Description

Carindacillin is a semi-synthetic penicillin antibiotic derived from carbenicillin. This compound is valued for its enhanced stability and spectrum of activity against a range of gram-negative and gram-positive bacteria. It is primarily utilized in pharmaceutical research and development, serving as a key intermediate or active pharmaceutical ingredient (API) in the formulation of antibacterial medications. Our supply ensures high purity and consistency, meeting the stringent demands of the global pharmaceutical and fine chemical industries.

Application

• Active Pharmaceutical Ingredient (API) in antibacterial injectable formulations.
• Key intermediate in the synthesis of advanced penicillin-based antibiotics.
• Reference standard for quality control and analytical testing in pharmaceutical laboratories.
• Research chemical for studying bacterial resistance mechanisms and developing new antimicrobial agents.
• Raw material for the preparation of veterinary medicinal products.

Basic Information

Product Name	Carindacillin
CAS No.	35531-88-5
Molecular Formula	C17H18N2O6S
Molecular Weight	378.40 g/mol
Synonyms	Carbenicillin indanyl sodium; Carindapen; Carindacillin sodium; (2S,5R,6R)-6-[[(2R)-2-Carboxy-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid indan-5-yl ester; Geopen; Geocillin; CP-15,664; Indanyl carbenicillin
EINECS	Contact for details

Quality Control

Our Carindacillin is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling via HPLC, to ensure it meets high-purity standards suitable for pharmaceutical use. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance with relevant guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 2.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm
Microbial Limits	Meets Ph. Eur. requirements

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.