Dimethyloctadecylchlorosilane - ≥97%(T) , CAS No.18643-08-8

CAS: 18643-08-8 Cat. No.: D155352 Peso molecular: 347.10 Beilstein Registry Number: 2246010 Número EC: 242-472-2

GRADE & PURITY ≥97%(T)

Synonyms

Silano, clorodimetiloctadecilsilano | Clorodimetilctadecilsilano | Cloro-dimetil-ctadecilsilano | C20H43ClSi | Clorodimetiloctadecilsilano | Cloro-dimetil-octadecilsilano | CD5636 | Dimetil-n-octadecilclorosilano | Ctadecildimetilclorosilano, 70

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

Silano, clorodimetiloctadecilsilano | Clorodimetilctadecilsilano | Cloro-dimetil-ctadecilsilano | C20H43ClSi | Clorodimetiloctadecilsilano | Cloro-dimetil-octadecilsilano | CD5636 | Dimetil-n-octadecilclorosilano | Ctadecildimetilclorosilano, 70

Especificaciones y pureza

≥97%(T)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥97%(T)

Nombres e identificadores

• Sonrisas canónicas: CCCCCCCCCCCCCCCCCC[Si](C)(C)Cl
• IUPAC Name: chloro-dimethyl-octadecylsilane
• InChIKey: GZGREZWGCWVAEE-UHFFFAOYSA-N
• INCHI: 1S/C20H43ClSi/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-22(2,3)21/h4-20H2,1-3H3
• Isómeros SMILES: CCCCCCCCCCCCCCCCCC[Si](C)(C)Cl
• WGK Alemania: 1
• Número ONU: 2987
• Grupo de embalaje: II
• Peso molecular: 347.10
• Beilstein: 2246010
• Reaxy-Rn: 2246012
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2246012&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Clase Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Organoheterosilanes
          • Level6 Trialkylheterosilanes
            • Level7 Trialkylchlorosilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Clase: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Organoheterosilanes - Trialkylheterosilanes
• Direct Parent: Trialkylchlorosilanes
• Alternative Parents: Silyl monohalides Organochlorosilanes Organic metalloid salts Alkylhalosilanes Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkylchlorosilane - Silyl monohalide - Organochlorosilane - Organic metalloid salt - Alkylhalosilane - Hydrocarbon derivative - Organic salt - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as trialkylchlorosilanes. These are organoheterosilanes, bearing a silicon atom linked to three alkyl groups and one chlorine atom.
• 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

• Sensibilidad: Moisture sensitive.
• Punto de inflamación (°F): 392 °F
• Punto de inflamación (°C): 201°C(lit.)
• Punto de fusión (°C): 29 °C
• Peso molecular: 347.100 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 17
• Exact Mass: 346.282 Da
• Monoisotopic Mass: 346.282 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 216.000
• 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

XLogP3

Referencias

1. Xiang Wan, Dian Wang, Yuqing He, Jiafei Wang, Qin Xu, Donglin Zhao, Fazhi Xie, Qishu Qu.  (2023)  Simple Preparation Method of Silica Core–Shell Spheres for HPLC in Undergraduate Chemistry.  JOURNAL OF CHEMICAL EDUCATION,      [PMID:] [10.1021/acs.jchemed.2c00956]

2. Likai Qi, Xinyi Jiang, Ning Wu, Jingjing Li, Bin Di, Fang Yan.  (2022)  Synthesis of a novel polydopamine and C18 dual-functionalized magnetic core-shell mesoporous nanocomposite for enrichment and analysis of widely abused illegal drugs in urine samples on site and in the laboratory.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:35168125] [10.1016/j.jpba.2022.114656]

3. Da Wang, Qinfu Zhao, Tongying Jiang, Luping Sha, Siling Wang, Yongbo Song.  (2019)  Large amino acid transporter 1 mediated glutamate modified mesoporous silica nanoparticles for chemophotothermal therapy.  JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.jddst.2019.05.043]

4. Luping Sha, Da Wang, Yuling Mao, Wei Shi, Tianbin Gao, Qinfu Zhao, Siling Wang.  (2018)  Hydrophobic interaction mediated coating of pluronics on mesoporous silica nanoparticle with stimuli responsiveness for cancer therapy.  NANOTECHNOLOGY,  29  (34): (345101).  [PMID:29786605] [10.1088/1361-6528/aac6b1]

5. Yajun Du, Lingping Cheng, Long Chen, Yunchao He, Yaling Wu, Shanshan He, Yanxiong Ke.  (2017)  Preparation of sub-2 μm large-pore monodispersed mesoporous silica spheres using mixed templates and application in HPLC.  MICROPOROUS AND MESOPOROUS MATERIALS,      [PMID:] [10.1016/j.micromeso.2017.02.051]

6. Cailing Chu, Fei Tan, Xiuyan Zhu, Long Su, Zhenghe Xu, Dejun Sun.  (2024)  Temperature-Insensitive Nonpolar Suspensions of Polyoxyethylene Alkyl Ether-Grafted Silica Nanoparticles.  LANGMUIR,      [PMID:38867510] [10.1021/acs.langmuir.4c01270]

7. Jia Chen, Run-qin Wang, Bei-bei Guo, Li Yang, Shuang Hu.  (2026)  Magnetic C18-modified mesoporous silica as an efficient adsorbent for dispersive solid phase microextraction of cardiac glycosides in human plasma.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:41616397] [10.1016/j.chroma.2026.466736]