Protanal® LF - 200M

1 of 28 products in this brand
Protanal® LF- 200M is a versatile powder renowned for its role as a controlled release agent, gelling agent, thickener, stabilizer, and antacid in pharmaceutical and nutraceutical applications. Ensuring purity, it is swage-sludge-free, offering reliability in food ingredients.

Chemical Name: Sodium Alginate

Labeling Claims: APE-free, Allergen-free, Aluminum-free, Animal Products-free, Antibiotics-free, Artificial Flavor-Free, BSE-free, Bactericide-free, Barium-free, Bisphenol A-free, CMR Substances-free, Cadmium-free, Caffeine Free, Cobalt-free, Colorants-free, Conflict minerals-free, Copper-free, Dioxin-free, Endocrine Disruptor-free, Fungicide-free, GMO-free, Generally Recognized As Safe (GRAS), Gluten-free, Glycerin-free, Gold-Free, Halal, Herbicide-free, Hormones-free, Impurities-free, Irradiation-free, Kosher, Latex-free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, Mycotoxins-free, NPE-free, Nanomaterials-free, Natural Latex Rubber-Free, Naturally Derived, No Artificial Sweeteners, Non-GMO, Not Listed In California Proposition 65, PAH-free, PFAS-Free, PFOA-free, PFOS-free, PHO (Partially Hydrogenated Oil)-Free, PVC-free, Palm Oil-free, Paraben-free, Pareve, Perfluorocarbon (PFC)-free, Pesticide-free, Phthalates-free, Plant-Based, Plasticizer-free, Potassium-free, Preservative-free, Quaternary Ammonium Salt-Free, Radioactive-free, Residual Solvent -Free, Solvent-free, Steroids Free, Sugar-free, TSE-free, Tin-free, Tributyltin (TBT) - Free, Vegan, Vegetarian

Certifications & Compliance: British Pharmacopeia (BP), Clean Water Act (CWA) Certified, Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), Doping-Free, EU Cosmetic Regulation 1223/2009 Compliant, EXCiPACT, European Pharmacopeia (Ph. Eur.), European Regulation 396/2005/EC, FCC Compliant, FDA 21 CFR 117, FDA Compliant, FDA Food Safety Modernization Act (FSMA), FFDCA, Generally Recognized As Safe (GRAS), IFRA Compliant, JECFA (FAO/WHO), Japan Pharmacopeia (JP), National Formulary (NF), Regulation (EU) No. 231/2012, United States Pharmacopeia (USP), cGMP

Chemical Inventories: AICS (Australia), DSL (Canada), ECL (Korea), ENCS (Japan), IECSC (China), NDSL (Canada), PICCS (Phillipines)

  • TypeDocument Name
View All Documents

Enhanced TDS

Identification & Functionality

Features & Benefits

Applications & Uses

Properties

Physical Form
Physico-Chemical Properties
ValueUnitsTest Method / Conditions
Loss on Dryingmax. 15.0%2081
pH6.0 - 8.0-2070.0
Viscosity200 - 400mPa.s2170
Ash Content18.0 - 27.0%2095
Particle Size (through 200 mesh, BS)min. 95%2221
Identification*Passes Tests-44
Assay90.8 - 106%2706
Microbiological Values
ValueUnitsTest Method / Conditions
Total Plate Countmax. 200cfu/g140
SalmonellaNegative/10g156.0
E. coliNegative/10g130
Heavy Metals
ValueUnitsTest Method / Conditions
Arsenic Contentmax. 1.5ppm-
Lead Contentmax. 10ppm-
Note

*NF and Ph. Eur. ID tests; “A” and “B” on a quarterly basis. ID tests “C” (NF and Ph. Eur.) and “D” (Ph. Eur.) will be completed by exception only.

Regulatory & Compliance

Storage & Handling

Shelf Life
12 months
Storage and Shelf Life Conditions

Recommended store at cool and dry conditions. Keep containers sealed as material is hygroscopic. Re-evaluation date is 12 months from date of manufacture, if storage conditions stated above are observed.