13360-63-9 Usage
Description
Ethylbutylamine is a colorless to light yellow liquid with an ammonia-like odor. It is insoluble in water and less dense than water, with a flash point of 65°F. The vapors of this compound are much heavier than air, and both the liquid and its vapors can strongly irritate the skin, eyes, and mucous membranes. Contact with the liquid may cause burns.
Uses
Used in Chemical Synthesis:
Ethylbutylamine is used as an intermediate in the chemical synthesis industry for the production of various compounds and materials. Its ability to react with other chemicals makes it a versatile building block in the creation of different products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethylbutylamine is used as a building block for the synthesis of various drugs and medications. Its chemical properties allow it to be incorporated into the structure of pharmaceutical compounds, potentially enhancing their efficacy and performance.
Used in Agrochemical Industry:
Ethylbutylamine is also utilized in the agrochemical industry as an intermediate for the development of pesticides, herbicides, and other agricultural chemicals. Its role in these applications is to help create more effective and targeted products for crop protection and management.
Used in Surface Treatments:
In the surface treatment industry, Ethylbutylamine is used as a component in the formulation of various coatings, adhesives, and sealants. Its chemical properties contribute to the overall performance and durability of these materials, making them more suitable for their intended applications.
Used in Corrosion Inhibition:
Ethylbutylamine is employed in the oil and gas industry as a corrosion inhibitor. Its chemical properties help to protect metal surfaces from corrosion, extending the lifespan of pipelines, storage tanks, and other equipment used in the extraction, transportation, and processing of oil and gas.
Used in Dyes and Pigments:
In the dyes and pigments industry, Ethylbutylamine is used as an intermediate for the synthesis of various colorants. Its chemical structure allows it to be incorporated into the production of dyes and pigments, resulting in a wide range of colors and shades for various applications, including textiles, plastics, and printing inks.
Air & Water Reactions
Highly flammable. Insoluble in water.
Reactivity Profile
Ethylbutylamine can react vigorously with oxidizing materials . Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
Hazard
Flammable, dangerous fire risk. Toxic by
ingestion.
Health Hazard
INHALATION: Irritation of mucous membranes and lungs. EYES: Irritation. Corrosive, may cause blindness - Irreversible. SKIN: Irritation. Corrosive. INGESTION: Nausea and salivation.
Check Digit Verification of cas no
The CAS Registry Mumber 13360-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,6 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13360-63:
(7*1)+(6*3)+(5*3)+(4*6)+(3*0)+(2*6)+(1*3)=79
79 % 10 = 9
So 13360-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H15N/c1-3-5-6-7-4-2/h7H,3-6H2,1-2H3/p+1
13360-63-9Relevant articles and documents
Selective one-pot synthesis of asymmetric secondary amines via N-alkylation of nitriles with alcohols
Segobia,Trasarti,Apesteguía
, p. 178 - 185 (2019/11/13)
The synthesis of asymmetric secondary amines (ASA) is commonly achieved by N-alkylation of primary amines with alcohols. Here, we investigated the ASA synthesis via the direct amination of alcohols with nitriles, which avoids the synthesis, separation and purification of the primary amines in a first step. Specifically, the ASA synthesis via N-alkylation of butyronitrile (BN) with primary (n-propanol, iso-butanol and n-octanol) and secondary (2‐propanol, 2‐butanol and 2‐octanol) alcohols was studied on SiO2-supported Co, Ni and Ru catalysts. Competitive BN hydrogenation‐condensation reactions formed dibutylamine (the symmetric secondary amine) and tertiary amines as main secondary products. On Co/SiO2, the ASA selectivities for BN/primary alcohol reactions were between 49 and 58% at complete BN conversion, forming dibutylamine and tertiary amines as byproducts. For BN/secondary alcohol reactions, Co/SiO2 formed selectively (ASA + dibutylamine) mixtures containing 78–85% of ASA, thereby showing that the alcohol amination with nitriles is an attractive alternative route for the synthesis of valuable asymmetric secondary amines.
N-ethyl-n-butylamine production method
-
Paragraph 0047; 0050; 0053, (2017/01/05)
The invention relates to a production method of N-ethyl-n-butylamine. According to the production method, n-butanol and monoethylamine are taken as raw materials; a supported non-noble metal catalyst is used under hydrogen conditions; and amination synthe
Catalytic hydrogenation of amides to amines under mild conditions
Stein, Mario,Breit, Bernhard
supporting information, p. 2231 - 2234 (2013/03/28)
Under (not so much) pressure: A general method for the hydrogenation of tertiary and secondary amides to amines with excellent selectivity using a bimetallic Pd-Re catalyst has been developed. The reaction proceeds under low pressure and comparatively low temperature. This method provides organic chemists with a simple and reliable tool for the synthesis of amines. Copyright
