N-[Tris(hydroxymethyl)methyl]acrylamide(NAT) - ≥93%, ≤7% KCl , CAS No.13880-05-2

CAS: 13880-05-2 Cat. No.: I167157 Peso molecular: 175.18 Número EC: 237-645-4

GRADE & PURITY ≥93%, ≤7% KCl

Synonyms

AKOS015900619 | N-[Tris(hydroxymethyl)methyl]acrylamide | n-[tris(hydroxymethyl)methyl]-acrylamide | SCHEMBL105869 | C93420 | N-(1,3-Dihydroxy-2-(hydroxymethyl)propan-2-yl)acrylamide | 2-Propenamide, N-[2-hydroxy-1,1-bis(hydroxymethyl)ethyl]- | FT-0636974

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

AKOS015900619 | N-[Tris(hydroxymethyl)methyl]acrylamide | n-[tris(hydroxymethyl)methyl]-acrylamide | SCHEMBL105869 | C93420 | N-(1, 3-Dihydroxy-2-(hydroxymethyl)propan-2-yl)acrylamide | 2-Propenamide, N-[2-hydroxy-1, 1-bis(hydroxymethyl)ethyl]- | FT-0636974

Especificaciones y pureza

≥93%, ≤7% KCl

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥93%

Nombres e identificadores

• Pubchem Sid: 504755725
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755725
• Sonrisas canónicas: C=CC(=O)NC(CO)(CO)CO
• IUPAC Name: N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]prop-2-enamide
• InChIKey: MVBJSQCJPSRKSW-UHFFFAOYSA-N
• INCHI: 1S/C7H13NO4/c1-2-6(12)8-7(3-9,4-10)5-11/h2,9-11H,1,3-5H2,(H,8,12)
• Isómeros SMILES: C=CC(=O)NC(CO)(CO)CO
• Peso molecular: 175.18
• Reaxy-Rn: 2081162
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2081162&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Acrylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Acrylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Acrylic acids and derivatives
• Alternative Parents: Secondary carboxylic acid amides Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acrylic acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as acrylic acids and derivatives. These are organic compounds containing acrylic acid CH2=CHCO2H or a derivative thereof.
• 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

Propiedades químicas y físicas

• Solubilidad: Soluble in water.
• Sensibilidad: light & Moisture sensitive
• Punto de fusión (°C): 136-141℃（lit）
• Peso molecular: 175.180 g/mol
• XLogP3: -2.000
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 175.084 Da
• Monoisotopic Mass: 175.084 Da
• Topological Polar Surface Area: 89.800 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 157.000
• 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

Referencias

1. Kuilong Liu, Ziyi Zhou, Haibo Wang, Qin Li, Binling Chen, Xiaoyue Wang, Jun Nie, Guiping Ma.  (2025)  A Heterojunction Piezoelectric Antimicrobial Asymmetric Hydrogel for Dynamic Wound Healing and Monitoring.  Small,      [PMID:39981806] [10.1002/smll.202411265]

2. Hanjie Shao, Junjie Deng, Zeping Xu, Jiujun Zhu, Wei Jian, Peiru Zhang, Xinhua Zhou, Xie Zhang, Hao She, Jingyun Ma, Xiang Wu, Hong Li.  (2024)  A Janus hydrogel that enables wet tissue adhesion and resists abdominal adhesions.  Materials Today Bio,      [PMID:39318376] [10.1016/j.mtbio.2024.101248]

3. Chunyang Li, Jin-Tao Wang, Kuili Liu, Hongwei Ding, Qing-Feng Li, Gaofeng Liang, Lin Jin, Deyan He.  (2024)  Antibacterial and anti-inflammatory synergistic effects of double-layer hydrogel promoting bacterial wound healing.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.152513]

4. Jianwei Li, Mengkun Wang, Xiangzhong Tan, Yingxi Duanmiao, Xiang Zheng, Zhen Wang, Fei Gao, Yuqing Miao, Huipeng Li, Bo Liu, Mingjun Li, Tingbin Zhang, Huan Zhou, Jinfeng Xing, Lei Yang.  (2025)  A dual-component particulate dressing for simultaneous microenvironment modulation and tissue regeneration in infected diabetic wounds.  Materials Today Bio,      [PMID:40612277] [10.1016/j.mtbio.2025.102005]

5. Shuaiqi Gan, Zheng Zheng, Xinyi Li, Jia Xu, Xiaofei Gong, Shujiang Chen, Ping Zhang, Wenchuan Chen.  (2026)  Scab-Inspired Thermoresponsive Hydrogel Dressing for Accelerated Healing of Infected Wounds.  ACS Applied Materials & Interfaces,      [PMID:41511899] [10.1021/acsami.5c21571]