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22208-25-9

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  • Butanoic acid, 3-oxo-,1,1'-[2-[(1,3-dioxobutoxy)methyl]-2-ethyl-1,3-propanediyl] ester

    Cas No: 22208-25-9

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  • BUTANOIC ACID, 3-OXO-, 2-[(1,3-DIOXOBUTOXY)METHYL]-2-ETHYL-1,3-PROPANDIYL ESTER

    Cas No: 22208-25-9

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22208-25-9 Usage

Description

BUTANOIC ACID, 3-OXO-, 2-[(1,3-DIOXOBUTOXY)METHYL]-2-ETHYL-1,3-PROPANDIYL ESTER is a complex organic compound with a unique chemical structure. It is characterized by the presence of a butanoic acid backbone, with a 3-oxo group and a 2-ethyl-1,3-propandiol moiety. Additionally, it features a (1,3-dioxobutoxy)methyl group, which contributes to its distinct properties. This liquid compound is known for its reactive methylene groups, making it a versatile component in various chemical formulations.

Uses

Used in Adhesives, Sealants, or Coatings Industry:
BUTANOIC ACID, 3-OXO-, 2-[(1,3-DIOXOBUTOXY)METHYL]-2-ETHYL-1,3-PROPANDIYL ESTER is used as a trifunctional crosslinker for adhesives, sealants, or coatings. Its reactive methylene groups enable the formation of strong crosslinks, enhancing the overall performance and durability of these products.
Used as a Curative for Waterborne Coating Systems:
In the coatings industry, BUTANOIC ACID, 3-OXO-, 2-[(1,3-DIOXOBUTOXY)METHYL]-2-ETHYL-1,3-PROPANDIYL ESTER serves as a curative for waterborne coating systems. Its ability to crosslink with other components in the system improves the hardness, adhesion, and chemical resistance of the final coating.
Used as a Catalyst for Amine-based Epoxy Hardeners:
BUTANOIC ACID, 3-OXO-, 2-[(1,3-DIOXOBUTOXY)METHYL]-2-ETHYL-1,3-PROPANDIYL ESTER also functions as a catalyst for amine-based epoxy hardeners. Its catalytic properties accelerate the curing process, leading to faster and more efficient hardening of epoxy resins, which is particularly beneficial in industrial applications where time and efficiency are critical factors.

Hazard

A poison by ingestion and skin contact.

Flammability and Explosibility

Notclassified

Safety Profile

A poison by ingestion and skin contact. When heated to decomposition it emits acrid smoke and irritating vapors.

Check Digit Verification of cas no

The CAS Registry Mumber 22208-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,0 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22208-25:
(7*2)+(6*2)+(5*2)+(4*0)+(3*8)+(2*2)+(1*5)=69
69 % 10 = 9
So 22208-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H26O9/c1-5-18(9-25-15(22)6-12(2)19,10-26-16(23)7-13(3)20)11-27-17(24)8-14(4)21/h5-11H2,1-4H3

22208-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name BUTANOIC ACID, 3-OXO-, 2-[(1,3-DIOXOBUTOXY)METHYL]-2-ETHYL-1,3-PROPANDIYL ESTER

1.2 Other means of identification

Product number -
Other names Trimethylolpropane trisacetoacetate

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:22208-25-9 SDS

22208-25-9Downstream Products

22208-25-9Relevant articles and documents

Suppressing Creep and Promoting Fast Reprocessing of Vitrimers with Reversibly Trapped Amines

Van Lijsebetten, Filip,De Bruycker, Kevin,Spiesschaert, Yann,Winne, Johan M.,Du Prez, Filip E.

supporting information, (2022/01/19)

We report a straightforward chemical strategy to tackle current challenges of irreversible deformation in low Tg vitrimers at operating temperature. In particular, vinylogous urethane (VU) vitrimers were prepared where reactive free amines, necessary for material flow, were temporarily shielded inside the network backbone, by adding a small amount of dibasic ester to the curing mixture. The amines could be released as reactive chain ends from the resulting dicarboxamide bonds via thermally reversible cyclisation to an imide moiety. Indeed, (re)generation of the required nucleophilic amines as network defects ensured reprocessing and rapid material flow at higher temperature, where exchange dynamics are (re)activated. As a result, VU vitrimers were obtained with limited creep at service temperature, yet with good reprocessability at elevated temperatures. Thus, by exerting strong control on the molecular level over the availability of exchangeable functional groups, a remarkable improvement of VU properties was obtained.

PROCESS FOR PREPARING MICROCAPSULES

-

Page/Page column 23, (2020/02/16)

The present invention relates to a new process for the preparation of core-shell microcapsules. Microcapsules are also an object of the invention. Perfuming compositions and consumer products comprising said capsules, in particular perfumed consumer produ

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