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478-84-2

478-84-2 Structure

478-84-2 Structure
IdentificationBack Directory
[Name]

2-bromolysergic acid diethylamide
[CAS]

478-84-2
[Synonyms]

BOL
BOL-148
BromLSD
Bromo-LSD
2-bromo-lsd
Bromolysergide
Bromlysergamide
2-bromo LSD (solution)
2-Bromo-LSD 2-Bromo-LSD
2-bromolysergic acid diethylamide
D-2-Bromolysergic acid diethylamide
2-Bromo-D-lysergic acid diethylamide
(8β)-2-Bromo-N,N-diethyl-6-methyl-9,10-didehydroergoline-8-carboxamide
Ergoline-8-carboxaMide,2-broMo-9,10-didehydro-N,N-diethyl-6-Methyl-, (8b)-
Ergoline-8-carboxamide, 2-bromo-9,10-didehydro-N,N-diethyl-6-methyl-, (8β)-
[Molecular Formula]

C20H24BrN3O
[MDL Number]

MFCD01746231
[MOL File]

478-84-2.mol
[Molecular Weight]

402.34
Chemical PropertiesBack Directory
[Melting point ]

120-127°
[alpha ]

D20 +15° (c = 0.5 in pyridine); D20 +53° (c = 0.5 in chloroform)
[density ]

1.3040 (rough estimate)
[refractive index ]

1.6770 (estimate)
[solubility ]

DMSO: Soluble: =10 mg/ml
Ethanol: Soluble: =10 mg/ml
[Boiling point ]

580.7±50.0 °C(Predicted)
[form ]

Solid
[pka]

15.65±0.40(Predicted)
[color ]

Off-white to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H302+H312+H332-H319
[Precautionary statements ]

P210-P233-P240-P241-P242-P243-P261-P264-P270-P271-P280-P301+P312-P303+P361+P353-P304+P340-P305+P351+P338-P321-P330-P362+P364-P337+P313-P370+P378-P403+P235-P501
[Safety Profile]

Poison by intraperitoneal and intravenous routes. Experimental teratogenic and reproductive effects. Human systemic effects by ingestion: ddation of the arteries or veins. Many lysergic acid derivatives have central nervous system effects. When heated to decomposition it emits very toxic fumes such as Brand NOx. See other lysergic acid derivatives.
Hazard InformationBack Directory
[Uses]

2-Bromo-LSD (BOL-148; Bromolysergide) is a Dopamine Receptor antagonist that directly affects dopamine neurons in the substantia nigra neostriatum. 2-Bromo-LSD increases the hydroxylation of tyrosine in striatum and antagonizes the decrease of Apomorphine-induced DOPA accumulation. 2-Bromo-LSD also blocks the 5-HT Receptor mediated DOPA formation[1].
[in vivo]

2-Bromo-LSD (0.125-5.5mg/kg; i.p.; single dose) increases the in vivo tyrosine hydroxylation in the striatum of Male Sprague-Dawley rats, and increase the accumulation of DOPA with minimum effect dose of 0.125 mg/kg[1].

[References]

[1] Persson SA. The effect of LSD and 2-bromo LSD on the striatal DOPA accumulation after decarboxylase inhibition in rats. Eur J Pharmacol. 1977 May 1;43(1):73-83. DOI:10.1016/0014-2999(77)90162-5
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