D-101
(±)-2,5-二甲氧基-4-溴苯丙胺 盐酸盐 溶液
1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®
别名:
DL-DOB 盐酸盐
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关于此项目
经验公式（希尔记法）:
C11H16BrNO2 · HCl
化学文摘社编号:
分子量:
310.62
UNSPSC Code:
41116107
PubChem Substance ID:
EC Number:
200-659-6
MDL number:
InChI key
SPBBKPOIDQIWDZ-UHFFFAOYSA-N
InChI
1S/C11H16BrNO2.ClH/c1-7(13)4-8-5-11(15-3)9(12)6-10(8)14-2;/h5-7H,4,13H2,1-3H3;1H
SMILES string
NC(C)CC1=CC(OC)=C(Br)C=C1OC.Cl
grade
certified reference material
form
liquid
feature
(Snap-N-Spike®)
packaging
ampule of 1 mL
manufacturer/tradename
Cerilliant®
drug control
psicótropo (Spain); Decreto Lei 15/93: Tabela IIA (Portugal)
concentration
1.0 mg/mL in methanol (as free base)
technique(s)
gas chromatography (GC): suitable, liquid chromatography (LC): suitable
application(s)
pharmaceutical (small molecule)
format
single component solution
storage temp.
−20°C
General description
Also known as bromo-DMA or brolamfetamine, DOB is a D-substituted amphetamine of the phenethylamine family of psychedelics. This designer drug, often misrepresented as LSD, is an extremely potent hallucinogen with a long duration of action of up to several days. This certified Snap-N-Spike® solution is suitable for use as starting material in calibrators or controls for phenethylamine testing methods by LC/MS or GC/MS for clinical toxicology, forensic analysis, or urine drug testing applications.
Legal Information
CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
target_organs
Eyes
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
49.5 °F - closed cup
flash_point_c
9.7 °C - closed cup
法规信息
监管及禁止进口产品
此项目有
Danielle M Schultz et al.
Bioorganic & medicinal chemistry, 16(11), 6242-6251 (2008-05-10)
Phenylalkylamines that possess conformationally rigidified furanyl moieties in place of alkoxy arene ring substituents have been shown previously to possess the highest affinities and agonist functional potencies at the serotonin 5-HT(2A) receptor among this chemical class. Further, affinity declines when
Tatsuyuki Kanamori et al.
Journal of analytical toxicology, 26(2), 61-66 (2002-03-28)
The in vivo metabolism of 4-bromo-2,5-dimethoxyphenethylamine (2C-B), a ring-substituted psychoactive phenethylamine, in the rat was studied. Male Wistar rats were administered 10 mg/kg of 2C-B hydrochloride orally, and 24 h urine fractions were collected. After enzymatic hydrolysis of the urine
Marie Balíková
Forensic science international, 153(1), 85-91 (2005-06-28)
2,5-Dimethoxy-4-bromoamphetamine (DOB) is a strongly acting hallucinogen with an estimated effective dose of 2 mg for an 80 kg man. The case of two men who ingested a new "hallucinogen LSD-like" designer drug is reported here. They experienced intense hallucinations
Andreas H Ewald et al.
Journal of mass spectrometry : JMS, 41(4), 487-498 (2006-02-14)
Studies are described on the metabolism and the toxicological analysis of the amphetamine-derived designer drug 2,5-dimethoxy-4-bromo-amphetamine (DOB) and its corresponding N-methyl analogue 2,5-dimethoxy-4-bromo-methamphetamine (MDOB) in rat urine using gas chromatographic/mass spectrometric techniques. The identified metabolites indicated that DOB was metabolized
Michael A Benneyworth et al.
Psychopharmacology, 179(4), 854-862 (2005-01-13)
The drug discrimination procedure is the most frequently used in vivo model of hallucinogen activity. Historically, most drug discrimination studies have been conducted in the rat. With the development of genetically modified mice, a powerful new tool has become available
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