Liquid 1B-LSD 100mcg Drop Bottle

Liquid-1B-LSD
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CAS Number2349376-12-9 Chemical Classlysergamides Density1.2±0.1 g/cm3 Flash Point:300.5±30.1 °C IUPAC name(6aR,9R)-N,N-diethyl-6-methyl-4-butanoyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide Molar mass393.531 g·mol−1 Molar Refractivity:115.8±0.5 cm3 Not For Human ConsumptionNot For Human Consumption Chem Spider number82827098 Index of Refraction:1.624 Enthalpy of Vaporization:85.9±3.0 kJ/mol PubChem CID145875086 UNIIY6JQX3L6LP Vapour Pressure:0.0±1.6 mmHg at 25°C

1B-LSD (1-Butanoyl-d-lysergic acid diethylamide) is a molecule substance of the Lysergamide family. It is comparable to and 1P-LSD and other Lysergamides. 1B-LSD surfaced on the research chemical market in 2018. Very little data exists about the research chemical or about who discovered it.

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1B-LSD (1-Butanoyl-d-lysergic acid diethylamide) is a molecule substance of the Lysergamide family. It is comparable to and 1P-LSD and other Lysergamides. 1B-LSD surfaced on the research chemical market in 2018. Very little data exists about the research chemical or about who discovered it.

All Lysergamides are isolated from a fungus called ergo. Ergot contains compounds known as ergot alkaloids, each containing a system called the tetracyclic ergoline ring system. Modifying the ergoline ring system in the N1 position are the most frequently performed changes you’ll see. Indole nitrogen is easily accessible for reactions and additions. 1B-LSD is structurally similar to 1P-LSD and named for the butyryl group bound to the nitrogen of the polycyclic indole group. In contrast to LSD, 1B-LSD has an additional N1-butyryl group.

Like other acyl homologs (such as 1P-LSD), 1B-LSD is deacylated via CYP1A2 and CYP3A4 by the elimination of the butyric acid (the “B” in 1B-LSD). Why use butyric acid to begin with? Butyric acid is a fatty acid that helps break down the fibre. When the butyric acid is eliminated, you will end up with a different compound. 

1-akylated lysergamide derivatives are useful research chemicals. Lysergic acid N,N-dimethylamide is derived from lysergic acid amide, not LSD. Following this logic, we can assume that the 1-alkyl and 1-acyl derivatives of the N,N-dimethyl isomer do not fall under controlled substance laws. Ergo, we can modify the ergoline ring system in the N1 position to create derivatives like 1B-LSD.

A Research chemicals

CAS Number:
2349376-12-9
Chemical Class:
lysergamides
Chemical name:
1B-LSD (N1-butyryl-lysergic acid diethylamide)
Density:
1.2±0.1 g/cm3
Flash Point::
300.5±30.1 °C
Formula:
C24-H31-N3-O2
IUPAC name:
(6aR,9R)-N,N-diethyl-6-methyl-4-butanoyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide
Molar mass:
393.531 g·mol−1
Molar Refractivity::
115.8±0.5 cm3
Not For Human Consumption :
Not For Human Consumption
Purity:
99.97
Chem Spider number:
82827098
Index of Refraction::
1.624
InChI:
InChI=1S/C24H31N3O2/c1-5-9-22(28)27-15-16-13-21-19(18-10-8-11-20(27)23(16)18)12-17(14-25(21)4)24(29)26(6-2)7-3/h8,10-12,15,17,21H,5-7,9,13-14H2,1-4H3/t17-,21-/m1/s1 Key:SVRFNPSJPIDUBC-DYESRHJHSA-N
Enthalpy of Vaporization::
85.9±3.0 kJ/mol
PubChem CID:
145875086
UNII:
Y6JQX3L6LP
Vapour Pressure::
0.0±1.6 mmHg at 25°C
Canonical SMILES:
CCCC(=O)N1C=C2CC3C(=CC(CN3C)C(=O)N(CC)CC)C4=C2C1=CC=C4
Isomeric SMILES:
CCCC(=O)N1C=C2C[C@@H]3C(=C[C@H](CN3C)C(=O)N(CC)CC)C4=C2C1=CC=C4
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