N,N-Dimethyldodecylamine N-oxide - ≥95% , CAS No.1643-20-5

CAS: 1643-20-5 Cat. No.: D106281 Peso molecular: 229.41 Número EC: 216-700-6

GRADE & PURITY ≥95%

Synonyms

Ammonyx LO | Lauramine oxide | Lauryldimethylamine oxide | Ammonyx AO | LDAO | Lauryldimethylamine N-oxide | N,N-dimethyldodecan-1-amine oxide | Dodecyldimethylamine oxide | Empigen OB | 1-Dodecanamine, N,N-dimethyl-, N-oxide | 1643-20-5

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Specifications

Sinónimos

Ammonyx LO | Lauramine oxide | Lauryldimethylamine oxide | Ammonyx AO | LDAO | Lauryldimethylamine N-oxide | N, N-dimethyldodecan-1-amine oxide | Dodecyldimethylamine oxide | Empigen OB | 1-Dodecanamine, N, N-dimethyl-, N-oxide | 1643-20-5

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Store at -20°C, Argon charged

Enviado en

Ice chest + Ice pads

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

Pureza

≥95%

Nombres e identificadores

• Sonrisas canónicas: CCCCCCCCCCCC[N+](C)(C)[O-]
• IUPAC Name: N,N-dimethyldodecan-1-amine oxide
• InChIKey: SYELZBGXAIXKHU-UHFFFAOYSA-N
• INCHI: 1S/C14H31NO/c1-4-5-6-7-8-9-10-11-12-13-14-15(2,3)16/h4-14H2,1-3H3
• Isómeros SMILES: CCCCCCCCCCCC[N+](C)(C)[O-]
• RTECS: JR6650000
• Número ONU: 3249
• Grupo de embalaje: II
• Peso molecular: 229.41
• Reaxy-Rn: 1769927
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1769927&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Aminoxides

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Aminoxides
• Intermediate Tree Nodes: Not available
• Direct Parent: Long-chain alkyl amine oxides
• Alternative Parents: Trialkyl amine oxides Trisubstituted amine oxides and derivatives Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Long-chain alkyl amine oxide - Trialkyl amine oxide - Trisubstituted n-oxide - N-oxide - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as long-chain alkyl amine oxides. These are aminoxides that carry an alkyl chain ranging from C10 to C24.
• 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

Objetivos asociados (humanos)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

LSS Tchem Lanosterol synthase (305 Activities)

Discover Target: LSS

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

RBL-2H3 (1162 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Insoluble in water.
• Sensibilidad: Hygroscopic；Air sensitive
• Punto de fusión (°C): 132-133°C
• Peso molecular: 229.400 g/mol
• XLogP3: 5.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 11
• Exact Mass: 229.241 Da
• Monoisotopic Mass: 229.241 Da
• Topological Polar Surface Area: 18.100 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 146.000
• 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. Zhuo Zhang, Ting Liu, Yawen Li, Yang Yu, Lin Ning, Xuefan Qiu, Chencan Li, Ling Wang, Wenlong Xu.  (2023)  Temporal Control of Fluorescent EuW10 Aggregates for Autonomous DNA Capture and Information Encryption.  CHEMISTRY-A EUROPEAN JOURNAL,  29  (57): (e202301968).  [PMID:37486795] [10.1002/chem.202301968]

2. Hao Wu, Xiaoyu Cheng, Songjun Xie, Yan Huang, Raheel Ahmed Janjua, Xinzi Liu, Sailing He.  (2023)  Aluminum Quantum Dots with Surface Controlled Blue-UV Photoluminescence.  Journal of Physical Chemistry C,      [PMID:] [10.1021/acs.jpcc.2c08441]

3. Mengkai Hu, Teng Bao, Zhen Qin, Qiang Wang, Hengwei Zhang, Yujue Wang, Jiajia You, Zhenglian Xue, Rongzhen Zhang, Shang-Tian Yang, Xian Zhang, Zhiming Rao.  (2025)  Programmable Scaffold-Mediated Assembly Regulation Tool for Dynamic Control of a Multienzyme Biocatalyst.  ACS Catalysis,      [PMID:] [10.1021/acscatal.4c05420]

4. Hui Tang, Jiateng Hu, Qianqian Yang, Gang Yu.  (2026)  Highly Uniform and Thermal Stable Paper-Structured Catalyst by Using Glass/Mullite Hybrid Fibers as a Matrix for Efficient Soot Combustion.  Catalysts,  16  (1): (103).  [PMID:] [10.3390/catal16010103]