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G1535

Sigma-Aldrich

(3-Glycidyloxypropyl)trimethoxysilane

≥97% (GC)

Synonym(s):

3-(2,3-Epoxypropoxy)propyltrimethoxysilane, GLYMO, Glycidyl 3-(trimethoxysilyl)propyl ether

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About This Item

Empirical Formula (Hill Notation):
C9H20O5Si
CAS Number:
2530-83-8
Molecular Weight:
236.34
Beilstein:
4308125
EC Number:
219-784-2
MDL number:
MFCD00005144
UNSPSC Code:
12352300
PubChem Substance ID:
24895068
Pricing and availability is not currently available.

Assay

≥97% (GC)

form

liquid

refractive index

n20/D 1.429 (lit.)

bp

120 °C/2 mmHg (lit.)

density

1.07 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CO[Si](CCCOCC1CO1)(OC)OC

InChI

1S/C9H20O5Si/c1-10-15(11-2,12-3)6-4-5-13-7-9-8-14-9/h9H,4-8H2,1-3H3

InChI key

BPSIOYPQMFLKFR-UHFFFAOYSA-N

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Description
Pricing

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318,H412

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
077K3670
125K3716
055K3444
104K3680
128H3696

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From the end of the twentieth century, the growing interest in a new generation of wearable electronics with attractive application for military, medical and smart textiles fields has led to a wide investigation of chemical finishes for the production of
Min-Huey Chen et al.
Dental materials : official publication of the Academy of Dental Materials, 22(2), 138-145 (2005-07-26)
The aim of this study was to develop a low shrinkage visible light curable nanocomposite dental restorative material without sacrificing the other properties of conventional materials. This nanocomposite was developed by using an epoxy resin 3,4-epoxycyclohexylmethyl-(3,4-epoxy)cyclohexane carboxylate (ERL4221) matrix with
W H Siddiqui et al.
Toxicology, 31(1), 1-8 (1984-05-01)
The embryotoxic and teratogenic potential of gamma- glycidoxypropyltrimethoxysilane ( GPTS ) was evaluated in rats. Pregnant Sprague-Dawley rats were administered 0, 50, 500, or 1,000 mg/kg/day of GPTS by gavage on days 6 through 15 of gestation. No treatment related
Yuki Shirosaki et al.
Biomaterials, 26(5), 485-493 (2004-07-28)
Chitosan-silicate hybrids were synthesized using gamma-glycidoxypropyltrimethoxysilane (GPSM) as the agent for cross-linking the chitosan chains. CaCl2 was introduced in the hybrids in expectation that it would improve cell adhesion and differentiation of the hybrid surfaces. Fourier-transform infrared (FT-IR) spectroscopy and
Yongpan Shan et al.
International journal of molecular sciences, 20(6) (2019-03-20)
Environmental stimuli-responsive pesticide release is desirable for enhanced efficiency and reduced side effects. In most cases, the loading and release of pesticides mainly depends on hydrophobic interactions and hydrogen bonding. Electrostatic interaction is less investigated as a weapon for achieving
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