ChemicalBook--->CAS DataBase List--->2494-12-4

2494-12-4

2494-12-4 Structure

2494-12-4 Structure
IdentificationBack Directory
[Name]

N-acetyldopamine
[CAS]

2494-12-4
[Synonyms]

N-acetyldopamine
Acetamide, N-[2-(3,4-dihydroxyphenyl)ethyl]-
[Molecular Formula]

C10H13NO3
[MDL Number]

MFCD00150490
[MOL File]

2494-12-4.mol
[Molecular Weight]

195.22
Chemical PropertiesBack Directory
[Boiling point ]

486.7±35.0 °C(Predicted)
[density ]

1.235±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Oil
[pka]

9.80±0.10(Predicted)
[color ]

Colorless to light yellow
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H315-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[RTECS ]

AB7651000
Hazard InformationBack Directory
[Uses]

N-acetyldopamine (NADA) is a catecholamine that is used by insects as sclerotizing precursors to harden their cuticle[1].
[Definition]

ChEBI: N-acetyldopamine is a secondary carboxamide obtained by formal condensation of the carboxy group of acetic acid with the amino group of dopamine. A dopamine metabolite. It has a role as a human urinary metabolite and a marine metabolite. It is a secondary carboxamide, a member of acetamides, a member of catechols and a N-(fatty acyl)-dopamine. It is functionally related to a dopamine.
[IC 50]

Human Endogenous Metabolite
[References]

[1] Hanine Barek, et al. Unraveling Complex Molecular Transformations of N-β-alanyldopamine That Account for Brown Coloration of Insect Cuticle. Rapid Commun Mass Spectrom. 2017 Aug 30;31(16):1363-1373. DOI:10.1002/rcm.7914
Spectrum DetailBack Directory
[Spectrum Detail]

N-acetyldopamine(2494-12-4)1HNMR
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