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| Product | Description | |
|---|---|---|
| X-14667 A | 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-1-Acetate | Heterocyclic Organic Compound. CAS No. 125328-76-9. Molecular formula: C10H7BrClNO2. Mole weight: 288.53. Catalog: ACM125328769. |  |
| 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-396 | X-396 is an orally available small molecule inhibitor of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK) with potential antineoplastic activity. Upon oral administration, X-396 binds to and inhibits ALK kinase, ALK fusion proteins and ALK point mutation variants. Inhibition of ALK leads to the disruption of ALK-mediated signaling and eventually inhibits tumor cell growth in ALK-expressing tumor cells. ALK belongs to the insulin receptor superfamily and plays an important role in nervous system development. ALK is not expressed in healthy adult human tissue but ALK dysregulation and gene rearrangements are associated with a series of tumors; ALK mutations are associated with acquired resistance to small molecule tyrosine kinase inhibitors. Uses: Antineoplastic agents. Synonyms: X-376; (R)-6-Amino-5-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-N-(4-(4-methylpiperazine-1-carbonyl)phenyl)pyridazine-3-carboxamide; 3-Pyridazinecarboxamide, 6-amino-5-((1R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)-N-(4-((4-methyl-1-piperazinyl)carbonyl)phenyl)-; 6-Amino-5-[(1R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy]-N-{4-[(4-methyl-1-piperazinyl)carbonyl]phenyl}-3-pyridazinecarboxamide. Grades: ≥98%. CAS No. 1365267-27-1. Molecular formula: C25H25Cl2FN6O3. Mole weight: 547.41. | |
| X4-136 | X4-136 is a novel small-molecule inhibitor of C-X-C chemokine receptor type 4 (CXCR4). Study in C57BL/6J mice model indicated that it exhibited an effct of long term control on tumor and improved survival when synergistically used with anti-PD-1. Combination therapy of X4-136 and anti-PD-1 is superior to single anti-PD-1 therapy. Uses: Combination therapy of x4-136 and anti-pd-1. | |
| X58123-(C13,2H3) | X58123-(C13,2H3). Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C2613CH29D3FN9O2. Mole Weight: 537.61. Catalog: APB10188. |  |
| Xaa-Arg dipeptidase | 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 |
| XAC | XAC is an adenosine receptor antagonist (IC50 = 1.8 and 114 nM at A1 and A2 receptors, respectively). XAC inhibits adenosine-induced vasodilation and exhibits proconvulsant activity in vivo. Synonyms: N-(2-Aminoethyl)-2-[4-(2,3,6,7-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)phenoxy]-acetamide dihydrochloride. Grades: ≥98% by HPLC. Molecular formula: C21H28N6O4.2HCl. Mole weight: 501.41. | |
| Xaliproden hydrochloride | Xaliproden hydrochloride is a potent, selective and orally active 5-HT1A receptor agonist with a high affinity for 5-HT1A specific binding sites in the rat hippocampus (IC50 = 3 nM). It is also a selective dopamine D2 receptor antagonist with moderate affinity (IC50 = 0.1-1 μM). It has antidepressant and anti-anxiety effects, and may have therapeutic potential in neurodegenerative diseases research. Uses: Serotonin 5-ht1 receptor agonists. Synonyms: SR57746A; SR57746 hydrochloride; 1-[2-(2-Naphthyl)ethyl]-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine hydrochloride; 1,2,3,6-Tetrahydro-1-[2-(2-naphthalenyl)ethyl]-4-[3-(trifluoromethyl)phenyl]pyridine hydrochloride. Grades: ≥99%. CAS No. 90494-79-4. Molecular formula: C24H23ClF3N. Mole weight: 417.89. | |
| Xaliproden hydrochloride | Xaliproden hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 90494-79-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Xamoterol β-D-Glucuronide | Xamoterol Glucuronide is a metabolite of Xamoterol, which is an authentic β1-adrenoceptor (β1-AR) agonist that has been shown to mimic the autoantibody effect on rat atria β1-AR apoptosis. Synonyms: (2S, 3S, 4S, 5R, 6S) -3, 4, 5-Trihydroxy-6- (4- (2-hydroxy-3- ( (2- (morpholine-4-carboxamido) ethyl) amino) propoxy) phenoxy) tetrahydro-2H-pyran-2-carboxylic Acid; 4-[2-Hydroxy-3-[[2-[ (4-morpholinylcarbonyl) amino]ethyl]amino]propoxy]phenyl-β -D-glucopyranosiduronic Acid. CAS No. 93491-13-5. Molecular formula: C22H33N3O11. Mole weight: 515.51. | |
| Xamoterol hemifumarate | Xamoterol hemifumarate is a third generation β1-adrenoceptor-selective partial agonist (pA2 = 7.4 - 7.8 and 5.2 - 6.2 at β1- and β2-adrenoceptors, respectively). Synonyms: Xamoterol hemifumarate; ICI-118587 hemioxalate; ICI 118587 hemioxalate; ICI118587 hemioxalate; 1-(4-Hydroxyphenoxy)-3-[2-(4-morpholinocarboxamido)ethylamino]-2-propanol hemifumarate; Corwin; Xamoterol fumarate. Grades: ≥97% by HPLC. CAS No. 73210-73-8. Molecular formula: C16H25N3O5.1/2C4H4O4. Mole weight: 397.43. | |
| Xanomeline | Xanomeline is a Muscarinic M1 and M4 receptor agonist under the development of Eli Lilly, though it is also known to act as a M5 receptor antagonist. Xanomeline has been shown to have reasonable efficacy for the treatment of schizophrenia symptoms although gastrointestinal side effects led to a high drop-out rate in clinical trials. Recent studies showed robust improvements in verbal learning and short-term memory associated with xanomeline treatment. In Dec 1998, Phaes-III clinical trials for Alzheimer's disease in USA was discontinued. Uses: Alzheimer's disease. Synonyms: LY-246708; LY246708; LY 246708; Xanomeline; Memcor; NNC-110232; Hexyloxy-TZTP; HexyloxyTZTP;3-(hexyloxy)-4-(1-methyl-1,2,5,6-tetrahydropyridin-3-yl)-1,2,5-thiadiazole. Grades: 95%. CAS No. 131986-45-3. Molecular formula: C14H23N3OS. Mole weight: 281.42. | |
| 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 Impurity 1 | Xanomeline Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 174656-58-7. Molecular Formula: C14H23N3O2S. Mole Weight: 297.42. Catalog: APB174656587. | |
| Xanomeline Impurity 10 | Xanomeline Impurity 10. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C20H27D4N3O8S. Mole Weight: 477.57. Catalog: APB11430. | |
| 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 Impurity 3 | Xanomeline Impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 174656-57-6. Molecular Formula: C11H15N3O3S. Mole Weight: 269.32. Catalog: APB174656576. | |
| Xanomeline Impurity 4 | Xanomeline Impurity 4. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C11H11D4N3O3S. Mole Weight: 273.34. Catalog: APB11425. | |
| Xanomeline Impurity 5 | Xanomeline Impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 159058-46-5. Molecular Formula: C12H17N3O3S. Mole Weight: 283.35. Catalog: APB159058465. | |
| Xanomeline Impurity 6 | Xanomeline Impurity 6. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C12H14D3N3O3S. Mole Weight: 286.36. Catalog: APB11427. | |
| Xanomeline Impurity 7 | Xanomeline Impurity 7. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C12H13D4N3O3S. Mole Weight: 287.37. Catalog: APB11426. | |
| Xanomeline Impurity 8 | Xanomeline Impurity 8. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C20H31N3O8S. Mole Weight: 473.54. Catalog: APB11428. | |
| Xanomeline Impurity 9 | Xanomeline Impurity 9. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C20H28D3N3O8S. Mole Weight: 476.56. Catalog: APB11429. | |
| Xanomeline oxalate | Muscarinic receptors are G protein-coupled acetylcholine receptors that play diverse roles. Xanomeline oxalate is a potent agonist of muscarinic acetylcholine receptors (EC50 values are 0.3, 92.5, 5, 52, and 42 nM for M1, M2, M3, M4, and M5, respectively). It has antipsychotic-like activities in rats and Cebus monkeys. M1 selective agonists, like Xanomeline oxalate, enhance memory function and has utility in treating Alzheimer's Disease. Synonyms: LY246708; LY 246708; LY-246708; Memcor; Lumeron. Grades: >98%. CAS No. 141064-23-5. Molecular formula: C16H25N3O5S. Mole weight: 371.45. | |
| Xanomeline oxalate | Xanomeline oxalate. Group: Biochemicals. Grades: Purified. CAS No. 141064-23-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Xanomeline Oxalate (3-(hexyloxy)-4-(1-methyl-1,2,5,6-tetrahydropyridin-3-yl)-1,2,5-thiadiazole, Muscarinic Acetylcholine Receptor (mAChR) Agonist, Xanomeline) | 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 |
| 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 kind of microbial polysaccharide produced by Xanomonas campestris. The structure of xanthan is based on a cellulosic backbone of β-(1-4)-linked glucose units which have a trisaccharide side chain of mannose-glucuronic acid-mannose linked to every second glucose unit in the main chain. Some terminal mannose units are pyruvylated and some of the inner mannose units are acetylated. Due to its unique rheological and gelatinous properties, it is widely used in the food and petroleum industry as a food additive, thickener and stabilizer. Uses: Shampoo shower gel body care face care. Synonyms: Corn sugar gum; E415; Grindsted; Keldent; Keltrol; polysaccharide B-1459; Rhodicare S; Rhodigel; Vanzan NF; xanthani gummi; Xantural. CAS No. 11138-66-2. Molecular formula: (C35H49O29)n. | |
| 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. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner. |  California |
| 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: Heterocyclic organic compound. Alternative Names: Gum xanthan. CAS No. 11138-66-2. Molecular formula: C35H49O29. Mole weight: 933.75. Appearance: fine, white to cream-colored powder. IUPACName: 2-(2, 4-diaminophenoxy)ethanol; dihydrochloride. Canonical SMILES: C1=CC(=C(C=C1N)N)OCCO.Cl.Cl. ECNumber: 266-3 | |
| 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. Group: Food ingredients. Pack Sizes: 25kgs Cartons. |  |
| 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 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. CAS No. 11138-66-2. Pack Sizes: 55 lb. |  USA |
| Xanthan Gum BP/USP | Xanthan Gum BP/USP. CAS No. 11138-66-2. Molecular formula: C35H49O29. |  |
| Xanthan gum for pharmaceutical grade | Heterocyclic Organic Compound. CAS No. 11138-66-26. Molecular formula: (C35H49O29)n. Catalog: ACM111386626. | |
| 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. | |
| 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-methylamine | Heterocyclic Organic Compound. Alternative Names: XANTHENE-9-METHYLAMINE HYDROCHLORIDE;XANTHENE-9-METHYLAMINE. CAS No. 100866-28-2. Molecular formula: C14H13NO. Mole weight: 211.26. Catalog: ACM100866282. | |
| 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 | 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 | 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. Uses: Relax and widen certain breathing passages of the lungs. Synonyms: 2,6-Dihydroxypurine; Isoxanthine; Xanthin. Grades: >98%. CAS No. 69-89-6. Molecular formula: C5H4N4O2. Mole weight: 152.11. | |
| Xanthine-13C,15N2 | 13C Labeled Compounds. Alternative Names: 3,9-Dihydro-1H-purine-2,6-dione-13C15N2; 1H,3H,7H-Xanthine-13C15N2; 1H-Purine-2,6-diol; 3,9-Dihydro-1H-purine-2,6-dione-13C15N2; 9H-Purine-2,6(1H,3H)-dione-13C15N2; Isoxanthine-13C15N2; NSC 14664-13C15N2; Pseudoxanthine-13C15N2; Xanthic oxide-13C15N2. CAS No. 1262670-81-4. Molecular formula: C413CH4N215N2O2. Mole weight: 155.09. Catalog: ACM1262670814. | |
| 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 |
