(Lauryldimethylammonio)acetate - 25%-29% , CAS No.683-10-3

CAS: 683-10-3 Cat. No.: L196320 Peso molecular: 271.44 Número EC: 211-669-5

GRADE & PURITY 25%-29%

Synonyms

2-[dodecyl(dimethyl)azaniumyl]acetate | Rewoteric AM-DML | (Dodecyldimethylammonio)acetate | Betaine lauryldimethylaminoacetate | SCHEMBL594518 | Ammonium, (carboxymethyl)dodecyldimethyl-, hydroxide, inner salt | DTXSID6041266 | 1-Dodecanaminium, N-(carbo

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

2-[dodecyl(dimethyl)azaniumyl]acetate | Rewoteric AM-DML | (Dodecyldimethylammonio)acetate | Betaine lauryldimethylaminoacetate | SCHEMBL594518 | Ammonium, (carboxymethyl)dodecyldimethyl-, hydroxide, inner salt | DTXSID6041266 | 1-Dodecanaminium, N-(carbo

Especificaciones y pureza

25%-29%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Nombres e identificadores

• Pubchem Sid: 488194803
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488194803
• Sonrisas canónicas: CCCCCCCCCCCC[N+](C)(C)CC(=O)[O-]
• IUPAC Name: 2-[dodecyl(dimethyl)azaniumyl]acetate
• InChIKey: DVEKCXOJTLDBFE-UHFFFAOYSA-N
• INCHI: 1S/C16H33NO2/c1-4-5-6-7-8-9-10-11-12-13-14-17(2,3)15-16(18)19/h4-15H2,1-3H3
• Isómeros SMILES: CCCCCCCCCCCC[N+](C)(C)CC(=O)[O-]
• Peso molecular: 271.44
• Reaxy-Rn: 3670807
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3670807&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Alpha amino acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Alpha amino acids
• Alternative Parents: Tetraalkylammonium salts Carboxylic acid salts Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-amino acid - Quaternary ammonium salt - Tetraalkylammonium salt - Carboxylic acid salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - Organic nitrogen compound - Organic oxide - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
• 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

• Peso molecular: 271.440 g/mol
• XLogP3: 6.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 12
• Exact Mass: 271.251 Da
• Monoisotopic Mass: 271.251 Da
• Topological Polar Surface Area: 40.100 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 221.000
• 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. Xiaoping Li, Bo Hui, Quanyou Jin, Huaqiang Shi, Xinlong Lu, Li Jing, Dengwei Jing.  (2023)  Control of Both Ionic Properties and Micellar Structure for Enhanced Turbulent Drag Reduction Performance of Surfactant Solutions.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.3c02708]

2. Liang Shen, Yifang Liu, Jiabao Gong, Erle Qiao.  (2023)  Study on the Remediation of Pyrene-Contaminated Soil with Surfactants and their Mechanisms.  Processes,  11  (7): (2199).  [PMID:] [10.3390/pr11072199]

3. Zhixia Wang, Hang Song.  (2023)  Application of curcumin in mixed properties of quaternary N-alkyl tropine-based ionic liquid surfactant with nonionic, anionic and zwitterionic surfactants.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2023.136125]

4. Lei Ma, Qiuyan Bi, Wanji Zhou, Xingliang Liu, Fuju Qi, Hao Zhang, Yifan Gao, Shiai Xu.  (2023)  Nanofiltration membrane with a zwitterion-g-C3N4 composite interlayer for Mg2+/Li+ separation.  Journal of Water Process Engineering,      [PMID:] [10.1016/j.jwpe.2023.103751]

5. Jing Gao, Meng Hao, Tao Wu, Yujiang Li.  (2021)  Efficient treatment of crude oil-contaminated hydrodesulphurization catalyst by using surfactant/solvent mixture.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2021.105890]

6. Long Bai, Yue Chen, Hongyao Yin, Xiaoyuan Sui, Dianguo Wu, Yujun Feng.  (2020)  Insights into the stability of polytetrafluoroethylene aqueous dispersion: Role of surfactant.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2020.113662]

7. Dandan Han, Tarak Karmakar, Fei Liu, Yan Wang, Weiwei Tang, Junbo Gong.  (2019)  Uncovering the Role of Surfactants in Controlling the Crystal Growth of Pyridoxine Hydrochloride.  CRYSTAL GROWTH & DESIGN,      [PMID:] [10.1021/acs.cgd.9b01134]

8. Yi Zheng, Qiuya Zhang, Haoran Chi, Yize Liu, Hongwei Ren.  (2025)  Efficient treatment of naphthenic acids with radical/non-radical synergy–based on MoS2/Si-CQDs derived from fructose.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2025.115710]

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10. Zhiqiang Jiang, Zili Li, Bin Liang, Miao He, Weishou Hu, Jun Tang, Chao Song, Nanxin Zheng.  (2025)  Performance Analysis of Foamed Fracturing Fluids Based on Microbial Polysaccharides and Surfactants in High-Temperature and High-Salinity Reservoirs.  FDMP-Fluid Dynamics & Materials Processing,      [PMID:] [10.32604/fdmp.2025.062737]