What is the ACETOACETIC ACID HEXYL ESTER?

ACETOACETIC ACID HEXYL ESTER is , while it's Molecular Formula is C10H18O3. Used in Paints and Inks Industry: ACETOACETIC ACID HEXYL ESTER is used as a chemical compound for the production of paints and inks. Its distinct, fruity smell adds a pleasant aroma to these products, enhancing their overall appeal. Used in Perfumes and Fragrances Industry: ACETOACETIC ACID HEXYL ESTER is used as a fragrance ingredient in perfumes and other fragrance products. Its fruity scent contributes to the overall scent profile of these products, making them more attractive to consumers. Used in Safety Measures: Due to its potential to cause irritation upon skin contact or if ingested or inhaled, ACETOACETIC ACID HEXYL ESTER is used as a reminder for the importance of safety measures during its handling and usage. This ensures that individuals working with ACETOACETIC ACID HEXYL ESTER are aware of the potential risks and take necessary precautions to minimize exposure and protect their health.

What is the CAS number for ACETOACETIC ACID HEXYL ESTER?

The CAS number of ACETOACETIC ACID HEXYL ESTER is 13562-84-0.

What is ACETOACETIC ACID HEXYL ESTER (13562-84-0) used for?

ACETOACETIC ACID HEXYL ESTER, also known as Hexyl 3-oxobutanoate and Hexyl acetoacetate, is an organic compound that belongs to the ester group. Ester compounds are characterized by their distinct, often fruity odors. This chemical is frequently utilized in the production of various items, such as paints, inks, and other similar products. It is also found in perfumes and fragrance products, contributing to their pleasant scents. While mostly safe, it can cause irritation upon skin contact or if ingested or inhaled, necessitating safety measures during handling and usage.

What is the ACETOACETIC ACID HEXYL ESTER?

ACETOACETIC ACID HEXYL ESTER is , while it's Molecular Formula is C10H18O3. Used in Paints and Inks Industry: ACETOACETIC ACID HEXYL ESTER is used as a chemical compound for the production of paints and inks. Its distinct, fruity smell adds a pleasant aroma to these products, enhancing their overall appeal. Used in Perfumes and Fragrances Industry: ACETOACETIC ACID HEXYL ESTER is used as a fragrance ingredient in perfumes and other fragrance products. Its fruity scent contributes to the overall scent profile of these products, making them more attractive to consumers. Used in Safety Measures: Due to its potential to cause irritation upon skin contact or if ingested or inhaled, ACETOACETIC ACID HEXYL ESTER is used as a reminder for the importance of safety measures during its handling and usage. This ensures that individuals working with ACETOACETIC ACID HEXYL ESTER are aware of the potential risks and take necessary precautions to minimize exposure and protect their health.

What is the CAS number for ACETOACETIC ACID HEXYL ESTER?

The CAS number of ACETOACETIC ACID HEXYL ESTER is 13562-84-0.

What is ACETOACETIC ACID HEXYL ESTER (13562-84-0) used for?

ACETOACETIC ACID HEXYL ESTER, also known as Hexyl 3-oxobutanoate and Hexyl acetoacetate, is an organic compound that belongs to the ester group. Ester compounds are characterized by their distinct, often fruity odors. This chemical is frequently utilized in the production of various items, such as paints, inks, and other similar products. It is also found in perfumes and fragrance products, contributing to their pleasant scents. While mostly safe, it can cause irritation upon skin contact or if ingested or inhaled, necessitating safety measures during handling and usage.

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Product classification

ACETOACETIC ACID HEXYL ESTER

Name: ACETOACETIC ACID HEXYL ESTER
CAS: 13562-84-0
Purity: 99%

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Details

Factory Sells Best Quality ACETOACETIC ACID HEXYL ESTER 13562-84-0 with ISO standards

Molecular Formula: C10H18O3
Molecular Weight: 186.251
Refractive Index: 1.4320-1.4360
Boiling Point: 232.6 °C at 760 mmHg
PKA: 10.79±0.46(Predicted)
Flash Point: 92.3 °C
PSA： 43.37000
Density: 0.959g/cm³
LogP: 2.08900

13562-84-0 Relevant articles

Combined experimental and computational studies of heterobimetallic Bi-Rh paddlewheel carboxylates as catalysts for metal carbenoid transformations

Hansen, Jorn,Li, Bo,Dikarev, Evgeny,Autschbach, Jochen,Davies, Huw M. L.

, p. 6564 - 6571 (2009)

(Chemical Equation Presented) The cataly...

Synthesis of Fatty Acetoacetates Under Microwave Irradiation Catalysed by Sulfamic Acid in a Solvent-Free System

Weber, Andressa C. H.,Batista, Thaís C.,Gon?alves, Bruno,Hack, Carolina R. L.,Porciuncula, Larissa M.,Treptow, Tamara G. M.,D’Oca, Caroline Da R. Montes,Russowsky, Dennis,D’Oca, Marcelo G. Montes

, p. 1399 - 1406 (2016)

The 1,3-dicarbonyl compounds are importa...

Studies of the Electronic Effects of Zinc Cluster Catalysts and Their Application to the Transesterification of β-Keto Esters

Agura, Kazushi,Hayashi, Yukiko,Wada, Mari,Nakatake, Daiki,Mashima, Kazushi,Ohshima, Takashi

supporting information, p. 1548 - 1554 (2016/06/01)

The electronic effects of tetranuclear z...

Ag-Cu nanoparticles as efficient catalysts for transesterification of β-keto esters under acid/base-free conditions

Yue, Hongmei,Yu, Hao,Liu, Sheng,Xu, Chunli

, p. 19041 - 19051 (2016/03/01)

Transesterification of β-keto esters and...

Nano CuFe2O4: An efficient, magnetically separable catalyst for transesterification of β-ketoesters

Gohain, Mukut,Kumar, Vinod,Van Tonder, Johannes H.,Swart, Hendrik C.,Ntwaeaborwa, Odireleng M.,Bezuidenhoudt, Barend C. B.

, p. 18972 - 18976 (2015/03/04)

The preparation of a variety of β-ketoes...

13562-84-0 Process route

: 141-97-9
ethyl acetoacetate

: 111-27-3
hexan-1-ol

: 64-17-5
ethanol

: 13562-84-0
3-oxo-butyric acid-n-hexyl ester

Conditions

Conditions	Yield
With 4 A molecular sieve; In toluene; for 4h; Heating;	95%

: 105-45-3
acetoacetic acid methyl ester

: 111-27-3
hexan-1-ol

: 13562-84-0
3-oxo-butyric acid-n-hexyl ester

Conditions

Conditions	Yield
With copper ferrite; In toluene; for 8h; Reflux;	94%
With aminosulfonic acid; In neat (no solvent); at 120 ℃; for 0.216667h; Microwave irradiation;	81%
With aminosulfonic acid; 1-methyl-3-propyl-1H-imidazolium chloride; at 80 ℃; for 3h;	95 % Chromat.

13562-84-0 Upstream products

674-82-8
4-methyleneoxetan-2-one
111-27-3
hexan-1-ol
141-97-9
ethyl acetoacetate
15159-48-5
2,4-oxetanedione

13562-84-0 Downstream products

104990-23-0
n-hexyl 2-(3-nitrobenzylidene)acetoacetate
1177774-66-1
n-hexyl 2,6-dimethyl-3-isopropylaminocarbonyl-4-(o-nitrophenyl)-1,4-dihydropyridine-5-carboxylate

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