U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C6H15ClO3Si
Molecular Weight 198.72
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of (3-CHLOROPROPYL)TRIMETHOXYSILANE

SMILES

CO[Si](CCCCl)(OC)OC

InChI

InChIKey=OXYZDRAJMHGSMW-UHFFFAOYSA-N
InChI=1S/C6H15ClO3Si/c1-8-11(9-2,10-3)6-4-5-7/h4-6H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C6H15ClO3Si
Molecular Weight 198.72
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The synthesis of chloropropyl-functionalized silica hybrid monolithic column with modification of N,N-dimethyl-N-dodecylamine for capillary electrochromatography separation.
2010-06-25
Utilization of rice husk ash as silica source for the synthesis of mesoporous silicas and their application to CO2 adsorption through TREN/TEPA grafting.
2010-03-15
Preconcentration and determination of Cu(II) in a fresh water sample using modified silica gel as a solid-phase extraction adsorbent.
2010-03-15
Use of chain transfer agent attached to silica particles in preparation of polystyrene-based stationary phases.
2010-03
Solid-phase extractors based on 8-aminoquinoline and 2-aminopyridine covalently bonded to silica gel for the selective separation and determination of calcium in natural water and pharmaceutical samples.
2010
Grafting of molecularly imprinted polymers on iniferter-modified carbon nanotube.
2009-11-15
Preparation and antibacterial characteristic of water-insoluble antibacterial material QPEI/SiO2.
2008-09
Lanthanide-centered covalently bonded hybrids through sulfide linkage: molecular assembly, physical characterization, and photoluminescence.
2008-07-07
Synthesis, characterization, and sorption properties of silica gel-immobilized Schiff base derivative.
2008-04-15
Adsorption of phenol on a novel adsorption material PEI/SiO2.
2008-04-15
Silica gel functionalized with 4-phenylacetophynone 4-aminobenzoylhydrazone: Synthesis of a new chelating matrix and its application as metal ion collector.
2008-02-11
n-Propylpyridinium chloride-modified poly(dimethylsiloxane) elastomeric networks: preparation, characterization, and study of metal chloride adsorption from ethanol solutions.
2007-10-01
Chelating adsorption properties of PEI/SiO(2) for plumbum ion.
2007-07-16
Ammonolysis of (3-chloropropyl)trimethoxysilane.
2006-08-25
Some features associated with organosilane groups grafted by the sol-gel process onto synthetic talc-like phyllosilicate.
2006-05-01
New stationary phase for anion-exchange chromatography.
2005-05-06
Proline-coated column for the capillary electrochromatographic separation of amino acids by in-column derivatization.
2004-10
Filler-elastomer interactions: influence of silane coupling agent on crosslink density and thermal stability of silica/rubber composites.
2003-11-01
Silica-titania sol-gel hybrid materials: synthesis, characterization and potential application in solid phase extraction.
2003-04-10
Synthesis, characterization and structure effects on selectivity properties of silica gel covalently bonded diethylenetriamine mono- and bis-salicyaldehyde and naphthaldehyde Schiff(,)s bases towards some heavy metal ions.
2001-04-12
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:10:35 GMT 2025
Edited
by admin
on Mon Mar 31 22:10:35 GMT 2025
Record UNII
T21BNL1S7F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(3-CHLOROPROPYL)TRIMETHOXYSILANE
Systematic Name English
NSC-83878
Preferred Name English
SILANE, (3-CHLOROPROPYL)TRIMETHOXY-
Systematic Name English
Code System Code Type Description
NSC
83878
Created by admin on Mon Mar 31 22:10:35 GMT 2025 , Edited by admin on Mon Mar 31 22:10:35 GMT 2025
PRIMARY
PUBCHEM
62449
Created by admin on Mon Mar 31 22:10:35 GMT 2025 , Edited by admin on Mon Mar 31 22:10:35 GMT 2025
PRIMARY
RXCUI
2368125
Created by admin on Mon Mar 31 22:10:35 GMT 2025 , Edited by admin on Mon Mar 31 22:10:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID4027490
Created by admin on Mon Mar 31 22:10:35 GMT 2025 , Edited by admin on Mon Mar 31 22:10:35 GMT 2025
PRIMARY
ECHA (EC/EINECS)
219-787-9
Created by admin on Mon Mar 31 22:10:35 GMT 2025 , Edited by admin on Mon Mar 31 22:10:35 GMT 2025
PRIMARY
CAS
2530-87-2
Created by admin on Mon Mar 31 22:10:35 GMT 2025 , Edited by admin on Mon Mar 31 22:10:35 GMT 2025
PRIMARY
FDA UNII
T21BNL1S7F
Created by admin on Mon Mar 31 22:10:35 GMT 2025 , Edited by admin on Mon Mar 31 22:10:35 GMT 2025
PRIMARY
DAILYMED
T21BNL1S7F
Created by admin on Mon Mar 31 22:10:35 GMT 2025 , Edited by admin on Mon Mar 31 22:10:35 GMT 2025
PRIMARY