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Home › Product Catalog › dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate]

dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate]

CAS 23564-05-8C12H14N4O4S2MW 342.4

dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate] (CAS 23564-05-8) — formula C12H14N4O4S2, molecular weight 342.4.

Product Overview

CAS Number23564-05-8
Molecular FormulaC12H14N4O4S2
Molecular Weight342.4
Melting Point172 °C (decomposes)
LogPlog Kow = 1.40
ApplicationsUses: Used as fungicide to control disease (vegetables, fruits, turf, and other crops) and protect wounds (fruit trees), [HSDB] Used as veterinary anthelmintic (nematodes), [Merck Index], Farming (Pesticides) [Category: Industry], For thiophanate methyl (USEPA, OPP Pesticide Code: 102001) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Used for plant disease control in vegetables, & turf., Fungicide, Wound protectant (fruit trees), For more Uses (Complete) data for THIOPHANATE METHYL (8 total), please visit the HSDB record page., This is a man-made compound that is used as a pesticide., Use Classification: Environmental transformation -> Pesticides (parent, predecessor), Fungicides, Household Products: Information on 10 consumer products that contain Dimethyl (1, 2-phenylene)bis(iminocarbonothioyl)bis(carbamate) in the following categories is provided:, • Landscaping, Yard, • Pesticides, Methods of Manufacturing: Thiophanate methyl is produced by reaction of o-phenylenediamine and methoxycarbonyl isothiocyanate., o-Phenylenediamine + potassium thiocyanate + methyl chloroformate (addition, dehydrochlorination), Formulations, Preparations: USEPA, OPP Pesticide Code 102001, Trade Names: Topsin, Cercobin M, Banrot, component of (with 084701), Fungo, TD-1771, NF-44, Enovit methyl., Thiophanate-methyl formulations include dust, granular, wettable powder, water-dispersible granular, and flowable concentrate, ranging from 1.5% to 90% active ingredient., Wettable powder, paste, flowable, granule, dust, ULV., Tops MZ Potato Dee-Piece Treatment Fungicide, Active ingredients 6.00% Mancozeb and 2.50% Thiophanate-methyl, For more Formulations, Preparations (Complete) data for THIOPHANATE METHYL (82 total), General Manufacturing Information: The WHO Recommended Classification of Pesticides by Hazard identifies Thiophanate-methyl as unlikely to present an acute hazard in normal use, Main Use: Fungicide (other than seed treatment)., Residential homeowners may use on lawns and ornamentals

Applications

Documented applications: Uses: Used as fungicide to control disease (vegetables, fruits, turf, and other crops) and protect wounds (fruit trees), [HSDB] Used as veterinary anthelmintic (nematodes), [Merck Index], Farming (Pesticides) [Category: Industry], For thiophanate methyl (USEPA, OPP Pesticide Code: 102001) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Used for plant disease control in vegetables, & turf., Fungicide, Wound protectant (fruit trees), For more Uses (Complete) data for THIOPHANATE METHYL (8 total), please visit the HSDB record page., This is a man-made compound that is used as a pesticide., Use Classification: Environmental transformation -> Pesticides (parent, predecessor), Fungicides, Household Products: Information on 10 consumer products that contain Dimethyl (1, 2-phenylene)bis(iminocarbonothioyl)bis(carbamate) in the following categories is provided:, • Landscaping, Yard, • Pesticides, Methods of Manufacturing: Thiophanate methyl is produced by reaction of o-phenylenediamine and methoxycarbonyl isothiocyanate., o-Phenylenediamine + potassium thiocyanate + methyl chloroformate (addition, dehydrochlorination), Formulations, Preparations: USEPA, OPP Pesticide Code 102001, Trade Names: Topsin, Cercobin M, Banrot, component of (with 084701), Fungo, TD-1771, NF-44, Enovit methyl., Thiophanate-methyl formulations include dust, granular, wettable powder, water-dispersible granular, and flowable concentrate, ranging from 1.5% to 90% active ingredient., Wettable powder, paste, flowable, granule, dust, ULV., Tops MZ Potato Dee-Piece Treatment Fungicide, Active ingredients 6.00% Mancozeb and 2.50% Thiophanate-methyl, For more Formulations, Preparations (Complete) data for THIOPHANATE METHYL (82 total), General Manufacturing Information: The WHO Recommended Classification of Pesticides by Hazard identifies Thiophanate-methyl as unlikely to present an acute hazard in normal use, Main Use: Fungicide (other than seed treatment)., Residential homeowners may use on lawns and ornamentals.

Technical Profile

What this product is

dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate] is a chemical compound with CAS registry number 23564-05-8 and molecular formula C12H14N4O4S2 (molecular weight 342.4).

Identification

CAS number: 23564-05-8

Its molecular formula C12H14N4O4S2 comprises 12 C, 14 H, 4 N, 4 O, 2 S atoms.

Also known as: dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate] · Thiophanate Methyl

Frequently Asked Questions

What is the CAS number of dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate]?

The CAS registry number of dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate] is 23564-05-8.

What is the molecular formula and molecular weight of dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate]?

Molecular formula C12H14N4O4S2, molecular weight 342.4.

What other names is dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate] known by?

It is also registered under: dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate], Thiophanate Methyl.

What are the documented applications of dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate]?

Recorded applications: Uses: Used as fungicide to control disease (vegetables, fruits, turf, and other crops) and protect wounds (fruit trees), [HSDB] Used as veterinary anthelmintic (nematodes), [Merck Index], Farming (Pesticides) [Category: Industry], For thiophanate methyl (USEPA, OPP Pesticide Code: 102001) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Used for plant disease control in vegetables, & turf., Fungicide, Wound protectant (fruit trees), For more Uses (Complete) data for THIOPHANATE METHYL (8 total), please visit the HSDB record page., This is a man-made compound that is used as a pesticide., Use Classification: Environmental transformation -> Pesticides (parent, predecessor), Fungicides, Household Products: Information on 10 consumer products that contain Dimethyl (1, 2-phenylene)bis(iminocarbonothioyl)bis(carbamate) in the following categories is provided:, • Landscaping, Yard, • Pesticides, Methods of Manufacturing: Thiophanate methyl is produced by reaction of o-phenylenediamine and methoxycarbonyl isothiocyanate., o-Phenylenediamine + potassium thiocyanate + methyl chloroformate (addition, dehydrochlorination), Formulations, Preparations: USEPA, OPP Pesticide Code 102001, Trade Names: Topsin, Cercobin M, Banrot, component of (with 084701), Fungo, TD-1771, NF-44, Enovit methyl., Thiophanate-methyl formulations include dust, granular, wettable powder, water-dispersible granular, and flowable concentrate, ranging from 1.5% to 90% active ingredient., Wettable powder, paste, flowable, granule, dust, ULV., Tops MZ Potato Dee-Piece Treatment Fungicide, Active ingredients 6.00% Mancozeb and 2.50% Thiophanate-methyl, For more Formulations, Preparations (Complete) data for THIOPHANATE METHYL (82 total), General Manufacturing Information: The WHO Recommended Classification of Pesticides by Hazard identifies Thiophanate-methyl as unlikely to present an acute hazard in normal use, Main Use: Fungicide (other than seed treatment)., Residential homeowners may use on lawns and ornamentals.

PubChem Public Data

Independent reference data for dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate] (CAS 23564-05-8), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number23564-05-8
PubChem CID3032791
Molecular formulaC12H14N4O4S2
IUPAC namemethyl N-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate
UNII (FDA)K4N81R84L8

Computed descriptors

Molecular Weight342.4
XLogP32.6
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count4
Exact Mass342.04564729
Monoisotopic Mass342.04564729
Topological Polar Surface Area165
Heavy Atom Count22

Physicochemical values on record

Melting Point172 °C (decomposes)
Melting PointMP: 181.5 - 182.5 °C
Melting Point342 °F
Vapor Pressure0.00000007 [mmHg]
Vapor Pressure7.13X10-8 mm Hg at 25 °C
Vapor Pressure<0.0000001 mmHg
LogPlog Kow = 1.40
LogP1.5
Ionization Efficiency2.52
Ionization Efficiency2.7

Documented uses on record

    Used as fungicide to control disease (vegetables, fruits, turf, and other crops) and protect wounds (fruit trees); [HSDB] Used as veterinary anthelmintic (nematodes); [Merck Index]Used for plant disease control in vegetables, fruits, & turf.

    Synonyms and trade names

    Thiophanate-methyl; 23564-05-8; Methylthiofanate; THIOPHANATE METHYL; Thiophanate M; Methyl topsin; Methylthiophanate; Mildothane; Neotopsin; Methyl thiophanate; Fungo; Cercobin methyl; Topsin Methyl; Caligran; Metoben; Enovit methyl

    GHS hazard classification

    Reported hazard statementsH317, H332, H341, H351, H400, H410, H373

    H317: May cause an allergic skin reaction [Warning Sensitization, Skin]

    H332: Harmful if inhaled [Warning Acute toxicity, inhalation]

    What the public record says

    dimethyl N,N'-[1,2-phenylenebis(iminocarbonothioyl)]bis[carbamate] · CAS 23564-05-8 · C12H14N4O4S2. UNII K4N81R84L8. Melting Point: 172 °C (decomposes); Melting Point: MP: 181.5 - 182.5 °C; Melting Point: 342 °F.

    Physical description and handling notes

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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