Ethopabate - ≥99% , CAS No.59-06-3

CAS: 59-06-3 Cat. No.: E136671 Fórmula: C12H15NO4 Peso molecular: 237.25 Beilstein Registry Number: 2808914 Número CE: 200-414-3
Disponível para encomenda
GRADE & PURITY ≥99%
Synonyms
ETHOPABATE [USP MONOGRAPH] | NCGC00160624-01 | Benzoic acid, 4-(acetylamino)-2-ethoxy-, methyl ester | DTXCID4026264 | Amprol Plus (veterinary) | ETHOPABATE [MI] | NCGC00160624-04 | SY226309 | Methyl 4-(acetylamino)-2-ethoxybenzoate | CHEBI:183844 | Ethop
Storage
Argon charged,Room temperature
Shipped In
Normal
Size
USA
Alemanha (EU)*
Price
Qty
25g
E136671-25g
5 Em stock

62,90US$

94,90US$
Gravar 32,00 US$ (33.72%)
100g
E136671-100g
5 Em stock

199,90US$

299,90US$
Gravar 100,00 US$ (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,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.

Specifications

Sinónimos
ETHOPABATE [USP MONOGRAPH] | NCGC00160624-01 | Benzoic acid, 4-(acetylamino)-2-ethoxy-, methyl ester | DTXCID4026264 | Amprol Plus (veterinary) | ETHOPABATE [MI] | NCGC00160624-04 | SY226309 | Methyl 4-(acetylamino)-2-ethoxybenzoate | CHEBI:183844 | Ethop
Especificações e pureza
≥99%
Condições de armazenamento de armazenamento
Argon charged,Room temperature
Enviado em
Normal
Tipo de ação
INHIBITOR
Pureza
≥99%
Nomes e identificadores
Pubchem Sid508810527
Sorrisos canónicosCCOC1=C(C=CC(=C1)NC(=O)C)C(=O)OC
IUPAC Namemethyl 4-acetamido-2-ethoxybenzoate
InChIKeyGOVWOKSKFSBNGD-UHFFFAOYSA-N
INCHI1S/C12H15NO4/c1-4-17-11-7-9(13-8(2)14)5-6-10(11)12(15)16-3/h5-7H,4H2,1-3H3,(H,13,14)
SMILES isoméricas CCOC1=C(C=CC(=C1)NC(=O)C)C(=O)OC
WGK Alemanha 3
Peso molecular 237.25
Beilstein 2808914
Reaxy-Rn 2808914
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2808914&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
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentAcylaminobenzoic acid and derivatives
Alternative Parents Benzoic acid esters  Acetanilides  N-acetylarylamines  Phenoxy compounds  Phenol ethers  Benzoyl derivatives  Alkyl aryl ethers  Methyl esters  Acetamides  Secondary carboxylic acid amides  Monocarboxylic acids and derivatives  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Acylaminobenzoic acid or derivatives - Acetanilide - Benzoate ester - N-acetylarylamine - Anilide - Phenoxy compound - Benzoyl - Phenol ether - N-arylamide - Alkyl aryl ether - Acetamide - Methyl ester - Carboxamide group - Carboxylic acid ester - Secondary carboxylic acid amide - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Organopnictogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
ABCB11 Tchem Bile salt export pump (2311 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alvos associados (não humanos)
NA Neuraminidase (1107 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
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.

4 results found

Lot NumberCertificate TypeDataItem
C23111020Certificate of AnalysisSep 01, 2026 E136671
C23111034Certificate of AnalysisSep 01, 2026 E136671
C23111035Certificate of AnalysisSep 01, 2026 E136671
C23111040Certificate of AnalysisSep 01, 2026 E136671
Propriedades químicas e físicas
SensibilidadeAir sensitive
Ponto de fusão (°C)148.5 °C
Peso molecular237.250 g/mol
XLogP31.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count5
Exact Mass237.1 Da
Monoisotopic Mass237.1 Da
Topological Polar Surface Area64.599 Ų
Heavy Atom Count17
Formal Charge0
Complexity280.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluções
Revisões

Avaliações dos Clientes

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