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| Product | Description | |
|---|---|---|
| Ophthalmic acid | Ophthalmic acid, an analogue of GSH, is a marker of oxidative stress and hepatic GSH consumption. Ophthalmic acid is an inhibitor of Glyoxalase I reaction [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 495-27-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-126752. |  |
| Ophthalmic Acid | Ophthalmic Acid. Group: Biochemicals. Alternative Names: H-γ-Glu-Abu-Gly-OH; H-Glu(Abu-Gly-OH)-OH. Grades: Highly Purified. CAS No. 495-27-2. Pack Sizes: 25mg, 50mg, 100mg, 250mg. US Biological Life Sciences. |  Worldwide |
| Ophthalmic Acid 98+% (TLC) | Ophthalmic Acid 98+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25mg, 100mg, 250mg. US Biological Life Sciences. | Worldwide |
| (11 β , ?17α )?-17-?[ (Ethoxycarbonyl)?oxy]?-?11-?hydroxy-?3-?oxo-?androsta-?1, ?4-?diene-?17-?carboxylic acid | (11 β , ?17α )?-17-?[ (Ethoxycarbonyl)?oxy]?-?11-?hydroxy-?3-?oxo-?androsta-?1, ?4-?diene-?17-?carboxylic acid is a derivative of Loteprednol Etabonate (L471400) which is an ophthalmic corticosteroid. Group: Biochemicals. Grades: Highly Purified. CAS No. 133991-63-6. Pack Sizes: 250mg, 2.5g. Molecular Formula: C23H30O7. US Biological Life Sciences. | Worldwide |
| (11 β , ?17α )?-17-?[ (Ethoxycarbonyl)?oxy]?-?11-?hydroxy-?3-?oxo-?androsta-?1, ?4-?diene-?17-?carboxylic Acid-d3 | (11 β , ?17α )?-17-?[ (Ethoxycarbonyl)?oxy]?-?11-?hydroxy-?3-?oxo-?androsta-?1, ?4-?diene-?17-?carboxylic Acid-d3 is an intermediate in the synthesis of Loteprednol Etabonate-d3 (L471402), whiich is a labelled Loteprednol Etabonate, an ophthalmic corticosteroid used as an anti-inflammatory. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 10mg. Molecular Formula: C23H27D3O7. US Biological Life Sciences. | Worldwide |
| (11 β , ?17α )?-17-?[ (Ethoxycarbonyl)?oxy]?-?11-?hydroxy-?3-?oxo-?androsta-?1, ?4-?diene-?17-?carboxylic acid-d5 | (11 β , ?17α )?-17-?[ (Ethoxycarbonyl)?oxy]?-?11-?hydroxy-?3-?oxo-?androsta-?1, ?4-?diene-?17-?carboxylic acid-d5 is labelled (11 β , ?17α )?-17-?[ (Ethoxycarbonyl)?oxy]?-?11-?hydroxy-?3-?oxo-?androsta-?1, ?4-?diene-?17-?carboxylic acid (E890570) which is a derivative of Loteprednol Etabonate (L471400) which is an ophthalmic corticosteroid. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 50mg. Molecular Formula: C23H25D5O7, Molecular Weight: 423.51. US Biological Life Sciences. | Worldwide |
| 17-Hydroxy-3,11-dioxo-androsta-1,4-diene-17 β-carboxylic Acid | 17-Hydroxy-3,11-dioxo-androsta-1,4-diene-17 β-carboxylic Acid is an intermediate used to prepare (11 β , ?17α )?-17-?[ (Ethoxycarbonyl)?oxy]?-?11-?hydroxy-?3-?oxo-?androsta-?1, ?4-?diene-?17-?carboxylic acid (E890570) which is a derivative of Loteprednol Etabonate (L471400), an ophthalmic corticosteroid. Group: Biochemicals. Grades: Highly Purified. CAS No. 78261-67-3. Pack Sizes: 1g, 10g. Molecular Formula: C20H24O5, Molecular Weight: 344.4. US Biological Life Sciences. | Worldwide |
| Aftobetin Hydrochloride | Aftobetin, also known as ANCA11 and NCE-11, is a novel amyloid-binding compound applied topically in the form of an ophthalmic ointment. Aftobetin may be of useful as an aid in the diagnosis Alzheimer's disease. Synonyms: Aftobetin Hydrochloride; NCE-11; Aftobetin Hydrochloride [USAN]; UNII-A1FCZ940WA; 1353222-83-9; A1FCZ940WA; 11-HCl; 2-Propenoic acid, 2-cyano-3-(6-(1-piperidinyl)-2-naphthalenyl)-, 2-(2-(2-methoxyethoxy)ethoxy)ethyl ester, hydrochloride (1:1), (2E)-; Aftobetin hydrochloride (USAN); 2-(2-(2-Methoxyethoxy)ethoxy)ethyl (2E)-2-cyano-3-(6-(piperidin-1-yl)naphthalen-2-yl)prop-2-enoate monohydrochloride; Aftobetin HCl; 2-[2-(2-Methoxyethoxy)ethoxy]ethyl (2E)-2-cyano-3-[6-(piperidin-1-yl)naphthalen-2-yl]prop-2-enoate monohydrochloride; aftobetin-hydrochloride; ANCA-11 HYDROCHLORIDE; CHEMBL2364602; DTXSID90159314; AKOS040750170; AFTOBETIN HYDROCHLORIDE [WHO-DD]; D10607; Q27273497. CAS No. 1353222-83-9. Molecular formula: C26H33ClN2O5. Mole weight: 489.009. |  |
| Alginic Acid | Alginic acid is a tasteless, practically odorless, white to yellowish white, fibrous powder. Synonyms: Acidum alginicum; E400; Kelacid; L-gulo-D-mannoglycuronan; polymannuronic acid; Protacid; Satialgine H8. CAS No. 9005-32-7. Product ID: PE-0139. Molecular formula: (C6H8O)n. Mole weight: 20000 ~ 240000. Category: Stabilizing Agents; Suspending Agents; Sustained Release Agents; Tablet Binder; Tablet Dsintegrant; Viscosity-increasing Agents. Product Keywords: Binder Excipients; Stabilizers; Suspending Agents; ; PE-0139; Alginic Acid; Stabilizing Agents; Suspending Agents; Sustained Release Agents; Tablet Binder; Tablet Dsintegrant; Viscosity-increasing Agents; (C6H8O)n; 9005-32-7. UNII: 8C3Z4148WZ. Chemical Name: Alginic acid. Grade: Pharmceutical Excipients. Administration route: Ophthalmic, oral. Dosage Form: Ophthalmic preparations, oral capsules, and tablets. Stability and Storage Conditions: Alginic acid hydrolyzes slowly at warm temperatures producing a material with a lower molecular weight and lower dispersion viscosity.Alginic acid dispersions are susceptible to microbial spoilage on storage, which may result in some depolymerization and hence a decrease in viscosity. Dispersions should therefore be preserved with an antimicrobial preservative such as benzoic acid; potassium sorbate; sodium benzoate; sorbic acid; or paraben. Concentrations of 0.1-0.2% are usually used. Alginic acid dispersions may be sterilize |  |
| Benoxaprofen-13C,d3 | Labeled Benoxaprofen. A non-steroidal anti-inflammatory ophthalmic agent. Group: Biochemicals. Alternative Names: 2-(4-Chlorophenyl)-α-(methyl-13C,d3)-5-benzoxazoleacetic Acid; (RS)-Benoxaprofen-13C,d3; (+/-)-Benoxaprofen-13C,d3; 2-[2- (4-Chlorophenyl) benzoxazol-5-yl]propanoic Acid-13C,d3; Compound 90459-13C,d3; Coxigon-13C,d3; LRCL 3794-13C,d3; Lilly 90459-13C,d3; NSC 299582-13C,d3; Opren-13C,d3; Oraflex-13C,d3; Uniprofen-13C,d3; dl-Benoxaprofen-13C,d3. Grades: Highly Purified. CAS No. 1329840-53-0. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Carbomer | Carbomers are white-colored, fluffy, acidic, hygroscopic powders with a characteristic slight odor. A granular carbomer is also available (Carbopol 71G). Synonyms: Acrypol; Acritamer; acrylic acid polymer; carbomera; Carbopol; carboxy polymethylene; polyacrylic acid; carboxyvinyl polymer; Pemulen; Tego Carbomer. CAS No. 9003-1-4. Product ID: PE-0469. Category: Bioadhesive Material; Controlled-release Agents; Emulsifying Agents; Emulsion Stabilizer; rheology modifier; Stabilizing Agents; Suspending Agents; Tablet Binder. Product Keywords: Suspending Agents; Emulsifier Excipients; Binder Excipients; ; PE-0469; Carbomer; Bioadhesive Material; Controlled-release Agents; Emulsifying Agents; Emulsion Stabilizer; rheology modifier; Stabilizing Agents; Suspending Agents; Tablet Binder; ; 9003-01-4. UNII: 9G2MAD7J6W. Chemical Name: Carbomer. Grade: Pharmceutical Excipients. Administration route: Oral; ophthalmic, rectal, topical, transdermal ; vaginal. Dosage Form: Oral suspensions, tablets; ophthalmic, rectal, topical, transdermal preparations; vaginal suppositories. Stability and Storage Conditions: Carbomers are stable, hygroscopic materials that may be heated at temperatures for up to 2 hours without affecting their thickening efficiency. However, exposure to excessive temperatures can result in discoloration and reduced stability. Complete decomposition occurs with heating for 30 minutes at 260°C. Dry powder forms of carbomer | |
| Carbomer 934 | Carbomer 934. Synonyms: Acritamer; acrylic acid polymer; Carbopol; carboxy polymethylene, polyacrylic acid; carboxyvinyl polymer; Pemulen; Ultrez. CAS No. 9003-1-4. Product ID: PE-0310. Molecular formula: (C3H4O2)n. Category: Suspending Agents; Thickener. Product Keywords: Excipients for Liquid Dosage Form; Suspending Agents; PE-0310; Carbomer 934; Suspending Agents; Thickener; (C3H4O2)n; 9003-01-4. UNII: Z135WT9208. Chemical Name: Cross-linked polyacrylic resin. Grade: Pharmceutical Excipients. Administration route: Oral administration; Rectum; Vagina; Local administration. Dosage Form: Oral suspensions and tablets, ophthalmic preparations, rectal preparations and topical preparations. Stability and Storage Conditions: Carbomer is a stable and hygroscopic substance that does not affect its thickening when heated at 104°C for 2 hours. However, exposure to excessive temperatures can reduce discoloration and stability. It is completely decomposed by heating at 260°C for 30 minutes. Dry powdery carbomer does not grow mildew. In contrast, microbes grow well in preservative-free aqueous dispersions. Therefore, preservatives such as 0.1%(W/V) of chlorocresol, 0.18% (W/V) of hydroxyphenylene methyl, 0.02%(W/V) of hydroxyphenylene propyl, or 0.1%(W/V) of thiomersal should be added. The addition of certain bacteriostatic agents, such as benzalammonium chloride or sodium benzoate, at high concentrations (0.1%W/V) caused turbidity | |
| Carbomer 940 | Carbomer 940. Synonyms: Acritamer; acrylic acid polymer; Carbopol; carboxy polymethylene, polyacrylic acid; carboxyvinyl polymer; Pemulen; Ultrez. CAS No. 9003-1-4. Product ID: PE-0637. Molecular formula: (C3H4O2)n. Category: Suspending Agents; Thickener. Product Keywords: Excipients for Liquid Dosage Form; Suspending Agents; PE-0637; Carbomer 940; Suspending Agents; Thickener; (C3H4O2)n; 9003-01-4. UNII: 4Q93RCW27E. Chemical Name: Cross-linked polyacrylic resin. Grade: Pharmceutical Excipients. Administration route: Topical; Ophthalmic; Transdermal. Dosage Form: Oral suspensions and tablets, ophthalmic preparations, rectal preparations and topical preparations. Stability and Storage Conditions: Carbomer is a stable and hygroscopic substance that does not affect its thickening when heated at 104°C for 2 hours. However, exposure to excessive temperatures can reduce discoloration and stability. It is completely decomposed by heating at 260°C for 30 minutes. Dry powdery carbomer does not grow mildew. In contrast, microbes grow well in preservative-free aqueous dispersions. Therefore, preservatives such as 0.1%(W/V) of chlorocresol, 0.18% (W/V) of hydroxyphenylene methyl, 0.02%(W/V) of hydroxyphenylene propyl, or 0.1%(W/V) of thiomersal should be added. The addition of certain bacteriostatic agents, such as benzalammonium chloride or sodium benzoate, at high concentrations (0.1%W/V) caused turbidity and decreased viscosity | |
| Carbomer 974P | Carbomer 974P. Synonyms: Acritamer; acrylic acid polymer; Carbopol; carboxy polymethylene, polyacrylic acid; carboxyvinyl polymer; Pemulen; Ultrez. CAS No. 2594-32-2. Product ID: PE-0638. Molecular formula: (C3H4O2)n. Category: Suspending Agents; Thickener. Product Keywords: Excipients for Liquid Dosage Form; Suspending Agents; PE-0638; Carbomer 974P; Suspending Agents; Thickener; (C3H4O2)n; 2594-32-2. UNII: NA. Chemical Name: Cross-linked polyacrylic resin. Grade: Pharmceutical Excipients. Administration route: Topical; Ophthalmic; Transdermal. Dosage Form: Oral suspensions and tablets, ophthalmic preparations, rectal preparations and topical preparations. Stability and Storage Conditions: Carbomer is a stable and hygroscopic substance that does not affect its thickening when heated at 104°C for 2 hours. However, exposure to excessive temperatures can reduce discoloration and stability. It is completely decomposed by heating at 260°C for 30 minutes. Dry powdery carbomer does not grow mildew. In contrast, microbes grow well in preservative-free aqueous dispersions. Therefore, preservatives such as 0.1%(W/V) of chlorocresol, 0.18% (W/V) of hydroxyphenylene methyl, 0.02%(W/V) of hydroxyphenylene propyl, or 0.1%(W/V) of thiomersal should be added. The addition of certain bacteriostatic agents, such as benzalammonium chloride or sodium benzoate, at high concentrations (0.1%W/V) caused turbidity and decreased viscosity of c | |
| Carbomer 980P | Carbomers are white-colored, fluffy, acidic, hygroscopic powders with a characteristic slight odor. A granular carbomer is also available (Carbopol 71G). CAS No. 139637-85-7. Product ID: PE-0470. Category: Carrier Excipients. Product Keywords: Pharmaceutical Excipients; Other Materials; Carbomer 980P; Carrier Excipients; Carrier Excipients; 139637-85-7; 139637-85-7. UNII: NA. Chemical Name: Carbomer 980. Grade: Pharmceutical Excipients. Administration route: Oral; ophthalmic, rectal, topical, transdermal. vaginal. Dosage Form: Oral suspensions, tablets; ophthalmic, rectal, topical, transdermal preparations. vaginal suppositories. Stability and Storage Conditions: Carbomers are stable, hygroscopic materials that may be heated at temperatures below 1048C for up to 2 hours without affecting their thickening efficiency. However, exposure to excessive temperatures can result in discoloration and reduced stability. Complete decomposition occurs with heating for 30 minutes at 260°C. Dry powder forms of carbomer do not support the growth of molds and fungi. In contrast, microorganisms grow well in unpreserved aqueous dispersions, and therefore an antimicrobial preservative such as 0.1% w/v chlorocresol, 0.18% w/v methylparaben-0.02% w/v propylparaben, or 0.1% w/v thimerosal should be added. The addition of certain antimicrobials, such as benzalkonium chloride or sodium benzoate, in high concentrations (0.1% w/v) can cause cl | |
| Carbomer 980P | Carbomers are white-colored, fluffy, acidic, hygroscopic powders with a characteristic slight odor. A granular carbomer is also available (Carbopol 71G). CAS No. 139637-85-7. Product ID: PE-0566. Category: Thickeners; Binders; Emulsifiers; Suspending Agentss; Carrier Bases, etc. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0566; Carbomer 980P; Thickeners; Binders; Emulsifiers; Suspending Agentss; Carrier Bases, etc; ; 139637-85-7. UNII: NA. Chemical Name: Carbomer 980. Grade: Pharmceutical Excipients. Administration route: Oral; ophthalmic, rectal, topical, transdermal ; vaginal. Dosage Form: Oral suspensions, tablets; ophthalmic, rectal, topical, transdermal preparations; vaginal suppositories. Stability and Storage Conditions: Carbomers are stable, hygroscopic materials that may be heated at temperatures for up to 2 hours without affecting their thickening efficiency. However, exposure to excessive temperatures can result in discoloration and reduced stability. Source and Preparation: Carbomers are synthetic, high-molecular-weight, crosslinked polymers of acrylic acid. These acrylic acid polymers are crosslinked with allyl sucrose or allyl pentaerythritol. The polymerization solvent used previously was benzene; however, some of the newer commercially available grades of carbomer are manufactured using either ethyl acetate or a cyclohexane-ethyl acetate cosolvent mixture. The Carbo | |
| Carboxymethyl cellulose sodium - Viscosity 1400 - 2000cps | Carboxymethyl cellulose sodium is an esteemed compound boasting a mesmerizing viscosity spanning the range of 1400 to 2000cps. Within the realms of pharmaceutical preparations, particularly oral suspensions and ophthalmic solutions, it acts as a thickening compound, stabilizer and binder. Synonyms: Cellulose Glycolic Acid Sodium Salt; Sodium Tylose; Sodium Cellulose Glycolate; Sodium Carboxymethyl Cellulose. Molecular formula: (C6H7O2(OH)x(OCH2COONa)y)n. | |
| Cetyl Alcohol, Cetanol | Cetyl alcohol occurs as waxy, white flakes, granules, cubes, or castings. It has a faint characteristic odor and bland taste. Synonyms: Alcohol cetylicus; Avol; Cachalot; Crodacol C70; Crodacol C90; Crodacol C95; ethal; ethol; HallStar CO-1695; 1-hexadecanol; nhexadecyl alcohol; Hyfatol 16-95; Hyfatol 16-98; Kessco CA; Lanette 16; Lipocol C; Nacol 16-95; palmityl alcohol; Rita CA; Speziol C16 Pharma; Tego Alkanol 16; Vegarol 1695. CAS No. 36653-82-4. Product ID: PE-0530. Molecular formula: C16H34O. Mole weight: 242.44. Category: Coating Agents; Emulsifying Agents; Stiffening Agents. Product Keywords: Surfactant Excipients; Emulsifier Excipients; PE-0530; Cetyl Alcohol, Cetanol; Coating Agents; Emulsifying Agents; Stiffening Agents; C16H34O; 36653-82-4. UNII: 936JST6JCN. Chemical Name: Hexadecan-1-ol. Grade: Pharmceutical Excipients. Administration route: Ophthalmic, oral, otic and rectal, topical aerosols, vaginal. Dosage Form: Ophthalmic preparations, oral capsules and tablets, otic and rectal preparations, topical aerosols, creams, emulsions, ointments and solutions, and vaginal preparations. Stability and Storage Conditions: Cetyl alcohol is stable in the presence of acids, alkalis, light, and air; it does not become rancid. It should be stored in a well-closed container in a cool, dry place. Source and Preparation: Cetyl alcohol may be manufactured by a number of methods such as esterification and hydrog | |
| Citric Acid | Citric acid monohydrate occurs as colorless or translucent crystals, or as a white crystalline, efflorescent powder. It is odorless and has a strong acidic taste. The crystal structure is orthorhombic. Synonyms: Acidum citricum monohydricum; E330; 2-hydroxypropane-1, 2, 3-tricarboxylic acid monohydrate. CAS No. 5949-29-1. Product ID: PE-0015. Molecular formula: C6H8O7·H2O. Mole weight: 210.14. Category: Acidifying Agents; Antioxidant; Buffering Agents; Chelating Agents; Flavor enhancer; Preservative. Product Keywords: Flavoring Agents; Stabilizers; Effervescents; ; PE-0015; Citric Acid; Acidifying Agents; Antioxidant; Buffering Agents; Chelating Agents; Flavor enhancer; Preservative; C6H8O7·H2O; 5949-29-1. UNII: 2968PHW8QP. Chemical Name: 2-Hydroxy-1, 2, 3-propanetricarboxylic acid monohydrate. Grade: Pharmceutical Excipients. Administration route: Inhaled, intramuscular, intravenous or other injectable, ocular preparation, nasal preparation, oral administration, local administration. Dosage Form: Inhalations; IM, IV, and other injections; ophthalmic preparations; oral capsules, solutions, suspensions and tablets; topical and vaginal preparations. Stability and Storage Conditions: Citric acid monohydrate loses water of crystallization in dry air or when heated to about 40°C. It is slightly deliquescent in moist air.Dilute aqueous solutions of citric acid may ferment on standing. The bulk monohydrate or anhydrous materia | |
| Ketotifen Fumarate | Ketotifen is a second-generation noncompetitive H1-antihistamine and mast cell stabilizer. It is most commonly sold as a salt with fumaric acid, ketotifen fumarate, and is available in two forms. In its ophthalmic form, it is used to treat allergic conjunctivitis,or the itchy red eyes caused by allergies. In its oral form, it is used to preventasthma attacks. Uses: Antipruritics. Synonyms: Zaditen; Zaditor. Grades: >98%. CAS No. 34580-14-8. Molecular formula: C19H19NOS.C4H4O4. Mole weight: 425.5. | |
| Lanolin Alcohols | Lanolin Alcohols. Synonyms: wool wax alcohols. CAS No. 8027-33-6. Product ID: PE-0545. Category: Emulsifier; Ointment Base. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0545; Lanolin Alcohols; Emulsifier; Ointment Base; ; 8027-33-6. UNII: 884C3FA9HE. Chemical Name: Lanolin alcohols. Grade: Pharmceutical Excipients. Administration route: Ophthalmic and topical. Dosage Form: Ophthalmic and topical preparations. Stability and Storage Conditions: Lanolin alcohol can gradually autoxize during storage. It should be filled in an airtight container and kept in a cool and dry place away from light. The normal storage period is about 2 years. Source and Preparation: Lanolin is saponified and separated to remove cholesterol and other alcohols. Applications: Lanolin alcohol is used in topical preparations and cosmetics. It is a hydrophobic substrate with soft and lubricating properties, such as preparations for dry skin and dry eyes. It is also used in oil-in-water (w/o) creams and ointments in concentrations as low as 2% w/w. Adding 5% lanolin alcohol can increase the amount of water added to mineral oil by 3.times. This emulsion is not destroyed when citric acid, lactic acid or tartaric acid is added. | |
| Levofloxacin Hemihydrate ((-)-(S)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid, Hemihydrate) | Levofloxacin is a synthetic chemotherapeutic antibiotic of the fluoroquinolone drug class[1][2] and is used to treat severe or life-threatening bacterial infections or bacterial infections that have failed to respond to other antibiotic classes.[3][4] It is sold under various brand names, such as Levaquin and Tavanic, the most common. In form of ophthalmic solutions it is known as Oftaquix, Quixin and Iquix. Group: Biochemicals. Alternative Names: (-)-(S)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid, Hemihydrate. Grades: Highly Purified. CAS No. 138199-71-0. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Mannitol | Mannitol is D-mannitol. It is a hexahydric alcohol related to mannose and is isomeric with sorbitol. Mannitol occurs as a white, odorless, crystalline powder, or freeflowing granules. It has a sweet taste, approximately as sweet as glucose and half as sweet as sucrose, and imparts a cooling sensation in the mouth. Synonyms: Cordycepic acid; E421; Emprove; manna sugar; D-mannite; mannite; mannitolum; Mannogem; Pearlitol. CAS No. 69-65-8. Product ID: PE-0479. Molecular formula: C6H14O6. Mole weight: 182.17. Category: Diluent; Plasticizer; Sweetening Agents; Tablet and Capsule Diluent. Product Keywords: Sweeteners Excipients; Stabilizers; PE-0479; Mannitol; Diluent; Plasticizer; Sweetening Agents; Tablet and Capsule Diluent; C6H14O6; 69-65-8. UNII: 3OWL53L36A. Chemical Name: D-Mannitol. Grade: Pharmceutical Excipients. Administration route: IP, IM, IV, and SC; infusions; buccal, oral and sublingual; ophthalmic; topical. Dosage Form: IP, IM, IV, and SC injections; infusions; buccal, oral and sublingual tablets, powders and capsules; ophthalmic preparations; topical solutions. Stability and Storage Conditions: Mannitol is stable in the dry state and in aqueous solutions. Solutions may be sterilized by filtration or by autoclaving and if necessary may be autoclaved repeatedly with no adverse physical or chemical effects. In solution, mannitol is not attacked by cold, dilute acids or alkalis, nor by atmospheric oxygen in the abs | |
| Methylcellulose | Methylcellulose occurs as a white, fibrous powder or granules. It is practically odorless and tasteless. It should be labeled to indicate its viscosity type (viscosity of a 1 in 50 solution). Synonyms: Benecel; Cellacol; Culminal MC; E461; Mapolose; Methocel; methylcellulosum; Metolose; Tylose; Viscol. CAS No. 9004-67-5. Product ID: PE-0457. Category: Coating Agents; Emulsifying Agents; Suspending Agents; Tablet and Capsule Disintegrant; Tablet Binder; Viscosity-increasing Agents. Product Keywords: Binder Excipients; Suspending Agents; Emulsifier Excipients; ; PE-0457; Methylcellulose; Coating Agents; Emulsifying Agents; Suspending Agents; Tablet and Capsule Disintegrant; Tablet Binder; Viscosity-increasing Agents; ; 9004-67-5. UNII: NA. Chemical Name: Cellulose methyl ether. Grade: Pharmceutical Excipients. Administration route: Sublingual; IM; intrasynovial; nasal; ophthalmic; oral ; topical and vaginal. Dosage Form: Sublingual tablets; IM injections; intrasynovial injections; nasal preparations; ophthalmic preparations; oral capsules, oral suspensions, and oral tablets; topical and vaginal preparations. Stability and Storage Conditions: Methylcellulose powder is stable, although slightly hygroscopic. The bulk material should be stored in an airtight container in a cool, dry place. Solutions of methylcellulose are stable to alkalis and dilute acids at pH 3-11, at room temperature. At pH less than 3, acid-catalyze | |
| Nonoxinol 4 | Nonoxinol 4. Synonyms: Nonoxynol-4; polyoxyethylene nonylphenol ether; NP-4; Nonyl phenol ether; Nonyl Phenol Ethyleneoxide. CAS No. 26027-38-3. Product ID: PE-0625. Molecular formula: C9H19C6H4(OCH2CH2)nOH (n=4). Mole weight: 616.87. Category: Surfactant. Product Keywords: Excipients for Liquid Dosage Form; Surfactant Excipients; PE-0625; Nonoxinol 4; Surfactant; C9H19C6H4(OCH2CH2)nOH (n=4); 26027-38-3. UNII: 48Q180SH9T. Chemical Name: α -(p-Nonylphenyl)-ω -hydroxynona(oxyethylene). Grade: Pharmceutical Excipients. Stability and Storage Conditions: Gradually saponification under strong acid or base conditions; Stable in a weak acid or base. Store in an airtight container in a cool and dry place. Commonly used amount and the maximum amount: Ophthalmic solution: 0.12%; Topical solution: 0.01%. Source and Preparation: It is an admixture of nonanphenol and ethylene oxide, and its alkyl carbon number is about 4. Applications: Surfactant, spermicide. | |
| Nonoxinol 9 | Colorless to yellowish oily liquid. Synonyms: Nonoxynol-9; polyoxyethylene nonylphenol ether; NP-9; Nonyl phenol ether; Nonyl Phenol Ethyleneoxide. CAS No. 26027-38-3. Product ID: PE-0626. Molecular formula: C9H19C6H4(OCH2CH2)nOH (n=9). Mole weight: 616.82. Category: Surfactant. Product Keywords: Excipients for Liquid Dosage Form; Surfactant Excipients; PE-0626; Nonoxinol 9; Surfactant; C9H19C6H4(OCH2CH2)nOH (n=9); 26027-38-3. UNII: 48Q180SH9T. Chemical Name: α -(p-Nonylphenyl)-ω -hydroxynona(oxyethylene). Grade: Pharmceutical Excipients. Administration route: Inhalant oral, topical. Dosage Form: Local administration solution; Local sponge; Ordinary topical preparations. Stability and Storage Conditions: Gradually saponification under strong acid or base conditions; Stable in a weak acid or base. Store in an airtight container in a cool and dry place. Commonly used amount and the maximum amount: Ophthalmic solution: 0.12%; Topical solution: 0.01%. Source and Preparation: It is an admixture of nonanphenol and ethylene oxide, and its alkyl carbon number is about 9. | |
| Olopatadine | This active molecular is an antihistamine, anticholinergic and mast cell stabilizer. Olopatadine blocks the action of endogenous histamine. It is used to treat itching associated with allergic conjunctivitis (eye allergies). In Dec 2014, Alcon Research planed a phase III trial for Allergic conjunctivitis in China.In Jan 2015,Registered for Allergic conjunctivitis in USA was completed (Ophthalmic, 0.7%). In Oct 2015, Alcon Research completeD phase III trial in Allergic conjunctivitis in China. Uses: Antiallergic; antihistaminic;for the treatment of ocular itching associated with allergic conjunctivitis. Synonyms: (Z)-11-[3-(Dimethylamino)propylidene]-6,11-dihydrodibenz[b,e]oxepin-2-acetic Acid; 11-[(Z)-3-(Dimethylamino)propylidene]-6,11-dihydrodibenz[b,e]oxepin-2-acetic Acid; Opatanol; Pataday; Patanol; KW-4679, KW 4679; KW4679; KW-4943A. Grades: 98%. CAS No. 113806-05-6. Molecular formula: C21H23NO3. Mole weight: 337.41. | |
| Poloxamer 124 | Poloxamers generally occur as white, waxy, free-flowing prilled granules, or as cast solids. They are practically odorless and tasteless. At room temperature, poloxamer 125 occurs as a colorless liquid. Synonyms: Lutrol; Monolan; Pluronic; poloxalkol; poloxamera; polyethylene-propylene glycol copolymer; polyoxyethylene-polyoxypropylene copolymer; Supronic; Synperonic. CAS No. 9003-11-6. Product ID: PE0390. Molecular formula: HO(C2H4O)a(C3H6O)b(C2H4O)aH. Mole weight: 2 090-2 360. Category: Dispersant; Emulsifier; Solubilizer; Lubricant; Humectant. Product Keywords: Dispersion Excipients; Emulsifier Excipients; Solubilizer Excipients; ; PE0390; Poloxamer 124; Dispersant; Emulsifier; Solubilizer; Lubricant; Humectant; HO(C2H4O)a(C3H6O)b(C2H4O)aH; 9003-11-6. UNII: 1S66E28KXA. Chemical Name: a-Hydro-o-hydroxypoly (oxyethylene)poly (oxypropylene) poly-(oxyethylene) block copolymer. Grade: Pharmceutical Excipients. Administration route: Oral, topical administration. Dosage Form: IV injections; inhalations, ophthalmic preparations; oral powders, solutions, suspensions, and syrups; topical preparations. Stability and Storage Conditions: Poloxamers are stable materials. Aqueous solutions are stable in the presence of acids, alkalis, and metal ions. However, aqueous solutions support mold growth. The bulk material should be stored in a well-closed container in a cool, dry place. Source and Preparation: Poloxamer polymers are prep | |
| Poloxamer 188 | Poloxamers generally occur as white, waxy, free-flowing prilled granules, or as cast solids. They are practically odorless and tasteless. Synonyms: Lutrol; Monolan; Pluronic; poloxalkol; poloxamera; polyethylene-propylene glycol copolymer; polyoxyethylene-polyoxypropylene copolymer; Supronic; Synperonic. CAS No. 9003-11-6. Product ID: PE0391. Molecular formula: HO(C2H4O)a(C3H6O)b(C2H4O)aH. Mole weight: 7 680-9 510. Category: Dispersant; Emulsifier; Solubilizer; Lubricant; Humectant. Product Keywords: Dispersion Excipients; Emulsifier Excipients; Solubilizer Excipients; ; PE0391; Poloxamer 188; Dispersant; Emulsifier; Solubilizer; Lubricant; Humectant; HO(C2H4O)a(C3H6O)b(C2H4O)aH; 9003-11-6. UNII: LQA7B6G8JG. Chemical Name: a-Hydro-o-hydroxypoly (oxyethylene)poly (oxypropylene) poly-(oxyethylene) block copolymer. Grade: Pharmceutical Excipients. Administration route: Injection, ophthalmic, oral, periodontal, topical. Dosage Form: IV injections; inhalations, ophthalmic preparations; oral powders, solutions, suspensions, and syrups; topical preparations. Stability and Storage Conditions: Poloxamers are stable materials. Aqueous solutions are stable in the presence of acids, alkalis, and metal ions. However, aqueous solutions support mold growth. The bulk material should be stored in a well-closed container in a cool, dry place. Source and Preparation: Poloxamer polymers are prepared by reacting propylene oxide with propyl | |
| Poloxamer 237 | Poloxamers generally occur as white, waxy, free-flowing prilled granules, or as cast solids. They are practically odorless and tasteless. Synonyms: Lutrol; Monolan; Pluronic; poloxalkol; poloxamera; polyethylene-propylene glycol copolymer; polyoxyethylene-polyoxypropylene copolymer; Supronic; Synperonic. CAS No. 9003-11-6. Product ID: PE0392. Molecular formula: HO(C2H4O)a(C3H6O)b(C2H4O)aH. Mole weight: 6 840-8 830. Category: Dispersant; Emulsifier; Solubilizer; Lubricant; Humectant. Product Keywords: Dispersion Excipients; Emulsifier Excipients; Solubilizer Excipients; ; PE0392; Poloxamer 237; Dispersant; Emulsifier; Solubilizer; Lubricant; Humectant; HO(C2H4O)a(C3H6O)b(C2H4O)aH; 9003-11-6. UNII: NA. Chemical Name: a-Hydro-o-hydroxypoly (oxyethylene)poly (oxypropylene) poly-(oxyethylene) block copolymer. Grade: Pharmceutical Excipients. Administration route: Topical administration. Dosage Form: IV injections; inhalations, ophthalmic preparations; oral powders, solutions, suspensions, and syrups; topical preparations. Stability and Storage Conditions: Poloxamers are stable materials. Aqueous solutions are stable in the presence of acids, alkalis, and metal ions. However, aqueous solutions support mold growth. The bulk material should be stored in a well-closed container in a cool, dry place. Source and Preparation: Poloxamer polymers are prepared by reacting propylene oxide with propylene glycol to form polyoxypropylene | |
| Poloxamer 338 | Poloxamers generally occur as white, waxy, free-flowing prilled granules, or as cast solids. They are practically odorless and tasteless. Synonyms: Lutrol; Monolan; Pluronic; poloxalkol; poloxamera; polyethylene-propylene glycol copolymer; polyoxyethylene-polyoxypropylene copolymer; Supronic; Synperonic. CAS No. 9003-11-6. Product ID: PE0393. Molecular formula: HO(C2H4O)a(C3H6O)b(C2H4O)aH. Mole weight: 12 700-17 400. Category: Dispersant; Emulsifier; Solubilizer; Lubricant; Humectant. Product Keywords: Dispersion Excipients; Emulsifier Excipients; Solubilizer Excipients; ; PE0393; Poloxamer 338; Dispersant; Emulsifier; Solubilizer; Lubricant; Humectant; HO(C2H4O)a(C3H6O)b(C2H4O)aH; 9003-11-6. UNII: NA. Chemical Name: a-Hydro-o-hydroxypoly (oxyethylene)poly (oxypropylene) poly-(oxyethylene) block copolymer. Grade: Pharmceutical Excipients. Administration route: Oral. Dosage Form: IV injections; inhalations, ophthalmic preparations; oral powders, solutions, suspensions, and syrups; topical preparations. Stability and Storage Conditions: Poloxamers are stable materials. Aqueous solutions are stable in the presence of acids, alkalis, and metal ions. However, aqueous solutions support mold growth. The bulk material should be stored in a well-closed container in a cool, dry place. Source and Preparation: Poloxamer polymers are prepared by reacting propylene oxide with propylene glycol to form polyoxypropylene glycol. Ethylen | |
| Poloxamer 407 | Poloxamers generally occur as white, waxy, free-flowing prilled granules, or as cast solids. They are practically odorless and tasteless. Synonyms: Lutrol; Monolan; Pluronic; poloxalkol; poloxamera; polyethylene-propylene glycol copolymer; polyoxyethylene-polyoxypropylene copolymer; Supronic; Synperonic. CAS No. 9003-11-6. Product ID: PE0394. Molecular formula: HO(C2H4O)a(C3H6O)b(C2H4O)aH. Mole weight: 9 840-14 600. Category: Dispersant; Emulsifier; Solubilizer; Lubricant; Humectant. Product Keywords: Dispersion Excipients; Emulsifier Excipients; Solubilizer Excipients; ; PE0394; Poloxamer 407; Dispersant; Emulsifier; Solubilizer; Lubricant; Humectant; HO(C2H4O)a(C3H6O)b(C2H4O)aH; 9003-11-6. UNII: TUF2IVW3M2. Chemical Name: a-Hydro-o-hydroxypoly (oxyethylene)poly (oxypropylene) poly-(oxyethylene) block copolymer. Grade: Pharmceutical Excipients. Administration route: Ophthalmic, oral, periodontal, topical. Dosage Form: IV injections; inhalations, ophthalmic preparations; oral powders, solutions, suspensions, and syrups; topical preparations. Stability and Storage Conditions: Poloxamers are stable materials. Aqueous solutions are stable in the presence of acids, alkalis, and metal ions. However, aqueous solutions support mold growth. The bulk material should be stored in a well-closed container in a cool, dry place. Source and Preparation: Poloxamer polymers are prepared by reacting propylene oxide with propylene glycol | |
| Poly(butyl acrylate) solution | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Our hydrophobic polymers are used as coatings, adhesives, fibers, films and engineering plastics. furthermore, they are widely used as biomedical polymers for vascular grafts, implants and ophthalmic applications. Group: Hydrophobic polymersreference-calibration standards. Alternative Names: Butyl acrylate homopolymer, Butyl acrylate polymer, Poly(n -butyl acrylate), Acrylic acid butyl ester polymer. CAS No. 9003-49-0. Pack Sizes: 50 g in glass bottle. Product ID: butyl prop-2-enoate. Molecular formula: average Mw ~99,000 by GPC. Mole weight: (C7H12O2)n. CCCCOC(=O)C=C. 1S/C7H12O2/c1-3-5-6-9-7(8)4-2/h4H, 2-3, 5-6H2, 1H3. CQEYYJKEWSMYFG-UHFFFAOYSA-N. |  |
| Polycarbophil | Polycarbophil occurs as fluffy, white to off-white, mildly acidic polymer powder with slightly acetic odor. Synonyms: Noveon AA-1. CAS No. 9003-97-8. Product ID: PE0366. Category: Adsorbents; Controlled-release agents; Suspending agents; Binders; Thickeners. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Filler Excipients; Absorbent; Polycarbophil; PE0366; W25LM17A4W; 9003-97-8; 9003-97-8. UNII: W25LM17A4W. Chemical Name: Polycarbophil. Grade: Pharmceutical Excipients. Administration route: Buccal; Ophhalmic; Topical. Dosage Form: Film; Tablet; Gel; Solution; Suspension/Drops. Stability and Storage Conditions: Polycarbophil polymers are stable, hygroscopic materials. They do not undergo hydrolysis or oxidation under normal conditions. ners necessitates a pH greater than 7.7 to prolong polycarbophil stability. Applications: Conventionally, polycarbophil is used as a thickening agent at very low concentrations (less than 1%) to produce a wide range of viscosities and flow properties in topical lotions, creams, and gels, in oral suspensions, and in transdermal gel reservoirs. It is also used as an emulsifying agent in topical oil-in-water systems. Polycarbophil is an excellent bioadhesive in buccal, ophthalmic, intestinal, nasal, vaginal, and rectal applications. Buccal tablets prepared using polycarbophil have shown high bioadhesive force and prolonged residence time, and proved to be no | |
| Poly(ethylene adipate) | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Our hydrophobic polymers are used as coatings, adhesives, fibers, films and engineering plastics. furthermore, they are widely used as biomedical polymers for vascular grafts, implants and ophthalmic applications. Group: Polyethylene (pe). Alternative Names: Ethylene glycol adipate, Poly(ethylene adipate), dihydroxy terminated. CAS No. 24938-37-2. Product ID: ethane-1,2-diol; hexanedioic acid. Molecular formula: average Mw ~10,000 by GPC. Mole weight: [OCH2CH2O2C(CH2)4CO]n. C(CCC(=O)O)CC(=O)O.C(CO)O. InChI=1S/C6H10O4. C2H6O2/c7-5(8)3-1-2-4-6(9)10; 3-1-2-4/h1-4H2, (H, 7, 8)(H, 9, 10); 3-4H, 1-2H2. FZWBABZIGXEXES-UHFFFAOYSA-N. | |
| Poly(ethylene succinate) | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Our hydrophobic polymers are used as coatings, adhesives, fibers, films and engineering plastics. furthermore, they are widely used as biomedical polymers for vascular grafts, implants and ophthalmic applications. Group: Hydrophobic polymerspolymers. Alternative Names: Ethylene glycol succinate. CAS No. 25569-53-3. Product ID: butanedioic acid; ethane-1,2-diol. Molecular formula: average Mw 10,000. Mole weight: (OCH2CH2O2CCH2CH2CO)n. OCCO.OC(=O)CCC(O)=O. 1S/C4H6O4.C2H6O2/c5-3(6)1-2-4(7)8; 3-1-2-4/h1-2H2, (H, 5, 6)(H, 7, 8); 3-4H, 1-2H2. VJVOPINBJQWMNY-UHFFFAOYSA-N. | |
| Poly(methyl methacrylate-co-methacrylic acid) | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Our hydrophobic polymers are used as coatings, adhesives, fibers, films and engineering plastics. furthermore, they are widely used as biomedical polymers for vascular grafts, implants and ophthalmic applications. Group: Bioelectronic materials hydrophobic polymersself assembly and lithography. Alternative Names: Poly(methacrylic acid-co-methyl methacrylate). CAS No. 25086-15-1. Pack Sizes: 1 kg in poly bottle. Product ID: methyl 2-methylprop-2-enoate; 2-methylprop-2-enoic acid. Molecular formula: average Mn ~15,000 by GPC average Mw ~34,000 by GPC. Mole weight: C9H14O4. CC(=C)C(=O)O.CC(=C)C(=O)OC. 1S/C5H8O2.C4H6O2/c1-4(2)5(6)7-3; 1-3(2)4(5)6/h1H2, 2-3H3; 1H2, 2H3, (H, 5, 6). IWVKTOUOPHGZRX-UHFFFAOYSA-N. | |
| Poly(vinyl cinnamate) | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Our hydrophobic polymers are used as coatings, adhesives, fibers, films and engineering plastics. furthermore, they are widely used as biomedical polymers for vascular grafts, implants and ophthalmic applications. Group: Hydrophobic polymerspolymers. Alternative Names: Ethenol,homopolymer,3-phenyl-2-propenoate; Vinylalcohol, cinnamoylchloridereactionproduct; POLY(VINYL CINNAMATE); VINYL CINNAMATE POLYMER; POLY(VINYL CINNAMATE), AVERAGE MW CA. 20 0,000 (GPC); vinyl cinnamate homopolymer; Poly(vinyl cinnamate) average Mn 40,000. CAS No. 9050-06-0. Product ID: ethenol; (E)-3-phenylprop-2-enoic acid. Molecular formula: average Mn 40,000. Mole weight: [CH2CH(O2CCH=CHC6H5)]n. C=COC(=O)\C=C\c1ccccc1. 1S/C9H8O2. C2H4O/c10-9(11)7-6-8-4-2-1-3-5-8; 1-2-3/h1-7H, (H, 10, 11); 2-3H, 1H2/b7-6+. HCCVHWNULIPQNY-UHDJGPCESA-N. | |
| Proparacaine Hydrochloride | Topical anesthetic (ophthalmic). Group: Biochemicals. Alternative Names: 3-Amino-4-propoxybenzoic Acid. Grades: Highly Purified. CAS No. 499-67-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Propylene Glycol | Propylene glycol is a clear, colorless, viscous, practically odorless liquid, with a sweet, slightly acrid taste resembling that of glycerin. Synonyms: 1, 2-Dihydroxypropane; E1520; 2-hydroxypropanol; methyl ethylene glycol; methyl glycol; propane-1, 2-diol; propylenglycolum. CAS No. 57-55-6. Product ID: PE-0178. Molecular formula: C3H8O2. Mole weight: 76.09. Category: Antimicrobial Preservative; Disinfectant; Humectant; Plasticizer; Solvent; Stabilizing Agents; Water-miscible Cosolvent. Product Keywords: Plasticizer Excipients; Emulsifier Excipients; Humectants Excipients; Stabilizers; PE-0178; Propylene Glycol; Antimicrobial Preservative; Disinfectant; Humectant; Plasticizer; Solvent; Stabilizing Agents; Water-miscible Cosolvent; C3H8O2; 57-55-6. UNII: 6DC9Q167V3. Chemical Name: 1, 2-Propanediol. Grade: Pharmceutical Excipients. Administration route: Intramuscular injection, intravenous injection, nasal administration, oral administration, ophthalmic administration, ear administration, external application. Stability and Storage Conditions: At cool temperatures, propylene glycol is stable in a well-closed container, but at high temperatures, in the open, it tends to oxidize, giving rise to products such as propionaldehyde, lactic acid, pyruvic acid, and acetic acid. Propylene glycol is chemically stable when mixed with ethanol (95%), glycerin, or water; aqueous solutions may be sterilized by autoclaving. Propyle | |
| Sodium Bicarbonate | Sodium bicarbonate occurs as an odorless, white, crystalline powder with a saline, slightly alkaline taste. The crystal structure is monoclinic prisms. Grades with different particle sizes, from a fine powder to free-flowing uniform granules, are commercially available. Synonyms: Baking soda; E500; Effer-Soda; monosodium carbonate; natrii hydrogenocarbonas; Sal de Vichy; sodium acid carbonate; sodium hydrogen carbonate. CAS No. 144-55-8. Product ID: PE-0619. Molecular formula: NaHCO3. Mole weight: 84.01. Category: Alkalizing Agents; therapeutic AgentsAcid-Base regulator; Effervescent Disintegrant; Buffer (in solution); Freeze-drying Stabilizer; Gas forming Agents. Product Keywords: Other Materials; Stabilizers; PE-0619; Sodium Bicarbonate; Alkalizing Agents; therapeutic AgentsAcid-Base regulator; Effervescent Disintegrant; Buffer (in solution); Freeze-drying Stabilizer; Gas forming Agents; NaHCO3; 144-55-8. UNII: 8MDF5V39QO. Chemical Name: Carbonic acid monosodium salt. Grade: Pharmceutical Excipients. Administration route: Injections; ophthalmic; oral. Dosage Form: Injections; ophthalmic preparations; oral capsules, solutions, and tablets. Stability and Storage Conditions: When heated to about 50°C, sodium bicarbonate begins to dissociate into carbon dioxide, sodium carbonate, and water; on heating to 250-300°C, for a short time, sodium bicarbonate is completely converted into anhydrous sodium carbonate. Source a | |
| Sodium Carbonate | Sodium carbonate is used as an alkalizing agent in injectable, ophthalmic, oral and rectal preparations, and as an oral antacid and buffering agent. Synonyms: Carbonic Acid Disodium Salt; Bisodium Carbonate; Calcined Soda; Carbonic acid Sodium Salt; Disodium Carbonate; Snowlite 1; Sodium carbonate, Anhydrous. Grades: ≥95%. CAS No. 497-19-8. Molecular formula: CH2O3.2Na. Mole weight: 105.99. | |
| Sodium Carbonate Monohydrate | Sodium Carbonate Monohydrate is used as an alkalizing agent in injectable, ophthalmic, oral and rectal preparations, and as an oral antacid and buffering agent. Synonyms: Carbonic Acid Disodium Salt, Monohydrate; Disodium Carbonate Monohydrate. CAS No. 5968-11-6. Molecular formula: CH2O3.H2O.2Na. Mole weight: 124.00. | |
| Sodium Citrate | Sodium citrate dihydrate consists of odorless, colorless, monoclinic crystals, or a white crystalline powder with a cooling, saline taste. It is slightly deliquescent in moist air, and in warm dry air it is efflorescent. Although most pharmacopeias specify that sodium citrate is the dihydrate, the USP states that sodium citrate may be either the dihydrate or anhydrous material. Synonyms: Citric acid trisodium salt; E331; natrii citras; sodium citrate tertiary; trisodium citrate. CAS No. 6132-4-3. Product ID: PE-0124. Molecular formula: C6H5Na3O7·2H2O. Mole weight: 294.1. Category: Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents. Product Keywords: Flavoring Agents; Stabilizers; pH Modifier Excipients; ; PE-0124; Sodium Citrate; Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents; C6H5Na3O7·2H2O; 6132-04-03. UNII: 1Q73Q2JULR. Chemical Name: Trisodium 2-hydroxypropane-1, 2, 3-tricarboxylate dihydrate. Grade: Pharmceutical Excipients. Administration route: Inhalations; injections; ophthalmic; oral; nasal, otic, rectal, topical, transdermal, and vaginal. Dosage Form: Inhalations; injections; ophthalmic products; oral solutions, suspensions, syrups and tablets; nasal, otic, rectal, topical, transdermal, and vaginal preparations. Stability and Storage Conditions: Sodium citrate dihydrate is a stable material. Aqueous solutions may be sterilized by autoclaving. On storag | |
| Sodium Citrate Dihydrate | Sodium citrate dihydrate consists of odorless, colorless, monoclinic crystals, or a white crystalline powder with a cooling, saline taste. It is slightly deliquescent in moist air, and in warm dry air it is efflorescent. Although most pharmacopeias specify that sodium citrate is the dihydrate, the USP states that sodium citrate may be either the dihydrate or anhydrous material. Synonyms: Citric acid trisodium salt; E331; natrii citras; sodium citrate tertiary; trisodium citrate. CAS No. 6132-4-3. Product ID: PE-0542. Molecular formula: C6H5Na3O7·2H2O. Mole weight: 294.1. Category: Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0542; Sodium Citrate Dihydrate; Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents; C6H5Na3O7·2H2O; 6132-04-3. UNII: 1Q73Q2JULR. Chemical Name: Trisodium 2-hydroxypropane-1, 2, 3-tricarboxylate dihydrate. Grade: Pharmceutical Excipients. Administration route: Inhalations; injections; ophthalmic; oral; nasal, otic, rectal, topical, transdermal, and vaginal. Dosage Form: Inhalations; injections; ophthalmic products; oral solutions, suspensions, syrups and tablets; nasal, otic, rectal, topical, transdermal, and vaginal preparations. Stability and Storage Conditions: Sodium citrate dihydrate is a stable material. Aqueous solutions may be sterilized by au | |
| Sodium Phosphate Monobasic | The hydrated forms of monobasic sodium phosphate occur as odorless, colorless or white, slightly deliquescent crystals. The anhydrous form occurs as a white crystalline powder or granules. Synonyms: Acid sodium phosphate; E339; Kalipol 32; monosodium orthophosphate; monosodium phosphate; natrii dihydrogenophosphas dihydricus; phosphoric acid, monosodium salt; primary sodium phosphate; sodium biphosphate; sodium dihydrogen orthophosphate; sodium dihydrogen phosphate. Product ID: PE-0557. Category: Buffering Agents; Emulsifying Agents; Sequestering Agents. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0557; Sodium Phosphate Monobasic; Buffering Agents; Emulsifying Agents; Sequestering Agents;. UNII: 3980JIH2SW. Grade: Pharmceutical Excipients. Administration route: Injections; infusions; ophthalmic, oral, topical, and vaginal. Dosage Form: Injections; infusions; ophthalmic, oral, topical, and vaginal preparations. Stability and Storage Conditions: Monobasic sodium phosphate is chemically stable, although it is slightly deliquescent. On heating at 100°C, the dihydrate loses all of its water of crystallization. On further heating, it melts with decomposition at 205°C, forming sodium hydrogen pyrophosphate, Na2H2P2O7. At 250°C it leaves a final residue of sodium metaphosphate, NaPO3. Aqueous solutions are stable and may be sterilized by autoclaving. Monobasic sodium phosphate sho | |
| Sorbitan Monostearate | Cream solid. Synonyms: Ablunol S-60; Alkamuls SMS; 1, 4-Anhydro-D-glucitol, 6-octadecanoate; anhydrosorbitol monostearate; Arlacel 60; Armotan MS; Atlas 110K; Capmul S; Crill 3; Dehymuls SMS; Drewmulse SMS; Drewsorb 60K; Durtan 6O; Durtan 60K; E491; Famodan MS Kosher; Glycomul S FG; Glycomul S KFG; Hodag SMS; Lamesorb SMS; Liposorb S; Liposorb SC; Liposorb S-K; Montane 60; Nissan Nonion SP-60R; Norfox Sorbo S-60FG; Pol. CAS No. 1338-41-6. Product ID: PE-0535. Molecular formula: C24H46O6. Mole weight: 431. Category: Dispersing Agents; Emulsifying Agents; Nonionic Surfactant; solubilizing Agents; Suspending Agents; Wetting Agents. Product Keywords: Surfactant Excipients; Emulsifier Excipients; Solubilizer Excipients; ; PE-0535; Sorbitan Monostearate; Dispersing Agents; Emulsifying Agents; Nonionic Surfactant; solubilizing Agents; Suspending Agents; Wetting Agents; C24H46O6; 1338-41-6. UNII: NVZ4I0H58X. Chemical Name: Sorbitan mono-octadecanoate. Grade: Pharmceutical Excipients. Administration route: Administration of topical preparations, sublingual administration, rectal cavity urethral administration, dental external application and tablet use. Dosage Form: Inhalation, intramuscular, ophthalmic, oral, topical and vaginal formulations. Stability and Storage Conditions: Gradually saponified under strong acid or strong base; stable in weak acid or weak base. Sorbitan ethoxylate should be packed in airtight conta | |
| Sorbitan oleate(Span 80) | Sorbitan oleate(Span 80). CAS No. 1338-43-8. Product ID: PE-0627. Molecular formula: C24H44O6. Mole weight: 429. Category: Surfactant. Product Keywords: Excipients for Liquid Dosage Form; Surfactant Excipients; PE-0627; Sorbitan oleate(Span 80); Surfactant; C24H44O6; 1338-43-8. UNII: 06XEA2VD56. Chemical Name: (Z)-Sorbitan mono-9-octadecenoate. Grade: Pharmceutical Excipients. Administration route: Oral administration, local administration, rectal administration. Dosage Form: Inhalants, intramuscular injections, ophthalmic, oral, topical and vaginal preparations. Stability and Storage Conditions: Gradually saponification under strong acid or base conditions; Stable in a weak acid or base. Sorbitan ester should be packed in an airtight container and stored in a cool and dry place. Source and Preparation: Sorbitol is dehydrated to form 1, 4-sorbitan, which is then esterified with oleic acid. Applications: Sorbitan ester, as a lipophilic nonionic surfactant, is widely used in cosmetics, food and pharmaceuticals. They are used primarily as emulsifiers in the preparation of creams, emulsions and ointments for topical applications. When used alone, sorbitan ester can produce stable water-in-oil emulsions and microemulsions, but when combined with polysorbitan ester in different proportions, various water-in-oil or oil-in-water emulsions or creams can be prepared. Safety: Sorbitan ester is widely used in cosmetic | |
| Sorbitan Sesquioleate | Sorbitan esters occur as cream- to amber-colored liquids or solids with a distinctive odor and taste. Synonyms: Span-83. CAS No. 8007-43-0. Product ID: PE0388. Molecular formula: C33H60O6.5. Mole weight: 561. Category: Dispersants; Emulsifiers; Surfactants; Suspending Agentss; Wetting Agentss. Product Keywords: Dispersion Excipients; Humectants Excipients; Emulsifier Excipients; Solubilizer Excipients; PE0388; Sorbitan Sesquioleate; Dispersants; Emulsifiers; Surfactants; Suspending Agentss; Wetting Agentss; C33H60O6.5; 8007-43-0. UNII: 0W8RRI5W5A. Chemical Name: (Z)-Sorbitan sesqui-9- octadecenoate. Grade: Pharmceutical Excipients. Administration route: Oral administration, intravenous injection, general topical preparation administration, transdermal administration, sublingual administration, rectal cavity urethral administration. Dosage Form: Inhalations; IM injections; ophthalmic, oral, topical, and vaginal preparations. Stability and Storage Conditions: Gradual soap formation occurs with strong acids or bases; sorbitan esters are stable in weak acids or bases. Sorbitan esters should be stored in a well-closed container in a cool, dry place. Source and Preparation: Sorbitol is dehydrated to form a hexitan (1, 4-sorbitan), which is then esterified with the desired fatty acid. Applications: Sorbitan monoesters are a series of mixtures of partial esters of sorbitol and its mono- and dianhydrides with fatty ac | |
| Ursodiol | 3a,7ß-dihydroxy-5ß-cholan-24-oic Ursodeoxycholic acid Actigall. Antiallergic, ophthalmic. CAS No. 128-13-2. Product ID: 8-01419. Molecular formula: C24H40O4. Mole weight: 392.56. Source : |  |
| Hyaluronic acid sodium salt | HAS. Grades: ophthalmic grade. CAS No. 9067-32-7. Product ID: 8-01735. Mole weight: high Mw. | |
| Ibopamine Hydrochloride | Ibopamine Hydrochloride, the prodrug of epinine, is a sympathomimetic drug used in ophthalmology. It induces mydriasis. It acts as an agonist on Dopamine receptor D1 and α-adrenergic receptors and has been studied for the treatment of congestive heart failure. Synonyms: 2-Methylpropanoic Acid 1,1'-[4-[2-(Methylamino)ethyl]-1,2-phenylene] Ester Hydrochloride; 3,4-Di-O-isobutyrylepinine Hydrochloride; Inopamil; Scandine. Grades: ≥95%. CAS No. 75011-65-3. Molecular formula: C17H26ClNO4. Mole weight: 343.85. | |
| Poly(dimer acid-co-alkyl polyamine) | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Our hydrophobic polymers are used as coatings, adhesives, fibers, films and engineering plastics. furthermore, they are widely used as biomedical polymers for vascular grafts, implants and ophthalmic applications. Group: Hydrophobic polymers. | |
| Pranoprofen | Pranoprofen is a non-steroidal anti-inflammatory agent ( NSAID ) for the research of keratitis or other ophthalmology diseases. Pranoprofen inhibit COX-1 and COX-2 enzymes, thus blocking arachidonic acid converted to eicosanoids and reducing prostaglandins synthesis [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 52549-17-4. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0336. | |
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