(3-Bromopropyl)trimethoxysilane - ≥98%(GC) , CAS No.51826-90-5

CAS: 51826-90-5 Cat. No.: B152651 Peso molecular: 243.17 Número EC: 257-453-4

GRADE & PURITY ≥98%(GC)

Synonyms

D88998 | AKOS015836207 | SCHEMBL446835 | SY050526 | gamma-bromopropyltrimethoxysilane | (3-bromopropyl)(trimethoxy)silane | EINECS 257-453-4 | (3-Bromopropyl)trimethoxysilane | DTXSID20199783 | 3-bromopropyl(trimethoxy)silane | STL373390 | 3-bromopropyltr

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

Product Introduction

3-bromopropyl trimethoxysilane is a bromo silane. It is popularly used as a silane coupling agent.
3-bromopropyl trimethoxysilane (BPTS) acted as initiating sites for functionalization magnetite (Fe3O4) nanoparticles. A study reports the role of BPTS in attaching a polyelectrolyte to an inorganic alumina substrate during the fabrication of a polymeric humidity sensor.

Specifications

Sinónimos

D88998 | AKOS015836207 | SCHEMBL446835 | SY050526 | gamma-bromopropyltrimethoxysilane | (3-bromopropyl)(trimethoxy)silane | EINECS 257-453-4 | (3-Bromopropyl)trimethoxysilane | DTXSID20199783 | 3-bromopropyl(trimethoxy)silane | STL373390 | 3-bromopropyltr

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%(GC)

Nombres e identificadores

• Sonrisas canónicas: CO[Si](CCCBr)(OC)OC
• IUPAC Name: 3-bromopropyl(trimethoxy)silane
• InChIKey: GLISZRPOUBOZDL-UHFFFAOYSA-N
• INCHI: 1S/C6H15BrO3Si/c1-8-11(9-2,10-3)6-4-5-7/h4-6H2,1-3H3
• Isómeros SMILES: CO[Si](CCCBr)(OC)OC
• WGK Alemania: 3
• Peso molecular: 243.17
• Reaxy-Rn: 4952577
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4952577&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Clase Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Alkoxysilanes
          • Level6 Trialkoxysilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Clase: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Alkoxysilanes
• Direct Parent: Trialkoxysilanes
• Alternative Parents: Silyl ethers Organoheterosilanes Organic metalloid salts Organooxygen compounds Organobromides Hydrocarbon derivatives Alkyl bromides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkoxysilane - Silyl ether - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organobromide - Organohalogen compound - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as trialkoxysilanes. These are organosilicon compounds with the general formula RO[Si](R')(OR'')OR''' (R-R''' = aliphatic organyl group).
• 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.
• Índice de refracción: n20/D 1.440
• Punto de inflamación (°F): 179.6 °F
• Punto de inflamación (°C): 82°C
• Punto de ebullición (°C): 130 °C/45 mmHg
• Peso molecular: 243.170 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 241.997 Da
• Monoisotopic Mass: 241.997 Da
• Topological Polar Surface Area: 27.700 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 89.600
• 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. Xue Li, Yuan-Yuan Cui, Cheng-Xiong Yang.  (2020)  Covalent coupling fabrication of microporous organic network bonded capillary columns for gas chromatographic separation.  TALANTA,      [PMID:33379116] [10.1016/j.talanta.2020.121914]

2. Xinxin Xu, Qiang Lou, Jiahao Wu, Haocheng Huang, Hao Zhang, Bosen Zhang, Maojun Sun, Lin Zhao, Jingyi Xu, Hang Zhou.  (2025)  Buried Interface Passivation of Regular Perovskite Solar Cells Using Trimethoxysilane-Based Small Molecule Materials.  ACS Applied Materials & Interfaces,      [PMID:40101194] [10.1021/acsami.5c01522]

3. Xin Wang, Lihong He, Jianrong Huang, Nanjing Zhong.  (2020)  Immobilization of lipases onto the halogen & haloalkanes modified SBA-15: Enzymatic activity and glycerolysis performance study.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:33345972] [10.1016/j.ijbiomac.2020.12.111]