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Merck
CN

D031

Supelco

N,N-Dipropyldopamine hydrobromide

solid

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About This Item

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

SMILES string

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

Gene Information

Biochem/physiol Actions

Dopamine receptor agonist.

Packaging

Packaged under argon.

Disclaimer

Photosensitive

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

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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
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
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

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