Carbendazim - ≥97% , CAS No.10605-21-7

Name: Carbendazim - ≥97% , CAS No.10605-21-7
SKU: C140191
Availability: InStock

CAS: 10605-21-7 Cat. No.: C140191 Fórmula: C₉H₉N₃O₂ Peso molecular: 191.19 Beilstein Registry Number: 649044 Número EC: 234-232-0

148 Citations COA

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Carbendazim - ≥97% CAS No(10605-21-7) by Aladdin Scientific

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Disponible para pedir

GRADE & PURITY ≥97%

Synonyms

Storage

Room temperature

Shipped In

Normal

Descripción general Specifications Nombres e identificadores Documentation Advanced Data Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Preguntas frecuentes y artículos Citations of This Product Calculadoras de soluciones Reseñas

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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 148 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Carbendazim (metil 2-benzimidazolecarbamato, metil benzimidazol-2-ilcarbamato) se ha utilizado en los siguientes estudios:

- Como control positivo en ensayo de contacto directo (ensayo de inhibición del crecimiento radial del micelio).

- Como plaguicida y se ha estudiado su efecto en las respuestas de transcripción de Enchytraeus albidus.

- Como compuesto antifúngico de amplio espectro, para estudiar la acción antibacteriana de los fármacos antituberculosos contra Mycobacterium tuberculosis en el medio de cultivo caldo Dubos.

Specifications

Sinónimos

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Tipo de acción

INHIBITOR

Pureza

≥97%

Nombres e identificadores

Pubchem Sid	488182963
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488182963
Sonrisas canónicas	COC(=O)NC1=NC2=CC=CC=C2N1
IUPAC Name	methyl N-(1H-benzimidazol-2-yl)carbamate
InChIKey	TWFZGCMQGLPBSX-UHFFFAOYSA-N
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)
Isómeros SMILES	COC(=O)NC1=NC2=CC=CC=C2N1
WGK Alemania	3
RTECS	DD6500000
Número ONU	3082
Grupo de embalaje	III
Peso molecular	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=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Clase Benzimidazoles
    - Subclass 2-benzimidazolylcarbamic acid esters

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Clase	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
Descripción	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
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Estructura 3D

Objetivos asociados (humanos)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

Discover Target: THRB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CXCL8 Tchem Interleukin-8 (642 Activities)

Discover Target: CXCL8

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

METAP1 Tchem Methionine aminopeptidase 1 (614 Activities)

Discover Target: METAP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AHR Tclin Aryl hydrocarbon receptor (1071 Activities)

Discover Target: AHR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

METAP2 Tchem Methionine aminopeptidase 2 (1512 Activities)

Discover Target: METAP2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

Discover Target: TP53

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A498 (42825 Activities)

Lot Number	Certificate Type	Fecha	Articulo
J2213324	Certificate of Analysis	Jul 06, 2026	C140191
J2213449	Certificate of Analysis	Jul 06, 2026	C140191
J2213474	Certificate of Analysis	Jul 06, 2026	C140191
H2131170	Certificate of Analysis	Jun 09, 2025	C140191
H1517076	Certificate of Analysis	Apr 12, 2023	C140191
B2310285	Certificate of Analysis	Feb 16, 2023	C140191
B2310286	Certificate of Analysis	Feb 16, 2023	C140191
D2518077	Certificate of Analysis	Jul 21, 2022	C140191
D2613018	Certificate of Analysis	Jul 21, 2022	C140191
G2510022	Certificate of Analysis	Jul 21, 2022	C140191
J2213475	Certificate of Analysis	Jul 21, 2022	C140191
F2221235	Certificate of Analysis	Aug 12, 2021	C140191
J2323081	Certificate of Analysis	Aug 12, 2021	C140191

Punto de fusión (°C)	>300°C
Peso molecular	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 Å²
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

Carbendazim - ≥97% , CAS No.10605-21-7

Storage & shipping

Quality documents

Literature proof

Descripción general

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Reseñas de cliente

📚 Citations by Application

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