Alkyl dimethyl benzyl ammonium chloride - ≥80% , CAS No.68424-85-1

CAS: 68424-85-1 Cat. No.: A194586 Número EC: 270-325-2

GRADE & PURITY ≥80%

Synonyms

DSSTox_GSID_28460 | Miristalkonium chloride (INN) | MYRISTALKONIUM CHLORIDE [INCI] | HSDB 5627 | N-Benzyl-N,N-dimethyl-1-tetradecanaminium chloride | Alpagelle (TN) | CAS-68424-85-1 | MIRISTALKONIUM CHLORIDE [MART.] | MIRISTALKONIUM CHLORIDE [WHO-DD] | N,

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

DSSTox_GSID_28460 | Miristalkonium chloride (INN) | MYRISTALKONIUM CHLORIDE [INCI] | HSDB 5627 | N-Benzyl-N, N-dimethyl-1-tetradecanaminium chloride | Alpagelle (TN) | CAS-68424-85-1 | MIRISTALKONIUM CHLORIDE [MART.] | MIRISTALKONIUM CHLORIDE [WHO-DD] | N,

Especificaciones y pureza

≥80%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥80%

Nombres e identificadores

• Pubchem Sid: 488180876
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180876
• Sonrisas canónicas: CCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1.[Cl-]
• IUPAC Name: benzyl-dimethyl-tetradecylazanium;chloride
• InChIKey: OCBHHZMJRVXXQK-UHFFFAOYSA-M
• INCHI: 1S/C23H42N.ClH/c1-4-5-6-7-8-9-10-11-12-13-14-18-21-24(2,3)22-23-19-16-15-17-20-23;/h15-17,19-20H,4-14,18,21-22H2,1-3H3;1H/q+1;/p-1
• Isómeros SMILES: CCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1.[Cl-]
• CAS alternativo: 68391-01-5
• Reaxy-Rn: 4062599
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4062599&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Alkyldimethylbenzylammonium halides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Alkyldimethylbenzylammonium halides
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkyldimethylbenzylammonium chlorides
• Alternative Parents: Phenylmethylamines Benzylamines Aralkylamines Tetraalkylammonium salts Organopnictogen compounds Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Alkyldimethylbenzylammonium chloride - Phenylmethylamine - Benzylamine - Aralkylamine - Tetraalkylammonium salt - Quaternary ammonium salt - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organic chloride salt - Organic salt - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as alkyldimethylbenzylammonium chlorides. These are organic compounds consisting of a quaternary ammonium group substituted with a benzyl group, two methyl groups as well as an alkyl chain. These compounds also contain a chlorine ion and have the general structure R1[N+](CH3)(CH3)R2.[Cl-], where R1 = benzyl group and R2 = alkyl chain.
• 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)

ALB Tchem Serum albumin (2651 Activities)

Discover Target: ALB

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

Objetivos asociados (no humanos)

Pseudomonas aeruginosa (123386 Activities)

Explore this target

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

Staphylococcus aureus (210822 Activities)

Explore this target

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

Escherichia coli (133304 Activities)

Explore this target

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

Aspergillus niger (16508 Activities)

Explore this target

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

Plasmodium falciparum (966862 Activities)

Explore this target

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

Mecanismos de acción

Propiedades químicas y físicas

• Peso molecular: 368.000 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 15
• Exact Mass: 367.301 Da
• Monoisotopic Mass: 367.301 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 25
• Formal Charge: 0
• Complexity: 265.000
• 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: 2

XLogP3

Referencias

1. Yimei Tang, Kuan Yang, Siyu Zhao, Qingqing Chen, Lan Qin, Bei Qin.  (2023)  Evaluation of Solubility, Physicochemical Properties, and Cytotoxicity of Naproxen-Based Ionic Liquids.  ACS Omega,      [PMID:36910967] [10.1021/acsomega.2c07044]

2. Xiyu Zang, Mingfeng Chang, Lan Zheng, Yingying Zhou, Yuqi Wang, Jiahao Ren, Le Wu, Xiaolong Han, Qian Wang, Jinqiao Wu.  (2019)  Synthesis and characterization of novel poly(ionic liquid)s and their viscosity-increasing effect.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2019.112044]

3. Lingxi Yang, Lina Zou, Gaiping Li, Baoxian Ye.  (2015)  Simple and rapid determination of trace iodide by cathodic stripping voltammetry.  TALANTA,      [PMID:26592656] [10.1016/j.talanta.2015.09.048]

4. Jiadi Wang, Zhirui Zhang, Yue Liu, Beiting Zong, Yixuan Lu, Yuhang Li, Jing Yao.  (2025)  Identification of ferroptosis-related genes in dry eye disease and their effects on inflammatory response and immune infiltration.  GENE,      [PMID:41151658] [10.1016/j.gene.2025.149853]