1. GPCR/G Protein Neuronal Signaling
  2. Adrenergic Receptor Trace Amine-associated Receptor (TAAR)
  3. Ractopamine hydrochloride

Ractopamine hydrochloride  (Synonyms: LY031537)

Cat. No.: HY-B1421 Purity: 99.2%
Handling Instructions Technical Support

Ractopamine hydrochloride (LY031537) is a potent and orally active β-adrenergic receptor (βAR) agonist with Kd value of ~25 nM for pig β1AR and β2AR. Ractopamine hydrochloride also is a mTAAR1 agonist with an EC50 of 16 μM. Ractopamine hydrochloride promotes muscle mass development, limits fat deposition, reduces feed consumption, increases total cellular protein synthesis, and improves growth rate and feed efficiency in finishing swine. Ractopamine hydrochloride can be used for researching to increase lean tissue growth and improve production efficiency in pigs.

For research use only. We do not sell to patients.

Ractopamine hydrochloride

Ractopamine hydrochloride Chemical Structure

CAS No. : 90274-24-1

Size Price Stock Quantity
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
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Solution
10 mM * 1 mL in DMSO In-stock
Solid
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25 mg In-stock
50 mg In-stock
100 mg In-stock
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Based on 1 publication(s) in Google Scholar

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Description

Ractopamine hydrochloride (LY031537) is a potent and orally active β-adrenergic receptor (βAR) agonist with Kd value of ~25 nM for pig β1AR and β2AR. Ractopamine hydrochloride also is a mTAAR1 agonist with an EC50 of 16 μM. Ractopamine hydrochloride promotes muscle mass development, limits fat deposition, reduces feed consumption, increases total cellular protein synthesis, and improves growth rate and feed efficiency in finishing swine. Ractopamine hydrochloride can be used for researching to increase lean tissue growth and improve production efficiency in pigs[1][2][3][4][5].

In Vitro

Ractopamine (50 nM-100 μM) hydrochloride acts as a full agonist of mouse trace amine-associated receptor 1 (mTAAR1) in Xenopus laevis oocytes coexpressing hCFTR and mTAAR1, with an EC50 of 16 μM, via a cAMP-dependent pathway[1].
Ractopamine hydrochloride increases protein accumulation and synthesis in postfusion ELC5 myotubes in a concentration-dependent manner[3].
Ractopamine hydrochloride shows Kd value of ~25 nM for pig β1AR and β2AR[5].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Ractopamine (5-10 mg/kg; oral; divided into 3 daily portions; 28 days) hydrochloride supplementation in finishing pigs causes minimal changes to specific behaviors, no changes to stress-related cortisol or lactate levels or skin/carcass lesions, but doubles serum creatine kinase concentrations, indicating potential muscular effects[2].
Ractopamine (5-20 mg/kg; p.o.; daily; 48 days) hydrochloride administered in the diet of finishing swine linearly improves average daily gain, increases carcass weight and loin eye are[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: crossbred Camborough 25 × AGPIC 337 (170 barrows, 170 gilts, average initial body weight 107.3 kg)[2]
Dosage: 5 mg/kg; 10 mg/kg
Administration: oral; divided into 3 daily portions; 28 days
Result: Increased the average percentage of pigs nosing pen mates to 6.73% (vs control 5.62%) at 5 mg/kg.
Reduced the average percentage of pigs playing to 0.06% (vs control 0.26%) at 5 mg/kg.
Increased the average percentage of pigs drinking water to 2.06% (vs control 1.58%) at 5 mg/kg.
Increased the average percentage of pigs standing to 1.39% (vs control 0.85%) at 10 mg/kg.
Increased serum CK-MB concentration to 4361 U/L (vs control 2341 U/L) and serum CK-total concentration to 12,436 U/L (vs control 5811 U/L) at 5 mg/kg.
Increased serum CK-MB concentration to 4510 U/L (vs control 2341 U/L) and serum CK-total concentration to 10,707 U/L (vs control 5811 U/L) at 10 mg/kg.
Showed no significant effect on overall pig behavior classification, skin/carcass lesions, blood cortisol or lactate concentrations.
Molecular Weight

337.84

Formula

C18H24ClNO3

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

OC(CNC(C)CCC1=CC=C(O)C=C1)C2=CC=C(O)C=C2.Cl

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

-20°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Solvent & Solubility
In Vitro: 

DMSO : 100 mg/mL (296.00 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.9600 mL 14.7999 mL 29.5998 mL
5 mM 0.5920 mL 2.9600 mL 5.9200 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

V2

In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 2.5 mg/mL (7.40 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

    Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
  • Protocol 2

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 2.5 mg/mL (7.40 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

    Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
%
DMSO +
+
%
Tween-80 +
%
Saline
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Calculation results:
Working solution concentration: mg/mL
Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).
Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
 If the continuous dosing period exceeds half a month, please choose this protocol carefully.
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Purity & Documentation

Purity: 99.2%

References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.9600 mL 14.7999 mL 29.5998 mL 73.9995 mL
5 mM 0.5920 mL 2.9600 mL 5.9200 mL 14.7999 mL
10 mM 0.2960 mL 1.4800 mL 2.9600 mL 7.4000 mL
15 mM 0.1973 mL 0.9867 mL 1.9733 mL 4.9333 mL
20 mM 0.1480 mL 0.7400 mL 1.4800 mL 3.7000 mL
25 mM 0.1184 mL 0.5920 mL 1.1840 mL 2.9600 mL
30 mM 0.0987 mL 0.4933 mL 0.9867 mL 2.4667 mL
40 mM 0.0740 mL 0.3700 mL 0.7400 mL 1.8500 mL
50 mM 0.0592 mL 0.2960 mL 0.5920 mL 1.4800 mL
60 mM 0.0493 mL 0.2467 mL 0.4933 mL 1.2333 mL
80 mM 0.0370 mL 0.1850 mL 0.3700 mL 0.9250 mL
100 mM 0.0296 mL 0.1480 mL 0.2960 mL 0.7400 mL
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Ractopamine hydrochloride
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