2C-P (hydrochloride) (CAS 1359704-27-0) | Cayman Chemical
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2C-P (hydrochloride)

Item № 11696
CAS № 1359704-27-0
Purity ≥98%

Formulation:  A crystalline solid

SIZE PRICE QUANTITY SUBTOTAL
CART TOTAL
     5 mg $44.00 0.00
     10 mg $68.00 0.00
     50 mg $264.00 0.00

Pricing updated 2018-10-21. Prices are subject to change without notice.

Description
Synonyms
  • 2,5-Dimethoxy-4-propylphenethylamine

A series of 2,5-dimethoxy phenethylamines, collectively referred to as 2Cs, have psychoactive effects.1,2 The most effective 2C compounds are substituted at the 4 position of the aromatic ring; many are scheduled as illegal substances.3,4 2C-P is described formally as 2,5-dimethoxy-4-propylphenethylamine and is structurally analogous to the psychedelic drug 2C-B. The physiological and toxicological properties of this compound are not known. LC-MS/MS screening methods for this designer drug have been developed.5 This product is intended for forensic and research purposes.

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Technical Information
Formal Name
2,5-dimethoxy-4-propyl-benzeneethanamine, monohydrochloride
CAS Number
1359704-27-0
Synonyms
  • 2,5-Dimethoxy-4-propylphenethylamine
Molecular Formula
C13H21NO2 • HCl
Formula Weight
259.8
Purity
≥98%
Formulation
A crystalline solid
λmax
204, 227, 292 nm
SMILES
NCCC1=CC(OC)=C(CCC)C=C1OC.Cl
InChI Code
InChI=1S/C13H21NO2.ClH/c1-4-5-10-8-13(16-3)11(6-7-14)9-12(10)15-2;/h8-9H,4-7,14H2,1-3H3;1H
InChI Key
GTAHFPSNRIBSFT-UHFFFAOYSA-N
Schedule
I

Warning - this product is not for human or veterinary use.

Shipping & Storage
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Stability
≥ 2 years
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Additional Information

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References & Product Citations
Product Description References

1. Bruno, R., Matthews, A.J., Dunn, M., et al. Emerging psychoactive substance use among regular ecstasy users in Australia. Drug and Alcohol Dependence 124(1-2), 19-25 (2012).

2. Moya, P.R., Berg, K.A., Gutiérrez-Hernandez, M.A., et al. Functional selectivity of hallucinogenic phenethylamine and phenylisopropylamine derivatives at human 5-hydroxytryptamine (5-HT)2A and 5-HT2C receptors. Journal of Pharmacology and Experimental Therapeutics 321, 1054-1061 (2007).

3. Meyer, M.R., and Maurer, H.H. Metabolism of designer drugs of abuse: An updated review. Curr. Drug Metab. 11(5), 468-482 (2010).

4. Nagai, F., Nonaka, R., and Satoh Hisashi Kamimura, K. The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain. European Journal of Pharmacology 559(2-3), 132-137 (2007).

5. Wohlfarth, A., Weinmann, W., and Dresen, S. LC-MS/MS screening method for designer amphetamines, tryptamines, and piperazines in serum. Anal. Bioanal. Chem. 396(7), 2403-2414 (2010).

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