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Triethyl orthoformate - anhydrous,98%, high purity , CAS No.122-51-0

In stock
Item Number
T119719
Grouped product items
SKU Size
Availability
Price Qty
T119719-25ml
25ml
2
$19.90
T119719-100ml
100ml
2
$51.90
T119719-500ml
500ml
2
$179.90

Basic Description

Synonyms 1,1',1''-[methanetriyltris(oxy)]triethane | Triethyl ortho formate | Orthoformic acid triethyl ester | orthoformic acidtriethyl ester | Triethyl orthoformate | tri-ethyl orthoformate | triethyl ortho-formate | NCGC00166027-01 | Triethyl orthoformate, reag
Specifications & Purity Anhydrous, ≥98%
Storage Temp Room temperature,Argon charged
Shipped In Normal
Grade anhydrous
Product Description

Triethyl orthoformate is a useful organic synthesis reagent for acetylization, imidic ester formation, and activated aromatic species formation.
A reagent useful for acetylization and imidic ester formation.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class Organooxygen compounds
Subclass Ortho esters
Intermediate Tree Nodes Not available
Direct Parent Ortho esters
Alternative Parents Carboxylic acid orthoesters  Hydrocarbon derivatives  
Molecular Framework Aliphatic acyclic compounds
Substituents Ortho ester - Carboxylic acid orthoester - Orthocarboxylic acid derivative - Hydrocarbon derivative - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as ortho esters. These are compounds having the general structure RC(OR')3 ( R' not H), or the structure C(OR')4 ( R' not H).
External Descriptors Not available

Associated Targets(Human)

THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name diethoxymethoxyethane
INCHI InChI=1S/C7H16O3/c1-4-8-7(9-5-2)10-6-3/h7H,4-6H2,1-3H3
InChIKey GKASDNZWUGIAMG-UHFFFAOYSA-N
Smiles CCOC(OCC)OCC
Isomeric SMILES CCOC(OCC)OCC
WGK Germany 1
RTECS RM6475000
PubChem CID 31214
UN Number 2524
Packing Group III
Molecular Weight 148.2
Beilstein 605384
Reaxy-Rn 605384

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.

15 results found

Lot Number Certificate Type Date Item
H2413587 Certificate of Analysis Jul 19, 2024 T119719
H2413588 Certificate of Analysis Jul 19, 2024 T119719
H2413589 Certificate of Analysis Jul 19, 2024 T119719
E2517009 Certificate of Analysis Jul 19, 2024 T119719
A2509160 Certificate of Analysis Jul 19, 2024 T119719
C2526026 Certificate of Analysis Jul 19, 2024 T119719
H2413586 Certificate of Analysis Jul 19, 2024 T119719
H2413590 Certificate of Analysis Jul 19, 2024 T119719
C1914128 Certificate of Analysis Jan 11, 2023 T119719
L2202540 Certificate of Analysis Nov 21, 2022 T119719
L2202541 Certificate of Analysis Nov 21, 2022 T119719
L2202533 Certificate of Analysis Nov 21, 2022 T119719
G2405003 Certificate of Analysis Nov 21, 2022 T119719
L2202543 Certificate of Analysis Nov 21, 2022 T119719
L1820024 Certificate of Analysis Oct 20, 2022 T119719

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Chemical and Physical Properties

Sensitivity Moisture sensitive.
Refractive Index 1.39
Flash Point(°F) 30℃
Flash Point(°C) 30℃
Boil Point(°C) 146°C
Melt Point(°C) -61°C
Molecular Weight 148.200 g/mol
XLogP3 1.200
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 6
Exact Mass 148.11 Da
Monoisotopic Mass 148.11 Da
Topological Polar Surface Area 27.700 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 51.600
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

Citations of This Product

1. Baojin Tan, Chao Zhao, Jing Wang, Aliya Tiemuer, Yuanyuan Zhang, Hui Yu, Yi Liu.  (2023)  Rational design of pH-activated upconversion luminescent nanoprobes for bioimaging of tumor acidic microenvironment and the enhancement of photothermal therapy.  Acta Biomaterialia,  155  (554). 
2. Ruiji Li, Dong Wang, Xiaoyun Li, Zehui Zhang, Wei Li.  (2022)  A visible-light-responsive DiSCn(3)-type fluorescent probe for the rapid, sensitive, and specific detection of tin(II) ions in aqueous solution.  JOURNAL OF CHEMICAL RESEARCH,     
3. Liu Chun-Yu, Yuan Shang-Fu, Wang Song, Guan Zong-Jie, Jiang De-en, Wang Quan-Ming.  (2022)  Structural transformation and catalytic hydrogenation activity of amidinate-protected copper hydride clusters.  Nature Communications,  13  (1): (1-8). 
4. Si-Fu Tang, Xiao-Bo Pan, Xiao-Xia Lv, Xue-Bo Zhao.  (2013)  Investigation on three new metal carboxydiphosphonates: Syntheses, structures, magnetic and luminescent properties.  JOURNAL OF SOLID STATE CHEMISTRY,  197  (139). 
5. Xuan Liu, Lixia Yang, Rao Chen, Mei Han, Chaoqun Yao, Guangwen Chen.  (2024)  Continuous alkylation of 1,3,5-trihydroxy-2,4,6-trinitrobenzene in microreactor: Process intensification and reaction kinetics.  CHEMICAL ENGINEERING JOURNAL,  495  (153544). 

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