94231-37-5

Basic information

• Product Name: ethyl L-ornithine monohydrochloride
• Synonyms: ethyl L-ornithine monohydrochloride;(S)-Ethyl 2,5-diaminopentanoate hydrochloride
• CAS NO: 94231-37-5
• Molecular Formula: C₇H₁₆N₂O₂*2ClH
• Molecular Weight: 196.67508
• EINECS: 303-854-5
• Mol File: 94231-37-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: ethyl L-ornithine monohydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl L-ornithine monohydrochloride(94231-37-5)
• EPA Substance Registry System: ethyl L-ornithine monohydrochloride(94231-37-5)

Safety Data

• Hazardous Substances Data: 94231-37-5(Hazardous Substances Data)

Usage

General Description

Ethyl L-ornithine monohydrochloride is a chemical compound that belongs to the class of organic compounds known as alpha amino acids and derivatives. It is an ethyl ester derivative of L-ornithine and contains a hydrochloride salt. L-ornithine is a non-essential amino acid that plays a key role in the urea cycle, which is responsible for detoxifying ammonia in the body. ethyl L-ornithine monohydrochloride has been studied for its potential use in pharmaceuticals, particularly as a treatment for liver diseases and as a nutritional supplement to support athletic performance. Additionally, it has been investigated for its potential benefits in wound healing and tissue repair. Ethyl L-ornithine monohydrochloride is often used in research and development as a chemical reagent and is of interest for its potential therapeutic applications.

Upstream product

• 64-17-5 ethanol 
• 3184-13-2 L-ornithine hydrochloride 
• 1069-31-4 DL-ornithine hydrochloride 

Downstream Products

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• 80822-62-4 4-(3-aminopropyl)-1H-imidazol-2-ylamine dihydrochloride 
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• 84772-28-1 2,3,4,4a,5,11-hexahydro-6H-pyrido<2,3-b><1,4>benzodiazepin-6-one hydrochloride 

Relevant articles and documents

Diastereoselective pictet-spengler reactions of a tethered 2-aminoimidazole

The diastereoselective Pictet-Spengler reaction of aminopropyl-2- aminoimidazole with enantiopure aldehydes has been investigated. With amino acid-derived aldehydes, anti stereochemistry is favoured, with a diastereoselectivity up to 92% achievable. The absolute stereochemistry of the products was determined through synthesis of a rigid derivative and from NMR data in combination with molecular modelling. The diastereoselectivity was shown to be dependent on the steric bulk of the amino acid side chain and independent of the nitrogen protecting group. Lewis acids catalysed the reaction but did not affect the diastereoselectivity.

CERTAIN 3-PHOSPHINYL-AMINO-2-OXO-1H-AZEPINE-1-ACETIC ACID DERIVATIVES HAVING ANTI-HYPERTENSIVE ACTIVITY

Phosphonamide substituted lactams of the formula STR1 are disclosed. These compounds are useful as hypotensive agents.