ResidualSolventsGCQualityChecker

Residual Solvents GC

LabEx laboratory QC CSV→JSON URS & FS chromatography microbiology utilities / cleanroom
Open selection

Residual Solvents GC Quality Checker — Residual Solvents Control (GC)

ℹ️ Utility checks residual solvent content according to ICH Q3C guidelines:
• Class 1 (Avoid): Benzene (≤2 ppm) — carcinogen
• Class 2 (Limit): Methanol (≤3000 ppm), Acetonitrile (≤410 ppm), Dichloromethane (≤600 ppm), Hexane (≤290 ppm)
• Class 3 (Low Toxicity): Ethyl Acetate (≤5000 ppm), Acetone (≤5000 ppm)
• Total Solvents (≤5000 ppm or 0.5%)

⚠️ CRITICAL: Benzene exceedance (>2 ppm) is unacceptable due to high carcinogenicity!
Exceedance of total solvents indicates insufficient drying or purification.

Usage:
ResidualSolventsGCQualityChecker.exe → demo mode (console output)
ResidualSolventsGCQualityChecker.exe input.csv output.json → evaluate your data

Input format:
BatchNumber,ProductName,MethanolPPM,AcetonitrilePPM,DichloromethanePPM,HexanePPM,EthylAcetatePPM,AcetonePPM,BenzenePPM,TotalSolventsPPM

Example:
API-2026-RS-001,Active Ingredient X,1500.0,200.0,300.0,100.0,2500.0,1000.0,0.5,5600.5

— WHY IS THIS NEEDED?
Residual solvents may be present in Active Pharmaceutical Ingredients (APIs) and excipients after synthesis or purification.
According to ICH Q3C, they are classified by toxicity:
• Class 1: Solvents to be avoided (known carcinogens or environmental toxins).
• Class 2: Solvents to be limited (non-genotoxic animal carcinogens or causing other irreversible toxic effects).
• Class 3: Solvents with low potential toxicity to humans.

⚠️ CRITICAL:
• Benzene ≤2 ppm — strict limit due to carcinogenicity. Even trace amounts are dangerous.
• Total Solvents ≤5000 ppm (0.5%) — standard limit for most APIs unless justified otherwise.
• Methanol ≤3000 ppm — often used in synthesis but toxic upon accumulation.
• Dichloromethane ≤600 ppm — potential carcinogen, requires strict control.

Key features:
• Check of solvents from all three ICH Q3C classes
• Strict control of Benzene (Class 1)
• Calculation and check of total solvents
• Generation of reports compatible with LIMS LabWare
• Support for multiple samples in one file

Critical parameters:
• Benzene: ≤2 ppm (Class 1)
• Methanol: ≤3000 ppm (Class 2)
• Acetonitrile: ≤410 ppm (Class 2)
• Dichloromethane: ≤600 ppm (Class 2)
• Hexane: ≤290 ppm (Class 2)
• Ethyl Acetate: ≤5000 ppm (Class 3)
• Acetone: ≤5000 ppm (Class 3)
• Total Sum: ≤5000 ppm

💡 Usage tips:
1. Analysis method: Gas Chromatography with Flame Ionization Detector (GC-FID) or Mass Spectrometry (GC-MS).
2. Sample preparation: Usually direct solution injection or HeadSpace method.
3. If the sum of individual solvents exceeds 5000 ppm, the batch is rejected, even if each individual solvent is within limits.
4. For Class 3 solvents, the limit may be higher if justified by the manufacturing process, but 5000 ppm is used by default.
5. Benzene must be determined with high sensitivity due to its low limit.

⚠️ Note: The presence of Class 1 solvents (e.g., benzene) should be completely excluded from the manufacturing process if possible. If their presence is unavoidable, they must be controlled using validated analytical procedures with detection limits appropriate to the level of toxicity.

input.csv

BatchNumber,ProductName,MethanolPPM,AcetonitrilePPM,DichloromethanePPM,HexanePPM,EthylAcetatePPM,AcetonePPM,BenzenePPM,TotalSolventsPPM
API-2026-RS-001,Active Pharmaceutical Ingredient X,1500.0,200.0,300.0,100.0,2500.0,1000.0,0.5,5600.5
API-2026-RS-002,Intermediate Compound Y,2800.0,400.0,550.0,280.0,4800.0,4900.0,1.8,4900.0

URS & FS — Residual Solvents GC

This document describes the user requirements and functional specification for ResidualSolventsGCQualityChecker. The utility is intended for QC laboratory use as a rule-based check of data prepared from an instrument, LIMS, ELN, MES or an approved input.csv.

URS — User Requirements Specification

IDRequirementCriticalityAcceptance criterion
URS-001The utility shall accept input.csv with approved columns: BatchNumber, ProductName, MethanolPPM, AcetonitrilePPM, DichloromethanePPM, HexanePPM, EthylAcetatePPM, AcetonePPM, BenzenePPM, TotalSolventsPPM.HighThe CSV file is processed without manual header editing.
URS-002The utility shall perform deterministic evaluation for “Residual Solvents GC” without machine learning.HighThe same input data produce the same JSON result.
URS-003The utility shall validate mandatory fields, numeric formats, flags, ranges and domain plausibility.HighSchema and conversion errors are explicitly reported.
URS-004The utility shall generate output.json with PASS / WARNING / FAIL statuses, source values, warnings and failures.HighThe JSON result is suitable for review, deviation investigation and integration.
URS-005The documentation shall support IQ/OQ/PQ or CSV/CSA verification.MediumURS/FS, CSV/JSON contract and test scenarios are supplied with the utility.

input.csv contract

#FieldSamplePurpose
1BatchNumberAPI-2026-RS-001Input parameter for deterministic QC evaluation.
2ProductNameActive Pharmaceutical Ingredient XInput parameter for deterministic QC evaluation.
3MethanolPPM1500.0Input parameter for deterministic QC evaluation.
4AcetonitrilePPM200.0Input parameter for deterministic QC evaluation.
5DichloromethanePPM300.0Input parameter for deterministic QC evaluation.
6HexanePPM100.0Input parameter for deterministic QC evaluation.
7EthylAcetatePPM2500.0Input parameter for deterministic QC evaluation.
8AcetonePPM1000.0Input parameter for deterministic QC evaluation.
9BenzenePPM0.5Input parameter for deterministic QC evaluation.
10TotalSolventsPPM5600.5Input parameter for deterministic QC evaluation.

FS — Functional Specification

IDFunctionImplementation
FS-001CSV importRead input.csv; validate header, column count and encoding.
FS-002Schema validationCheck required fields and permitted input values.
FS-003Rule engineApply domain rules, limits and system suitability/specification checks described in the source utility description.
FS-004Status aggregationProduce final status: FAIL for critical failure, WARNING for non-critical deviation, PASS for conformance.
FS-005JSON exportWrite machine-readable output.json for LIMS/ELN/MES and QA/QC review.

OQ/PQ scenarios

  • OQ-001: a valid sample row shall be processed without schema error.
  • OQ-002: a missing mandatory column shall produce a schema error.
  • OQ-003: a non-numeric value in a numeric field shall produce a conversion error.
  • OQ-004: a critical parameter outside the limit shall produce FAIL or a critical finding.
  • PQ-001: user real batches shall be checked with retention of input.csv, output.json, utility version and checksum.

Included in packages

Addiction Medicine & Controlled Substances QC Suite

QC utility package for addiction medicine and regulated medicinal products: addiction-treatment medicines, opioids, benzodiazepines, stimulants, sedatives, volatile impurities, assay/identity/dissolution/release checks.

Open

Biopharmaceuticals Extended QC Suite

Extended QC utility coverage for mAbs, biosimilars, proteins, insulins, vaccines, mRNA/LNP, HCP, sterile release, microbiology, water, cleanroom and stability workflows.

Open

Dental & Dental Materials QC Suite

QC utility package for dental medicinal products, oral-care products and dental materials: anaesthetics, antiseptics, analgesic/anti-infective products, polymers/minerals, resins, bonding workflows, microbiology, stability and material QC.

Open

Infectious Diseases QC Suite

QC utility package for infectious diseases: antibacterial, antiviral, antifungal and antiparasitic products, microbiology, sterility, endotoxins, viral safety and vaccine release checks.

Open

LabEx QC Suite

LabEx package for laboratory QC methods: chromatography, spectroscopy, microbiology, sterility, endotoxins, particles, dissolution, water, cleanrooms and sample preparation.

Open

Radiology QC Suite

QC package for radiology and diagnostic imaging: radiopharmaceuticals, PET/SPECT, contrast media, iodinated and gadolinium products, plus particle, sterility and endotoxin checks.

Open

Toxicology QC Suite

QC utility package for toxicologically relevant risks: genotoxic impurities, residual solvents, elemental impurities, heavy metals, mercury, mycotoxins, pesticides, extractables/leachables and degradation impurities.

Open