous system)
Specific target organ toxicity - Repeated exposureCategory 1 (blood system, liver)
Hazardous to the aquatic environment (Acute)Category 1
Hazardous to the aquatic environment (Long-term)Category 1

Selected source-reported endpoints. Other endpoints, rationales and conditions remain in the original classification. Missing or unlisted information does not mean non-hazardous. This is not a global classification or transport decision.

Read the original NITE classification

Mass ↔ amount of substance

Calculated from sourced mass
Equivalent amount
0.00616207 mol

Uses 162.283 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.

Elemental composition

Theoretical mass fractions
S
Sulfur · 2 atoms
39.52%
C
Carbon · 5 atoms
37.00%
N
Nitrogen · 2 atoms
17.26%
H
Hydrogen · 10 atoms
6.21%

Calculated theoretical mass fractions from the reported formula and PubChem periodic-table atomic masses. These are not assay or purity results.

Research & patent references

Selected source associations

Sources & record history

Checked 27 Sep 2026
EMBL-EBI ChEBI · CHEBI:75212

Release 255, 9 September 2026. ChEBI three-star (manually annotated) source entry. View original record ↗ · CC BY 4.0

NCBI PubChem · CID 10788 · retrieved 2026-09-27

PubCAS formats source data, connects references and computes explicitly labelled conversions. CAS cross-references are supplied by ChEBI; they do not constitute CAS verification or endorsement.