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53581-53-6

53581-53-6 Structure

53581-53-6 Structure
IdentificationBack Directory
[Name]

(+/-)-2,5-DIMETHOXY-4-BROMO-AMPHETAMINE HYDROBROMIDE
[CAS]

53581-53-6
[Synonyms]

dob
[+/-]-DOB HYDROBROMIDE
KOUBEZAODVTFTG-UHFFFAOYSA-N
4-bromo-2,5-dimethoxyamphetamine hydrobromide
dl-4-bromo-2,5-dimethoxyamphetaminehydrobromide
dl-2,5-dimethoxy-4-bromoamphetaminehydrobromide
(+-)-2,5-dimethoxy-4-bromoamphetamine*hydrobromid
(+/-)-2,5-DIMETHOXY-4-BROMO-AMPHETAMINE HYDROBROMIDE
(+/-)-2,5-Dimethyoxy-4-bromo-amphetamine hydrobromide
dl-4-bromo-2,5-dimethoxy-alpha-methylphenethylaminehydrobromide
TIANFU-CHEM (+/-)-2,5-DIMETHOXY-4-BROMO-AMPHETAMINE HYDROBROMIDE
4-bromo-2,5-dimethoxy-alpha-methyl-,hydrobromide,dl-phenethylamin
Benzeneethanamine,4-bromo-2,5-dimethoxy-a-methyl-, hydrobromide (1:1)
Phenethylamine, 4-bromo-2,5-dimethoxy-alpha-methyl-, hydrobromide, DL-
[Molecular Formula]

C11H17Br2NO2
[MDL Number]

MFCD00069251
[MOL File]

53581-53-6.mol
[Molecular Weight]

355.07
Safety DataBack Directory
[Symbol(GHS) ]


GHS06
[Signal word ]

Danger
[Hazard statements ]

H302-H310-H330
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P262-P264-P270-P280-P302+P350-P310-P322-P361-P363-P405-P501-P260-P271-P284-P304+P340-P310-P320-P403+P233-P405-P501
[Hazard Codes ]

T+
[Risk Statements ]

26/27/28
[Safety Statements ]

28-36/37-45
[RIDADR ]

UN 2811 6.1/PG 2
[WGK Germany ]

3
[RTECS ]

SH0300000
[HazardClass ]

6.1(a)
[PackingGroup ]

I
[Toxicity]

A hallucinogenic (psychedelic) agent that is obtained by chemical synthesis. It may catalyze severe emotional problems or psychosis in predisposed individuals, and in large doses, produces peripheral arterial spasm which, if not treated, can lead to gangrene. DOB is a potent serotonin 5-HT2 agonist, and although the underlying mechanism of action for hallucinogens is not well understood, this may be related to its actions in the CNS. Symptoms include hyperreflexia, restlessness, perceptual alterations, and illusions, including changes in touch, taste, and odor, and the thinking process is substantially altered. At high doses, it causes hallucinations, loss of contact with reality, and pain and coldness in the extremities at toxic levels. Therapeutically, peripheral arterial spasm has been treated with intraarterial tolazoline hydrochloride. Its LD50 is in mice 80 mg/kg, i.v., in rats 8 mg/kg, i.p., in dogs 4 mg/kg. i.v., and in monkeys 2 mg/kg, i.v.
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