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ChemicalBook >  Product Catalog >  Analytical Chemistry >  Standard >  Standard Substance >  2,5-DIMETHOXY-4-(PROPYLTHIO)BENZENEETHANAMINE, YDROCHLORIDE

2,5-DIMETHOXY-4-(PROPYLTHIO)BENZENEETHANAMINE, YDROCHLORIDE

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2,5-DIMETHOXY-4-(PROPYLTHIO)BENZENEETHANAMINE, YDROCHLORIDE Basic information

Product Name:
2,5-DIMETHOXY-4-(PROPYLTHIO)BENZENEETHANAMINE, YDROCHLORIDE
Synonyms:
  • 2,5-DIMETHOXY-4-(PROPYLTHIO)BENZENEETHANAMINE, YDROCHLORIDE
  • 2,5-Dimethoxy-4-(n)-propylthiophenethylamine hydrochloride solution
  • 2C-T-7 (hydrochloride)
  • 2C-T-7 (hydrochloride) (exempt preparation)
  • 2-(2,5-dimethoxy-4-propylsulfanylphenyl)ethanamine:hydrochloride
  • 2,5-Dimethoxy-4-(propylthio)benzeneethanaminehydrochloride
  • 2,5-Dimethoxy-4-(propylsulfanyl)phenethylamine Hydrochloride
  • 2,5-Dimethoxy-4-(propylthio)phenethylamine Hydrochloride
CAS:
850140-15-7
MF:
C13H22ClNO2S
MW:
291.83
Product Categories:
  • Amines
  • Inhibitors
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Sulfur & Selenium Compounds
Mol File:
850140-15-7.mol
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2,5-DIMETHOXY-4-(PROPYLTHIO)BENZENEETHANAMINE, YDROCHLORIDE Chemical Properties

Flash point:
2℃
storage temp. 
-20°C
solubility 
DMF: 20 mg/ml
DMSO: 16 mg/ml
Ethanol: 11 mg/mlPBS (pH 7.2): 5 mg/ml
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Safety Information

Hazard Codes 
F,Xn
Risk Statements 
11-20/21/22-36
Safety Statements 
16-26-36/37
RIDADR 
UN 1648 3 / PGII
WGK Germany 
2
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2,5-DIMETHOXY-4-(PROPYLTHIO)BENZENEETHANAMINE, YDROCHLORIDE Usage And Synthesis

Description

A series of 2,5-dimethoxy phenethylamines, collectively referred to as 2Cs, have psychoactive effects. The most effective 2C compounds are substituted at the 4 position of the aromatic ring. Many are regulated as illegal substances. 2C-T-7 is a 2,5-dimethoxy phenethylamine with a propylthio group in the 4 position. Its metabolism has been described. LC-MS/MS screening methods for this designer drug have been developed. This product is intended for forensic and research purposes.

Uses

Phenethylamine derivative. Inhibits monoamine oxidase A (MAO-A) and monoamine oxidase B (MAO-B)

References

[1] MARKUS R MEYER  Hans H M. Metabolism of designer drugs of abuse: an updated review.[J]. Current drug metabolism, 2010, 11 5: 468-482. DOI: 10.2174/138920010791526042
[2] ARIANE WOHLFARTH  Sebastian D  Wolfgang Weinmann. LC-MS/MS screening method for designer amphetamines, tryptamines, and piperazines in serum[J]. Analytical and Bioanalytical Chemistry, 2010, 396 7: 2403-2414. DOI: 10.1007/s00216-009-3394-4
[3] RAIMONDO BRUNO . Emerging psychoactive substance use among regular ecstasy users in Australia[J]. Drug and alcohol dependence, 2012, 124 1: Pages 19-25. DOI: 10.1016/j.drugalcdep.2011.11.020
[4] PABLO R MOYA. Functional selectivity of hallucinogenic phenethylamine and phenylisopropylamine derivatives at human 5-hydroxytryptamine (5-HT)2A and 5-HT2C receptors.[J]. Journal of Pharmacology and Experimental Therapeutics, 2007, 321 3: 1054-1061. DOI: 10.1124/jpet.106.117507
[5] FUMIKO NAGAI  Kanako S H K  Ryouichi Nonaka. The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain[J]. European journal of pharmacology, 2007, 559 2: Pages 132-137. DOI: 10.1016/j.ejphar.2006.11.075

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