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1,3-Cyclohexanedione (1,3-CHD) (six-membered cyclic beta-diketone), a largelly used as a building block in organic synthesis, pharmaceutical & agrochemical intermediates. Also referred to as (Dihydroresorcinol, Hydroresorcinol) by speciality chemical suppliers. 1,3 Cyclohexanedione participates in condensation, alkylation, and cyclization reactions, providing access to heterocyclic scaffolds for drug design and fine chemicals. Cyclohexane-1,3-dione is a cyclohexanedione carrying oxo substituents at positions 1 and 3. This is a beta-diketone and a cyclohexanedione. With its high chemical stability and versatile reactivity make it a preferred precursor in the preparation of CNS-active agents, herbicides, and specialty intermediates. Supplied in technical grade (B2B Advantage) with consistent quality for reproducible synthetic applications. We are among the trusted 1,3-Cyclohexanedione manufacturers and suppliers worldwide, with reliable lead times and global supply capability.
1,3-Cyclohexanedione (1,3-CHD) (six-membered cyclic beta-diketone), a largelly used as a building block in organic synthesis, pharmaceutical & agrochemical intermediates. Also referred to as (Dihydroresorcinol, Hydroresorcinol) by speciality chemical suppliers. 1,3 Cyclohexanedione participates in condensation, alkylation, and cyclization reactions, providing access to heterocyclic scaffolds for drug design and fine chemicals. Cyclohexane-1,3-dione is a cyclohexanedione carrying oxo substituents at positions 1 and 3. This is a beta-diketone and a cyclohexanedione. With its high chemical stability and versatile reactivity make it a preferred precursor in the preparation of CNS-active agents, ...
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Pharmaceutical, Agrochemicals
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Pharmaceutical Actives & Precursors, Agrochemical Intermediates
Intermediates & Precursors, Specialty & Advanced Intermediates
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Chemical Properties & Specifications
Eye Irritation (Category 2A), Skin Irritation (Category 2), Acute Toxicity: Category 4 (oral)
P280, P305+P351+P338, P261, P264
H302, H315, H319
Used as a key heterocyclic building block for synthesizing pharmaceuticals and fine chemicals.
Participates in reactions to form CNS-active agents, anti-inflammatory compounds, and herbicide precursors. Used to synthesize drugs such as Ondansetron (antiemetic), Carvedilol (beta-blocker for hypertension), and Nitisinone
Serves in Michael addition, Knoevenagel condensation, and alkylation reactions for diverse chemical scaffolds.
Provides structural motifs for medicinal chemistry research in neuroactive and cardiovascular drug candidates.
Used in the preparation of ligands, dyes, and agrochemical intermediates
Compatible with multiple organic transformations including alkylation and condensation.
Forms key intermediates for heterocyclic compound libraries.
Critical intermediate for manufacturing HPPD inhibitor herbicides, which are used for selective grass weed control in crops like corn and rice. Examples include Mesotrione and Sulcotrione
Serves as a derivatizing agent for the analysis of low-molecular-weight aldehydes in food and environmental samples
Store at 15–30 °C in a dry, ventilated space
Protect from moisture, sunlight, and strong oxidizers
1 kg, 5 kg, 25 kg sealed HDPE drums or fiberboard containers
2 years under recommended storage conditions; maintain sealed packaging
Palletized, stack ≤2 drums; comply with local chemical transport regulations
It is used as a heterocyclic building block in pharmaceuticals, herbicide precursors, and specialty organic synthesis.
No, it is primarily an intermediate for further chemical synthesis, not a final formulation.
Handle in a well-ventilated area with gloves and eye protection; avoid dust inhalation.
SDS, CoA, TDS, and ISO/GMP certification for research or industrial applications.
Soluble in ethanol, acetone, dichloromethane, sparingly soluble in water; compatible with standard organic reaction media.
RoHS: Not applicable (industrial chemical).
