Carbendazim (CAS 10605-21-7) — formula C9H9N3O2, molecular weight 191.19.
| CAS Number | 10605-21-7 |
|---|---|
| Molecular Formula | C9H9N3O2 |
| Molecular Weight | 191.19 |
| Melting Point | Decomposes at 300 °C |
| LogP | log Kow = 1.52 |
| Applications | Uses: Used as a fungicide in cereals, fruits, vines, hops, vegetables, ornamentals, coffee, cotton, rice, flax, beet, sugar cane, peanuts, oilseed rape, cucurbits, rubber, tobacco, turf, mushrooms, and other crops, [HSDB], Farming (Pesticides) [Category: Industry], For carbendazim (USEPA, OPP Pesticide Code: 128872) 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., Fungicide, Systemic leaf and soil fungicide, absorbed through the roots and green tissues., Carbendazim is, used as a preservative in paint, papermaking and leather industry, and as a preservative of fruits., Antimicrobial in caulks, concrete, grouts, inks, paints, sealants, stains and textiles, It is a systemic fungicide that is selectively toxic to microorganisms and invertebrates. It is also employed as a casting worm control agent in amenity turf situations such as golf greens and tennis courts. It is also used to control plant diseases in cereals and fruits, including citrus, bananas, strawberries, pineapples, and pomes., Use Classification: Pesticides -> Fungicides -> Benzimidazole fungicides, Environmental transformation -> Pesticides (parent, predecessor), Environmental transformation -> Pesticide transformation products (metabolite, successor), Fungicides, Transformation products, Household Products: Information on 19 consumer products that contain Carbendazim in the following categories is provided:, • Home Maintenance, Methods of Manufacturing: Prepn: H.M. Loux, United States of America patent 3010968 (1961 to du Pont), Carbendazim is produced by the reaction of o-phenylenediamine with methoxycarbonylcyanamide or with methoxycarbonyl isocyanide dichloride (formed from cyanogen chloride, phosgene, and methanol) in the presence of a base., Impurities: 2, 3-Diaminophenazine, 2-Amino-3-hydroxyphenazine, Formulations, Preparations: Mergal BCM (Troy Chemical Company Limited): Active ingredient: Carbendazim 99.0%., Mergal BCM Technical (Troy Chemical Company Limited): Active ingredient: Carbendazim 98.6%., Rocima 63 Industrial Microbicide (Rohm & Hass Company): Active ingredient: Diuron 20.0%, Octhilinone 2.7%, and Carbendazim 7.5%., Rocima 65 Industrial Microbicide (Rohm & Hass Company): Active ingredient: 3(2H)-Isothiazolone, 4, 5-dichloro-2-octyl- 5.0%, Carbendazim 9.0%, and 1, 3, 5-Triazine-2, 4-diamine, N-cyclopropyl-N'-(1, 1-dimethylethyl)-6-(methylthio)- 3.5%., For more Formulations, Preparations (Complete) data for CARBENDAZIM (25 total), please visit the HSDB record page., U.S. Production: Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Carbamic acid, N-1H-benzimidazol-2-yl-, methyl ester. National Production Volume: Withheld., General Manufacturing Information: Carbamic acid, methyl ester: ACTIVE, The WHO Recommended Classification of Pesticides by Hazard identifies carbendazim (technical grade) as unlikely to present an acute hazard in normal use, Main Use: fungicide., Marine pollutant., Degradation product of benomyl. |
Documented applications: Uses: Used as a fungicide in cereals, fruits, vines, hops, vegetables, ornamentals, coffee, cotton, rice, flax, beet, sugar cane, peanuts, oilseed rape, cucurbits, rubber, tobacco, turf, mushrooms, and other crops, [HSDB], Farming (Pesticides) [Category: Industry], For carbendazim (USEPA, OPP Pesticide Code: 128872) 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., Fungicide, Systemic leaf and soil fungicide, absorbed through the roots and green tissues., Carbendazim is, used as a preservative in paint, papermaking and leather industry, and as a preservative of fruits., Antimicrobial in caulks, concrete, grouts, inks, paints, sealants, stains and textiles, It is a systemic fungicide that is selectively toxic to microorganisms and invertebrates. It is also employed as a casting worm control agent in amenity turf situations such as golf greens and tennis courts. It is also used to control plant diseases in cereals and fruits, including citrus, bananas, strawberries, pineapples, and pomes., Use Classification: Pesticides -> Fungicides -> Benzimidazole fungicides, Environmental transformation -> Pesticides (parent, predecessor), Environmental transformation -> Pesticide transformation products (metabolite, successor), Fungicides, Transformation products, Household Products: Information on 19 consumer products that contain Carbendazim in the following categories is provided:, • Home Maintenance, Methods of Manufacturing: Prepn: H.M. Loux, United States of America patent 3010968 (1961 to du Pont), Carbendazim is produced by the reaction of o-phenylenediamine with methoxycarbonylcyanamide or with methoxycarbonyl isocyanide dichloride (formed from cyanogen chloride, phosgene, and methanol) in the presence of a base., Impurities: 2, 3-Diaminophenazine, 2-Amino-3-hydroxyphenazine, Formulations, Preparations: Mergal BCM (Troy Chemical Company Limited): Active ingredient: Carbendazim 99.0%., Mergal BCM Technical (Troy Chemical Company Limited): Active ingredient: Carbendazim 98.6%., Rocima 63 Industrial Microbicide (Rohm & Hass Company): Active ingredient: Diuron 20.0%, Octhilinone 2.7%, and Carbendazim 7.5%., Rocima 65 Industrial Microbicide (Rohm & Hass Company): Active ingredient: 3(2H)-Isothiazolone, 4, 5-dichloro-2-octyl- 5.0%, Carbendazim 9.0%, and 1, 3, 5-Triazine-2, 4-diamine, N-cyclopropyl-N'-(1, 1-dimethylethyl)-6-(methylthio)- 3.5%., For more Formulations, Preparations (Complete) data for CARBENDAZIM (25 total), please visit the HSDB record page., U.S. Production: Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Carbamic acid, N-1H-benzimidazol-2-yl-, methyl ester. National Production Volume: Withheld., General Manufacturing Information: Carbamic acid, methyl ester: ACTIVE, The WHO Recommended Classification of Pesticides by Hazard identifies carbendazim (technical grade) as unlikely to present an acute hazard in normal use, Main Use: fungicide., Marine pollutant., Degradation product of benomyl..
Carbendazim is a chemical compound with CAS registry number 10605-21-7 and molecular formula C9H9N3O2 (molecular weight 191.19).
CAS number: 10605-21-7
Its molecular formula C9H9N3O2 comprises 9 C, 9 H, 3 N, 2 O atoms.
Also known as: Carbendazim · 多菌灵
The CAS registry number of Carbendazim is 10605-21-7.
Molecular formula C9H9N3O2, molecular weight 191.19.
It is also registered under: Carbendazim, 多菌灵.
Recorded applications: Uses: Used as a fungicide in cereals, fruits, vines, hops, vegetables, ornamentals, coffee, cotton, rice, flax, beet, sugar cane, peanuts, oilseed rape, cucurbits, rubber, tobacco, turf, mushrooms, and other crops, [HSDB], Farming (Pesticides) [Category: Industry], For carbendazim (USEPA, OPP Pesticide Code: 128872) 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., Fungicide, Systemic leaf and soil fungicide, absorbed through the roots and green tissues., Carbendazim is, used as a preservative in paint, papermaking and leather industry, and as a preservative of fruits., Antimicrobial in caulks, concrete, grouts, inks, paints, sealants, stains and textiles, It is a systemic fungicide that is selectively toxic to microorganisms and invertebrates. It is also employed as a casting worm control agent in amenity turf situations such as golf greens and tennis courts. It is also used to control plant diseases in cereals and fruits, including citrus, bananas, strawberries, pineapples, and pomes., Use Classification: Pesticides -> Fungicides -> Benzimidazole fungicides, Environmental transformation -> Pesticides (parent, predecessor), Environmental transformation -> Pesticide transformation products (metabolite, successor), Fungicides, Transformation products, Household Products: Information on 19 consumer products that contain Carbendazim in the following categories is provided:, • Home Maintenance, Methods of Manufacturing: Prepn: H.M. Loux, United States of America patent 3010968 (1961 to du Pont), Carbendazim is produced by the reaction of o-phenylenediamine with methoxycarbonylcyanamide or with methoxycarbonyl isocyanide dichloride (formed from cyanogen chloride, phosgene, and methanol) in the presence of a base., Impurities: 2, 3-Diaminophenazine, 2-Amino-3-hydroxyphenazine, Formulations, Preparations: Mergal BCM (Troy Chemical Company Limited): Active ingredient: Carbendazim 99.0%., Mergal BCM Technical (Troy Chemical Company Limited): Active ingredient: Carbendazim 98.6%., Rocima 63 Industrial Microbicide (Rohm & Hass Company): Active ingredient: Diuron 20.0%, Octhilinone 2.7%, and Carbendazim 7.5%., Rocima 65 Industrial Microbicide (Rohm & Hass Company): Active ingredient: 3(2H)-Isothiazolone, 4, 5-dichloro-2-octyl- 5.0%, Carbendazim 9.0%, and 1, 3, 5-Triazine-2, 4-diamine, N-cyclopropyl-N'-(1, 1-dimethylethyl)-6-(methylthio)- 3.5%., For more Formulations, Preparations (Complete) data for CARBENDAZIM (25 total), please visit the HSDB record page., U.S. Production: Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Carbamic acid, N-1H-benzimidazol-2-yl-, methyl ester. National Production Volume: Withheld., General Manufacturing Information: Carbamic acid, methyl ester: ACTIVE, The WHO Recommended Classification of Pesticides by Hazard identifies carbendazim (technical grade) as unlikely to present an acute hazard in normal use, Main Use: fungicide., Marine pollutant., Degradation product of benomyl..
Independent reference data for Carbendazim (CAS 10605-21-7), compiled from public chemistry databases.
| CAS Registry Number | 10605-21-7 |
|---|---|
| PubChem CID | 25429 |
| Molecular formula | C9H9N3O2 |
| IUPAC name | methyl N-(1H-benzimidazol-2-yl)carbamate |
| UNII (FDA) | H75J14AA89 |
| Molecular Weight | 191.19 |
|---|---|
| XLogP3 | 1.5 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 191.069476538 |
| Monoisotopic Mass | 191.069476538 |
| Topological Polar Surface Area | 67 |
| Heavy Atom Count | 14 |
| Melting Point | Decomposes at 300 °C |
|---|---|
| Melting Point | MP: 302-307 °C (decomposes) |
| Melting Point | 302 - 307 °C |
| Solubility | 29 mg/L @ 24C (exp) |
| Density | 1.45 g/cu cm at 25 °C |
| Density | 0.27 g/cm³ |
| Vapor Pressure | 7.5X10-10 mm Hg at 20 °C |
| LogP | log Kow = 1.52 |
| LogP | 1.52 |
| LogP | 1.49 |
Carbendazim; 10605-21-7; Carbendazole; Mecarzole; Bavistin; Thicoper; Carbendazime; Derosal; Bavistan; Carbendazol; Funaben; Supercarb; Delsene; Kolfugo; Medamine; Battal
| GHS notification summary | 0.3% (2 / 692) |
|---|
| GHS notification summary | 0.3% (2 / 692) |
|---|---|
| Reported hazard statements | H317, H340, H400, H410, H360 (74%), H371, H373, H319 |
H317: May cause an allergic skin reaction [Warning Sensitization, Skin]
H340: May cause genetic defects [Danger Germ cell mutagenicity]
Carbendazim · CAS 10605-21-7 · C9H9N3O2. UNII H75J14AA89. Melting Point: Decomposes at 300 °C; Melting Point: MP: 302-307 °C (decomposes); Melting Point: 302 - 307 °C.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 多菌灵