Albendazole Oxide - ≥98% , CAS No.54029-12-8

CAS: 54029-12-8 Cat. No.: A129901 Peso molecular: 281.33 Número EC: 628-805-8
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
Methyl (5-propylsulfoxy)2-benzimidazolecarbamate | Albendazole oxyde [INN-French] | Albendazole sulfoxide, VETRANAL(TM), analytical standard | methyl 5-(propylsulfinyl)-1H-benzo[d]imidazol-2-ylcarbamate | SR-05000001502 | Tox21_113873 | Methoxy-N-[5-(prop
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
A129901-1g
9

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
5g
A129901-5g
4

26,90US$

40,90US$
Guardar 14,00 US$ (34.23%)
10g
A129901-10g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

47,90US$

71,90US$
Guardar 24,00 US$ (33.38%)
25g
A129901-25g
4

104,90US$

157,90US$
Guardar 53,00 US$ (33.57%)
100g
A129901-100g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

164,90US$

247,90US$
Guardar 83,00 US$ (33.48%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Albendazole Oxide is a tubulin polymerization or assembly inhibitor
Ricobendazole is a methylcarbamate benzimidazole with a broad-spectrum anthelmintic activity. Ricobendazole is a key metabolite of albendazole;It has been shown to induce apoptosis in human cancer cell line HT-29, possibly by arresting the cell cycle at the G2/M phase.

Specifications

Sinónimos
Methyl (5-propylsulfoxy)2-benzimidazolecarbamate | Albendazole oxyde [INN-French] | Albendazole sulfoxide, VETRANAL(TM), analytical standard | methyl 5-(propylsulfinyl)-1H-benzo[d]imidazol-2-ylcarbamate | SR-05000001502 | Tox21_113873 | Methoxy-N-[5-(prop
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Ricobendazole is a key metabolite of albendazole and acts as an anthelmintic. It has been shown to induce apoptosis in human cancer cell line HT-29, possibly by arresting cell cycle at the G2/M phase.Broad spectrum anthelmintic agent. Microtubule depolyme
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488186218
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488186218
Sonrisas canónicasCCCS(=O)C1=CC2=C(C=C1)N=C(N2)NC(=O)OC
IUPAC Namemethyl N-(6-propylsulfinyl-1H-benzimidazol-2-yl)carbamate
InChIKeyVXTGHWHFYNYFFV-UHFFFAOYSA-N
INCHI1S/C12H15N3O3S/c1-3-6-19(17)8-4-5-9-10(7-8)14-11(13-9)15-12(16)18-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)
Isómeros SMILES CCCS(=O)C1=CC2=C(C=C1)N=C(N2)NC(=O)OC
WGK Alemania 3
Peso molecular 281.33
Reaxy-Rn 11333813
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11333813&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

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseBenzimidazoles
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzimidazoles
Alternative Parents Benzenoids  Imidazoles  Heteroaromatic compounds  Sulfoxides  Sulfinyl compounds  Propargyl-type 1,3-dipolar organic compounds  Carboximidic acids and derivatives  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Benzimidazole - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Sulfoxide - Carboximidic acid derivative - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfinyl compound - Organic nitrogen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzimidazoles. These are organic compounds containing a benzene ring fused to an imidazole ring (five member ring containing a nitrogen atom, 4 carbon atoms, and two double bonds).
External Descriptors a small molecule
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ABCG2 Tchem ATP-binding cassette sub-family G member 2 (4927 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Taenia crassiceps (97 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ido2 Indoleamine 2,3-dioxygenase 2 (105 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

6 results found

Lot NumberCertificate TypeFechaArticulo
C1523008Certificate of AnalysisMar 20, 2026 A129901
E2516800Certificate of AnalysisMay 19, 2025 A129901
H2127054Certificate of AnalysisMay 24, 2023 A129901
C2304161Certificate of AnalysisMar 11, 2023 A129901
E2315584Certificate of AnalysisSep 20, 2022 A129901
C2304163Certificate of AnalysisAug 30, 2021 A129901
Propiedades químicas y físicas
SolubilidadSoluble in DMSO (11 mg/ml at 25 °C), water (<1 mg/ml at 25 °C), and ethanol (<1 mg/ml at 25 °C).
Punto de fusión (°C)226 °C(dec.)
Peso molecular281.330 g/mol
XLogP31.400
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count5
Exact Mass281.083 Da
Monoisotopic Mass281.083 Da
Topological Polar Surface Area103.000 Ų
Heavy Atom Count19
Formal Charge0
Complexity353.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
Reseñas

Reseñas de cliente

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.