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58035

Sigma-Aldrich

(3-Iodopropyl)trimethoxysilane

≥95.0% (GC)

Synonym(s):

3-Iodo-n-propyl-1-trimethoxysilane, Iodopropyltrimethoxysilane, Trimethoxy(iodopropyl)silane

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About This Item

Empirical Formula (Hill Notation):
C6H15IO3Si
CAS Number:
14867-28-8
Molecular Weight:
290.17
Beilstein:
969628
MDL number:
MFCD00054838
UNSPSC Code:
12352103
PubChem Substance ID:
57651637
NACRES:
NA.22

Quality Level

100

Assay

≥95.0% (GC)

refractive index

n20/D 1.473 (lit.)

density

1.482 g/mL at 20 °C (lit.)

SMILES string

CO[Si](CCCI)(OC)OC

InChI

1S/C6H15IO3Si/c1-8-11(9-2,10-3)6-4-5-7/h4-6H2,1-3H3

InChI key

NILZGRNPRBIQOG-UHFFFAOYSA-N

Related Categories

Application

(3-iodopropyl)trimethoxysilane may be used to organically modify mesoporous silica support by grafting method.{85} The product may be used to synthesize heavy atom-concentrated organically modified silica nanoparticles.{86}

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

172.4 °F - closed cup

Flash Point(C)

78 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Ugochukwu C Okeke et al.
Molecules (Basel, Switzerland), 24(8) (2019-04-25)
Methacrylate analogs of quaternary ammonium salts functionalized with carboxylic (AMadh1 68.8% yield, AMadh2 53.2% yield) and methoxysilane (AMsil1 94.8% yield, AMsil2 36.0% yield) groups were synthesized via Menschutkin reaction. Fourier-transform infrared spectroscopy (FTIR), nuclear magnetic resonance spectroscopy (1H, 13C and
Goutam Ghosh et al.
Photochemistry and photobiology, 95(1), 293-305 (2018-08-17)
There is a major need for light-activated materials for the release of sensitizers and drugs. Considering the success of chiral columns for the separation of enantiomer drugs, we synthesized an S,S-chiral linker system covalently attached to silica with a sensitizer
Epoxidation of olefins catalyzed by novel Mn(III) and Mo(IV) Salen complexes immobilized on mesoporous silica gel: Part I. Synthesis and characterization of homogeneous and immobilized Mn(III) and Mo(IV) Salen complexes
Luts T, et al.
J. Mol. Catal. A: Chem., 261(1), 16-23 (2007)
Mari Miura Sugii et al.
Materials science & engineering. C, Materials for biological applications, 73, 340-346 (2017-02-12)
The antibiofilm effect of iodide quaternary ammonium methacryloxy silicate (IQAMS) in Transbond XT Light Cure Adhesive resin used for braces cementation was evaluated. Fourier Transform Infrared (FTIR) spectroscopy confirmed IQAMS formation and Scanning Electron Microscopy coupled to Energy-Dispersive X-ray Spectroscopy
Sandra Jimenez-Falcao et al.
Journal of materials chemistry. B, 7(30), 4669-4676 (2019-08-01)
We report herein the assembly of an integrated nanodevice with bi-enzymatic cascade control for on-command cargo release. This nanocarrier is based on Au-mesoporous silica Janus nanoparticles capped at the mesoporous face with benzimidazole/β-cyclodextrin-glucose oxidase pH-sensitive gate-like ensembles and functionalized with
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