2-bromolysergic acid diethylamide
2-bromolysergic acid diethylamide Basic information
- Product Name:
- 2-bromolysergic acid diethylamide
- Synonyms:
-
- Ergoline-8-carboxaMide,2-broMo-9,10-didehydro-N,N-diethyl-6-Methyl-, (8b)-
- 2-Bromo-LSD 2-Bromo-LSD
- 2-bromo-lsd
- Ergoline-8-carboxamide, 2-bromo-9,10-didehydro-N,N-diethyl-6-methyl-, (8β)-
- 2-bromolysergic acid diethylamide
- BOL-148
- BromLSD
- Bromlysergamide
- CAS:
- 478-84-2
- MF:
- C20H24BrN3O
- MW:
- 402.34
- Mol File:
- 478-84-2.mol
2-bromolysergic acid diethylamide Chemical Properties
- 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 - form
- Solid
- Boiling point:
- 580.7±50.0 °C(Predicted)
- pka
- 15.65±0.40(Predicted)
- color
- Off-white to light yellow
2-bromolysergic acid diethylamide Usage And Synthesis
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].
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.
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
[2] PAUL CARVEY . LSD and other related hallucinogens elicit myoclonic jumping behavior in the guinea pig[J]. Progress in Neuro-Psychopharmacology & Biological Psychiatry, 1989, 13 1: Pages 199-210. DOI: 10.1016/0278-5846(89)90017-1
[3] WACHEŁKO O, NOWAK K, TUSIEWICZ K, et al. A highly sensitive UHPLC-MS/MS method for determining 15 designer LSD analogs in biological samples with application to stability studies†[J]. Analyst, 2024, 2: 290-308. DOI: 10.1039/d4an01361a
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