MedKoo Cat#: 561664 | Name: DL-Adrenaline
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

DL-Adrenaline is a non-selective adrenoceptor agonist. It induces lipolysis and systemic muscle contraction, and shows systemic vasoconstrictive, bronchodilatory, positive chronotropic and gastrointestinal relaxant effects in vivo.

Chemical Structure

DL-Adrenaline
DL-Adrenaline
CAS#329-65-7 (free base)

Theoretical Analysis

MedKoo Cat#: 561664

Name: DL-Adrenaline

CAS#: 329-65-7 (free base)

Chemical Formula: C9H13NO3

Exact Mass: 183.0895

Molecular Weight: 183.21

Elemental Analysis: C, 59.00; H, 7.15; N, 7.65; O, 26.20

Price and Availability

Size Price Availability Quantity
1g USD 250.00 2 Weeks
5g USD 650.00 2 weeks
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Synonym
DL-Adrenaline; DL Adrenaline; Racepinefrine; Racepinephrine; DL-Epinephrine; DL Epinephrine; (+/-)-Adrenaline;
IUPAC/Chemical Name
4-[1-Hydroxy-2-(methylamino)ethyl]benzene-1,2-diol
InChi Key
UCTWMZQNUQWSLP-UHFFFAOYSA-N
InChi Code
InChI=1S/C9H13NO3/c1-10-5-9(13)6-2-3-7(11)8(12)4-6/h2-4,9-13H,5H2,1H3
SMILES Code
OC1=CC=C(C(O)CNC)C=C1O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Product Data
Biological target:
DL-Adrenaline is a non-selective adrenoceptor agonist.
In vitro activity:
TBD
In vivo activity:
TBD
Solvent mg/mL mM
Solubility
5% TFA 20.0 109.17
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 183.21 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
TBD
In vitro protocol:
TBD
In vivo protocol:
TBD
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