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CAS 3815-86-9

Malonic Acid Dihydrazide TCI M3206

Malonic Acid Dihydrazide TCI M3206
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TCI M3206 Malonic Acid Dihydrazide, bearing CAS number 3815-86-9, is a dihydrazide compound derived from malonic acid, a three-carbon dicarboxylic acid whose two carboxyl groups have both been converted into hydrazide functionalities. It belongs to the family of highly versatile non-heterocyclic building blocks used in synthetic chemistry. In the laboratory, the presence of a hydrazide group at each end of the molecule makes it a bifunctional reagent, meaning a single molecule is able to bind two other molecules simultaneously. This property makes it useful for constructing extended chains, molecular bridges, and new heterocyclic ring systems.

The characteristic that makes this compound a preferred choice is the high and dependable reactivity of the hydrazide group toward carbonyl functions. Hydrazides react rapidly with aldehydes and ketones to form stable hydrazones, and this reaction proceeds under mild conditions without requiring complicated catalysts. The hydrazide group is also a common precursor to a variety of nitrogen-containing heterocyclic rings such as pyrazolones, oxadiazoles, and triazoles through cyclisation with suitable reagents. In addition, its paired nitrogen and oxygen atoms are capable of coordinating metal ions, so the compound is frequently employed as a ligand framework in research work.

In Indonesian laboratories, this building block is typically found in university and institutional research settings where organic synthesis, heterocyclic chemistry, and coordination chemistry are studied. It serves researchers preparing hydrazone derivatives, building nitrogen heterocycle libraries, or assembling ligand scaffolds for metal complex investigations. As a TCI-branded reagent supplied by AMI Scientific, it suits synthesis groups that need a reliable bifunctional starting material for multi-step preparative work.

  • Hydrazone synthesis: the two terminal hydrazide groups condense rapidly with aldehydes and ketones under mild conditions to give stable hydrazone products without complex catalysts.
  • Heterocyclic ring construction: the hydrazide functionality serves as a common precursor for building nitrogen-containing rings such as pyrazolones, oxadiazoles, and triazoles through cyclisation with appropriate reagents.
  • Ligand framework preparation: the paired nitrogen and oxygen atoms coordinate metal ions, making this compound a frequently chosen scaffold for preparing ligands in coordination chemistry research.
  • Bifunctional linking and bridging: because one molecule can bind two partner molecules simultaneously, it is well suited to assembling extended chains and molecular bridges in preparative work.
  • General building block chemistry: as a versatile non-heterocyclic building block derived from a three-carbon dicarboxylic acid, it supports multi-step organic synthesis routes requiring a symmetrical difunctional core.

Brand TCI
CAS number 3815-86-9
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes available in standard laboratory research pack sizes; please confirm the currently offered packing when ordering
Physical form —
Storage store in a closed container under the conditions indicated on the manufacturer's label
  • Product code: M3206

Store this reagent in a tightly closed original container, kept in a cool, dry place away from direct sunlight, moisture, and sources of heat or ignition. Hydrazide compounds are reactive toward carbonyl-containing substances, so keep the container well sealed and separated from aldehydes, ketones, and strong oxidising agents. Handle the material in a well-ventilated area or inside a fume hood, and wear standard laboratory personal protective equipment including safety glasses, gloves, and a laboratory coat. Avoid generating dust, avoid inhalation and direct skin or eye contact, and wash hands thoroughly after handling. Always consult the manufacturer's Safety Data Sheet before use and follow institutional procedures for chemical waste disposal.

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