82560-46-1

Basic information

• Product Name: Ethyl N-(2-butyl)glycinate
• Synonyms: ETHYL N-(2-BUTYL)GLYCINATE;N-(2-Butyl)glycine ethyl ester
• CAS NO: 82560-46-1
• Molecular Formula: C₈H₁₇NO₂
• Molecular Weight: 159.23
• Mol File: 82560-46-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethyl N-(2-butyl)glycinate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl N-(2-butyl)glycinate(82560-46-1)
• EPA Substance Registry System: Ethyl N-(2-butyl)glycinate(82560-46-1)

Safety Data

• Hazardous Substances Data: 82560-46-1(Hazardous Substances Data)

Usage

General Description

Ethyl N-(2-butyl)glycinate is a chemical compound with the molecular formula C9H19NO2. It is an ester derived from ethyl alcohol and glycine, with a butyl group attached to the nitrogen atom. This chemical is commonly used as a fragrance ingredient and can be found in various cosmetic and personal care products. It has a mild, sweet, and fruity odor, making it a popular choice for adding a pleasant scent to perfumes, lotions, and other beauty products. Ethyl N-(2-butyl)glycinate is also utilized in the manufacturing of soaps, detergents, and other household cleaning products. Additionally, it can be used as a flavoring agent in food products and as a chemical intermediate in the synthesis of other compounds.

Upstream product

• 33966-50-6 SEC-BUTYLAMINE 
• 105-36-2 ethyl bromoacetate 
• 78-93-3 butanone 
• 459-73-4 GlyOEt*HCl 

Downstream Products

• 7253-47-6 N-sec-butyl-N-nitroso-glycine 

Relevant articles and documents

A quantitative structure-activity relationship study of herbicidal analogues of α-hydroxy-substituted 3-benzylidenepyrrolidene-2,4-diones

A series of pyrrolidine-2,4-dione and piperidine-2,4-dione derivatives were prepared and evaluated for their herbicidal activities where some of these compounds exhibited good bioactivity against Echinochloa crus-galli in comparison with sulcotrione. Quan

Reductive amination of aldehydes and ketones with sodium triacetoxyborohydride. Studies on direct and indirect reductive amination procedures

Sodium triacetoxyborohydride is presented as a general reducing agent for the reductive amination of aldehydes and ketones. Procedures for using this mild and selective reagent have been developed for a wide variety of substrates. The scope of the reaction includes aliphatic acyclic and cyclic ketones, aliphatic and aromatic aldehydes, and primary and secondary amines including a variety of weakly basic and nonbasic amines. Limitations include reactions with aromatic and unsaturated ketones and some sterically hindered ketones and amines. 1,2-Dichloroethane (DCE) is the preferred reaction solvent, but reactions can also be carried out in tetrahydrofuran (THF) and occasionally in acetonitrile. Acetic acid may be used as catalyst with ketone reactions, but it is generally not needed with aldehydes. The procedure is carried out effectively in the presence of acid sensitive functional groups such as acetals and ketals; it can also be carried out in the presence of reducible functional groups such as C-C multiple bonds and cyano and nitro groups. Reactions are generally faster in DCE than in THF, and in both solvents, reactions are faster in the presence of AcOH. In comparison with other reductive amination procedures such as NaBH3CN/MeOH, borane-pyridine, and catalytic hydrogenation, NaBH(OAc)3 gave consistently higher yields and fewer side products. In the reductive amination of some aldehydes with primary amines where dialkylation is a problem we adopted a stepwise procedure involving imine formation in MeOH followed by reduction with NaBH4.