395-29-9

Basic information

• Product Name: Isoxsuprine base
• Synonyms: 2-[3-Phenoxy-2-propylamino]-1-[p-hydroxyphenyl]-1-propanol;Isoxsuprine base;1-(4-Hydroxyphenyl)-2-(1-methyl-2-phenoxyethylamino)propanol;4-Hydroxy-alpha-(1-((1-methyl-2-phenoxyethyl)amino)ethyl)benzenemethanol;Benzyl alcohol, p-hydroxy-alpha-(1-((1-methyl-2-phenoxyethyl)amino)ethyl)-;Einecs 206-898-2;Erythro-1-(p-hydroxyphenyl)-2-(alpha-methyl-beta-phenoxyethylamino)propanol
• CAS NO: 395-29-9
• Molecular Formula: C18H23NO3
• Molecular Weight: 301.38012
• Mol File: 395-29-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Isoxsuprine base(CAS DataBase Reference)
• NIST Chemistry Reference: Isoxsuprine base(395-29-9)
• EPA Substance Registry System: Isoxsuprine base(395-29-9)

Safety Data

• Hazardous Substances Data: 395-29-9(Hazardous Substances Data)

Upstream product

• 621-87-4 3-phenoxy-2-propanone 
• 552-85-2 p-hydroxynorepherdine 
• 552-85-2 (1RS,2RS)-2-amino-1-(4-hydroxy-phenyl)-propan-1-ol 
• 25070-02-4 (1RS,2RS)-2-dibenzylamino-1-(4-benzyloxy-phenyl)-propan-1-ol 
• 552-85-2 (+/-)-p-Hydroxy-norephedrin 
• 35205-54-0 1-methyl-2-phenoxyethylamine 
• 395-28-8 (+/-)-1-<4-Hydroxyphenyl>-2-<1-methyl-2-phenoxyaethylamino>-propan-1-ol 
• 35081-45-9 1-<4-(benzyloxy)phenyl>-2-bromo-1-propanone 
• 45972-73-4 S-(+)-1-phenoxy-2-propanamine 
• 552-85-2 4-((1R,2S)-2-amino-1-hydroxypropyl)phenol 
• 45972-74-5 R-(-)-1-phenoxy-2-propanamine 
• 1926-72-3 (+/-)-4-Hydroxynorephedrin 
• 123777-67-3 (1RS,2SR)-1-(4-benzyloxy-phenyl)-2-((RS)-β-phenoxy-isopropylamino)-propan-1-ol; hydrochloride 
• 35205-50-6 1-(4-benzyloxy-phenyl)-2-(β-phenoxy-isopropylamino)-propan-1-one; hydrochloride 

Relevant articles and documents

Phenethanolamine-derived haptens, immunogens and conjugates comprising them and antibodies recognising said immunogenes and conjugates

The present invention relates to a method for preparing haptens of formulae I and II that are useful in the preparation of immunogens, antibodies and conjugates, for use in competitive immunoassays for the detection of ractopamine, isoxsuprine and ritodrine. The haptens are prepared by reacting a phenylethanolamine derivative of formula D with a phenylalkylcarbonyl derivative of formula E: in which, in formula I, Z1 is a crosslinker and Z2 is H and, in formula II, Z1 is H and Z2 is a crosslinker.