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Carbendazim solution - analytical standard,100ug/ml,u=3% in ethanol, high purity , CAS No.10605-21-7

In stock
Item Number
C102517
Grouped product items
SKU Size
Availability
Price Qty
C102517-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$62.90

Basic Description

Synonyms BCM | Carbendazim D3 | Thicoper | BAS-3460 | Bavistin | methyl-2-benzimidazole carbamate | Preventol BCM | Antibac MF | Garbenda | Pillarstin | Sarfun | Kolfugo 25 FW | Subeej | EK 578 | Methyl 2-benzimidazolylcarbamate | Supercarb | A 118 (pesticide) | C
Specifications & Purity analytical standard, 100ug/ml,u=3% in ethanol
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade analytical standard

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Benzimidazoles
Subclass 2-benzimidazolylcarbamic acid esters
Intermediate Tree Nodes Not available
Direct Parent 2-benzimidazolylcarbamic acid esters
Alternative Parents Benzenoids  Imidazoles  Heteroaromatic compounds  Carbamate esters  Organic carbonic acids and derivatives  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents 2-benzimidazolylcarbamic acid ester - Benzenoid - Azole - Imidazole - Carbamic acid ester - Heteroaromatic compound - Carbonic acid derivative - Azacycle - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as 2-benzimidazolylcarbamic acid esters. These are aromatic heteropolycyclic compounds that contain a carbamic acid ester group, which is N-linked to the C2-atom of a benzimidazole moiety.
External Descriptors Carbamate fungicides

Associated Targets(Human)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
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THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
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CXCL8 Tchem Interleukin-8 (642 Activities)
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METAP1 Tchem Methionine aminopeptidase 1 (614 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AHR Tclin Aryl hydrocarbon receptor (1071 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
METAP2 Tchem Methionine aminopeptidase 2 (1512 Activities)
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TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
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A498 (42825 Activities)
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ACHN (49357 Activities)
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CAKI-1 (44928 Activities)
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CCRF-CEM (65223 Activities)
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COLO 205 (50209 Activities)
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DU-145 (51482 Activities)
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HL-60 (67320 Activities)
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HT-29 (80576 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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M14 (47487 Activities)
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MCF7 (126967 Activities)
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MOLT-4 (49676 Activities)
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OVCAR-3 (48710 Activities)
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OVCAR-4 (44535 Activities)
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OVCAR-5 (45555 Activities)
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OVCAR-8 (47708 Activities)
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PC-3 (62116 Activities)
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RPMI-8226 (44974 Activities)
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RXF 393 (41971 Activities)
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SF-295 (48000 Activities)
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SK-MEL-2 (46422 Activities)
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SK-MEL-28 (48833 Activities)
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SK-MEL-5 (47095 Activities)
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SK-OV-3 (52876 Activities)
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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
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TK-10 (45540 Activities)
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U-251 (51189 Activities)
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UACC-257 (46019 Activities)
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UACC-62 (47335 Activities)
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UO-31 (46270 Activities)
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786-0 (47912 Activities)
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A549 (127892 Activities)
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NCI/ADR-RES (33767 Activities)
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T47D (39041 Activities)
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EKVX (44102 Activities)
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NCI-H322M (45589 Activities)
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HCC 2998 (41480 Activities)
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HCT-116 (91556 Activities)
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HEK293 (82097 Activities)
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HOP-92 (41141 Activities)
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Associated Targets(non-human)

map Methionine aminopeptidase (444 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Alternaria solani (773 Activities)
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Oculimacula yallundae (312 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Bipolaris oryzae (287 Activities)
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Thanatephorus cucumeris (609 Activities)
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Cercospora beticola (433 Activities)
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Pyricularia grisea (1253 Activities)
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Pseudomonas aeruginosa (123386 Activities)
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Fusarium solani (1274 Activities)
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Klebsiella pneumoniae (43867 Activities)
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Staphylococcus aureus (210822 Activities)
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Acinetobacter baumannii (41033 Activities)
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Escherichia coli (133304 Activities)
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Streptococcus pyogenes (16140 Activities)
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Aspergillus flavus (8875 Activities)
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Aspergillus niger (16508 Activities)
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Nicotiana tabacum (382 Activities)
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Phytophthora infestans (820 Activities)
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Aspergillus sp. (177 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Penicillium citrinum (522 Activities)
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Aspergillus fumigatus (16427 Activities)
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Entamoeba histolytica (2676 Activities)
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Cryptococcus neoformans (21258 Activities)
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Candida albicans (78123 Activities)
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Fusarium oxysporum (3998 Activities)
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Trichoderma (92 Activities)
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Giardia intestinalis (1290 Activities)
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Trichinella spiralis (212 Activities)
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Talaromyces funiculosus (619 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Blumeria graminis (462 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Botrytis cinerea (4183 Activities)
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Bipolaris maydis (114 Activities)
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Fusarium verticillioides (912 Activities)
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Alternaria alternata (757 Activities)
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Alternaria mali (94 Activities)
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Athelia rolfsii (768 Activities)
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Ceratobasidium cereale (139 Activities)
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Curvularia lunata (722 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Colletotrichum fragariae (147 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Colletotrichum gloeosporioides (560 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Fusarium culmorum (260 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Fusarium equiseti (38 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Fusarium oxysporum f. sp. vasinfectum (242 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Fusarium fujikuroi (210 Activities)
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Helminthosporium (185 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Macrophomina phaseolina (474 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Pyricularia oryzae (1832 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mycosphaerella arachidis (441 Activities)
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Phytophthora cactorum (113 Activities)
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Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name methyl N-(1H-benzimidazol-2-yl)carbamate
INCHI InChI=1S/C9H9N3O2/c1-14-9(13)12-8-10-6-4-2-3-5-7(6)11-8/h2-5H,1H3,(H2,10,11,12,13)
InChIKey TWFZGCMQGLPBSX-UHFFFAOYSA-N
Smiles COC(=O)NC1=NC2=CC=CC=C2N1
Isomeric SMILES COC(=O)NC1=NC2=CC=CC=C2N1
WGK Germany 3
RTECS DD6500000
UN Number 3082
Packing Group III
Molecular Weight 191.19
Beilstein 649044
Reaxy-Rn 649044
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=649044&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot Number Certificate Type Date Item
G2219292 Certificate of Analysis Apr 07, 2024 C102517
C2223188 Certificate of Analysis Dec 25, 2023 C102517

Chemical and Physical Properties

Melt Point(°C) >300°C
Molecular Weight 191.190 g/mol
XLogP3 1.500
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 2
Exact Mass 191.069 Da
Monoisotopic Mass 191.069 Da
Topological Polar Surface Area 67.000 Ų
Heavy Atom Count 14
Formal Charge 0
Complexity 222.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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