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ETHYL FORMATE-D1 is a deuterated form of ethyl formate, an ester with the chemical formula CH3CH2O2C. It is characterized by a higher abundance of deuterium, a hydrogen isotope, compared to regular ethyl formate. This unique isotopic composition makes it valuable for various applications in chemical and biological research, as well as in NMR spectroscopy for studying molecular structures and dynamics. Despite its deuterated nature, ETHYL FORMATE-D1 retains the same chemical properties as regular ethyl formate, including its use as a solvent and a flavoring agent in the food industry.

35976-76-2

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35976-76-2 Usage

Uses

Used in Chemical and Biological Research:
ETHYL FORMATE-D1 is used as a tracer in chemical and biological research for its unique isotopic composition. The presence of deuterium allows for more accurate tracking and analysis of chemical reactions and biological processes, providing valuable insights into the underlying mechanisms.
Used in NMR Spectroscopy:
In NMR spectroscopy, ETHYL FORMATE-D1 serves as a valuable tool for studying molecular structures and dynamics. The deuterated form of ethyl formate enables researchers to observe细微的 changes in molecular behavior that may be obscured in the presence of the more abundant hydrogen isotope. This capability is particularly useful in the investigation of complex molecular systems and the development of new materials and compounds.
Used in the Food Industry:
ETHYL FORMATE-D1 is used as a flavoring agent in the food industry, providing a unique taste and aroma to various food products. Its use as a solvent in food processing also aids in the extraction and preservation of flavors and other desirable properties in food products.
Used in the Solvent Industry:
As a solvent, ETHYL FORMATE-D1 is utilized in various industrial applications, including the production of chemicals, pharmaceuticals, and other specialty products. Its unique properties make it a versatile and effective solvent for a wide range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 35976-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35976-76:
(7*3)+(6*5)+(5*9)+(4*7)+(3*6)+(2*7)+(1*6)=162
162 % 10 = 2
So 35976-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H6O2/c1-2-5-3-4/h3H,2H2,1H3/i3H

35976-76-2 Well-known Company Product Price

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  • Aldrich

  • (489328)  Ethylformate-d  98 atom % D

  • 35976-76-2

  • 489328-5G

  • 4,463.55CNY

  • Detail

35976-76-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL FORMATE-D1

1.2 Other means of identification

Product number -
Other names Deuterio-ameisensaeure-ethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35976-76-2 SDS

35976-76-2Relevant academic research and scientific papers

THE SYNTHETIC UTILITY OF DIOXYPHOSPHORANES IN ORGANIC SYNTHESIS

Robinson, Philip L.,Kelly, Jeffery W.,Evans, Slayton A.

, p. 15 - 24 (2007/10/02)

Diethoxytriphenylphosphorane, DTPP, prepared by reaction of triphenylphosphine and diethyl peroxide, is a "hydrolytically active" dioxyphosphorane which promotes mild and efficient cyclodehydration of diols to cyclic ethers in neutral media.Simple 1,2-, 1,4-, and 1,5-diols afford good yields of the cyclic ethers but 1,3-propanediol and 1,6-hexanediol give mainly 3-ethoxy-1-propanol and 6-ethoxy-1-hexanol, respectively, with DTPP.Tri- and tetra-substituted 1,2-diols afford the relatively stable 1,3,2-dioxaphospholanes in the presence of DTPP and the reaction conditions dictate whether epoxides, ketones, or allylic alcohols are obtained.

THE KINETIC ISOTOPE EFFECT IN THE RADICAL FRAGMENTATION OF LINEAR ORTHO ESTERS

Pastushenko, E. V.,Kostyukevich, L. L.,Kurbanov, D.,Zlot-skii, S. S.,Rakhmankulov, D. L.

, p. 28 - 30 (2007/10/02)

The substitution of hydrogen atoms of deuterium in triethoxymethane leads to a change in the formation rate of diethyl carbonate and ethyl formate.The magnitude of the kinetic isotope effect lies in the range of 2-3 and coincides with the known values for the free-radical reactions of linear and cyclic acetals.

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