6291-85-6

Basic information

• Product Name: 3-Ethoxy-1-propanamine
• Synonyms: 3-ethoxy-1-propanamin;3-Ethoxy-1-propylamine;3-ethoxy-propylamin;Propylamine, 3-ethoxy-;3-AMINOPROPYL ETHYL ETHER;(3-AMINOPROPOXY)ETHANE;3-ETHOXYPROPYLAMINE;3-ETHOXY-1-PROPANAMINE
• CAS NO: 6291-85-6
• Molecular Formula: C₅H₁₃NO
• Molecular Weight: 103.16
• EINECS: 228-545-1
• Product Categories: Amino Alcohols;Organic Building Blocks;Oxygen Compounds;Amines;C2 to C6;Nitrogen Compounds
• Mol File: 6291-85-6.mol

Chemical Properties

• Melting Point: -70 °C
• Boiling Point: 136-138 °C(lit.)
• Flash Point: 91 °F
• Appearance: Clear colourless liquid
• Density: 0.861 g/mL at 25 °C(lit.)
• Vapor Pressure: 7.19mmHg at 25°C
• Refractive Index: n20/D 1.418(lit.)
• Storage Temp.: Flammables area
• PKA: 9.79±0.10(Predicted)
• Explosive Limit: 0.8-8.1%(V)
• Water Solubility: miscible
• BRN: 1732287
• CAS DataBase Reference: 3-Ethoxy-1-propanamine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Ethoxy-1-propanamine(6291-85-6)
• EPA Substance Registry System: 3-Ethoxy-1-propanamine(6291-85-6)

Safety Data

• Hazard Codes: C
• Statements: 10-22-34-35
• Safety Statements: 26-36/37/39-45-36-28A-23-16
• RIDADR: UN 2734 8/PG 2
• WGK Germany: 1
• RTECS: UI2700000
• TSCA: Yes
• HazardClass: 3
• PackingGroup: III
• Hazardous Substances Data: 6291-85-6(Hazardous Substances Data)

Usage

Uses

Used in Dye Industry:
3-Ethoxy-1-propanamine is used as an intermediate for the production of disperse red 90, a dye used in the textile industry. Its role in the synthesis process is crucial for creating the desired color properties in fabrics.
Used in Cosmetics Industry:
In the cosmetics industry, 3-Ethoxy-1-propanamine is used as an intermediate in the formulation of various cosmetic products. Its chemical properties contribute to the development of effective and stable formulations.
Used in Pharmaceutical Research:
3-Ethoxy-1-propanamine is used as a tool to partially open the rigid oxetane chain, which is essential in the study and development of new pharmaceutical compounds.
Used in Protein Research:
It is also employed in the identification of Hsp70 modulators, which are important for understanding the function and regulation of heat shock proteins, a family of proteins involved in cellular stress response and protein folding.

InChI:InChI=1/C5H13NO/c1-2-7-5-3-4-6/h2-6H2,1H3/p+1

Upstream product

• 15678-32-7 vinyloxypropionitrile 
• 64-17-5 ethanol 
• 107-13-1 acrylonitrile 
• 2141-62-0 3-(ethoxy)propionitrile 
• 22397-31-5 bis(2-(2-cyanoethoxy)ethyl)ether 
• 109-78-4 3-Hydroxypropionitrile 
• 3055-86-5 3-phenoxypropionitrile 
• 108-88-3 toluene 

Downstream Products

• 101428-23-3 1-(3-ethoxy-propyl)-4-(2-methoxy-phenyl)-piperazine 
• 66742-49-2 [1-(4-Benzyloxy-phenyl)-meth-(E)-ylidene]-(3-ethoxy-propyl)-amine 
• 66742-43-6 [1-(4-Benzyloxy-phenyl)-ethyl]-(3-ethoxy-propyl)-amine 
• 65261-21-4 N-(3-Ethoxy-propyl)-3-phenoxy-benzamide 
• 71416-84-7 Cyclohex-1-ene-1,2-dicarboxylic acid 1-[(4-chloro-2-fluoro-phenyl)-amide] 2-[(3-ethoxy-propyl)-amide] 
• 15029-47-7 N-(3-Ethoxy-propyl)-cyanacetamid 
• 78010-27-2 2,2'-dithiobis(N-3-ethyloxypropylbenzamide) 
• 116952-10-4 (E)-methyl 3-(3-ethoxypropylamino)-2-formyl-2-propenoate 
• 1039809-61-4 (4-Chloro-2-nitro-phenyl)-(3-ethoxy-propyl)-amine 
• 27911-33-7 (3-Ethoxy-propyl)-(3-ethyl-4-methoxy-benzyl)-amine 
• 1040329-50-7 (3-Ethoxy-propyl)-(2-nitro-phenyl)-amine 
• 200400-74-4 N-(3-ethoxypropyl)-2-<4-(3-pyridylcarbonyl)phenyl>-4-oxazolecarboxamide 

Relevant articles and documents

Preparation method of 3-ethoxypropylamine

The invention discloses a preparation method of 3-ethoxypropylamine. The preparation method comprises the following steps: 1) adding a catalyst A and ethanol into a reactor; 2) controlling the temperature of the reactor and dripping acrylonitrile; 3) preparing 3-ethoxy propionitrile with the content of more than 97%; 4) hydrogenating the prepared 3-ethoxy propionitrile in the presence of a catalyst B, hydrogen and an inhibitor; and 5) after the hydrogenation is qualified, carrying out vacuum vacuum distillation to obtain a finished product with a content greater than 99.5%. The preparation method has high selectivity, and excessive ethanol and the catalysts A and B in the process can be recycled, thus further reducing the production cost and reducing the discharge amount of waste liquid.

4-unsubstituted dihydroisoquinolinone derivatives and combinatorial libraries thereof

The present invention relates to novel dihydroisoquinolinone (DHQ) derivative compounds of the following formula: wherein R1to R7, X, Y, Z, b, c and d have the meanings provided herein. The invention further relates to combinatorial libraries containing two or more such compounds, as well as methods of preparing DHQ derivative compounds.

2-aminopyridine derivatives and combinatorial libraries thereof

The present invention relates to novel 2-aminopyridine derivative compounds of the following formula: wherein R1to R5have the meanings provided herein. The invention further relates to combinatorial libraries containing two or more such compounds, as well as methods of preparing 2-aminopyridine derivative compounds.

Process for the preparation of 2-nitrobenzaldehydes

The new process for the preparation of 2-nitrobenzaldehydes of the general formula STR1 in which X1 and X2 either independently of one another represent hydrogen or halogen or one of the substituents represents nitro and the other substituent then represents hydrogen, by oxidation of 2-nitrotoluenes of the general formula STR2 in which X1 and X2 have the meaning indicated above is characterized in that the oxidation with oxygen or an oxygen-containing gas is carried out in the presence of at least one alkoxyalkylamine as a solvent and in the presence of strong bases.

Aldose epimerization by Ni(II): effect of ether-containig alkylenediamine ligands

Several N-substituted ethylenediamine (en) Ni(II) derivatives containing ether linkages were prepared in order to study the effect of ligand structure on C-2 epimerization of aldohexoses.The reagent consisted of a Ni(II)-alkyenediamine derivative in methanol.The presence of ether linkages in the ligand increased the solubilty of the complexes, and resulted in an increase in the rate of epimerization.Epimerization occured rapidly under mild conditions, and the same equilibrium point was reached regardless of whether the reaction was started from glucose or mannose.Among the ligands studied, N,N'-dialkylethylenediamine was the most effective in C-2 epimerization.

Triazinyl reactive dyestuffs in which triazinyl group is further substituted with a beta-chloroethylsulfonyl- or vinylsulfonylbutyrylamino moiety

Reactive dyes of the formula STR1 in which D is the radical of an organic dye of the monoazo, polyazo, metal complex azo, anthraquinone, phthalocyanine, formazan, azomethine, dioxazine, phenazine, stilbene, triphenylmethane, xanthene, thioxanthrone, nitroaryl, naphthoquinone, pyrenequinone or perylenetetracarbimide series, R is hydrogen or substituted or unsubstituted C1-4 -alkyl, X is a substituent which is detachable as an anion, B is a radical of the formula STR2 R1 and R2, independently of each other, are hydrogen or substituted or unsubstituted C1-4 -alkyl or phenyl, A is a substituted or unsubstituted aliphatic or aromatic bridge member, Y is a --CO--Z or --SO2 --Z radical, Z is an aliphatic, aromatic or heterocyclic reactive radical, and n is 1 or 2, are suitable for dyeing or printing cellulose-containing and nitrogen-containing materials and in high dyeing yield produce dyeings and prints having good fastness properties.