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Contract Laboratory has received the following Chemicals and Functional Products Laboratory Test Requests which need to be fulfilled! These Laboratory Test Requests are received from a variety of sources ranging from start-up companies to large, multinational Fortune 500 corporations, international organizations, well-respected universities and government agencies that are actively seeking Independent, Third-Party Chemicals and Functional Products Laboratories to perform their Chemicals and Functional Products Testing, Analysis, Assays, Product Development, Scientific Research Experiments, Inspections, Certifications, and Engineering Projects. If you are a Chemicals and Functional Products laboratory that would like more information on these Chemicals and Functional Products projects, please visit our registration page or call toll us free 1-855-377-6821.
Analytical Chemistry Laboratory needed for Chemical Analysis of High Purity Red Oxide powder.
The following parameters need to be checked for Red Iron Oxide powder:
Fe203 content by % wt
Si02 content by % wt and ppm value
MnO content by % wt and ppm Value
CaO content by % wt and ppm value
Cl content by % wt and ppm value
P content by % wt and ppm Value
Al content by % wt and ppm value
PH of the samples.
Loss on Ignition.
Please check for the same and as well as inform us the Cost so that we can prepare Demand Draft.
Looking for an analytical chemistry lab that can perform the following tests-
Oxidation Test Method Limits
Acid AOCS Cd 3d-63 NMT 3.0 KOH/g
Peroxide AOCS Cd 8b-90 NMT 5.0 meq/kg
Anisidine AOCS Cd 18-90 NMT 20.0
Totox (Total Oxidation) Calculation NMT 26.0 meq/kg
Heavy Metals Test Method Limits
Arsenic USEPA 1638 NMT 0.1 mg/kg (ppm)
Cadmium USEPA 1638 NMT 0.1 mg/kg (ppm)
Lead USEPA 1638 NMT 0.1 mg/kg (ppm)
Mercury USEPA 1631 NMT 0.1 mg/kg (ppm)
Environmental Toxins Test Method Limits
Polychlorinated Biphenyls (PCBs) USEPA 1668 A/C NMT 0.09 mg/kg (ppm)
Dioxin-Like PCBs (non-ortho & mono-ortho) USPEA 1668 A/C NMT 1.0 pg/g (ppt)
Dioxins & Furans (WHO TEQ) USEPA 1613B NMT 2.0 pg/g (ppt)
Microbial Analysis Test Method Limits
Plate Count USP 37 <2021> <1000 cfu/g
Staphylococcus Aureus USP 37 <2022> Absent
Escherichia Coli USP 37 <2022> Absent
Salmonella USP 37 <2022> Absent
Yeast & Mold USP 37 <2021> <100 cfu/g
Fatty Acid Profile Test Method Label Claim (mg/serving)
Eicosapentaenoic Acid (EPA;20:5 (n-3)) AOCS CE 1b-89 180 mg
Docosahexaenoic Acid (DHA;22:6(n-3)) AOCS CE 1b-89 320 mg
Total Omega-3 AOCS CE 1b-89 570 mg
Other Omegas AOCS CE 1b-89 70 mg
USA VIROLOGY LABORATORY NEEDED FOR VIRUCIDAL EFFICACY TESTING AGAINST PEDV (Porcine epidemic diarrhea vírus) AND DILUTION TEST AGAINST APP ( Actinobacillus Pleuronemoniae). PLEASE LET ME KNOW THE COST AS WELL AS THE TIME REQUIRED FROM SUBMISSION TO FINAL REPORT.
Small chemical company that imports research chemicals needs laboratory to have incoming shipments tested for purity and to validate that it is the correct compound. Proton NMR may be sufficient in most cases. Since H-NMR is not the best for determining purity then it may also require quantification by NMR or LCMS
Australia analytical chemistry laboratory needed for agrochemical analysis of five batches of an active used in agrochemicals. The active technical grade constituent is Linuron, and the tests to be performed would be as follows:
1) Assay: this would include assay method development and validation.
- Validation parameters: specificity, precision, linearity, accuracy and range.
2) Impurities: This would include:
- Identification of any impurities above 1.0% levels (by area normalization) through PDA-LC/MS, GC/MS or any other suitable technique.
- Validation for all specified impurities and active at low levels (surrogate for unknown/unspecified impurities) . Validation parameters: specificity, precision, linearity, accuracy, range, LOD and LOQ.
3) Sulphated Ash
4) Water Content: by Karl Fischer
5) Residual solvents: by Headspace GC, using appropriate validated methodology.
For the assay and impurities, I would suggest HPLC as the substance is not very volatile, and may decompose upon heating. The water content and residual solvent test may be substituted by loss on drying.
Analytical Chemistry Laboratory needed for organic salt compound testing of organic compound is presented in the form of a hydrochloride salt.
The compound's molar mass: (approximate) 247.33 g/mol Only carbon , hydrogen, nitrogen, and possibly halides are expected to be found.
Please let me know the procedure for sending a sample to you and payment methods.
Many thanks in advance.
Canada microbiology laboratory needed for DIN registration testing Against Salmonella enterica (ATCC 10708), AOAC use-dilution method: 955.14, 955.15 (1 batch, 60 carriers); - Against Staphylococcus aureus (ATCC 6538), AOAC use-dilution method: 955.14, 955.15 (1 batch, 60 carriers); - ASTM E1053, AOAC use-dilution methods (UDM) modified for viruses (1 batch, 1 carrier); - Against Trichophyton mentagrophytes (ATCC9533), AOAC 955.17, AOAC use-dilution methods (UDM) modified for fungi (1 batch, 10 carriers).
Pharmaceutical Laboratory needed for Residual Moisture Content analysis (e.g. Karl-Fisher analysis ) on lyophilized cake. All excipients in the formulation safely handled under BL 1 conditions. Fast Turn Around Times a must. Laboratory should be in the contiguous United States.
Bioanalytical Laboratory needed for Vitamin detection on Fetal Bovine Serum. Following is a list of vitamins and detectable units:
Vitamin B-12 pg/mL
Folic Acid ng/mL
Vitamin B-6 ng/mL
Thiamin B-1 ng/mL
Vitamin H Biotin pg/mL
Riboflavin B2 ng/mL
Vitamin A Retinol ng/mL
Vitamin C ng/mL
Microbiology Laboratory needed for microbial analysis SB 3112. The test material consisted of only the bacterial spores at a count of 55 x 107 cfu/ml. The tests were run in compliance with the following protocols: 1 USEPA FIFRA;GLP Standards 40 CFR 160 2 USEPA TSCA 40 CFR 792 3 Org. Economic Coop. and Dev. Principles of GLP, Annex 2, C(97)186 4 Japan Ministry of Ag, Forestry & Fisheries, Notification No. 59 Noshan 3850, Director-General of Agricultural Prod. Bureau, 10 Aug 84
Preclinical toxicology laboratory needed for Cytotoxicity studies: MEM Elution Sample Amount: 120 cm2 or 4 grams Irritation: Intracutaneous Reactivity (ISO) (w/2 extracts) Sample Amount: 240 cm2 or 8 grams Sensitization: Magnusson-Kligman (w/2 extracts) Sample Amount 600 cm2 or 32 grams (6 samples minimum) Sensitization: Local Lymph Node Assay: Sample Amount 400 cm2 or 20 grams