2319-29-1

Basic information

• Product Name: DECANAMIDE
• Synonyms: DECANOYLAMIDE;DECAMIDE CAPRAMIDE;DECANAMIDE;N-DECANAMIDE;Capramide;capramidecrystalline;Decanoic acid amide;decan-1-amide
• CAS NO: 2319-29-1
• Molecular Formula: C₁₀H₂₁NO
• Molecular Weight: 171.28
• EINECS: 219-029-7
• Mol File: 2319-29-1.mol
• Article Data: 19

Chemical Properties

• Melting Point: 98
• Boiling Point: 301.29°C (rough estimate)
• Flash Point: 138.4°C
• Appearance: /
• Density: 0.8220
• Vapor Pressure: 0.000836mmHg at 25°C
• Refractive Index: 1.4621
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 16.63±0.40(Predicted)
• CAS DataBase Reference: DECANAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: DECANAMIDE(2319-29-1)
• EPA Substance Registry System: DECANAMIDE(2319-29-1)

Safety Data

• Hazard Codes: Xn
• Statements: 22-37/38
• Safety Statements: 22-24/25-36/37
• Hazardous Substances Data: 2319-29-1(Hazardous Substances Data)

Usage

General Description

Decanamide, also known as capric acid, is a chemical compound classified as an amide. It is a white, waxy solid with a faint odor. Decanamide is commonly used as a flavoring agent in the food industry, particularly in the production of fruit flavors and essences. It is also used as an additive in cosmetic and personal care products, such as shampoos and lotions, due to its emollient and moisturizing properties. Decanamide is known for its ability to enhance the creamy texture and mouthfeel of food products and is often used in combination with other flavoring agents to create a more complex flavor profile. Additionally, it has antimicrobial properties that make it useful in certain pharmaceutical and medical applications.

InChI:InChI=1/C10H21NO/c1-2-3-4-5-6-7-8-9-10(11)12/h2-9H2,1H3,(H2,11,12)

Upstream product

• 143-10-2 decylthiol 
• 598-94-7 1,1-Dimethylurea 
• 334-48-5 1-decanoic acid 
• 1975-78-6 n-decanenitrile 
• 110-38-3 decanoic acid ethyl ester 
• 110-42-9 Methyl decanoate 
• 872-05-9 1-Decene 
• 7664-41-7 ammonia 
• 112-30-1 1-Decanol 
• 621-71-6 capric acid triglyceride 
• 2016-57-1 1-aminodecane 
• 112-31-2 caprinaldehyde 
• 73488-76-3 N-t-butyloxycarbonyl-alanine-N'-hydroxysuccinimide ester 
• 80251-02-1 C₁₀H₂₀ClNO 

Downstream Products

• 112-20-9 n-Nonylamin 
• 2016-57-1 1-aminodecane 
• 1975-78-6 n-decanenitrile 
• 1120-49-6 didecylamine 
• 2243-27-8 nonanonitrile 
• 112-30-1 1-Decanol 
• 1407496-77-8 N,N'-((4-(diethylamino)phenyl)methylene)bis(decanamide) 
• 1391847-97-4 C₁₉H₃₁NO₃ 
• 31078-36-1 Vanillyl N-decoylamide 
• 1039559-62-0 C₂₄H₄₁NO₂Si 

Relevant articles and documents

On some bifunctional derivatives of delta-lactones.

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Ring Opening/Site Selective Cleavage in N-Acyl Glutarimide to Synthesize Primary Amides

A LiOH-promoted hydrolysis selective C-N cleavage of twisted N-acyl glutarimide for the synthesis of primary amides under mild conditions has been developed. The reaction is triggered by a ring opening of glutarimide followed by C-N cleavage to afford primary amides using 2 equiv of LiOH as the base at room temperature. The efficacy of the reactions was considered and administrated for various aryl and alkyl substituents in good yield with high selectivity. Moreover, gram-scale synthesis of primary amides using a continuous flow method was achieved. It is noted that our new methodology can apply under both batch and flow conditions for synthetic and industrial applications.

Atomically Dispersed Ru on Manganese Oxide Catalyst Boosts Oxidative Cyanation

There is a strong incentive for environmentally benign and sustainable production of organic nitriles to avoid the use of toxic cyanides. Here we report that manganese oxide nanorod-supported single-site Ru catalysts are active, selective, and stable for oxidative cyanation of various alcohols to give the corresponding nitriles with molecular oxygen and ammonia as the reactants. The very low amount of Ru (0.1 wt %) with atomic dispersion boosts the catalytic performance of manganese oxides. Experimental and theoretical results show how the Ru sites enhance the ammonia resistance of the catalyst, bolstering its performance in alcohol dehydrogenation and oxygen activation, the key steps in the oxidative cyanation. This investigation demonstrates the high efficiency of a single-site Ru catalyst for nitrile production.

Ti-superoxide catalyzed oxidative amidation of aldehydes with saccharin as nitrogen source: Synthesis of primary amides

A new heterogeneous catalytic system (Ti-superoxide/saccharin/TBHP) has been developed that efficiently catalyzes oxidative amidation of aldehydes to produce various primary amides. The protocol employs saccharin as amine source and was found to tolerate a wide range of substrates with different functional groups. Moderate to excellent yields, catalyst reusability and operational simplicity are the main highlights. A possible mechanism and the role of the catalyst in oxidative amidation have also been discussed.