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IFF Pharma Solutions
Avicel® CE-15
Chemical Name:
Guar Gum, Calcium Hydrogen Phosphate, Cellulose, Microcrystalline
Dosage Form:
Soft Chews, Tablets
Labeling Claims:
Not Tested on Animals, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Plasticizer-free, Gluten-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Genotoxic-free, Flavor Free, Melamine-free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, Free of Major Allergens, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, TSE-free, Vegetarian, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, Tributyl Tin Compounds-Free, Kosher, Perchlorate-free, Amine-free, Dehp (Diethylhexyl Phthalate)-Free, Not Engineered With Nanomaterials, Preservative-free, PFAS-Free, Vegan
Certifications & Compliance:
Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, EC No. 1935/2004, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, EU Directive 2002/72/EC, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1334/2008, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 10/2011 (PIM), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, Halal, Central Islamic Council of Thailand, FCC Compliant, British Pharmacopeia (BP), ISO 45001, Directive 1895/2005/EC, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, EC No. 2023/2006, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003, IFANCA Halal, IFRA Compliant
Manufacturing Technology:
Dry Granulation, Direct Compression, Wet Granulation
Avicel® CE-15 a non-animal-derived ingredient, is widely employed in tablet production. It's adaptable to various manufacturing methods like direct compression, dry granulation, and wet granulation. In pharmaceutical and nutraceutical applications, it acts as a binder, compression aid, filler, immediate release agent, and suspension aid. It's supplied in powder form for easy tablet formulation.
IFF Pharma Solutions
Protanal® CR - 8133
Chemical Name:
Sodium Alginate
Labeling Claims:
Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Solvent-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Barium-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-free, Gold-Free, Cobalt-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
Certifications & Compliance:
Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Protanal® CR - 8133 featuring sodium alginate, serves various functions in pharmaceuticals and nutraceuticals. It acts as an antacid, controlled release agent, emulsifying agent, gelling agent, thickener, and viscosity modifier, available in powder form.
IFF Pharma Solutions
Manugel® DMB
Chemical Name:
Sodium Alginate
Labeling Claims:
Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Gluten-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Barium-free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, Formaldehyde-free, PAH-free, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Gold-Free, Irradiation-free, Cobalt-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, Heavy Metal-free, PFAS-Free, Vegan
Certifications & Compliance:
European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Generally Recognized As Safe (GRAS), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Manugel® DMB is free from copper, cobalt, barium, and gold. It serves as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical applications.
IFF Pharma Solutions
Avicel® PH - 103
Chemical Name:
Cellulose, Microcrystalline
CAS Number:
9004-34-6
Dosage Form:
Granules, Tablets, Suspension
Labeling Claims:
Vegan, Bisphenol Derivatives-free, Fragrance allergen-free, Not Tested on Animals, Diethylene Glycol-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, Herbicide-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Iodide-free, Dye Free, Genotoxic-free, Ethylene Glycol-free, Flavor Free, Melamine-free, Monosodium Glutamate (MSG)-free, PAH-free, Free of Major Allergens, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Kosher, Amine-free, Dioxane-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, PFAS-Free, Potassium-free
Certifications & Compliance:
Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, FDA 21 CFR 117, Halal, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, Regulation (EC) No. 1334/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, Halal, Central Islamic Council of Thailand, Generally Recognized As Safe (GRAS), British Pharmacopeia (BP), Nagoya Compliant, ISO 45001, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1830/2003, IFANCA Halal
Manufacturing Technology:
Dry Granulation, Direct Compression, Wet Granulation
Avicel® PH - 103 is a microcrystalline cellulose used in direct compression, dry granulation, and wet granulation technologies. It serves the healthcare and pharma markets, particularly in oral drug delivery and care solutions. This product is available in granule form.
IFF Pharma Solutions
Protanal® LF - 240D
Chemical Name:
Sodium Alginate
Labeling Claims:
Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Solvent-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Barium-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-free, Gold-Free, Cobalt-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
Certifications & Compliance:
Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, ISO 14001, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Protanal® LF - 240D sourced from non-animal origins, aligns with modern labeling preferences, being free from aluminum, antibiotics, and APE. Its multifunctionality in pharmaceuticals and nutraceuticals includes serving as an antacid, controlled release agent, gelling agent, stabilizer, and thickener, offering versatility in various applications.
IFF Pharma Solutions
Manucol® LMT2
Chemical Name:
Sodium Alginate
Ingredient Name:
Sodium Alginate
CAS Number:
9005-38-3
Labeling Claims:
Aluminum-free, Endocrine Disruptor-free, Dye Free, Plasticizer-free, Nanomaterials-free, Copper-free, Barium-free, APE-free, Triphenyl Tin Compounds-Free, Halal, Paraben-free, Cadmium-free, Propylene Glycol-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Antibiotics-free, Latex-free, Aflatoxin-free, TSE-free, Mercury-Free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, Cobalt-free, PVC-free, Perfluorooctanoic Acid-free, Nitrosamines-free, Melamine-free, Gold-Free, PFAS-Free
Certifications & Compliance:
Generally Recognized As Safe (GRAS), Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), EC No. 2023/2006, European Regulation 396/2005/EC, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, European Pharmacopeia (Ph. Eur.), IFRA Compliant, EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EU) No. 1272/2008, Halal Food Council of Europe, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), FCC Compliant, ABNT NBR 14725, ISO 9000, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP
Chemical Inventories:
NDSL (Canada), ECL (Korea), PICCS (Phillipines), ENCS (Japan), IECSC (China), DSL (Canada), AICS (Australia)
Manucol® LMT2 is free from caffeine, colorants, dioxins, dyes, hormones, MSG, and natural latex rubber. It functions as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical formulations.
IFF Pharma Solutions
Manugel® LBB
Chemical Name:
Sodium Alginate
Functions:
Viscosity Modifier
Labeling Claims:
Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Gluten-free, APE-free, Caffeine Free, Dye Free, Barium-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-free, Allergen-free, Gold-Free, Cobalt-free, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, Kosher, Preservative-free, PFAS-Free
Certifications & Compliance:
European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Manugel® LBB boasts several labeling claims, including being free from aluminum, antibiotics, APE, bisphenol A, caffeine, and colorants. Additionally, it functions as a viscosity modifier in pharmaceutical and nutraceutical applications.
IFF Pharma Solutions
METHOCEL™ K100M Premium HPMC
Chemical Name:
Hydroxypropyl Methylcellulose
CAS Number:
9004-65-3
Functions:
Controlled Release Agent, Suspending Agent, Binder, Thickener, Mucoadhesive, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
Dosage Form:
Tablets
Labeling Claims:
VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free
Certifications & Compliance:
Directive 2009/48/EC, British Pharmacopeia (BP), National Bioengineered Food Disclosure Standard, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), JECFA (FAO/WHO), Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, USDA Organic, EXCiPACT
Manufacturing Technology:
Tablet Coating, Granulation
METHOCEL™ K100M Premium HPMC is employed in ceramics as a binder, utilizing granulation in its manufacturing process. Within pharmaceuticals and nutraceuticals, it serves as a suspension aid, thickener, and viscosity modifier, boasting water solubility for versatile application.
IFF Pharma Solutions
METHOCEL™ A4M Premium Methylcellulose - Specialty
Functions:
Binder, Emulsifier, Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid, Thickener
Chemical Name:
Methylcellulose
Chemical Family:
Cellulose & Cellulosics, Cellulose Ethers
End Uses:
Ceramics
Dosage Form:
Tablets
Certifications & Compliance:
ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS), EC No. 2023/2006, CFDA Compliant (China), Regulation (EC) No. 1333/2008, cGMP, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, EC No. 1935/2004, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), IFANCA Halal, Organic Certified, Chinese Pharmacopeia (ChP), European Pharmacopeia (Ph. Eur.), USDA Organic, FCC Compliant, FDA 21 CFR 182.1480, FFDCA, EU Directive 2002/72/EC, ICH Q3C, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, British Pharmacopeia (BP), EXCiPACT, Doping-Free, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Regulation (EU) No. 1272/2008
Features:
Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range, Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties
METHOCEL™ A4M Premium Methylcellulose - Specialty a water-soluble additive, is utilized in granulation and wet granulation manufacturing. It functions as a binder in ceramics and pharmaceuticals, serving as a binder, film former, and gelling agent in various applications.
IFF Pharma Solutions
METHOCEL™ E50 Premium LV HPMC - Specialty
Functions:
Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid, Thickener, Binder, Emulsifier
Chemical Name:
Hydroxypropyl Methylcellulose
Chemical Family:
Cellulose & Cellulosics, Cellulose Ethers
End Uses:
Ceramics
Dosage Form:
Tablets
Certifications & Compliance:
CFDA Compliant (China), Regulation (EC) No. 1333/2008, cGMP, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), IFANCA Halal, Organic Certified, Chinese Pharmacopeia (ChP), Regulation (EU) No. 2022/1396, European Pharmacopeia (Ph. Eur.), USDA Organic, FCC Compliant, FDA 21 CFR 182.1480, FFDCA, ICH Q3C, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, British Pharmacopeia (BP), EXCiPACT, Doping-Free, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Regulation (EU) No. 1272/2008, ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS)
Features:
Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties, Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range
METHOCEL™ E50 Premium LV HPMC - Specialty is a versatile ingredient suitable for various applications. In suspension dosage forms, it serves as a binder for ceramics, while its granulation and tablet coating manufacturing technologies make it adaptable for different production processes. With properties such as film formation, gelling, and mucoadhesion, it functions in pharmaceutical and nutraceutical applications, facilitating immediate release and solubilization when needed.
IFF Pharma Solutions
METHOCEL™ K15M S HPMC - Specialty
Functions:
Controlled Release Agent, Rheology Modifier
Chemical Name:
Hydroxypropyl Methylcellulose
Chemical Family:
Cellulose & Cellulosics, Cellulose Ethers
Labeling Claims:
Persistent Organic Pollutants (POP)-free, Natural Latex Rubber-Free, Phthalates-free, Hormones-free, Bisphenol Derivatives-free, Herbicide-free, VOC-free, Dioxane-free, TSE-free, Aflatoxin-free, Irradiation-free, PVC-free, Nitrosamines-free, APE-free, Caffeine Free, Paraben-free, Vegan, Iodide-free, Latex-free, PAH-free, Halal, Kosher, Mycotoxins-free, Sewage Sludge Free, CMR Substances-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Sugar-free, Fungicide-free, PFOA-free, Diethylene Glycol-free, Allergen-free, Gluten-free, Glycerin-free, Dairy-free, Organic, Monosodium Glutamate (MSG)-free, Potassium-free, Pesticide-free, Aluminum-free, Non-GMO, PFAS-Free, Ethylene Glycol-free, Vegetarian, Antibiotics-free, BSE-free, Quaternary Ammonium Salt-Free, PFOS-free, Dye Free, Palm Oil-free, Preservative-free, Plasticizer-free
Certifications & Compliance:
Regulation (EU) No. 10/2011 (PIM), ISO 9001, United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, Regulation (EU) No. 1169/2011, National Formulary (NF), GMP, Regulation (EU) No. 1829/2003, ISO 50001, Nagoya Compliant, FDA 21 CFR 174.5, USDA Organic, Turkish RoHS Regulation, Regulation (EC) No. 1333/2008, Halal, Directive 1333/2008/EC, FDA 21 CFR 175.300, Doping-Free, FDA 21 CFR 175.105, Directive 2009/48/EC, FDA 21 CFR 176.180, Chinese Pharmacopeia (ChP), FDA Compliant, cGMP, ISO 14001, OEKO-TEX Compliant, FSSC 22000, FDA 21 CFR 172.874, Generally Recognized As Safe (GRAS), European Pharmacopeia (Ph. Eur.), Swiss Ordinance (SR 817.023.21), ICH Q3C, Regulation (EU) No. 2022/1396, Organic Certified, FDA Food Safety Modernization Act (FSMA), FSC Certified, Waste Electrical & Electronic Equipment Directive (WEEE), Regulation (EU) No. 1830/2003, Regulation (EU) No. 231/2012, Kosher, FDA 21 CFR 101.9, Orthodox Union Kosher, Indian Pharmacopeia, EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 176.170
Dosage Form:
Tablets
METHOCEL™ K15M S HPMC - Specialty, identified as cellulose ethers and hypromellose, functions as a rheology modifier, ensuring consistency in formulations. Notably, it possesses the property of being water-soluble, making it suitable for various applications.
IFF Pharma Solutions
ETHOCEL™ Standard 10 Premium Ethylcellulose
Chemical Name:
Ethylcellulose
CAS Number:
9004-57-3
Functions:
Controlled Release Agent, Binder, Granulation Aid, Taste Masker
Dosage Form:
Tablets
Labeling Claims:
PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, Paraben-free, PAH-free, PFOS-free, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Antibiotics-free, 1,4-Dioxane-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, Formaldehyde-free, PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free
Certifications & Compliance:
Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), cGMP, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Canadian Environmental Protection Act (CEPA), Kosher, European Regulation 396/2005/EC, ICH Q3C, Clean Air Act (CAA) Certified, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, EuPIA Listed, Halal, Directive 2023/915/EU, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 573.420, Regulation (EU) No. 10/2011 (PIM), Organic Certified, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, FDA 21 CFR 172.868, Regulation (EU) No. 1272/2008, FDA 21 CFR 73.1001, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Majelis Ulama Indonesia Halal, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, FCC Compliant, FDA 21 CFR 163, USDA Organic, EXCiPACT, FDA 21 CFR 73.1, Directive 2009/48/EC, British Pharmacopeia (BP)
Manufacturing Technology:
Tablet Coating, Hot Melt Extrusion, Direct Compression, Granulation, Encapsulation
ETHOCEL™ Standard 10 Premium Ethylcellulose characterized by its white color, serves as a stabilizer and thickener in cosmetic ingredients. Utilizing encapsulation, granulation, hot melt extrusion, and tablet coating technologies, it is available in a powdered physical form.
IFF Pharma Solutions
Lattice® NTC 90 - Specialty
Chemical Family:
Cellulose & Cellulosics
Labeling Claims:
Bisphenol Derivatives-free, Dioxin-free, Non-GMO, PFAS-Free, Monosodium Glutamate (MSG)-free, Natural Latex Rubber-Free, Tributyltin (TBT) - Free, PFOA-free, Not Tested on Animals, Iodide-free, Vegetarian, Dye Free, PVC-free, Aflatoxin-free, Aluminum-free, TSE-free, Sugar-free, Halal, Irradiation-free, APE-free, PAH-free, Pesticide-free, Allergen-free, Non-Toxic, Plasticizer-free, Kosher, Artificial Flavor-Free, Antibiotics-free, Endocrine Disruptor-free, Phthalates-free, Vegan, CMR Substances-free, Preservative-free, Caffeine Free, Gluten-free, Latex-free, Palm Oil-free, BSE-free, PHO (Partially Hydrogenated Oil)-Free, Odor-free, Paraben-free, Quaternary Ammonium Salt-Free, Not Listed In California Proposition 65, Glycerin-free, Dioxane-free, Hormones-free, PFOS-free, Ethylene Oxide-free, Potassium-free
Physical Form:
Powder
Features:
Wide pH Compatibility, Excellent Freeze/Thaw Stability, Long Shelf Life, Works Over Wide pH Range, Wide pH Range, Freeze/Thaw Stable
Lattice® NTC 90 - Specialty stands out with its freeze/thaw stability, long shelf life, and compatibility across a wide pH range. Serving as a rheology modifier, stabiliser, and suspending agent, it ensures consistent performance. Identified as microcrystalline cellulose, it's available in powder form, making it perfect for suspension concentrate formulations.
IFF Pharma Solutions
ETHOCEL™ Standard 45 Industrial Ethylcellulose - Specialty
Chemical Family:
Cellulose Ethers, Cellulose & Cellulosics
Chemical Name:
Ethylcellulose
CAS Number:
9004-57-3
Pigment Type:
Metallic Effect
Dosage Form:
Tablets
Labeling Claims:
FSSC 22000, Not Listed In California Proposition 65, Sugar-free, Iodide-free, 1,4-Dioxane-free, Nitrosamines-free, Gluten-free, Quaternary Ammonium Salt-Free, Plasticizer-free, Halal, PFOS-free, Bisphenol Derivatives-free, Caffeine Free, Irradiation-free, Odor-free, VOC-free, PFAS-Free, Kosher, Tributyltin (TBT) - Free, PAH-free, Natural Latex Rubber-Free, Organic, Allergen-free, Dioxane-free, Antibiotics-free, Hormones-free, Dairy-free, Zero Calorie, Monosodium Glutamate (MSG)-free, Phthalates-free, Paraben-free, Non-Mutagenic, Non-Irritant, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, APE-free, Non-GMO, Dye Free, Aluminum-free, Sewage Sludge Free, Potassium-free, PFOA-free, PVC-free, Pesticide-free
Color (Properties):
White
Certifications & Compliance:
Chinese Pharmacopeia (ChP), Clean Water Act (CWA) Certified, ICH Q3C, EFSA (European Food Safety Authority) Certified, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, Kosher, ISO 9001, Organic Certified, Regulation (EU) No. 10/2011 (PIM), GMP, Directive 1333/2008/EC, Directive 2011/65/EU (RoHS 2), FDA 21 CFR 117, FSSC 22000, United States Pharmacopeia (USP), FDA Compliant, EuPIA Listed, Regulation (EU) No. 231/2012, USDA Organic, Regulation (EC) No. 1333/2008, FSC Certified, JECFA (FAO/WHO), cGMP, FDA 21 CFR 172.868, RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Directive 2012/19/EU, Regulation (EU) No. 1272/2008, Directive 2009/48/EC, Halal, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), FDA 21 CFR 101.9
Manufacturing Technology:
Tablet Coating, Direct Compression, Encapsulation, Granulation
ETHOCEL™ Standard 45 Industrial Ethylcellulose - Specialty is optimized for spray, phenolics, and modified rosins applications. It features good printability, reduced tack, and scuff resistance, ensuring high-quality finishes. Serving as a stabilizer and thickener, it is available in both powder and granule forms, presenting a white color for versatility in industrial processes.
IFF Pharma Solutions
ETHOCEL™ Hot Melt Ethylcellulose - Specialty
Chemical Family:
Cellulose Ethers, Cellulose & Cellulosics
Chemical Name:
Ethylcellulose
CAS Number:
9004-57-3
Pigment Type:
Metallic Effect
Dosage Form:
Tablets
Labeling Claims:
FSSC 22000, Sugar-free, Iodide-free, 1,4-Dioxane-free, Nitrosamines-free, Gluten-free, Quaternary Ammonium Salt-Free, Plasticizer-free, Halal, PFOS-free, Bisphenol Derivatives-free, Caffeine Free, Irradiation-free, Odor-free, VOC-free, PFAS-Free, Kosher, Tributyltin (TBT) - Free, PAH-free, Natural Latex Rubber-Free, Organic, Allergen-free, Dioxane-free, Antibiotics-free, Hormones-free, Dairy-free, Zero Calorie, Monosodium Glutamate (MSG)-free, Phthalates-free, Paraben-free, Non-Mutagenic, Non-Irritant, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, APE-free, Non-GMO, Dye Free, Aluminum-free, Sewage Sludge Free, Potassium-free, PFOA-free, PVC-free, Pesticide-free
Certifications & Compliance:
Chinese Pharmacopeia (ChP), ICH Q3C, EU Directive 2002/72/EC, EFSA (European Food Safety Authority) Certified, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, Kosher, ISO 9001, Organic Certified, Regulation (EU) No. 10/2011 (PIM), GMP, Directive 1333/2008/EC, Directive 2011/65/EU (RoHS 2), FDA 21 CFR 117, FSSC 22000, United States Pharmacopeia (USP), FDA Compliant, EuPIA Listed, Regulation (EU) No. 231/2012, USDA Organic, Regulation (EC) No. 1333/2008, JECFA (FAO/WHO), cGMP, FDA 21 CFR 172.868, RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), FDA Food Safety Modernization Act (FSMA), EC No. 1935/2004, EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Directive 2012/19/EU, Regulation (EU) No. 1272/2008, Directive 2009/48/EC, Halal, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), FDA 21 CFR 101.9, EC No. 2023/2006
Manufacturing Technology:
Tablet Coating, Direct Compression, Encapsulation, Granulation
ETHOCEL™ Hot Melt Ethylcellulose - Specialty finds versatile applications in spray, phenolics, modified rosins, and alkyds (Long Oil). As a stabilizer, rheology modifier, binder, dispersing agent, and anti-blocking agent, it offers robust performance. Identified as a cellulose ether and specifically ethylcellulose, it ensures consistency and efficacy in various formulations.
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