Erucamide - ≥85% , CAS No.112-84-5

CAS: 112-84-5 Cat. No.: E107867 Peso molecular: 337.58 Número EC: 204-009-2

GRADE & PURITY ≥85%

Synonyms

0V89VY25BN | cis-13-Docosenamide | Erucamide; erucylamide | erucic amide | 2-hydroxy-1,2-diphenyl-ethanone | Eflossato | Methylnitrophenol | Erucamide, analytical standard | plastic additive 13 | erucilamide | 13-Docosenamide, (Z)- | CHEBI:142245 | EC 204

Storage

Desiccated,Room temperature

Shipped In

Normal

Specifications

Sinónimos

0V89VY25BN | cis-13-Docosenamide | Erucamide; erucylamide | erucic amide | 2-hydroxy-1, 2-diphenyl-ethanone | Eflossato | Methylnitrophenol | Erucamide, analytical standard | plastic additive 13 | erucilamide | 13-Docosenamide, (Z)- | CHEBI:142245 | EC 204

Especificaciones y pureza

≥85%

Condiciones de almacenamiento de almacenamiento

Desiccated, Room temperature

Enviado en

Normal

Pureza

≥85%

Nombres e identificadores

• Pubchem Sid: 488195455
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488195455
• Sonrisas canónicas: CCCCCCCCC=CCCCCCCCCCCCC(=O)N
• IUPAC Name: (Z)-docos-13-enamide
• InChIKey: UAUDZVJPLUQNMU-KTKRTIGZSA-N
• INCHI: 1S/C22H43NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h9-10H,2-8,11-21H2,1H3,(H2,23,24)/b10-9-
• Isómeros SMILES: CCCCCCCC/C=C\CCCCCCCCCCCC(=O)N
• WGK Alemania: 1
• Peso molecular: 337.58
• Reaxy-Rn: 1728047
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1728047&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Fatty Acyls
      • Subclass Fatty amides

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Fatty Acyls
• Subclass: Fatty amides
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty amides
• Alternative Parents: Primary carboxylic acid amides Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty amide - Primary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as fatty amides. These are carboxylic acid amide derivatives of fatty acids, that are formed from a fatty acid and an amine.
• External Descriptors: Not available

Data sources

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Slightly soluble in ethanol and acetone.
• Punto de fusión (°C): 81 °C
• Peso molecular: 337.600 g/mol
• XLogP3: 8.800
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 19
• Exact Mass: 337.334 Da
• Monoisotopic Mass: 337.334 Da
• Topological Polar Surface Area: 43.100 Ų
• Heavy Atom Count: 24
• Formal Charge: 0
• Complexity: 286.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1

Referencias

1. Zhongan Zhu, Jing Liu, Yuhang Yang, Michael Adu-Frimpong, Hao Ji, Elmurat Toreniyazov, Qilong Wang, Jiangnan Yu, Ximing Xu.  (2021)  SMEDDS for improved oral bioavailability and anti-hyperuricemic activity of licochalcone A.  JOURNAL OF MICROENCAPSULATION,      [PMID:34338606] [10.1080/02652048.2021.1963341]

2. Yajing Hu, Zhenxia Du, Xuechun Sun, Xin Ma, Jingdan Song, Haixia Sui, Augustine Atta Debrah.  (2020)  Non-targeted analysis and risk assessment of non-volatile compounds in polyamide food contact materials.  FOOD CHEMISTRY,      [PMID:33601649] [10.1016/j.foodchem.2020.128625]

3. Chun Hui Zhou, Li Cun Jun, Will P. Gates, Ting Ting Zhu, Yu Wei Hua.  (2019)  Co-intercalation of organic cations/amide molecules into montmorillonite with tunable hydrophobicity and swellability.  APPLIED CLAY SCIENCE,      [PMID:] [10.1016/j.clay.2019.105157]

4. Peng Jiao, Liu Rongyan, Xu Junyi, Yao Yingjuan, Li Beibei, Chen Dengke, Chang Zhuangpeng, Zhao Rui, Feng Yanlin, Hou Ruigang, Lee Min, Zhang Xiao.  (2025)  Acid-responsive aggregated carrot-derived nanoantioxidants alleviate oxidative stress and restore osteoblast activity.  JOURNAL OF NANOBIOTECHNOLOGY,  23  (1): (1-27).  [PMID:40075427] [10.1186/s12951-025-03235-y]

5. Ping Li, Siyi Wang, Mengyuan Liu, Xue Dai, Huicong Shi, Weihong Zhou, Sheng Sheng, Fuan Wu.  (2024)  Antibacterial Activity and Mechanism of Three Root Exudates from Mulberry Seedlings against Ralstonia pseudosolanacearum.  Plants-Basel,  13  (4): (482).  [PMID:38498445] [10.3390/plants13040482]

6. Ke Wang, Xiaoyan Sun, Fayong Li, Dong Xie.  (2024)  Solid-phase synthesis of grafted carbon black for superior aging resistance in biodegradable poly(butylene adipate-co-butylene terephthalate) composite films.  JOURNAL OF VINYL & ADDITIVE TECHNOLOGY,      [PMID:] [10.1002/vnl.22173]