Description
1,4-Diacetyl-2,5-piperazinedione (CAS No. 3027-05-2) is a high-purity organic compound with the molecular formula C8H10N2O4, widely utilized in pharmaceutical and biochemical research. This crystalline solid, also known as 1,4-diacetylpiperazine-2,5-dione or N,N’-Diacetylglycine Anhydride, serves as a versatile intermediate in peptide synthesis and heterocyclic chemistry. Its unique structure, featuring two acetyl groups on a piperazinedione backbone, enables applications in drug development and material science. Our product is rigorously tested for purity (≥98% by HPLC) and stability, ensuring optimal performance in sensitive reactions. Packaged under inert conditions to prevent degradation, it is ideal for researchers requiring precise, reproducible results.
Properties
- CAS Number: 3027-05-2
- Complexity: 291
- IUPAC Name: 1,4-diacetylpiperazine-2,5-dione
- InChI: InChI=1S/C8H10N2O4/c1-5(11)9-3-8(14)10(6(2)12)4-7(9)13/h3-4H2,1-2H3
- InChI Key: CBBKKVPJPRZOCM-UHFFFAOYSA-N
- Exact Mass: 198.06405680
- Molecular Formula: C8H10N2O4
- Molecular Weight: 198.18
- SMILES: CC(=O)N1CC(=O)N(CC1=O)C(=O)C
- Topological: 74.8
- Monoisotopic Mass: 198.06405680
- Synonyms: 1,4-Diacetyl-2,5-piperazinedione, 664-262-3, 1,4-diacetylpiperazine-2,5-dione, 3027-05-2, N,N’-Diacetylglycine Anhydride, 1,4-diacetyltetrahydro-2,5-pyrazinedione, 2,5-Piperazinedione, 1,4-diacetyl-, 1,4-DIACETYL-PIPERAZINE-2,5-DIONE, MFCD00059789, 1,4-Diacetyl-2,5-diketopiperazine, 21827-92-9, SCHEMBL64071, CBBKKVPJPRZOCM-UHFFFAOYSA-, DTXSID90337231, 1,4-Diacetyl-2,5-dioxopiperazine, BCP19706, N,N’-diacetyl-2,5-piperazinedione, N,N’-Diacetyl-2,5-dioxopiperazine, SBB092274, STK955333, AKOS005069543, SY051121, DB-250072, CS-0033721, D1073, 1,4-diacetyl-2,5-dioxo-1,4-diazaperhydroine, D72581, 12B-033, 1,4-Diacetyl-2,5-piperazinedione, >=98% (HPLC), N,N inverted exclamation mark -Diacetylglycine Anhydride, InChI=1/C8H10N2O4/c1-5(11)9-3-8(14)10(6(2)12)4-7(9)13/h3-4H2,1-2H3
Application
1,4-Diacetyl-2,5-piperazinedione is primarily employed as a building block in the synthesis of complex heterocycles and peptidomimetics. It facilitates the study of enzyme inhibition mechanisms due to its structural similarity to peptide bonds. Researchers also utilize it to develop novel antimicrobial agents and investigate protein-protein interactions. Its anhydride functionality makes it valuable in polymer chemistry for crosslinking applications.
Safety and Hazards
GHS Hazard Statements
- H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
Precautionary Statements
- P261, P264, P264+P265, P270, P272, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P332+P317, P333+P317, P337+P317, P362+P364, and P501
Hazard Classes and Categories
- Acute Tox. 4 (100%)
- Skin Irrit. 2 (100%)
- Skin Sens. 1 (100%)
- Eye Irrit. 2 (100%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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