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X-14667 A is a monovalent polyether antibiotic of the spiroketal type isolated from fermented cultures of Streptomyces cinnamonensis subsp. Urethanofaciens. It shows activity against gram-positive bacteria. Synonyms: X 14667 A; X-14667A; X14667 A. Molecular formula: C44H69NO12. Mole weight: 804.02.
X-14667 B
X-14667 B is a monovalent polyether antibiotic of the spiroketal type isolated from fermented cultures of Streptomyces cinnamonensis subsp. Urethanofaciens. It shows activity against gram-positive bacteria. Synonyms: X 14667 B; X-14667B; X14667 B. Molecular formula: C45H70NO12Na. Mole weight: 840.02.
X-14766 A
X-14766 A is a monovalent polyether antibiotic of the spiroketal type isolated from fermented cultures of Streptomyces malachitofuscus subsp. downeyi. It shows activity against gram-positive bacteria. Synonyms: X 14766 A; X-14766A; X14766 A. Molecular formula: C44H63ClO14. Mole weight: 851.41.
X-14847
X-14847 is an aminoglycoside antibiotic isolated from Micromonospora echinospora. It shows weak activity against gram-positive bacteria. Synonyms: X 14847; 1D-myo-inositol 2-amino-2-deoxy-alpha-D-glucopyranoside; 1-O-(2-amino-2-deoxy-alpha-D-glucopyranosyl)-1D-myo-inositol. CAS No. 75802-23-2. Molecular formula: C12H23NO10. Mole weight: 341.31.
X-14868B
X-14868B is a polyether antibiotic produced by Nocardia sp. X-14868. It exhibits activity against gram-negative bacteria and coccidium. Synonyms: X 14868 B; X-14868 B; X14868 B. CAS No. 79296-11-0. Molecular formula: C48H82O17. Mole weight: 931.2.
X-14868C
X-14868C is a polyether antibiotic produced by Nocardia sp. X-14868. It exhibits activity against gram-negative bacteria. Synonyms: X 14868 C; X-14868 C; X14868 C. Molecular formula: C46H78O17. Mole weight: 903.1.
X-14868D
X-14868D is a polyether antibiotic produced by Nocardia sp. X-14868. It exhibits activity against gram-negative bacteria. Synonyms: X 14868 D; X-14868 D; X14868 D. CAS No. 79331-54-7. Molecular formula: C47H80O17. Mole weight: 917.1.
X-14873A
X-14873A is a polyether antibiotic produced by the fermentation of Streptomyces sp. X-14873. It is mainly active against Gram-positive bacteria. Synonyms: X 14873 A; X-14873 A; X14873 A; (5R)-4-Demethyl-4-ethyl-5-hydroxylysocellin. CAS No. 88263-37-0. Molecular formula: C35H62O11. Mole weight: 658.86.
X-14873G
X-14873G is a polyether antibiotic produced by the fermentation of Streptomyces sp. X-14873. It is mainly active against Gram-positive bacteria. Synonyms: X 14873 G; X-14873 G; X14873 G. CAS No. 88263-35-8. Molecular formula: C34H60O8. Mole weight: 596.8.
X-14873H
X-14873H is a polyether antibiotic produced by the fermentation of Streptomyces sp. X-14873. It is mainly active against Gram-positive bacteria. Synonyms: X 14873 H; X-14873 H; X14873 H. CAS No. 88263-36-9. Molecular formula: C34H62O9. Mole weight: 614.8.
X-14885A
X-14885A is a divalent cation ionophore produced by a Streptomyces culture isolated from soil sample collected in Wyoming. It is active against gram-positive bacteria and Treponema. Synonyms: X 14885 A; X-14885 A; X14885 A. CAS No. 83917-57-1. Molecular formula: C27H32N2O7. Mole weight: 496.6.
X-14885B
X-14885B is a macrolide antibiotic produced by Streptomyces sp. It shows antifungal activity. Synonyms: X 14885 B; X-14885 B; X14885 B. Molecular formula: C43H69NO12. Mole weight: 792.
X-206
X-206 is an ionophore antibiotic produced by Streptomyces sp. X 206. It acts as a potent and selective inhibitor of SARS-CoV-2. Synonyms: Antibiotic X-206. CAS No. 36505-48-3. Molecular formula: C47H82O14. Mole weight: 871.1.
X-34
X-34 is a lipophilic and bright yellow-green fluorescent derivative of Congo red (HY-D0236). X-34 can be used to stain neuritic and diffuse plaques, neurofibrillary tangles (NFTs), neuropil threads, and cerebrovascular amyloid in the brain. X-34 can be used for research of Alzheimers disease [1]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 215294-98-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-125962.
Widely distributed in mammals. Group: Enzymes. Synonyms: aminoacyl-lysine dipeptidase; N2-(4-amino-butyryl)-L-lysine hydrolase; X-Arg dipeptidase. Enzyme Commission Number: EC 3.4.13.4. CAS No. 37288-72-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4037; Xaa-Arg dipeptidase; EC 3.4.13.4; 37288-72-5; aminoacyl-lysine dipeptidase; N2-(4-amino-butyryl)-L-lysine hydrolase; X-Arg dipeptidase. Cat No: EXWM-4037.
Xaa-methyl-His dipeptidase
This enzyme catalyses the following chemical reaction: hydrolysis of anserine (beta-alanyl-Npi-methyl-L-histidine), carnosine, homocarnosine, glycyl-leucine and other dipeptides with broad specificity. Group: Enzymes. Synonyms: anserinase; aminoacyl-methylhistidine dipeptidase; acetylhistidine deacetylase; N-acetylhistidine deacetylase; α-N-acetyl-L-histidine aminohydrolase; X-methyl-His dipeptidase. Enzyme Commission Number: EC 3.4.13.5. CAS No. 9027-38-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4038; Xaa-methyl-His dipeptidase; EC 3.4.13.5; 9027-38-7; anserinase; aminoacyl-methylhistidine dipeptidase; acetylhistidine deacetylase; N-acetylhistidine deacetylase; α-N-acetyl-L-histidine aminohydrolase; X-methyl-His dipeptidase. Cat No: EXWM-4038.
Xaa-Pro aminopeptidase
A Mn2+-dependent, generally membrane-bound enzyme present in both mammalian and bacterial cells. In peptidase family M24 (methionyl aminopeptidase family). Group: Enzymes. Synonyms: proline aminopeptidase; aminopeptidase P; aminoacylproline aminopeptidase; X-Pro aminopeptidase. Enzyme Commission Number: EC 3.4.11.9. CAS No. 37288-66-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4029; Xaa-Pro aminopeptidase; EC 3.4.11.9; 37288-66-7; proline aminopeptidase; aminopeptidase P; aminoacylproline aminopeptidase; X-Pro aminopeptidase. Cat No: EXWM-4029.
Xaa-Pro dipeptidase
A Mn2+-activated enzyme, in peptidase family M24 (methionyl aminopeptidase family); cytosolic from most animal tissues. Group: Enzymes. Synonyms: prolidase; imidodipeptidase; proline dipeptidase; peptidase D; γ-peptidase; X-Pro dipeptidase. Enzyme Commission Number: EC 3.4.13.9. CAS No. 9025-32-5. Prolidase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4042; Xaa-Pro dipeptidase; EC 3.4.13.9; 9025-32-5; prolidase; imidodipeptidase; proline dipeptidase; peptidase D; γ-peptidase; X-Pro dipeptidase. Cat No: EXWM-4042.
Xaa-Pro dipeptidyl-peptidase
The intracellular enzyme from Lactococcus lactis (190-kDa) is the type example of peptidase family S15. The reaction is similar to that catalysed by dipeptidyl-peptidase IV of animals. Group: Enzymes. Synonyms: X-prolyl dipeptidyl aminopeptidase; PepX; X-prolyl dipeptidyl peptidase; X-Pro dipeptidyl-peptidase. Enzyme Commission Number: EC 3.4.14.11. CAS No. 54249-88-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4045; Xaa-Pro dipeptidyl-peptidase; EC 3.4.14.11; 54249-88-6; X-prolyl dipeptidyl aminopeptidase; PepX; X-prolyl dipeptidyl peptidase; X-Pro dipeptidyl-peptidase. Cat No: EXWM-4045.
Xaa-Trp aminopeptidase
A glycoprotein containing Zn2+, from renal and intestinal brush border membranes. Group: Enzymes. Synonyms: aminopeptidase W; aminopeptidase X-Trp; X-Trp aminopeptidase. Enzyme Commission Number: EC 3.4.11.16. CAS No. 137010-33-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4012; Xaa-Trp aminopeptidase; EC 3.4.11.16; 137010-33-4; aminopeptidase W; aminopeptidase X-Trp; X-Trp aminopeptidase. Cat No: EXWM-4012.
Xaa-Xaa-Pro tripeptidyl-peptidase
This cell-surface-associated serine exopeptidase is found in the Gram-negative, anaerobic bacterium Porphyromonas gingivalis, which has been implicated in adult periodontal disease. The enzyme releases the N-terminal tripeptide of peptides, such as interleukin-6. It has an absolute requirement for a proline residue at the P1 position but is completely inactivated by a proline residue at the P1' position. The size of the peptide does not affect the rate of reaction. Group: Enzymes. Synonyms: prolyltripeptidyl amino peptidase; prolyl tripeptidyl peptidase; prolyltripeptidyl aminopeptidase; PTP-A; TPP. Enzyme Commission Number: EC 3.4.14.12. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4046; Xaa-Xaa-Pro tripeptidyl-peptidase; EC 3.4.14.12; prolyltripeptidyl amino peptidase; prolyl tripeptidyl peptidase; prolyltripeptidyl aminopeptidase; PTP-A; TPP. Cat No: EXWM-4046.
XAC
XAC. Group: Biochemicals. Grades: Purified. CAS No. 96865-92-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
Worldwide
Xaliproden hydrochloride
Xaliproden hydrochloride (SR57746A) is a potent, selective and orally active agonist of 5-HT 1A receptor , shows a high affinity for 5-HT 1A specific binding sites in the rat hippocampus ( IC 50 =3 nM). Xaliproden hydrochloride is also a selective antagonist of dopamine D 2 receptor , has moderate affinity ( IC 50 =0.1-1 μM). Xaliproden hydrochloride exhibits anti-depression and anti-anxiety effects, and it may possess therapeutic potential for the research of neurodegenerative diseases [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SR57746A; SR57746 hydrochloride. CAS No. 90494-79-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14604.
Xaliproden hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 90494-79-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
Worldwide
X-alpha-Gal
X-alpha-Gal is a chromogenic substrate that is used to screen colonies with high activity of β-galactopyranoside [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 107021-38-5. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114522.
Xaluritamig
Xaluritamig is an anti- CD3E/STEAP1 monoclonal antibody [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2460399-39-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990688.
Xamoterol hemifumarate
Xamoterol hemifumarate is a selective and potent agonist of beta1-adrenergic receptor. Xamoterol hemifumarate has the potential for the research of arrhythmogenesis. Xamoterol hemifumarate has the potential for the investigating the relationship between β1-adrenergic stimulation and IKr [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Corwin hemifumarate; ICI 118587 hemifumarate. CAS No. 73210-73-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101327A.
Xamoterol hemifumarate
Xamoterol hemifumarate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethyl]morpholine-4-carboxamide. Appearance: Crystalline solid. CAS No. 73210-73-8. Molecular formula: C36H54N6O14. Mole weight: 794.85. Purity: 0.98. Product ID: ACM73210738. Alfa Chemistry ISO 9001:2015 Certified.
Xanomeline
Xanomeline. Uses: For analytical and research use. Group: Impurity standards. CAS No. 131986-45-3. Molecular formula: C14H23N3OS. Mole weight: 281.42. Catalog: APB131986453.
Xanomeline
Xanomeline, as an effective and selective muscarinic type 1 and type 4 ( M1/M4 ) receptor agonist, increases neuronal excitability. Xanomeline can be used for the research of neurological disorders, such as schizophrenia [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY-246708. CAS No. 131986-45-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-105182.
Xanomeline Impurity 11
Xanomeline Impurity 11. Uses: For analytical and research use. Group: Impurity standards. CAS No. 131986-66-8. Molecular formula: C15H25N3OS. Mole weight: 295.45. Catalog: APB131986668.
Xanomeline Impurity 2
Xanomeline Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 131986-96-4. Molecular formula: C13H21N3OS. Mole weight: 267.39. Catalog: APB131986964.
Xanomeline oxalate (LY246708 oxalate) is a potent and selective muscarinic receptor agonist (SMRA) and stimulates phosphoinositide hydrolysis in vivo. Xanomeline oxalate can be used for the research of Alzheimers disease [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY246708 oxalate. CAS No. 141064-23-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13410.
Xanomeline oxalate
Xanomeline oxalate. Group: Biochemicals. Grades: Purified. CAS No. 141064-23-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
An agonist selective for muscarinic acetylcholine receptor (mAChR) subtype M1 (EC50 = 0.3, 5, 42, 52 and 92.5nM at M1, M3, M5, M4 and M2 receptors respectively). An antipsychotic agent. Used in improving cognitive deficits and behavioral disturbances in Alzheimer's disease and schizophrenia. Group: Biochemicals. Grades: Highly Purified. CAS No. 141064-23-5. Pack Sizes: 10mg. Molecular Formula: C??H??N?OS C?H?O. US Biological Life Sciences.
Worldwide
Xanomeline tartrate
Xanomeline (LY 246708) is the potent agonist of muscarinic M1/M4 receptor with antipsychotic-like activity. Xanomeline (LY 246708) increases neuronal excitability. Xanomeline (LY 246708) can be used for the research of schizophrenia [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY 246708 tartrate. CAS No. 152854-19-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-105182A.
Xanthamide 8
Xanthamide 8. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-[2-(6-Methoxy-3-oxo-3H-xanthen-9-yl)-benzoyl]-piperidine-4-carboxylic acid. Product Category: Other Fluorophores. Appearance: Solid. CAS No. 442151-56-6. Molecular formula: C27H23NO6. Mole weight: 457.47. Purity: 95%+. Product ID: ACM442151566-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: 1-(O'-Methylfluoresceinyl)piperidine-4-carboxylic acid.
Xanthan from Xanthomonas campestris
4,500,000. Group: Polysaccharide.
Xanthan from Xanthomonas campestris
Xanthan gum is a monospore polysaccharide produced by the fermentation of Pseudomonas sp. It is made of carbohydrates as the main raw material from the cabbage black rot Xanthomonas spp. through aerobic fermentation bioengineering technology to cut 1,6 - Glycosidic bond, after opening the branched chain, an acidic extracellular polysaccharide composed of straight chains is synthesized by 1,4-bond. The structure and conformation of xanthan gum determine the functional properties of its solution: the complex aggregated structure and intermolecular forces of xanthan gum determine that its solution has high viscosity at low shear and low concentration, and is more viscous than other polysaccharide solutions. High modulus, as well as pseudoplastic behavior; Xanthan gum has hydrogen bonds, anions, and side chains entangled in the rigid and straight molecular chains of the molecular chain to protect the main chain, so that the solution has good heat and salt resistance. It also has good stability to acid-base and enzymatic hydrolysis. Due to its excellent physical and chemical properties, including high viscosity, thixotropy, and stability of dispersions, xanthan gum has been widely used in the food industry, oil extraction, coatings, and many other fields. Uses: ·useful matrix components for drug delivery systems: functional components in microencapsulated drug capsules ·used as food additives such as emulsi
Xanthan gum
Xanthan gum is a microbial polysaccharide produced by Xanthomonas campestris. The structure of xanthan gum is based on a cellulose backbone of β-(1-4)-linked glucose units with a trisaccharide side of mannose-glucuronic acid-mannose attached to every other glucose unit in the backbone chain. Some terminal mannose units are pyruvated and some internal mannose units are acetylated. Due to its unique rheology and gelling properties, it is widely used as a food additive, thickener and stabilizer in the food and petroleum industries. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 11138-66-2. Pack Sizes: 500 g. Product ID: HY-A0103.
Xanthan Gum
Xanthan gum is an anionic polysaccharide composed of a β-(1?4)-D-glucopyranose glucan backbone with side chains of (1?3)-α-D-mannopyranose-(2?1)- β-D-glucuronic acid-(4?1)- β-D-mannopyranose on alternating residues. Approximately half of the terminal mannose residues are 4,6-pyruvated while most of the inner mannose residues are 6-acetylated. Its properties make it a useful matrix component for drug delivery systems. It forms stable drug suspensions in aqueous media and soft gels with locust bean gum or guar gum. Xanthan gum mimics the texture of lipids and is used as a control in experiments where signaling pathways initiated by consumption of lipid-containing reagents are investigated in mice. Group: Biochemicals. Grades: Highly Purified. CAS No. 11138-66-2. Pack Sizes: 25g, 100g, 250g. US Biological Life Sciences.
Worldwide
Xanthan Gum
Xanthan gum is a complex carbohydrate, made from the fermentation of simple sugars by a bacterium called Xanthomonas campestris. Xanthan gum is a popular ingredient in gluten-free baking, providing the texture and consistency that is often lost without gluten. It is also used in personal care products like shampoo, toothpaste and cosmetics because of its ability to make the products thicker and more stable. Uses: 1. thickening agent: xanthan gum is commonly used as a food additive to thicken liquids and create a desired texture in products such as salad dressings, sauces, and dairy products. 2. stabilizer: it also acts as a stabilizer in food products, helping to prevent separation of oil and water or other ingredients. 3. gluten-free baking: as a gluten-free alternative for wheat flour, xanthan gum can be used to provide elasticity and texture in baked goods. 4. industrial applications: xanthan gum is also widely used in industrial applications, such as in the production of oil and gas, paper, and textiles. 5. personal care products: it can be found in personal care products, such as toothpaste, as a thickening agent. Group: Polymers. Alternative Names: Gum xanthan. CAS No. 11138-66-2. Product ID: 2-(2,4-diaminophenoxy)ethanol; dihydrochloride. Molecular formula: 933.75. Mole weight: C35H49O29. C1=CC(=C(C=C1N)N)OCCO.Cl.Cl. VXYWXJXCQSDNHX-UHFFFAOYSA-N. InChI=1S/C8H12N2O2. 2ClH/c9-6-1-2-8(7(10)5-6)12-4-3-11; ; /h1-2, 5, 11H, 3
Xanthan Gum
Xanthan gum occurs as a cream- or white-colored, odorless, freeflowing, fine powder. Synonyms: Corn sugar gum; E415; Grindsted; Keldent; Keltrol; polysaccharide B-1459; Rhodicare S; Rhodigel; Vanzan NF; xanthani gummi; Xantural. CAS No. 11138-66-2. Product ID: PE-0521. Molecular formula: (C35H49O29)n. Mole weight: 100000. Category: Gelling Agents; Stabilizing Agents; Suspending Agents; Sustained-release Agents; Viscosity-increasing Agents. Product Keywords: Emulsifier Excipients; Stabilizers; Suspending Agents; ; PE-0521; Xanthan Gum; Gelling Agents; Stabilizing Agents; Suspending Agents; Sustained-release Agents; Viscosity-increasing Agents; (C35H49O29)n; 11138-66-2. UNII: TTV12P4NEE. Chemical Name: Xanthan gum. Grade: Pharmceutical Excipients. Administration route: Oral; rectal and topical. Dosage Form: Oral solutions, suspensions, and tablets; rectal and topical preparations. Stability and Storage Conditions: Xanthan gum is a stable material. Aqueous solutions are stable over a wide pH range (pH 3-12), although they demonstrate maximum stability at pH 4-10 and temperatures of 10-60°C. Xanthan gum solutions of less than 1% w/v concentration may be adversely affected by higher than ambient temperatures: for example, viscosity is reduced. Xanthan gum provides the same thickening, stabilizing, and suspending properties during long-term storage at elevated temperatures as it does at ambient conditions. In addition, it ens
Xanthan Gum
Xanthan Gum. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner.
Xanthan Gum 200 Mesh is a frequently used product in food applications. It works as a fantastic emulsifier for liquids that do not normally mix well together. It can also be used as a thickener with no concentrations. Since it is plant-based, it is great to use in vegetarian or vegan products and has very low caloric value. Uses: Food, Beverages, Thickener, Emulsifier. Alternative Names: Polysacccharide Gum, E 415. Grades: Food. FCC. CAS No. 11138-66-2. Pack Sizes: 50 lb.
USA
Xanthan Gum 80 Mesh
Xanthan Gum 80 Mesh is a frequently used product in food applications. It works as a fantastic emulsifier for liquids that do not normally mix well together. It can also be used as a thickener with no concentrations. Since it is plant-based, it is great to use in vegetarian or vegan products and has very low caloric value. Uses: Food, Beverages, Thickener, Emulsifier. Alternative Names: Polysacccharide Gum, E 415. Grades: Food. FCC. CAS No. 11138-66-2. Pack Sizes: 50 lb.
USA
Xanthan Gum BP/USP
Xanthan Gum BP/USP. CAS No. 11138-66-2. Molecular formula: C35H49O29.
Xanthan gum from Xanthomonas campestris
Xanthan gum is a monospore polysaccharide produced by the fermentation of Pseudomonas sp. It is made of carbohydrates as the main raw material from the cabbage black rot Xanthomonas spp. through aerobic fermentation bioengineering technology to cut 1,6 - Glycosidic bond, after opening the branched chain, an acidic extracellular polysaccharide composed of straight chains is synthesized by 1,4-bond. The structure and conformation of xanthan gum determine the functional properties of its solution: the complex aggregated structure and intermolecular forces of xanthan gum determine that its solution has high viscosity at low shear and low concentration, and is more viscous than other polysaccharide solutions. High modulus, as well as pseudoplastic behavior; Xanthan gum has hydrogen bonds, anions, and side chains entangled in the rigid and straight molecular chains of the molecular chain to protect the main chain, so that the solution has good heat and salt resistance. It also has good stability to acid-base and enzymatic hydrolysis. Due to its excellent physical and chemical properties, including high viscosity, thixotropy, and stability of dispersions, xanthan gum has been widely used in the food industry, oil extraction, coatings, and many other fields. Uses: ·useful matrix components for drug delivery systems: functional components in microencapsulated drug capsules ·used as food additives such as em
xanthan ketal pyruvate transferase
Involved in the biosynthesis of the polysaccharide xanthan. 30-40% of the terminal mannose residues of xanthan have a 4,6-O-(1-carboxyethan-1,1-diyl) ketal group. It also acts on the 6-O-acetyl derivative of the inner mannose unit. Group: Enzymes. Synonyms: KPT. Enzyme Commission Number: EC 2.5.1.95. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2834; xanthan ketal pyruvate transferase; EC 2.5.1.95; KPT. Cat No: EXWM-2834.
xanthan lyase
In enzymology, a xanthan lyase (EC 4.2.2.12) is an enzyme that catalyzes the chemical reaction of cleaving the beta-D-mannosyl-beta-D-1,4-glucuronosyl bond on the polysaccharide xanthan. This enzyme belongs to the family of lyases, specifically those carbon-oxygen lyases acting on polysaccharides. Group: Enzymes. Enzyme Commission Number: EC 4.2.2.12. CAS No. 113573-69-6. Xanthan lyase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5087; xanthan lyase; EC 4.2.2.12; 113573-69-6. Cat No: EXWM-5087.
Xanthanoic acid
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Xanthate
Xanthate. Market: Mining. PK Chem Industries: We supply chemicals related to Cosmetic, Personal Care, Food, Pharmaceutical, Feed, Agriculture and Mining Industries.
Xanthatin
Xanthatin. Group: Biochemicals. Grades: Plant Grade. CAS No. 26791-73-1. Pack Sizes: 20mg. US Biological Life Sciences.
Worldwide
Xanthene-9-carboxylic Acid
Xanthene-9-carboxylic Acid is xanthrene derivative that is capable of inhibiting the TTR conformational changes facilitating amyloid fibril formation. Group: Biochemicals. Alternative Names: 9-Carboxyxanthene; 9H-Xanthen-9-carboxylic Acid; NSC 66208; Xanthanoic Acid; Xanthenecarboxylic Acid. Grades: Highly Purified. CAS No. 82-07-5. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Xanthene-9-carboxylic acid chloride
Xanthene-9-carboxylic acid chloride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: XANTHENE-9-CARBOXYLIC ACID CHLORIDE;9H-XANTHENE-9-CARBONYL CHLORIDE;9H-Xanthene-9-carbonyl chloride 97%. Product Category: Heterocyclic Organic Compound. CAS No. 26454-53-5. Molecular formula: C14H9ClO2. Mole weight: 244.67. Purity: 0.96. IUPACName: 9H-xanthene-9-carbonyl chloride. Density: 1.335g/cm³. Product ID: ACM26454535. Alfa Chemistry ISO 9001:2015 Certified.
Xanthiazone
Xanthiazone. Group: Biochemicals. Grades: Plant Grade. CAS No. 212701-97-8. Pack Sizes: 5mg. Molecular Formula: C11H13NO3S, Molecular Weight: 239.29. US Biological Life Sciences.
Worldwide
Xanthine
?99.5% (HPLC), purified by recrystallization. Group: Fluorescence/luminescence spectroscopy.
Xanthine
Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 69-89-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-W017389.
Xanthine
Found in animal organs, yeast, patatoes, coffee beans, tea. This drug can be used to relax and widen certain breathing passages of the lungs. It is also found that a large number of derivatives have adenoside receptor antagonist properties. Group: Biochemicals. Alternative Names: 3,9-Dihydro-1H-purine-2,6-dione; 1H,3H,7H-Xanthine; 1H,3H,9H-Xanthine; 1H-Purine-2,6-diol; 2,6-Dioxo-1,2,3,6-tetrahydropurine; 2,6-Dioxopurine; 3,9-Dihydro-1H-purine-2,6-dione; 3,9-Dihydropurine-2,6-dione; 9H-Purine-2,6(1H,3H)-dione; Isoxanthine; NSC 14664; Pseudoxanthine; Purine-2,6(1H,3H)-dione; Xan; Xanthic oxide; Xanthin. Grades: Highly Purified. CAS No. 69-89-6. Pack Sizes: 2.5g. US Biological Life Sciences.
Worldwide
Xanthine-[13C,15N2]
Xanthine-[13C,15N2] is the labelled analogue of Xanthine, which is a kind of purine compound, widely existed, and has been found to exhibit adenoside receptor antagonist activities. Synonyms: Xanthine-13C 15N2; 3,9-Dihydro-1H-purine-2,6-dione-13C,15N2. Grade: 95% by HPLC; 98% atom 13C; 98% atom 15N. CAS No. 1262670-81-4. Molecular formula: C4[13C]H4N2[15N]2O2. Mole weight: 155.09.
Xanthine (2,6-Dihydroxypurine)
25g Pack Size. Group: Biochemicals. Formula: C5H4N4O2. CAS No. 69-89-6. Prepack ID 30098252-25g. Molecular Weight 152.11. See USA prepack pricing.
Xanthine 99+% (HPLC)
Xanthine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences.
Worldwide
xanthine dehydrogenase
Acts on a variety of purines and aldehydes, including hypoxanthine. The mammalian enzyme can also convert all-trans retinol to all-trans-retinoate, while the substrate is bound to a retinoid-binding protein. The enzyme from eukaryotes contains [2Fe-2S], FAD and a molybdenum centre. The mammalian enzyme predominantly exists as the NAD-dependent dehydrogenase (EC 1.17.1.4). During purification the enzyme is largely converted to an O2-dependent form, xanthine oxidase (EC 1.17.3.2). The conversion can be triggered by several mechanisms, including the oxidation of cysteine thiols to form disulfide bonds [which can be catalysed by EC 1.8.4.7, enzyme-thiol transhydrogenase (glutathione-disulfide) in the presence of glutathione disulfide] or limited proteolysis, which results in irreversible conversion. The conversion can also occur in vivo. Group: Enzymes. Synonyms: NAD+-xanthine dehydrogenase; xanthine-NAD+ oxidoreductase; xanthine/NAD+ oxidoreductase; xanthine oxidoreductase. Enzyme Commission Number: EC 1.17.1.4. CAS No. 9054-84-6. XDH. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1082; xanthine dehydrogenase; EC 1.17.1.4; 9054-84-6; NAD+-xanthine dehydrogenase; xanthine-NAD+ oxidoreductase; xanthine/NAD+ oxidoreductase; xanthine oxidoreductase. Cat No: EXWM-1082.
xanthine dioxygenase
Requires Fe2+ and L-ascorbate. The enzyme, which was characterized from fungi, is specific for xanthine. Group: Enzymes. Synonyms: XanA; α-ketoglutarate-dependent xanthine hydroxylase. Enzyme Commission Number: EC 1.14.11.48. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0667; xanthine dioxygenase; EC 1.14.11.48; XanA; α-ketoglutarate-dependent xanthine hydroxylase. Cat No: EXWM-0667.
xanthine oxidase
An iron-molybdenum flavoprotein (FAD) containing [2Fe-2S] centres. Also oxidizes hypoxanthine, some other purines and pterins, and aldehydes, but is distinct from EC 1.2.3.1, aldehyde oxidase. Under some conditions the product is mainly superoxide rather than peroxide: RH + H2O + 2 O2 = ROH + 2 O2.- + 2 H+. The mammalian enzyme predominantly exists as an NAD-dependent dehydrogenase (EC 1.17.1.4, xanthine dehydrogenase). During purification the enzyme is largely converted to the O2-dependent xanthine oxidase form (EC 1.17.3.2). The conversion can be triggered by several mechanisms, including the oxidation of cysteine thiols to form disulfide bonds [which can be catalysed by EC 1.8.4.7, enzyme-thiol transhydrogenase (glutathione-disulfide) in the presence of glutathione disulfide] or limited proteolysis, which results in irreversible conversion. The conversion can also occur in vivo. Group: Enzymes. Synonyms: hypoxanthine o. Enzyme Commission Number: EC 1.17.3.2. CAS No. 9002-17-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1088; xanthine oxidase; EC 1.17.3.2; 9002-17-9; hypoxanthine oxidase; hypoxanthine:oxygen oxidoreductase; Schardinger enzyme; xanthine oxidoreductase; hypoxanthine-xanthine oxidase; xanthine:O2 oxidoreductase; xanthine:xanthine oxidase. Cat No: EXWM-1088.