Carbendazim

Carbendazim structural formula

CAS Number10605-21-7
Molecular FormulaC9H9N3O2
Molecular Weight191.191
InChI KeyTWFZGCMQGLPBSX-UHFFFAOYSA-N
LogP1.52
Synonyms
  • Carbendazim
  • Methyl 1H-benzimidazol-2-ylcarbamate
  • Carbamic acid, N-1H-benzimidazol-2-yl-, methyl ester
  • 10605-21-7
  • Carbamic acid, 1H-benzimidazol-2-yl-, methyl ester
  • MBC
  • 1H-Benzimidazol-2-ylcarbamic acid methyl ester
  • 1H-Benzimidazole-2-carbamic acid, methyl ester
  • 2-(Carbomethoxyamino)benzimidazole
  • 2-(Methoxycarbamoyl)benzimidazole
  • 2-(Methoxycarboxamido)benzimidazole
  • 2-[(Methoxycarbonyl)amino]benzimidazole
  • 2-Benzimidazolecarbamic acid, methyl ester
  • 2-CARBOMETHOXYAMINO-BENZIMIDAZOLE
  • 2-Methoxycarbonylamino-benzimidazole
  • Agrizim
  • Aimcozim
  • Antibac MF
  • Bavistan
  • Bavistin
  • Bavistin 25SD
  • Bavistin 3460
  • Bavistin 50SD
  • Bavistin FL
  • Bavistine
  • Bendazim
  • Bengard
  • Bercema-Bitosen
  • Bitosen
  • CARBAMATE, 1H-BENZIMIDAZOL-2-YL-, METHYL
  • Carbamic acid, N-1H-benzimidazol-2-yl-, methyl ester
  • Carbate
  • Carben VL
  • Carbendazime
  • carbendazina
  • Carbendazine
  • Carbendazol
  • Carbendazole
  • Carbendor
  • Carbenzdazim
  • Cekudazim
  • Defensor
  • Delsene
  • Derosal
  • Derosal 60PM
  • Derroprene
  • Dhanustin
  • Equitdazin
  • Falicarben
  • Ferazim
  • Funaben
  • Fungoxan
  • Garbenda
  • Jkstein
  • Karben flo Stefes
  • Karben Stefes Flo
  • Kemdazin
  • Kolfugo
  • Kolfugo 25FW
  • Kolfugo Super
  • Lignasan
  • Mecarzole
  • Medamine
  • Methoxycarbonylaminobenzimidazole
  • Methyl 1H-2-benzimidazolecarbaminate
  • Methyl 1H-benzimidazol-2-ylcarbamate
  • Methyl 1H-benzimidazole-2-carbamate
  • Methyl 2-benzimidazolecarbamate
  • Methyl 2-benzimidazolylcarbamate
  • Methyl benzimidazolylcarbamate
  • NSC 109874
  • Pillarstin
  • Preparation G 665
  • Preventol BCM
  • Spin Flo
  • Stempor
  • Supercarb
  • Thicoper
  • Triticol
  • Zhiweiling
  • Benzimidazolecarbamic
  • Benzimidazole-2-carbamic acid, methyl ester
  • BMK (VAN)
  • Carbendazym
  • EINECS 234-232-0
  • Kolfugo 25 FW
  • Kolfugo Extra
  • MBC (VAN)
  • Methyl N-2-benzimidazolecarbamate
  • Jkatein
  • Fungisol
  • EPA Pesticide Chemical Code 115001
  • EPA Pesticide Chemical Code 128872
  • Benzimidazole carbamate de methyle
  • UNII-H75J14AA89
  • 2-(Methoxy-carbonylamino)-benzimidazol
  • 2-(methoxycarbonylamino)-benzimidazole
  • 2-(methoxycarbonylamino)benzimidazole
  • 2-benzimidazolecarbamic acid methyl ester
  • BMC
  • methyl benzimidazol-2-ylcarbamate
  • 102040-01-7
  • 105268-95-9
  • 110342-67-1
  • 1135441-26-7
  • 1155875-94-7
  • 1203557-88-3
  • 212384-28-6
  • 276680-08-1
  • 39413-19-9
  • 59758-95-1
  • 63090-40-4
  • 63278-70-6

Applications:

HPLC Method for Analysis of Carbendazim on Primesep 100 Column

August 2, 2024

High Performance Liquid Chromatography (HPLC) Method for Analysis of Carbendazim on Primesep 100 by SIELC Technologies

Separation type: Liquid Chromatography Mixed-mode SIELC Technologies

HPLC Method for Analysis of Carbendazim on Primesep 100 Column


 High Performance Liquid Chromatography (HPLC) Method for Analysis of Carbendazim

Carbendazim is a fungicide widely used to control a variety of fungal diseases in crops.

arbendazim acts by inhibiting the development of fungi. It disrupts microtubule formation during mitosis, which prevents cell division and growth of the fungi.

Uses
Agricultural Applications:

Used on a variety of crops including fruits, vegetables, and cereals.
Controls a wide range of fungi, including those causing powdery mildew, leaf spots, and root rot.
Post-Harvest Treatment:

Used to treat fruits and vegetables after harvest to prevent spoilage during storage and transport.
Seed Treatment:

Applied to seeds before planting to protect against soil-borne fungal infections.

Carbendazim can be retained, separated and analyzed using a Primesep 100 mixed-mode stationary phase column. The analysis employs an isocratic method with a simple mobile phase comprising water, acetonitrile (MeCN), and sulfuric acid as a buffer. This method allows for detection using UV 200 nm.

You can find detailed UV spectra of Carbendazim and information about its various lambda maxima by visiting the following link.

ColumnPrimesep 100, 4.6 x 150 mm, 5 µm, 100 A
Mobile PhaseMeCN – 70%
BufferH2SO4 -0.1%
Flow Rate1.0 ml/min
DetectionUV 200 nm
Samples1.0 mg/ml in MP
Injection volume1 µl
LOD*40 ppb (200 nm)
* LOD was determined for this combination of instrument, method, and analyte, and it can vary from one laboratory to another even when the same general type of analysis is being performed.

Class of Compounds
Benzimidazoles
Analyzing CompoundsCarbendazim

Application Column

Primesep 100

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
Carbendazim

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Method for Analysis of Pesticides: Isoproturon, Diuron, Acenaphthene, Carbendazim

July 11, 2017

Isoproturon is an agricultural herbicide with a tendency to adsorb to soils, which leads to it entering bodies of water. In that water, it is highly toxic for algae and oysters, while long term exposure to the pesticide affects the growth of fish. Diuron is a pre-emergent that is used for non-crop areas as well as with many agricultural crops. It has a low acute toxicity to mammals. It can cause irritation of nose and throat.if inhaled and irritation of eyes if comes in contact with the eyes. Acenaphthene is derived from coal tar and has many used such as dyes, pharmaceuticals, insecticides, fungicides, and plastics. It is harmful if ingested, inhaled or comes in contact with skin, and can cause irritations to skin, eyes, upper respiratory tract, and mucous membranes Carbendazim, also known as mercazole, is a broad-spectrum benzimidazole fungicide. It’s used mostly as a worm control agent in places like tennis courts and golf greens. Sometimes it is also used to control plant diseases in cereals and fruits. Primesep 100, a reverse-phase column, contains embedded acidic ionizable groups and can retain Isoproturon, Diuron, Acenaphthene, and Carbendazim. The method is UV compatible and can be used as a general approach for analyzing similar compounds.

 

Condition

Column Primesep 100, 3.2×100 mm, 5 µm, 100A
Mobile Phase Gradient MeCN – 35-85%, 6 min , 4 min hold
Buffer Gradient H2SO4 – 0.05- 0.15%, 6 min, 4 min hold
Flow Rate 0.6 ml/min
Detection UV, 230 nm

 

Description

Class of Compounds
 Herbicide, Acid, Hydrophilic, Ionizable
Analyzing Compounds Isoproturon, Diuron, Acenaphthene, Carbendazim

 

Application Column

Primesep 100

The Primesep family of mixed-mode columns offers a wide variety of stationary phases, boasting unprecedented selectivity in the separation of a broad array of chemical compounds across multiple applications. Corresponding Primesep guard columns, available with all stationary phases, do not require holders. SIELC provides a method development service available to all customers. Inquire about our specially-tailored custom LC-phases for specific separations.

Select options
Application Analytes:
Acenaphthene
Carbendazim
Diuron
Isoproturon
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Separation of Bendazoles on Primesep P Column

August 22, 2008

Eight bendazoles are separated on Primesep P HPLC column by combination of reverse phase and ion-exchange mechanisms. Primesep P column can be used when mixed-mode mechanisms, including pi-pi interactions, can benefit separation. HPLC column and method is compatible with UV detection technique.

Application Column

Primesep P

The Primesep family of mixed-mode columns offers a wide variety of stationary phases, boasting unprecedented selectivity in the separation of a broad array of chemical compounds across multiple applications. Corresponding Primesep guard columns, available with all stationary phases, do not require holders. SIELC provides a method development service available to all customers. Inquire about our specially-tailored custom LC-phases for specific separations.

Select options
Application Analytes:
2-Aminosulphone Albendazole Metabolite
5-Hydroxy Thiabendazole
Albendazole
Cambendazole
Carbendazim
Fenbendazole
Mebendazole
Oxfendazole
Thiabendazole

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.