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Triethoxy(3-glycidyloxypropyl)silane - >96.0%(GC), high purity , CAS No.2602-34-8

    Grade & Purity:
  • ≥96%(GC)
In stock
Item Number
T162295
Grouped product items
SKU Size
Availability
Price Qty
T162295-5g
5g
5
$19.90
T162295-25g
25g
4
$42.90
T162295-100g
100g
1
$136.90
T162295-500g
500g
2
$615.90

Basic Description

Synonyms (3-(2,3-Epoxypropoxy)propyl)triethoxysilane | JXUKBNICSRJFAP-UHFFFAOYSA-N | TRIETHOXY(3-GLYCIDOXYPROPYL)SILANE | Q27894344 | (3-Glycidoxypropyl)triethoxysilane | Triethoxy(3-glycidyloxypropyl)silane | CCRIS 3046 | Glycidyl 3-Triethoxysilylpropyl Ether | s
Specifications & Purity ≥96%(GC)
Storage Temp Argon charged
Shipped In Normal
Product Description

(3-Glycidyloxypropyl)triethoxysilane (GPTES) can be used as a reagent in the synthesis of: • Polymer nanocomposite membranes for direct methanol fuel cells (DMFCs). • Azido terminated poly(ethylene glycol) silane that can be self-assembled on a metal-oxide surface to facilitate the orthogonal biofunctionalization. • Epoxy functionalized silsesquioxane nanoparticles (SQ-NPs). • Epoxy-functionalized mesoporous cellular foams (G-MCFs) as the support for the immobilization of penicillin G acylase (PGA). GPTES can also be used as a precursor to prepare water-repellent, self-cleaning coatings.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organometallic compounds
Class Organometalloid compounds
Subclass Organosilicon compounds
Intermediate Tree Nodes Alkoxysilanes
Direct Parent Trialkoxysilanes
Alternative Parents Silyl ethers  Oxacyclic compounds  Organoheterosilanes  Organic metalloid salts  Epoxides  Dialkyl ethers  Hydrocarbon derivatives  
Molecular Framework Aliphatic heteromonocyclic compounds
Substituents Trialkoxysilane - Silyl ether - Organoheterosilane - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Aliphatic heteromonocyclic compound
Description 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

Names and Identifiers

Pubchem Sid 488187315
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488187315
IUPAC Name triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane
INCHI InChI=1S/C12H26O5Si/c1-4-15-18(16-5-2,17-6-3)9-7-8-13-10-12-11-14-12/h12H,4-11H2,1-3H3
InChIKey JXUKBNICSRJFAP-UHFFFAOYSA-N
Smiles CCO[Si](CCCOCC1CO1)(OCC)OCC
Isomeric SMILES CCO[Si](CCCOCC1CO1)(OCC)OCC
WGK Germany 3
PubChem CID 102856
Molecular Weight 278.42
Beilstein 144145

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

23 results found

Lot Number Certificate Type Date Item
F2527260 Certificate of Analysis Mar 19, 2025 T162295
F2530380 Certificate of Analysis Mar 19, 2025 T162295
H1724031 Certificate of Analysis Mar 04, 2025 T162295
J2425687 Certificate of Analysis Sep 13, 2024 T162295
J2425694 Certificate of Analysis Sep 13, 2024 T162295
F2419347 Certificate of Analysis Jun 06, 2024 T162295
F2419346 Certificate of Analysis Jun 06, 2024 T162295
D2415317 Certificate of Analysis Mar 13, 2024 T162295
C2404042 Certificate of Analysis Jan 11, 2024 T162295
C2404041 Certificate of Analysis Jan 11, 2024 T162295
C2404043 Certificate of Analysis Jan 11, 2024 T162295
C2404049 Certificate of Analysis Jan 11, 2024 T162295
I2306779 Certificate of Analysis Aug 26, 2023 T162295
I2306778 Certificate of Analysis Aug 26, 2023 T162295
A2330013 Certificate of Analysis Nov 19, 2022 T162295
A2330023 Certificate of Analysis Nov 19, 2022 T162295
A2330027 Certificate of Analysis Nov 19, 2022 T162295
A2330072 Certificate of Analysis Nov 19, 2022 T162295
A2330056 Certificate of Analysis Nov 19, 2022 T162295
A2330055 Certificate of Analysis Nov 19, 2022 T162295
E2227062 Certificate of Analysis Mar 10, 2022 T162295
E2227069 Certificate of Analysis Mar 10, 2022 T162295
E2227061 Certificate of Analysis Mar 10, 2022 T162295

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Chemical and Physical Properties

Sensitivity air & Moisture sensitive
Refractive Index n20/D 1.427
Flash Point(°F) 291.2 °F
Flash Point(°C) 144 °C
Boil Point(°C) 135 °C/2 mmHg
Molecular Weight 278.420 g/mol
XLogP3
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 12
Exact Mass 278.155 Da
Monoisotopic Mass 278.155 Da
Topological Polar Surface Area 49.500 Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 198.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 1
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Chenfang Miao, Xin Zhou, Xiaoyang Huang, Jiyue Huang, Yanping Chen, Yuebin Liu, Xiaomu Hu, Lingjun Zeng, Shaohuang Weng, Huixing Chen.  (2023)  Effectively synthesized functional Si-doped carbon dots with the applications in tyrosinase detection and lysosomal imaging.  ANALYTICA CHIMICA ACTA,  1279  (341789). 
2. Kai He, Huanchen Liao, Zejia Liu, Yiping Liu, Liqun Tang, Bao Yang, Licheng Zhou, Zhenyu Jiang.  (2023)  Reinforcing efficiency of nanophases with various geometric shapes on interfacial bonding in multiscale composites.  COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING,  165  (107369). 
3. Jipeng Guan, Yaru Yang, Bolin Tang, Xiaojun Shen, Yongjin Li.  (2022)  The synthesis of functional Janus nanosheets as compatibilizers for the immiscible polyamide 6 /polystyrene (PA6/PS): Formation of the nanosilica monolayer at the interface.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,  643  (128788). 
4. Pei Lyu, Xiangyi Zhang, Xin Jiang, Bin Shang, Xin Liu, Ziwei Deng.  (2021)  One-Step Preparation of Hydrophobic Surfaces Containing Hydrophilic Groups for Efficient Water Harvesting.  LANGMUIR,  37  (31): (9630–9636). 
5. Yi Hao, Yuan Gao, Luyao Gao, Yulian He, Yingying Niu, Sameer Hussain, Ruixia Gao, Lisa D. Pfefferle, M. Shahid, Sicen Wang.  (2021)  Amphiphilic core–shell magnetic adsorbents for efficient removal and detection of phthalate esters.  CHEMICAL ENGINEERING JOURNAL,  423  (129817). 
6. Manoj B. Kale, Zhen Luo, Xu Zhang, D. Dhamodharan, Nidhin Divakaran, Suhail Mubarak, Lixin Wu, Ying Xu.  (2019)  Waterborne polyurethane/graphene oxide-silica nanocomposites with improved mechanical and thermal properties for leather coatings using screen printing.  POLYMER,  170  (43). 
7. Yueyue Zhu, Penghao Sun, Zhen Huang, He Liu, Xu Xu.  (2025)  Enhancing Barrier Properties of Cellulose Paper: A Rosin-Based Polymer Coating Approach.  ACS Applied Polymer Materials,  (5): (3043-3053). 
8. Jiaman Hu, Zihao Wang, Minglin Yang, Chuansong Yu, Siyu Li, Yinggang Miao, Xiangqian Quan, Jize Liu, Shiyang Shao.  (2024)  Long afterglow epoxidized soybean oil polymer composites with reversible dynamic cross-linking for intelligent coating.  Polymer Chemistry,  15  (48): (4982-4992). 
9. Haitao Shi, Rong Cao, Haijun Zhang, Jiajia Yang, Yanlin Fu, Jiping Chen.  (2024)  Molecule-level Design to Form Pocket Structures for Improving Amine Efficiency in CO2 Capture.  ADVANCED FUNCTIONAL MATERIALS,    (2415211). 
10. Chuanjuan Chen, Yicheng Zhang, Siqi Chen, Qinhui Chen.  (2025)  Unilateral thermosensitive Janus hemostatic dressing for matching coagulation physiological processes.  Journal of Materials Chemistry B,     

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