Allylamine hydrochloride

Base Information

• Chemical Name: Allylamine hydrochloride
• CAS No.: 10017-11-5
• Deprecated CAS: 204719-79-9,1619884-03-5,204075-67-2
• Molecular Formula: C₃H₈N*Cl
• Molecular Weight: 93.5562
• Hs Code.: 29211990
• European Community (EC) Number: 415-050-2,600-035-7,615-303-9
• UNII: R2H25ILF98
• DSSTox Substance ID: DTXSID60872280
• Wikipedia: Polyallylamine_hydrochloride
• Wikidata: Q903911
• Mol file: 10017-11-5.mol

Synonyms:Allylamine hydrochloride;10017-11-5;71550-12-4;3-Aminopropene hydrochloride;Allylamine HCl;Allylamine, hydrochloride;Allylammonium chloride;prop-2-en-1-amine hydrochloride;prop-2-en-1-amine;hydrochloride;2-Propen-1-amine hydrochloride;UNII-R2H25ILF98;R2H25ILF98;allylaminehydrochloride;2-PROPENYLAMINE HYDROCHLORIDE;2-Propen-1-amine, hydrochloride (1:1);N-2-PROPEN-1-AMINE HYDROCHLORIDE;EC 415-050-2;2-Propen-1-amine, hydrochloride;allyl amine hydrochloride;C3H7N.ClH;monoallylamine hydrochloride;C3-H7-N.Cl-H;Allylamine hydrochloride, 98%;(C3-H7-N.Cl-H)x-;Allylamine hydrochloride (1:1);PROP-2-EN-1-AMINE HCL;DTXSID60872280;AMY22118;CS-AM-00207;MFCD00054329;AKOS015847154;CS-W016666;LS-16408;2-Propen-1-amine hydrochloride, AldrichCPR;A0226;FT-0622039;FT-0724079;A914416;Q903911

Chemical Property of Allylamine hydrochloride

Chemical Property:

• Vapor Pressure: 247mmHg at 25°C
• Melting Point: 106 °C
• Refractive Index: 1.414
• Boiling Point: 54.3 °C at 760mmHg
• Flash Point: >110℃
• PSA: 26.02000
• Density: 0.743g/cm³
• LogP: 1.63340
• Water Solubility.: almost transparency
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 93.0345270
• Heavy Atom Count: 5
• Complexity: 17.2

Purity/Quality:

50%，60% ^*data from raw suppliers

Prop-2-en-1-amineHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 23/24/25-51/53-25-36
• Safety Statements: 26-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Plastics & Rubber -> Polymers
• Canonical SMILES: C=CCN.Cl
• Uses: Allylamine hydrochloride is an organic intermediate that can be used to prepare polymer nanocomposites and sevelamer carbonate.

Technology Process of Allylamine hydrochloride

There total 10 articles about Allylamine hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

N,N-bis(trimethylsilyl)allylamine (7688-51-9) → Hexamethyldisiloxane (107-46-0) + allylammonium chloride (10017-11-5,110507-15-8,71550-12-4)

Guidance literature:

With hydrogenchloride; In diethyl ether;

Reference yield: 99.0%

N-tert-butoxycarbonylprop-2-en-1-amine (78888-18-3) → allylammonium chloride (10017-11-5,110507-15-8,71550-12-4)

Guidance literature:

With sulfuric acid; sodium chloride; In neat (no solvent); at 20 ℃; for 1h; Sealed tube;

DOI:10.1039/d1ob00728a

Reference yield: 67.0%

C12H24NO5P (85231-93-2) → allylammonium chloride (10017-11-5,110507-15-8,71550-12-4)

Guidance literature:

With hydrogenchloride; In benzene; Ambient temperature;

DOI:10.1055/s-1982-29997

upstream raw materials:

N,N-bis(trimethylsilyl)allylamine

C₁₂H₂₄NO₅P

N-tritylprop-2-en-1-amine

1-bromo dodecane

Downstream raw materials:

(S,R)-3-bromo-5-aminomethyl-4,5-dihydroisoxazole

(R)-(3-bromo-4,5-dihydroisoxazol-5-yl)methanamine

(S)-(3-bromo-4,5-dihydroisoxazol-5-yl)methanamine

N-allylphenethylamine

Refernces

• 1、 De Borggraeve, Wim M.,Gilles, Philippe,Van Mileghem, Seger,Verschueren, Rik H.. "Solvent-freeN-Boc deprotection byex situgeneration of hydrogen chloride gas". supporting information. p. 5782 - 5787. Retrieved 2021/07/12.
• 2、 Theodorou, Vassiliki,Ragoussis, Valentine,Strongilos, Alexandros,Zelepos, Evangelos,Eleftheriou, Argyro,Dimitriou, Maria. "A convenient method for the preparation of primary amines using tritylamine". . p. 1357 - 1360. Retrieved 2007/10/03.