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1,1-diethoxyundecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53405-97-3

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53405-97-3 Usage

Physical state

Colorless, oily liquid

Solubility

Insoluble in water, soluble in organic solvents

Usage

a. Raw material or intermediate in the synthesis of other organic compounds
b. Solvent in laboratory and industrial processes
c. Potential applications in cosmetics and personal care products
d. Formulation of certain types of coatings and adhesives

Hazards

a. Flammability
b. Skin irritation

Safety precautions

Handle with care to avoid exposure and potential hazards

Check Digit Verification of cas no

The CAS Registry Mumber 53405-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,0 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53405-97:
(7*5)+(6*3)+(5*4)+(4*0)+(3*5)+(2*9)+(1*7)=113
113 % 10 = 3
So 53405-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H32O2/c1-4-7-8-9-10-11-12-13-14-15(16-5-2)17-6-3/h15H,4-14H2,1-3H3

53405-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-diethoxyundecane

1.2 Other means of identification

Product number -
Other names EINECS 258-539-4

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:53405-97-3 SDS

53405-97-3Downstream Products

53405-97-3Relevant academic research and scientific papers

Practical acetalization and transacetalization of carbonyl compounds catalyzed by recyclable PVP-I

Cao, Fu-Rong,Lu, Guangying,Ren, Jiangmeng,Wang, Di,Zeng, Bu-Bing

, (2021/06/21)

A novel PVP-I catalyzed acetalizations/transacetalizations of carbonyl compounds has been developed processing with a mild and easy handling fashion. Different types of Acyclic and cyclic acetals were prepared from carbonyl compounds or their acetals successfully. Further applications of newly developed catalytic combination were testified. This protocol featured with simplicity of operation, mild reaction condition, short reaction time, recyclable of catalyst and broad substrates scope with excellent yields.

Quantitation, Organoleptic Contribution, and Potential Origin of Diethyl Acetals Formed from Various Aldehydes in Cognac

Thibaud, Fannie,Shinkaruk, Svitlana,Darriet, Philippe

, p. 2617 - 2625 (2019/03/12)

Cognac wine distillate (WD), especially that produced during aging, is marked by complex and elegant aroma. This work aimed at expanding the knowledge on the Cognac WD aroma by a sensory-guided approach, involving a fractional-distillation technique and gas chromatography coupled to olfactometry and mass spectrometry (GC-O-MS). In doing so, a fruity-odor zone was highlighted in WD extracts that was attributed to the diethyl acetal family. Ten additional diethyl acetals were detected by GC-MS. Next, an assay method was developed and validated for seven of these diethyl acetals. Their detection thresholds were evaluated in a model solution of water/ethanol (60:40, v/v). 1,1-Diethoxy-3-methylbutane was shown to present a significant organoleptic impact because its olfactory-detection threshold (323 μg/L) is lower than its range of concentrations in WD (461 to 3337 μg/L). Given that diethyl acetals result from reactions between ethanol and aldehydes, quantitative correlations between diethyl acetals and corresponding aldehydes were considered.

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