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Triethyl orthobutyrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 24964-76-9 Structure
  • Basic information

    1. Product Name: Triethyl orthobutyrate
    2. Synonyms: Triethyl orthobutyra;Ethyl Orthobutyrate Orthobutyric Acid Triethyl Ester 1,1,1-Triethoxybutane;The originalbutyric acidethyl ester three;Triethyl orthobutyrate≥ 99% (GC);N-BUTYRIC ACID TRIETHYL ORTHO ESTER;ORTHO-N-BUTYRIC ACID TRIETHYL ESTER;O-N-BUTYRIC ACID TRIETHYL ESTER;TRIETHYL ORTHOBUTYRATE
    3. CAS NO:24964-76-9
    4. Molecular Formula: C10H22O3
    5. Molecular Weight: 190.28
    6. EINECS: 221-641-4
    7. Product Categories: Organic synthesis;Intermediates of Dyes and Pigments;Orthoesters
    8. Mol File: 24964-76-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 63 °C / 10mmHg
    3. Flash Point: 58°C
    4. Appearance: colorless Liquid
    5. Density: 0,88 g/cm3
    6. Vapor Pressure: 0.496mmHg at 25°C
    7. Refractive Index: 1.4040-1.4080
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Triethyl orthobutyrate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Triethyl orthobutyrate(24964-76-9)
    12. EPA Substance Registry System: Triethyl orthobutyrate(24964-76-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. RIDADR: 3272
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 3
    8. PackingGroup: III
    9. Hazardous Substances Data: 24964-76-9(Hazardous Substances Data)

24964-76-9 Usage

Chemical Properties

Colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 24964-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,6 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24964-76:
(7*2)+(6*4)+(5*9)+(4*6)+(3*4)+(2*7)+(1*6)=139
139 % 10 = 9
So 24964-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O3/c1-5-9-10(11-6-2,12-7-3)13-8-4/h5-9H2,1-4H3

24964-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-triethoxybutane

1.2 Other means of identification

Product number -
Other names triethyl orthobutyrate

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:24964-76-9 SDS

24964-76-9Relevant articles and documents

A Process for Preparation of High Flash Point Frothing Agent

-

Paragraph 0039-0041, (2017/07/14)

The present invention discloses a process for preparing high flash point frothing agent by treating an aldehyde with an alcohol in the presence of an acid catalyst at elevated temperature and further adding a carbonate salt to obtain the frothing agent and polymer.

Orthoester exchange: A tripodal tool for dynamic covalent and systems chemistry

Brachvogel, Ren-Chris,Von Delius, Max

, p. 1399 - 1403 (2015/02/05)

Reversible covalent reactions have become an important tool in supramolecular chemistry and materials science. Here we introduce the acid-catalyzed exchange of O,O,O-orthoesters to the toolbox of dynamic covalent chemistry. We demonstrate that orthoesters readily exchange with a wide range of alcohols under mild conditions and we disclose the first report of an orthoester metathesis reaction. We also show that dynamic orthoester systems give rise to pronounced metal template effects, which can best be understood by agonistic relationships in a three-dimensional network analysis. Due to the tripodal architecture of orthoesters, the exchange process described herein could find unique applications in dynamic polymers, porous materials and host-guest architectures.

Process for preparation of adjacently disubstituted ketones

-

, (2008/06/13)

A novel 7-hydroxyprostaglandin E1, or a stereoisomer thereof, or a protected derivative thereof, having the following formula: STR1 wherein R8 represents H, CH3 or C2 H5, R9 represents H or CH3, R10 and R11 are identical or different, and each represents H, tetrahydropyranyl or t-butyldimethylsilyl. Also provided is a process for producing an adjacently disubstituted ketone including the above compounds, i.e. 7-oxoprostaglandin, etc. which comprises reacting an α,β-unsaturated carbonyl compound with a cuprous salt and an organolithium compound in an aprotic inert organic medium in the presence of trialkylphosphine, the amounts of said cuprous salt and said organolithium compound being substantially equimolar, and reacting the product with a protected acetal derivative of an organic carbonyl compound or an aldehyde in the presence of a Lewis acid, if necessary, followed by reacting the product with a proton donor.

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