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538-65-8

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  • butyl cinnamate/factory price direct CAS NO.538-65-8 CAS NO.538-65-8

    Cas No: 538-65-8

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538-65-8 Usage

Description

N-BUTYL CINNAMATE, also known as Butyl cinnamate, is an organic compound commonly used in the fragrance industry due to its pleasant, balsamic, and slightly cocoa-like odor. It is a colorless to pale yellow liquid at room temperature and is characterized by its distinctive scent.

Uses

Used in Fragrance Industry:
N-BUTYL CINNAMATE is used as a fragrance ingredient for its pleasant, balsamic, and slightly cocoa-like odor. It is widely utilized in the creation of perfumes, colognes, and other scented products to provide a unique and appealing aroma.
Used in Flavor Industry:
N-BUTYL CINNAMATE is also used as a flavor additive in the food and beverage industry, where it imparts a sweet, balsamic, and slightly cocoa-like taste to various products. It is often used in the production of candies, chewing gums, and other confectionery items to enhance their flavor profile.
Used in Cosmetics Industry:
In the cosmetics industry, N-BUTYL CINNAMATE is used as a component in various personal care products, such as lotions, creams, and shampoos. Its pleasant scent makes it an ideal addition to these products, providing a sensory experience that is both enjoyable and appealing to consumers.
Used in Pharmaceutical Industry:
N-BUTYL CINNAMATE is also utilized in the pharmaceutical industry, where it serves as a solvent or carrier for various drugs and medications. Its chemical properties make it suitable for use in the formulation of certain pharmaceutical products, enhancing their stability and effectiveness.

Production Methods

Butyl cinnamate is produced by the direct esterification of n-butanol with cinnamic acid under azeotropic conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 538-65-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 538-65:
(5*5)+(4*3)+(3*8)+(2*6)+(1*5)=78
78 % 10 = 8
So 538-65-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O2/c1-2-3-11-15-13(14)10-9-12-7-5-4-6-8-12/h4-10H,2-3,11H2,1H3/b10-9+

538-65-8 Well-known Company Product Price

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  • Alfa Aesar

  • (L07362)  n-Butyl cinnamate, 98%   

  • 538-65-8

  • 50g

  • 654.0CNY

  • Detail
  • Alfa Aesar

  • (L07362)  n-Butyl cinnamate, 98%   

  • 538-65-8

  • 250g

  • 2337.0CNY

  • Detail
  • USP

  • (1082617)  Butyl cinnamate  United States Pharmacopeia (USP) Reference Standard

  • 538-65-8

  • 1082617-500MG

  • 4,647.24CNY

  • Detail

538-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-BUTYL CINNAMATE

1.2 Other means of identification

Product number -
Other names Butylcinnamat

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:538-65-8 SDS

538-65-8Relevant articles and documents

Palladium supported aminobenzamide modified silica coated superparamagnetic iron oxide as an applicable nanocatalyst for Heck cross-coupling reaction

Fatahi, Yousef,Ghaempanah, Aram,Ma?mani, Leila,Mahdavi, Mohammad,Bahadorikhalili, Saeed

, (2021/01/26)

An applicable palladium-based nanocatalyst was constructed through the immobilization of palladium onto 2-aminobenzamide functionalized silica coated superparamagnetic iron oxide magnetic nanoparticles. The nanocatalyst (named as Pd@ABA@SPIONs@SiO2) was characterized by several characterization methods, including scanning electron microscope (SEM), transmission electron microscopy (TEM), vibrating-sample magnetometry (VSM), energy-dispersive X-ray spectroscopy (EDS), dynamic light scattering (DLS), X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), inductively coupled plasma (ICP), and X-ray photoelectron spectroscopy (XPS) analyses. Microscopy results showed that the nanoparticles are spherical in shape with 20–25 nm size. The size of the nanoparticles was confirmed by the DLS method. The superparamagnetic nature of the catalyst was confirmed by the VSM method. The successful functionalization of SPIONs@SiO2 was confirmed by FT-IR spectroscopy. The presence of palladium in the structure of the nanocatalyst was illustrated by XRD and EDS analysis. Also using XPS technique, the oxidation state of palladium in Pd@ABA@SPIONs@SiO2 was determined zero before and after the catalyst was applied in Mizoroki-Heck reaction. Several aryl halides and alkenes were reacted in the presence of the nanocatalyst and formed the corresponding products in high isolated yields. The nanocatalyst showed very good reusability and did not decrease its activity after 10 sequential runs. Density functional theory (DFT) calculation was performed to provide a mechanism for the reaction and confirmed the role of the palladium catalyst in the reaction function.

NiFe2O4@SiO2@ZrO2/SO42-/Cu/Co nanoparticles: A novel, efficient, magnetically recyclable and bimetallic catalyst for Pd-free Suzuki, Heck and C-N cross-coupling reactions in aqueous media

Alavi G., Seyyedeh Ameneh,Nasseri, Mohammad Ali,Kazemnejadi, Milad,Allahresani, Ali,Hussainzadeh, Mahdi

, p. 7741 - 7757 (2021/05/13)

The novel heterogeneous bimetallic nanoparticles of Cu-Co were synthesized based on magnetic nanoparticles, and the magnetic nanocatalyst was characterized by XRD, FE-SEM, EDX mapping, BET, TEM, HRTEM, FTIR, TGA, and VSM. This catalyst was successfully applied as a recyclable magnetically catalyst in Heck, Suzuki, and C-N cross-coupling reactions with various aryl halides (iodides, bromides, and chlorides as challengeable substrates), with olefins, phenylboronic acid, and amines, respectively. We considered the rise of synergetic effects from the different Lewis acid and Br?nsted acid sites present in the catalyst. The catalyst was synthesized with cheap, available materials and a simple synthesis method. The catalyst can be separated easily using an external magnet. It was recycled for more than ten runs without a sensible loss of its catalytic activity, and no significant leaching of the Cu and Co quantity was observed. The significant benefits of the method are high-level generality, simple operation, and there are no heavy metals and toxic solvents. This is a quick, easy, efficacious and environmentally friendly protocol, and no by-products are formed in the reaction. These features make it an appropriate practical alternative protocol. In comparison with recent works, the other advantage of this catalyst is the synthesis of a wide variety of C-C and C-N bond derivatives (more than 40 derivatives). The other significant advantage is the low temperature of the reaction and the use of the least possible amount of the catalyst (0.003 g). The efficiency was good to excellent and the catalyst selectivity has been high. We aspire that our study inspires more interest to design novel catalysts based on using low-cost metal ions (such as cobalt and copper) in the cross-coupling reactions. This journal is

Palladium and silk fibroin-containing magnetic nano-biocomposite: a highly efficient heterogeneous nanocatalyst in Heck coupling reactions

Nouri Parouch, Ahmad,Koukabi, Nadiya,Abdous, Elham,Shobeiri, Seyed Amin

, p. 3165 - 3177 (2021/05/21)

Supported metal catalysts, for instance, palladium, are one of the foundations of chemical reactions, especially in C–C bond formation. The present study reports preparation of a magnetically separable palladium-supported nano-biocomposite with a low cost and easy immobilization technique. Fibroin, a natural biodegradable polymer, was used through an in situ method to cover the Fe3O4 nanoparticles to make a nano-biocomposite followed by anchoring palladium on the fibroin surface. The morphology and the structure of palladium-supported nano-biocomposite Fe3O4@fibroin-Pd were characterized by FT-IR, XRD, TGA, SEM, EDX, and TEM techniques. Consequently, the nanocatalyst activity was evaluated in the Heck coupling reactions. Only a very small amount of the nanocatalyst was employed in the reaction, and it showed excellent catalytic activity; in most cases more than 90% efficiency. The significant advantages of employing this nanocatalyst include high catalytic activity, short reaction times, easy separation of the nanocatalyst with an external magnet and great reusability. The results demonstrated that the used nanocatalysts were very active for four consecutive reaction rounds.

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