An internal standard for the quantification of ractopamine
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Ractopamine-d3 (hydrochloride)

Item No. 37207

Technical Information
Formal Name
4-hydroxy-α-[[[3-(4-hydroxyphenyl)-1-methylpropyl]amino]methyl-d2]-benzenemethan-d-ol, monohydrochloride
CAS Number
1219794-72-5
Synonyms
  • LY031537-d3
Molecular Formula
C18H20D3NO3 • HCl
Formula Weight
Purity
≥99% deuterated forms (d1-d3)
Formulation
A solid
DMSO: soluble with sonicationWater: soluble with heat
SMILES
OC(C=C1)=CC=C1CCC(C)NC([2H])([2H])C(C2=CC=C(C=C2)O)([2H])O.Cl
InChi Code
InChI=1S/C18H23NO3.ClH/c1-13(2-3-14-4-8-16(20)9-5-14)19-12-18(22)15-6-10-17(21)11-7-15;/h4-11,13,18-22H,2-3,12H2,1H3;1H/i12D2,18D;
InChi Key
JHGSLSLUFMZUMK-AKLJGQCDSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Ractopamine-d3 is intended for use as an internal standard for the quantification of ractopamine (Item No. 27613) by GC- or LC-MS. Ractopamine is a trace amine-associated receptor 1 (TAAR1) agonist.1 It increases chloride conductance in X. laevis oocytes expressing the human cystic fibrosis transmembrane conductance regulator (CFTR) and mouse TAAR1 (EC50 = 16 µM), an effect that can be blocked by the TAAR1 antagonist EPPTB (Item No. 34330). It selectively induces chloride conductance in TAAR1- and CFTR-expressing oocytes over those expressing the human β2-adrenergic receptor (β2-AR) and CFTR at 36 µM. However, it is also considered a β2-AR agonist that binds to β2-ARs (Ki = 0.18 µM for the recombinant human receptor expressed in Sf9 cells) and induces relaxation of isolated guinea pig trachea with an EC50 value of 9.1 nM.2 Formulations containing ractopamine have been used as food additives in livestock to increase weight gain and leanness and improve feed efficiency.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Liu, X., Grandy, D.K., and Janowsky, A. Ractopamine, a livestock feed additive, is a full agonist at trace amine-associated receptor 1. J. Pharmacol. Exp. Ther. 350(1), 124-129 (2014).

    2. Kern, C., Meyer, T., Droux, S., et alSynthesis and pharmacological characterization of β2-adrenergic agonist enantiomers: Zilpaterol. J. Med. Chem. 52(6), 1773-1777 (2009).