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Merck
CN

D031

N,N-Dipropyldopamine hydrobromide

solid

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About This Item

Empirical Formula (Hill Notation):
C14H23NO2 · HBr
CAS Number:
Molecular Weight:
318.25
UNSPSC Code:
41116107
MDL number:
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SMILES string

Br.CCCN(CCC)CCc1ccc(O)c(O)c1

form

solid

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

color

white

solubility

aqueous base: unstable, ethanol: soluble (Solutions should be freshly prepared and kept at 4 °C.), oxygen-free water containing 0.1% sodium metabisulfite or other antioxidant: soluble (Solutions should be freshly prepared and kept at 4 °C.)

application(s)

forensics and toxicology
veterinary

storage temp.

2-8°C

Gene Information

Biochem/physiol Actions

Dopamine receptor agonist.

Packaging

Packaged under argon.

Disclaimer

Photosensitive

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

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I Cavero et al.
Life sciences, 31(11), 1059-1069 (1982-09-13)
Relatively selective dopamine receptor agonists, like bromocriptine, lergotrile, pergolide and N,N-di-n-propyl-dopamine, lower arterial pressure in conscious spontaneously hypertensive rats and in several anesthetized animal preparations. This effect has been attributed to stimulation of dopamine receptors since it can be specifically
R A Hahn et al.
The Journal of pharmacology and experimental therapeutics, 229(1), 132-138 (1984-04-01)
Administration of N,N-di-n-propyldopamine (DPDA) (1-100 micrograms/kg i.v.) and LY171555 (1-100 micrograms/kg i.v.) produced dose-related arterial hypotension accompanied by bradycardia in anesthetized rhesus monkey. The cardiovascular effects of DPDA were of brief duration, whereas hypotension and bradycardia induced by LY171555 were
A Hilditch et al.
Journal of cardiovascular pharmacology, 6(3), 460-469 (1984-05-01)
The interactions between several putative dopamine receptor agonists and antagonists have been examined at neuronal and vascular dopamine receptors in the femoral and mesenteric vascular beds, respectively, of anaesthetised dogs. N,N-di-n- propyldopamine (DPDA) and apomorphine caused vasodilatation in both vascular

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