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Dipentoxyethane, also known as diethylene glycol methyl ether, is a clear, colorless liquid with a faint odor. It is a versatile chemical with a wide range of industrial applications, including as a solvent in paint, varnish, and dye production, a coupling agent in agricultural and household products, and a cleaning agent in industrial and commercial settings. Although it is considered to have low toxicity and minimal risk to human health and the environment when used according to safety guidelines, prolonged or high-level exposure may cause irritation to the skin, eyes, and respiratory system.

13002-08-9

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13002-08-9 Usage

Uses

Used in Paint and Varnish Production:
Dipentoxyethane is used as a solvent in paint and varnish production for its ability to dissolve various substances and improve the flow and application properties of the coatings.
Used in Dye Production:
In the dye industry, Dipentoxyethane is used as a solvent to facilitate the dissolution and application of dyes onto different substrates.
Used in Agricultural and Household Products:
Dipentoxyethane is used as a coupling agent in agricultural and household products to enhance the effectiveness of these products by improving the binding of active ingredients.
Used in Industrial and Commercial Cleaning Agents:
In industrial and commercial settings, Dipentoxyethane is utilized as a cleaning agent due to its ability to dissolve a wide range of soils and contaminants, making it effective for various cleaning applications.
Used in Solvent Applications:
Dipentoxyethane is used as a solvent in various industries for its capacity to dissolve a broad spectrum of compounds, which makes it suitable for a multitude of applications where solubility of substances is required.

Check Digit Verification of cas no

The CAS Registry Mumber 13002-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,0 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13002-08:
(7*1)+(6*3)+(5*0)+(4*0)+(3*2)+(2*0)+(1*8)=39
39 % 10 = 9
So 13002-08-9 is a valid CAS Registry Number.

13002-08-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name DIPENTOXYETHANE

1.2 Other means of identification

Product number -
Other names Acetaldehyde dipentyl acetal

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:13002-08-9 SDS

13002-08-9Relevant academic research and scientific papers

FRAGMENTATION OF LINEAR ACETALS IN HOMOLYTIC LIQUID-PHASE TRANSFORMATIONS

Kalashnikov, S. M.,Imashev, U. B.,Zlotskii, S. S.,Rakhmankulov, D. L.

, p. 783 - 786 (2007/10/02)

The kinetics of the accumulation of the products formed by fragmentation of linear acetals in free-radical liquid-phase reactions initiated by thermal decomposition of tert-butyl peroxide were investigated.The products from the transformation of 1,1-dimethoxyethane are methyl acetate and methane, whereas ethanal, pentanal, and 1-ethoxypentane are formed in addition to amyl acetate and pentane in the case of 1,1-dipentyloxyethane, and ethanal, hexanal, and 1-ethoxyethane are formed in addition to hexyl acetate and hexane from 1,1-dihexyloxyethane.The initial formation rate of pentane and hexane was measured for the first time, and it was shown that the sum of the accumlation rate of the alkane and the initiation rate is close to the accumlation rate of the ester.A scheme which takes account of all the products is proposed for the fragmentation of linear acetals.The C1-H bond in the linear acetals is an order of magnitude more reactive than the other C-H bonds.The difference in the activation energies for the cleavage of the active C-H bonds was evaluated, and the lenght of the chains, the activation energies for decomposition of tert-butyl peroxide in the acetals, and the kinetic parameters of the homolytic liquid-phase reactions of the acetals were determined.

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