{"id":245,"date":"2026-08-29T08:54:21","date_gmt":"2026-08-29T08:54:21","guid":{"rendered":"https:\/\/nex-chems.com\/?post_type=product&p=245"},"modified":"2026-09-01T14:01:08","modified_gmt":"2026-09-01T14:01:08","slug":"buy-3-cmc-pellets-220mg","status":"publish","type":"product","link":"https:\/\/nex-chems.com\/it\/product\/buy-3-cmc-pellets-220mg\/","title":{"rendered":"3-CMC Pellets \u2013 220mg"},"content":{"rendered":"

Buy 3-CMC Pellets \u2013 220mg<\/h1>\n

3-CMC Chemical Purchase Description<\/h2>\n

When you buy 3-CMC<\/a><\/strong>, also known as 3-chloromethcathinone<\/strong> or clophedrone<\/strong>, it is a synthetic cathinone belonging to a broader class of \u03b2-keto phenethylamine derivatives. From a chemical perspective, 3-CMC contains a substituted phenyl ring, a ketone group, and a methylamino side chain. The compound is structurally related to other methcathinone derivatives, but the position of its chlorine substituent distinguishes 3-CMC from positional isomers such as 2-CMC and 4-CMC.<\/p>\n

3-CMC Chemical Name and Molecular Formula<\/h3>\n

The IUPAC name for 3-CMC is 1-(3-chlorophenyl)-2-(methylamino)propan-1-one<\/strong>. Its molecular formula is C\u2081\u2080H\u2081\u2082ClNO<\/strong>, and its molecular weight is approximately 197.66 g\/mol<\/strong>. The compound has the CAS number 1049677-59-9<\/strong>. These identifiers are useful for analytical chemistry, forensic testing, compound identification, and scientific literature searches.<\/p>\n

The molecular structure can be represented using the SMILES notation:<\/p>\n

O=C(C1=CC(Cl)=CC=C1)C(C)NC<\/strong><\/p>\n

Its InChIKey is VOEFELLSAAJCHJ-UHFFFAOYSA-N<\/strong>, providing another standardized identifier for database and analytical applications.<\/p>\n

Chemical Structure of 3-CMC<\/h3>\n

The structure of 3-CMC can be understood by examining its principal functional components.<\/p>\n

First, the molecule contains a phenyl ring<\/strong>. A chlorine atom is attached to the third position of this aromatic ring, giving the compound its “3-chloro” designation.<\/p>\n

Second, the molecule contains a \u03b2-keto group<\/strong>. This carbonyl-containing feature is characteristic of cathinone compounds and distinguishes synthetic cathinones from their corresponding phenethylamine analogues.<\/p>\n

Third, 3-CMC contains a methylamino group<\/strong> attached to the carbon adjacent to the carbonyl group. The presence of this N-methylamino substituent is responsible for the “methcathinone” component of its chemical classification.<\/p>\n

Together, these structural elements place 3-CMC within the synthetic cathinone family. The European Union Drugs Agency describes synthetic cathinones as \u03b2-keto analogues of corresponding phenethylamines.<\/p>\n

3-CMC and Synthetic Cathinones<\/h3>\n

Synthetic cathinones are chemically related to cathinone<\/strong><\/a>, a naturally occurring compound associated with the khat plant (Catha edulis<\/em>). Synthetic derivatives modify the basic cathinone structure through substitutions on the aromatic ring, nitrogen atom, or carbon side chain.<\/p>\n

The \u03b2-keto group is particularly important from a chemical perspective. According to the EUDA, this feature makes cathinone derivatives more polar than corresponding phenethylamine derivatives, which can influence their ability to cross the blood-brain barrier and consequently affect their pharmacological characteristics.<\/p>\n

However, the pharmacology of many ring-substituted synthetic cathinones remains incompletely characterized. Therefore, structural similarity between compounds should not be interpreted as evidence that two substances have identical biological effects.<\/p>\n

3-CMC Chirality and Stereochemistry<\/h3>\n

An important chemical characteristic of 3-CMC is chirality<\/strong>.<\/p>\n

The molecule contains a chiral center within its side chain. As a result, two possible enantiomers exist: (R)-3-CMC<\/strong> and (S)-3-CMC<\/strong>. These molecules have the same molecular formula and connectivity but differ in their three-dimensional spatial arrangement.<\/p>\n

The World Health Organization’s Expert Committee on Drug Dependence noted that information concerning the enantiomeric composition of 3-CMC encountered on the drug market was limited. Consequently, analytical characterization can be important when determining the precise composition of a sample.<\/p>\n

This stereochemical property matters in analytical chemistry because different enantiomers can interact differently with biological targets. Consequently, researchers studying 3-CMC may need analytical techniques that can distinguish stereoisomers when stereochemical composition matters.<\/p>\n

3-CMC Positional Isomers<\/h3>\n

3-CMC belongs to a group of chloromethcathinone positional isomers. The number in the name identifies the location of the chlorine atom on the phenyl ring.<\/p>\n

For example:<\/p>\n