Description

DOB Also known as:

• 2,5-Dimethoxy-4-bromoamphetamine[Wiki]

• (±)-1-(4-Bromo-2,5-dimethoxyphenyl)-2-aminopropane

• (±)-1-(4-Bromo-2,5-dimethoxyphenyl)-2-aminopropane

• (±)-2,5-Dimethoxy-4-bromoamphetamine

• (±)-2,5-Dimethoxy-4-bromoamphetamine

• (±)-4-Bromo-2,5-dimethoxy-α-methylphenethylamine

• 1-(4-Brom-2,5-dimethoxyphenyl)-2-propanamin[German][ACD/IUPAC Name]

• 1-(4-Bromo-2,5-dimethoxyphenyl)-2-propanamine[ACD/IUPAC Name]

• 1-(4-Bromo-2,5-diméthoxyphényl)-2-propanamine[French][ACD/IUPAC Name]

• 1-(4-Bromo-2,5-dimethoxyphenyl)propan-2-amine

• 4-Bromo-2,5-dimethoxy-amphetamine

• 5874

• 64638-07-9[RN]

• Benzeneethanamine, 4-bromo-2,5-dimethoxy-α-methyl-[ACD/Index Name]

• Benzeneethanamine, 4-bromo-2,5-dimethoxy-α-methyl-, (±)-

• brolamfetamine[INN]

• brolamfétamine[French][INN]

• BROLAMFETAMINE, (R)-

• BROLAMFETAMINE, (S)-

• Brolamfetaminum[Latin][INN]

• brolamphetamine

• brolanfetamina[Spanish][INN]

• dl-2,5-Dimethoxy-4-bromoamphetamine

• броламфетамин[Russian][INN]

• برولامفيتامين[Arabic][INN]

• 布苯丙胺[Chinese][INN]

• (±)2-(4-Bromo-2,5-dimethoxy-phenyl)-1-methyl-ethylamine

• (±)-2,5-Dimethoxy-4-bromoamphetamine

• (±)-4-Bromo-2,5-dimethoxy-α-methylphenethylamine

• [³H](+)DOB

• 1-(4-bromo-2,5-dimethoxyphenyl)-2-aminopropane

• 2-(2-Methoxy-Phenyl)-1-Methyl-Ethylamine

• 2-(4-Bromo-2,5-dimethoxy-phenyl)-1-methyl-ethylamine

• 2-(5-Bromo-2,4-dimethoxy-phenyl)-1-methyl-ethylamine

• 2,5-dimethoxy-(4-bromo)phenylisopropylamine

• 2,5-DIMETHOXY-4-BROMAMPHETAMIN

• 2,5-DIMETHOXY-4-BROMAMPHETAMINE

• 2,5-dimethoxy-4-bromoamphetamine|DOB

• 2,5-DIMETHOXY-4-BROMOAMPHETAMINE-D6

• 32156-26-6[RN]

• 43061-15-0[RN]

• 43061-16-1[RN]

• 4-Bromo-2,5-dimethoxy-a-methylbenzeneethanamine

• 4-Bromo-2,5-dimethoxyamphetamine

• 4-bromo-2,5-dimethoxyphenylisopropylamine

• 4-bromo-2,5-dimethoxyphenylisopropylaminerolamfetamine

• 4-bromo-2,5-dimethoxy-α-methylbenzeneethanamine

• 4-Bromo-DMA

• Benzeneethanamine,4-bromo-2,5-dimethoxy-α-methyl-(±)-

• DOB

• DOB-4

DOB is a relatively uncommon synthetic psychedelic. It is best known for its very low doses and long duration. Historically it has rarely been taken deliberately, but in place of LSD, however it has recently found its own place in the research chemical scene.

Summary

It is a member of the DOx family of psychedelic amphetamines. While DOB had first been synthesized in 1967 and briefly tested in 1971, it took until the 1991 publication of the book PiHKAL ("Phenethylamines I Have Known And Loved") by Alexander Shulgin to be documented in-depth. Today, DOB is used as a recreational drug and an entheogen.

It is still rarely sold online but is more commonly found in the streets the form of misrepresented LSD due to its ability to fit onto similar-sized blotter paper. Very little data exists about the pharmacological properties, metabolism, and toxicity of DOB in humans. Along with its sensitive dose-response, unusually long and unpredictable duration, many reports also suggest that this substance may be overly difficult to use safely for those who are not already very experienced with using hallucinogens.

It is highly advised to use harm reduction practices if using this substance.

Chemistry

Amphetamines are substituted phenethylamines containing a phenyl ring bound to an amino (NH2) group through an ethyl chain and a methyl group bound to the alpha carbon Rα.

DOB contains methoxy functional groups OCH3 attached to carbons R2 and R5 as well as a bromine atom attached to carbon R4 of the phenyl ring.

DOB is the amphetamine analogue of the phenethylamine 2C-B.

Dose Chart

Duration Chart

Interactions

Legal Status

Internationally, DOB is a Schedule I drug under the Convention on Psychotropic Substances.

Sources