Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| Sodium lactate | Pharmacopeia & Metrological Institutes Standards. Uses: For analytical and research use. Group: Reagents. CAS No. 867-56-1. Pack Sizes: 200MG. |  |
| Sodium lactate | Sodium lactate. Uses: For analytical and research use. Group: Impurity standards. CAS No. 312-85-6/72-17-3. Molecular Formula: C3H5NaO3. Mole Weight: 112.06. Catalog: APB312856. | |
| Sodium Lactate | Sodium lactate occurs as a clear, colorless, slightly syrupy liquid. It is odorless, or has a slight odor with a characteristic saline taste. It is hygroscopic. Synonyms: E325; 2-hydroxypropanoic acid monosodium salt; Lacolin; lactic acid monosodium salt; lactic acid sodium salt; natrii lactatis solutio; Patlac; Purasal; Ritalac NAL; sodium a-hydroxypropionate. CAS No. 72-17-3. Product ID: PE-0556. Molecular formula: C3H5NaO3. Mole weight: 112.06. Category: Antimicrobial Preservative; Buffering Agents; Emulsifying Agents; flavoring Agents; Humectant. Product Keywords: Stabilizers; Emulsifier Excipients; PE-0556; Sodium Lactate; Antimicrobial Preservative; Buffering Agents; Emulsifying Agents; flavoring Agents; Humectant; C3H5NaO3; 72-17-3. UNII: TU7HW0W0QT. Chemical Name: Sodium lactate. Grade: Pharmceutical Excipients. Administration route: Infiltration; Intraperitoneal; Intravenous; Oral; Intracardiac; Intramuscular; Subcutaneous. Dosage Form: Epidural, IM, IV, and SC injections; oral suspensions; topical gels and solutions. Stability and Storage Conditions: Sodium lactate should be stored in a well-closed container in a cool, dry, place. Sodium lactate is combustible and decomposes upon heating. Commonly used amount and the maximum amount: The maximum dosage for intravenous injection: 50mg; the maximum dosage for general topical preparations: 51.3mg/g. Source and Preparation: Add sodium hydroxide to lactic acid u |  |
| Sodium Lactate BP/USP | Sodium Lactate BP/USP. CAS No. 72-17-3. Molecular formula: C3H5NaO3. |  |
| Sodium lactate, powder | 100g Pack Size. Group: Biochemicals, Carbohydrates. Formula: C3H5NaO3. CAS No. 72-17-3. Prepack ID 90018783-100g. Molecular Weight 112.06. See USA prepack pricing. |  |
| Lactate-d3 (sodium) (60% in water) | Lactate-d 3 sodium (60% in water) is the deuterium labeled Lactate sodium (60% in water). Lactate sodium (60% in water) is the product of glycogenolysis and glycolysis. Lactate sodium (60% in water) functions in a variety of biochemical processes [1] [2]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Lactic acid-d3 sodium. CAS No. 1219802-24-0. Pack Sizes: 1 mg (5.20 M * 1.67 μL in Water); 5 mg (5.20 M * 8.36 μL in Water); 10 mg (5.20 M * 16.71 μL in Water). Product ID: HY-B2227BS1. |  |
| Lactate (sodium) (60% in water) | Lactate (60% in water) (Lactic acid) sodium is the product of glycogenolysis and glycolysis [1]. Lactate sodium (60% in water) is an organic salt that is mainly used as a buffer and pH adjuster for injection solutions. Lactate sodium (60% in water) can be metabolized by the body into sodium bicarbonate, which in turn acts to increase the pH of the blood. Lactate sodium (60% in water) is used to improve metabolic acidosis and hypovolemic states. In terms of pharmaceutical preparations, Lactate sodium (60% in water) is often used in combination with sodium chloride, glucose, etc. to form normal saline or compound liquid intravenous injection [2] [3] [4] [5]. Lactate sodium (60% in water) also has antimicrobial activity, which can be used as a food preservative [6]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lactic acid sodium. CAS No. 72-17-3. Pack Sizes: 100 mg (5.34 M * 167 μL in Water); 250 mg (5.34 M * 418 μL in Water); 500 mg (5.34 M * 835 μL in Water); 1 g (5.34 M * 1.67 mL in Water). Product ID: HY-B2227B. | |
| Sodium DL-Lactate-3,3,3-d3 (60% w/w in H2O) | Deuterium Labeled Products-Medical Research. Alternative Names: Sodium (±)-2-hydroxypropionate; Lacolin. CAS No. 1219802-24-0. Molecular formula: CD3CH(OH)COONa. Mole weight: 115.08. Catalog: ACM1219802240. |  |
| Sodium DL-Lactate(60% in Water) | Sodium DL-Lactate(60% in Water). Group: Molecular Biology. CAS No. 72-17-3. Pack Sizes: 500g. Molecular Formula: C3H6O3. US Biological Life Sciences. |  Worldwide |
| Sodium DL-Lactate-d3 | Sodium DL-Lactate-d3. Group: Biochemicals. Alternative Names: 2-Hydroxypropanoic Acid Sodium Salt-d3; Monosodium Salt Lactic Acid-d3; 2-Hydroxy-Propanoic Acid Monosodium Salt-d3; Sodium Lactate-d3; E 325; Lacolin-d3; Lactic Acid Sodium Salt-d3; Monosodium Lactate-d3; NSC 31718-d3; Per-glycerin-d3; Purasal Powder S 98JS-d3; Purasal S-d3; Purasal S/HQ 60-d3; Purasal S/SP 60-d3; Purasal-Purac Spray 80-d3; Sodium α-Hydroxypropionate-d3; Wilclear-d3. Grades: Highly Purified. CAS No. 1219802-24-0. Pack Sizes: 10mg. Molecular Formula: C3H2D3NaO3, Molecular Weight: 115.08. US Biological Life Sciences. | Worldwide |
| 2-Hydroxybutanoic-d3 Acid Sodium Salt | 2-Hydroxybutanoic-d3 Acid Sodium Salt is the labeled analogue of a degredation product of isotactic P[(R)-2-hydroxybutyrate] and Its copolymer with (R)-Lactate. Group: Biochemicals. Grades: Highly Purified. CAS No. 1219798-97-6. Pack Sizes: 10mg, 100mg. Molecular Formula: C4H4D3NaO3, Molecular Weight: 129.1. US Biological Life Sciences. | Worldwide |
| DCA | DCA is a mitochondrial pyruvate dehydrogenase kinase (PDK) inhibitor that shifts pyruvate metabolism from glycolysis and lactate production to glucose oxidation in the mitochondria. DCA also induces apoptosis and reverses the KV1.5 channels downregulation in cancer. Synonyms: Sodium dichloroacetate; Sodium 2,2-dichloroacetate; Dichloroacetic acid sodium salt. CAS No. 2156-56-1. Molecular formula: C2HCl2NaO2. Mole weight: 150.92. |  |
| Glycerokinase from Cellulomonas sp. | Glycerol kinase is a phosphotransferase enzyme involved in triglycerides and glycerophospholipids synthesis. Glycerol kinase catalyzes tge MgATP-dependent phosphorylation of glycerol to produce sn-glycerol-3-phosphate and is the rate limiting enzyme in the utilization of glycerol. It is also subject to feedback regulation by fructose-1,6-bisphosphate. Phosphoryl moiety of atp to one of the primary hydroxyl group of glycerol, forming sn-glycerol-3-p. the enzyme has the highest specificity for glycerol, and also phosphorylates dihydroxyacetone and glyceraldehyde (table 1,2). mg++ is essentially required for the reaction. Applications: This enzyme is useful for enzymatic deter...se, g3o-301, g3o-311, g3o-321) or pyruvate kinase (pyk-301) and lactate dehydrogenase (lcd-209, lcd-211), lipoprotein lipase (lpl-311, lpl-314) in clinical analysis. Group: Enzymes. Synonyms: EC 2.7.1.30; glycerokinase; GK; ATP:glycerol-3-phosphotransferase; glycerol kinase (phosphorylating); glyceric kinase; 9030-66-4. Enzyme Commission Number: EC 2.7.1.30. CAS No. 9030-66-4. Activity: 20 U/mg-solid or more. Storage: -20°C. Form: Lyophilized powder containing phosphate buffer salts and sodium gluconate. Source: Cellulomonas sp. EC 2.7.1.30; glycerokinase; GK; ATP:glycerol-3-phosphotransferase; glycerol kinase (phosphorylating); glyceric kinase; 9030-66-4. Cat No: NATE-0287. |  |
| Glycolic Acid-13C Sodium Salt | Glycolic Acid-13C Sodium Salt is the isotope labelled analog of Glycolic Acid Sodium Salt; a compound that increases the glycolate oxidase activity in the liver when fed to rats. It also increases the lactate dehydrogenase activity in the liver and kidney. Group: Biochemicals. Grades: Highly Purified. CAS No. 1706469-52-4. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C13CH3NaO3, Molecular Weight: 99.03. US Biological Life Sciences. | Worldwide |
| JNJ-19567470 | JNJ-19567470 is a selective Corticotropin releasing factor (CRF) receptor antagonist. It is a novel target for developing anti-panic drugs. JNJ-19567470 is as effective as benzodiazepines in treatment of a panic attack which prevents sodium lactate-induced acute panic-like responses. In Oct 2009, preclinical development in Anxiety disorders was ongoing in Japan. Uses: Anxiety disorders. Synonyms: JNJ-19567470; JNJ19567470; JNJ 19567470; TAI-041; TAI 041; TAI041; R-317573;1-(7-(4-bromo-2,6-dimethylphenyl)-2,5-dimethyl-7H-pyrrolo(2,3-d)pyrimidin-4-yl)-4-Piperidinemethanol. Grades: 98%. CAS No. 724471-26-5. Molecular formula: C22H27BrN4O. Mole weight: 443.38. | |
| Lactate potassium | Lactate (Lactic acid) potassium is used as a sodium chloride substitute in the elaboration of dry meat products. Lactate potassium (56%) and sodium diacetate (4%) mixture inhibit the development of L. sake and L. monocytogenes bacteria at 4°C to extend the shelf life of food [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lactic acid potassium. CAS No. 996-31-6. Pack Sizes: 50 g; 100 g. Product ID: HY-B2227C. | |
| L-Lactic acid-13C3 (sodium) (20% in water) | L-Lactic acid- 13 C 3 ((S)-2-hydroxypropanoic- 13 C 3 ) sodium (20% in water) is the 13 C labeled L-Lactic acid. L-Lactic acid- 13 C 3 sodium (20% in water) can be used for lactate metabolism research [1]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: (S)-2-hydroxypropanoic- 13 C3 sodium. CAS No. 201595-71-3. Pack Sizes: 1 mg (200 mg/mL * 5 μL in Water); 5 mg (200 mg/mL * 25 μL in Water); 10 mg (200 mg/mL * 50 μL in Water); 25 mg (200 mg/mL * 125 μL in Water); 50 mg (200 mg/mL * 250 μL in Water). Product ID: HY-Y0479AS. | |
| L+Lactic Acid, Calcium Salt, Pentahydrate | Lactic acid (2-hydroxypropanoic acid), also known as milk acid, is a chemical compound that plays a role in several biochemical processes. It was first isolated in 1780 by a Swedish chemist, Carl Wilhelm Scheele, and is a carboxylic acid with a chemical formula of C3H6O3. It has a hydroxyl group adjacent to the carboxyl group, making it an alpha hydroxy acid (AHA). In solution, it can lose a proton from the acidic group, producing the lactate ion CH3CH(OH)COO?. It is miscible with water or ethanol, and is hygroscopic. Lactic acid is chiral and has two optical isomers. One is known as L-(+)-lactic acid or (S)-lactic acid and the other, its mirror image, is D-(-)-lactic ac...or Hartmann's Solution in the UK). This intravenous fluid consists of sodium and potassium cations, with lactate and chloride anions, in solution with distilled water in concentration so as to be isotonic compared to human blood. It is most commonly used for fluid resuscitation after blood loss due to trauma, surgery, or a burn injury. Group: Biochemicals. Alternative Names: Lactic Acid Calcium Salt (2:1) Pentahydrate; Propanoic Acid 2-Hydroxycalcium Salt Pentahydrate; Calcium Lactate Pentahydrate; Puracal DC. Grades: USP. CAS No. 5743-47-5. Pack Sizes: 100g, 250g, 500g, 1Kg, 2.5Kg. Molecular Formula: C6H10O6 Ca 5H2O, Molecular Weight: 308.29. US Biological Life Sciences. | Worldwide |
| Native Cellulomonas sp. Glycerokinase | Glycerol kinase is a phosphotransferase enzyme involved in triglycerides and glycerophospholipids synthesis. Glycerol kinase catalyzes tge MgATP-dependent phosphorylation of glycerol to produce sn-glycerol-3-phosphate and is the rate limiting enzyme in the utilization of glycerol. It is also subject to feedback regulation by fructose-1,6-bisphosphate. Phosphoryl moiety of atp to one of the primary hydroxyl group of glycerol, forming sn-glycerol-3-p. the enzyme has the highest specificity for glycerol, and also phosphorylates dihydroxyacetone and glyceraldehyde (table 1,2). mg++ is essentially required for the reaction. Applications: This enzyme is useful for enzymatic dete...1) and lactate dehydrogenase (lcd-209, lcd-211), lipoprotein lipase (lpl-311, lpl-314) in clinical analysis. Group: Enzymes. Synonyms: EC 2.7.1.30; glycerokinase; GK; ATP:glycerol-3-phosphotransferase; glycerol kinase (phosphorylating); glyceric kinase; 9030-66-4. Enzyme Commission Number: EC 2.7.1.30. CAS No. 9030-66-4. GK. Mole weight: mol wt ~128 kDa ((by gel filtration). Activity: 25-75 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing phosphate buffer salts and sodium gluconate. Source: Cellulomonas sp. EC 2.7.1.30; glycerokinase; GK; ATP:glycerol-3-phosphotransferase; glycerol kinase (phosphorylating); glyceric kinase; 9030-66-4. Cat No: NATE-0287. | |
| Native Microorganism Glycerol Kinase | The activity of glycerol kinase is found widely in nature. In microorganisms GK makes possible the utilization of glycerol as a carbon source. In mammals the enzyme represents a juncture of sugar and fat metabolism; The enzyme is important to the clinical chemist in the determination of glycerol. GK is also useful in the assay of glyceraldehydes and dihydroxyacetone following their quantitative reduction to glycerol with sodium borohydride. Applications: This enzyme is useful for enzymatic determination of glycerol and triglyceride when coupled with glycerol-3-phosphate dehydrogenase, glycerol-3-phosphate oxidase or pyruvate kinase and lactate dehydrogenase, lipoprotein lipase in clinical analysis. Group: Enzymes. Synonyms: glycerokinase; GK; ATP: glycerol-3-phosphotransferase; glycerol kinase phosphorylating; glyceric kinase; EC 2.7.1.30. Enzyme Commission Number: EC 2.7.1.30. CAS No. 9030-66-4. GK. Mole weight: approx. 220 kDa (by gel filtration). Activity: Grade? 30 U/mg-solid or more. Stability: Stable at-20°C. Appearance: White amorphous powder, lyophilized. Form: Freeze dried powder. Source: Microorganism. glycerokinase; GK; ATP: glycerol-3-phosphotransferase; glycerol kinase phosphorylating; glyceric kinase; EC 2.7.1.30. Cat No: DIA-149. | |
| Oxamic acid sodium | Oxamic acid (oxamate) sodium salt is a lactate dehydrogenase-A ( LDH-A ) inhibitor. Oxamic acid sodium salt shows anti-tumor activity, and anti-proliferative activity against cancer cells, and can induce apoptosis [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sodium oxamate. CAS No. 565-73-1. Pack Sizes: 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-W013032A. | |
| Sodium 2-Hydroxypropiomate Solution | Sodium lactate occurs as a clear, colorless, slightly syrupy liquid. It is odorless, or has a slight odor with a characteristic saline taste. It is hygroscopic. Synonyms: E325; 2-hydroxypropanoic acid monosodium salt; Lacolin; lactic. acid monosodium salt; lactic acid sodium salt; natrii lactatis solutio. Patlac; Purasal; Ritalac NAL; sodium a-hydroxypropionate. CAS No. 72-17-3. Product ID: PE0407. Molecular formula: C3H5NaO3. Mole weight: 112.06. Category: Humectants; Stabilizers; pH adjuster; Wetting agents. Product Keywords: Pharmaceutical Excipients; Other Materials; Humectants; Sodium 2-Hydroxypropiomate Solution; PE0407; TU7HW0W0QT; 72-17-3; 72-17-3. UNII: TU7HW0W0QT. Chemical Name: Sodium lactate. Grade: Pharmceutical Excipients. Administration route: Infiltration; Intraperitoneal; Intravenous; Oral; Intracardiac; Intramuscular; Subcutaneous. Dosage Form: Epidural, IM, IV, and SC injections; oral. suspensions; topical gels and solutions. Stability and Storage Conditions: Sodium lactate should be stored in a well-closed container in a cool,dry, place. Sodium lactate is combustible and decomposes upon heating. Commonly used amount and the maximum amount: The maximum dosage for intravenous injection: 50mg; the maximum dosage for general topical preparations: 51.3mg/g. Source and Preparation: Add sodium hydroxide to lactic acid under cooling conditions to carry out neutralization reaction, th | |
| Sodium Lauroyl Lactylate | Sodium salt of the lauric acid ester of lactyl lactate. Acts as a foamy anionic surfactant. It is extremely mild to skin and eyes. Melting point: 55-59?C. Uses: Liquid soaps, shampoos, skin lotions and creams, bar soaps. Group: Surfactants/emulsifiers. Alternative Names: Dodecanoic acid, 2-(1-carboxyethoxy)-1-methyl-2-oxoethyl ester, sodium salt. CAS No. 13557-75-0. Molecular formula: C18H31NaO6. Mole weight: 366.42 g/mol. Appearance: Waxy solid. IUPACName: Sodium;2-(2-dodecanoyloxypropanoyloxy)propanoate. Canonical SMILES: CCCCCCCCCCCC (=O)OC (C)C (=O)OC (C)C (=O)[O-]. [Na+]. Catalog: CI-SC-0200. | |
| Sodium Oxamate | Sodium oxamate is an inhibitor of lactate dehydrogenase (LDH), a key regulator of glycolysis, reversibly catalyzing the conversion of pyruvate to lactate. Synonyms: Sodium 2-amino-2-oxoacetate; Oxamic acid sodium salt. Grades: ≥95%. CAS No. 565-73-1. Molecular formula: C2H2NO3·Na. Mole weight: 111. | |
| Sodium Stearoyl Lactylate | Acts as an emulsifier, conditioner and mild anionic cleansing agent. The sodium salt of the stearic acid ester of lactyl lactate is vegetable derived. It boosts foam and conditions hair and skin. It offers an elegant feel to cleansing systems and cosmetic emulsions. Melting point: 47-53 deg.C. Uses: Creams, lotions, facial cleansers, shampoos and bath products such as bath butters & scrubs. Group: Surfactants/emulsifiers. CAS No. 18200-72-1/25383-99-7. Appearance: Light tan powder. Catalog: CI-SC-0236. | |
| SODIUM STEAROYL LACTYLATE | SODIUM STEAROYL LACTYLATE. Synonyms: Octadecanoicacid, 2-(1-carboxyethoxy)-1-methyl-2-oxoethylester, sodiumsalt; sodium2-stearoyllactate; SODIUMSTEAROYLLACTYLATE, FCC; SODIUM STEAROYL LACTYLATE(SSL);Natrium-2-stearoyllactat;Sodium stearyl 2-lactylate;sodium stearoyl lactate(SSL);SODIUM STEAROYL-2-LACTYLATE. CAS No. 25383-99-7. Pack Sizes: 1 kg. Product ID: CDF4-0110. Molecular formula: C21H39NaO4. Category: Food Emulsifiers. Product Keywords: Food Ingredients; Food Emulsifiers; SODIUM STEAROYL LACTYLATE; CDF4-0110; 25383-99-7; C21H39NaO4; 246-929-7; 25383-99-7. Purity: 0.99. EC Number: 246-929-7. Storage: Inert atmosphere,Room Temperature. Application: sodium stearoyl lactylate is an emulsifier. It can be obtained from natural or synthetic sources. Density: 1.002[at 20°C]. | |
| Tris(hydroxymethyl)aminomethane | Tris(hydroxymethyl)aminomethane. Synonyms: Tris(Hydroxymethyl)Aminomethane. CAS No. 77-86-1. Product ID: CDC10-0247. Molecular formula: C4H11NO3. Category: Buffering Agents. Product Keywords: Cosmetic Ingredients; Buffering Agents; Tris(hydroxymethyl)aminomethane; CDC10-0247; 77-86-1; C4H11NO3; Tris(Hydroxymethyl)Aminomethane; 201-064-4; MFCD00004679; 77-86-1. Grade: AR. Purity: 0.995. Color: White Crystalline. EC Number: 201-064-4. Physical State: Powder. Quality Level: 200. Storage: Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Application: Tris(hydroxymethyl)aminomethane has been used as a buffer solution for lactate dehydrogenase assay, in situ hybridization procedure and protein extraction from cells. Melting Point: 168.0-171.0. Product Description: Tris(hydroxymethyl)aminomethane is used as buffers in biochemistry and molecular biology laboratories. It is used as a primary standard to standardize acid solutions for chemical analysis. It finds application in cell membranes to increase its permeability. As an alternative to sodium bicarbonate, it used in the treatment of metabolic acidosis. | |
| Acetylcholine iodide | Acetylcholine iodide is a muscarinic receptor modulator. Acetylcholine iodide specifically binds to muscarinic receptors, inhibits sodium absorption, and induces chloride secretion. Acetylcholine iodide changes intestinal ion transport, enhances intestinal secretory function, induces or maintains mammary gland development and lactation. Acetylcholine iodide can be used for intestinal ion transport regulation and mammary gland physiological function research [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: ACh iodide. CAS No. 2260-50-6. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-101086. | |
| Chlorophyllin sodium copper salt | Chlorophyllin sodium copper salt. Synonyms: Chlorophyllin, coppered trisodium salt. CAS No. 11006-34-1. Pack Sizes: 5, 25, 100 g in glass bottle. Product ID: CDC10-0144. Molecular formula: C34H31CuN4Na3O6. Category: Cosmetic Color Additives. Product Keywords: Cosmetic Ingredients; Cosmetic Color Additives; Chlorophyllin sodium copper salt; CDC10-0144; 11006-34-1; C34H31CuN4Na3O6; Chlorophyllin, coppered trisodium salt; 234-242-5; 11006-34-1. Grade: commercial grade. Purity: 0.99. Color: Dark Green to Black. EC Number: 234-242-5. Physical State: Powder. Solubility: H2O: 100 mg/mL, dark green. Quality Level: 200. Storage: 2-8°C. Application: Chlorophyllin sodium copper salt has been used to study the effect of chlorophyllin against radiation-induced hematopoietic syndrome. It has been used to study the effect of chlorophyllin on the excretion of PhIP (2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine) and its metabolites into the breast-milk of lactating rats. Boiling Point: N/A. Melting Point: >300°C. | |
Our database is helping our users find suppliers everyday.
