Protanal® PH - 1322

1 of 28 products in this brand

Protanal® PH - 1322 is a versatile powder offering various functions for pharmaceuticals and nutraceuticals. It serves as a controlled-release agent, gelling agent, thickener, stabilizer, and antacid. It's also sewage-sludge-free, ensuring purity.

Chemical Name: Sodium Alginate

Labeling Claims: APE-free, Allergen-free, Aluminum-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, Copper-free, Dioxin-free, Endocrine Disruptor-free, Fungicide-free, GMO-free, Generally Recognized As Safe (GRAS), Gluten-free, Glycerin-free, Gold-Free, Herbicide-free, Hormones-free, Impurities-free, Kosher, Mercury-Free, Monosodium Glutamate (MSG)-free, NPE-free, Natural Latex Rubber-Free, No Artificial Sweeteners, Non-GMO, PAH-free, PFAS-Free, PFOA-free, PFOS-free, PHO (Partially Hydrogenated Oil)-Free, PVC-free, Palm Oil-free, Paraben-free, Perfluorocarbon (PFC)-free, Pesticide-free, Phthalates-free, 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, Vegetarian

Certifications & Compliance: British Pharmacopeia (BP), 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, Japan Pharmacopeia (JP), National Formulary (NF), Regulation (EU) No. 231/2012, United States Pharmacopeia (USP), cGMP

Technical Data Sheet Safety Data Sheet Brochure

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Enhanced TDS

Properties

Physical Form

Powder

Physico-Chemical Properties


	Value	Units	Test Method / Conditions
Loss on Drying	7 - 14	%	SOM 1
Viscosity (at 0.5% solution)	500 - 1000	mPa.s	SOM 82Q
pH (at 0.5%)	6.4 - 8.5	-	SOM 6
Particle Size (through 250 micron)	min. 98	%	SOM 106
Particle Size (through 180 micron)	min. 91	%	SOM 106
Calcium Content	2 - 4	%	SOM 7
Ash Content (at 800°C, on dry matter)	18.0 - 27.0	%	SOM 8C
Sodium Alginate Content (Assay)	90.8 - 106	%	SOM 2F
Powder Color	64 - 80	-	SOM 105

Microbiological Values


	Value	Units	Test Method / Conditions
Total Viable Mesophilic Aerobic Count	max. 200	cfu/g	201C (EP), Usp
Yeast and Mold Count	max. 200	cfu/g	203A (EP)
Salmonella	Absent	/25g	205 (EP)
Staphlococcus aureus	Absent	/0.5g	206 (EP)
E. coli	Absent	/25g	204 (EP)
Pseudomonas aeruginosa	Absent	/0.5g	207 (EP)
Coliform	Negative	MPN	204 (EP)

Heavy Metals


	Value	Units	Test Method / Conditions
Lead Content	max. 5	ppm	22
Arsenic Content	max. 1.5	ppm	22

Regulatory & Compliance

Certifications & Compliance: British Pharmacopeia (BP),
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,
Japan Pharmacopeia (JP),
National Formulary (NF),
Regulation (EU) No. 231/2012,
United States Pharmacopeia (USP),
cGMP

Packaging & Availability

Packaging Type: Drums

Storage & Handling

Shelf Life: 9 months
Storage and Shelf Life Conditions: Recommended store at cool and dry conditions. Keep containers sealed as material is hygroscopic. Re-evaluation date is 9 months from date of manufacture, if storage conditions stated above are observed.