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1kg Pack Size. Group: Analytical Reagents, Bioactive Small Molecules, Biochemicals, Building Blocks, Carbohydrates. Formula: C6H14O6. CAS No. 87-78-5. Prepack ID 89993169-1kg. Molecular Weight 182.2. See USA prepack pricing.
Mannitol
Cas No. 69-65-8.
Mannitol
MANNITOL, ACS Reagent, powder, Formula: HOCH2(CHOH)4CH2OH. CAS No. 69-65-8. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today!
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Mannitol
Mannitol. CAS No. 69-65-8. Molecular Formula HOCH2(CHOH)4CH2OH. Chemical Reagents
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
Mannitol
Mannitol. Uses: For analytical and research use. Group: Impurity standards. CAS No. 87-78-5. Molecular Formula: C6H14O6. Mole Weight: 182.17. Catalog: APB87785.
Mannitol
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Mannitol
Pharmacopeia & Metrological Institutes Standards; API Standards; British Pharmacopoeia; Impurity Standards; Pharmaceutical Toxicology; Pharmacopoeial Standards. Uses: For analytical and research use. Group: Reagents. Alternative Names: Osmitrol, Pearlitol 100, Mannitol 60, Bronchitol, Mannit S, Mannitol 35, D-Mannitol, Manicol, Resectisol, Cordycepic acid (6CI,7CI), Partek M, d-Mannitol, Parteck 300, PharmMannidex 16701, Mannit P, Mannitol P 60, Pearlitol 100SD, Mannidex 16700, Nonpareil 108, Nonpareil 108(200), Mannitolum, Pearlitol, Parteck M 200, Maniton S, Pearlitol 50C, Mannitol, D- (8CI), Mannitol SD 200, Orocell 200, Brightmoon, Cerestar 16700, E 421, Pearlitol 160C, Parteck M 100, Osmosal, Parteck Delta M, D-(-)-Mannitol, Mannidex, Parteck M 300, Mannistol, Mannogem 2080, Mannit,Mannitol, Pearlitol 200SD, Perteck M, Pearlitol 2005D, Manna sugar, Mannite, Isotol, D-Mannit, Perlitol SD 200, Mannigen, Diosmol, Pearlitol SD 100, Pearlitol 25C, PharmMannidex, Mannogem EZ, Mannit 60, Marine Crystal. CAS No. 69-65-8. Pack Sizes: 1.5G. IUPAC Name: (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol.
This enzyme belongs to the family of hydrolases, specifically those acting on phosphoric monoester bonds. The systematic name of this enzyme class is D-mannitol-1-phosphate phosphohydrolase. This enzyme is also called mannitol-1-phosphate phosphatase. This enzyme participates in fructose and mannose metabolism. Group: Enzymes. Synonyms: mannitol-1-phosphate phosphatase. Enzyme Commission Number: EC 3.1.3.22. CAS No. 9055-29-2. 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-3625; mannitol-1-phosphatase; EC 3.1.3.22; 9055-29-2; mannitol-1-phosphate phosphatase. Cat No: EXWM-3625.
mannitol-1-phosphate 5-dehydrogenase
This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is D-mannitol-1-phosphate:NAD+ 2-oxidoreductase. Other names in common use include hexose reductase, mannitol 1-phosphate dehydrogenase, D-mannitol-1-phosphate dehydrogenase, and fructose 6-phosphate reductase. This enzyme participates in fructose and mannose metabolism. Group: Enzymes. Synonyms: hexose reductase; mannitol 1-phosphate dehydrogenase; D-mannitol-1-phosphate dehydrogenase; fructose 6-phosphate reductase. Enzyme Commission Number: EC 1.1.1.17. CAS No. 9028-24-4. 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-0073; mannitol-1-phosphate 5-dehydrogenase; EC 1.1.1.17; 9028-24-4; hexose reductase; mannitol 1-phosphate dehydrogenase; D-mannitol-1-phosphate dehydrogenase; fructose 6-phosphate reductase. Cat No: EXWM-0073.
mannitol 2-dehydrogenase
This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is D-mannitol:NAD+ 2-oxidoreductase. Other names in common use include D-mannitol dehydrogenase, and mannitol dehydrogenase. This enzyme participates in fructose and mannose metabolism. Group: Enzymes. Synonyms: D-mannitol dehydrogenase; mannitol dehydrogenase. Enzyme Commission Number: EC 1.1.1.67. CAS No. 9001-65-4. Mannitol Dehydrogenase. 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-0352; mannitol 2-dehydrogenase; EC 1.1.1.67; 9001-65-4; D-mannitol dehydrogenase; mannitol dehydrogenase. Cat No: EXWM-0352.
mannitol 2-dehydrogenase (NADP+)
This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is D-mannitol:NADP+ 2-oxidoreductase. This enzyme is also called mannitol 2-dehydrogenase (NADP+). This enzyme participates in fructose and mannose metabolism. Group: Enzymes. Synonyms: mannitol 2-dehydrogenase (NADP). Enzyme Commission Number: EC 1.1.1.138. CAS No. 37250-68-3. 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-0042; mannitol 2-dehydrogenase (NADP+); EC 1.1.1.138; 37250-68-3; mannitol 2-dehydrogenase (NADP). Cat No: EXWM-0042.
Mannitol BP/USP/FCC
Mannitol BP/USP/FCC. CAS No. 69-65-8. Molecular formula: C6H14O6.
mannitol dehydrogenase
The enzyme from Apium graveolens (celery) oxidizes alditols with a minimum requirement of 2R chirality at the carbon adjacent to the primary carbon undergoing the oxidation. The enzyme is specific for NAD+ and does not use NADP+. Group: Enzymes. Synonyms: MTD; NAD-dependent mannitol dehydrogenase. Enzyme Commission Number: EC 1.1.1.255. CAS No. 144941-29-7. 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-0160; mannitol dehydrogenase; EC 1.1.1.255; 144941-29-7; MTD; NAD-dependent mannitol dehydrogenase. Cat No: EXWM-0160.
Mannitol Dehydrogenase (Crude Enzyme)
This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD + or NADP + as acceptor. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Diagnostics; biotechnology. Group: Enzymes. Synonyms: MTD; NAD-dependent mannitol dehydrogenase. Enzyme Commission Number: EC 1.1.1.255. CAS No. 144941-29-7. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. MTD; NAD-dependent mannitol dehydrogenase. Pack: 100ml. Cat No: NATE-1796.
mannitol dehydrogenase (cytochrome)
The enzyme from the bacterium Gluconobacter oxydans acts on polyols with a D-lyxo configuration, such as D-mannitol and D-sorbitol, with preference towards the former. Group: Enzymes. Synonyms: polyol dehydrogenase. Enzyme Commission Number: EC 1.1.2.2. CAS No. 37250-78-5. 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-0384; mannitol dehydrogenase (cytochrome); EC 1.1.2.2; 37250-78-5; polyol dehydrogenase. Cat No: EXWM-0384.
Mannitol EP Impurity A
Mannitol EP Impurity A. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: D-Sorbitol; D-Glucitol; (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexaol. CAS No. 50-70-4. Molecular Formula: C6H14O6. Mole Weight: 182.17. Catalog: APB50704.
Mannitol EP impurity B
Mannitol EP impurity B. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Maltitol/Erythritol EP Impurity A. CAS No. 585-88-6. Molecular Formula: C12H24O11. Mole Weight: 344.31. Catalog: APB585886.
Alfa Chemistry offers 1,2,3,4,5,6-Hexa-O-[11-[4-(4-hexylphenylazo)phenoxy]undecanoyl]-D-mannitol products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: Photochromic materials are further developed for a light-modulating materials, optical recording media, optical switches, and functional inks. Group: Azobenzenes. CAS No. 1093077-77-0. Molecular formula: C180H254N12O18. Mole weight: 2874.08. Appearance: Light yellow to Brown powder to crystaline. Purity: >97.0%(HPLC). Catalog: ACM1093077770.
1,2,3,4,5,6-Hexa-O-acetyl-D-mannitol
1,2,3,4,5,6-Hexa-O-acetyl-D-mannitol is an intermediate compound. This molecule orients itself towards the synthesis of intricate glycoside antibiotics. Synonyms: D-Mannitol hexaacetate. CAS No. 642-00-2. Molecular formula: C18H26O12. Mole weight: 434.39.
1,2:3,4:5,6-Tri-O-isopropylidene-D-mannitol
1,2:3,4:5,6-Tri-O-isopropylidene-D-mannitol: An indispensible entity in the biomedical sector, this highly esteemed compound showcases an array of paramount utilities. Regarded as a proficient safeguarding agent for diverse functional molecules, it unravels its true potential. CAS No. 3969-59-3. Molecular formula: C15H26O6. Mole weight: 302.4.
1,2:4,5-Di-O-isopropylidene-D-mannitol
1,2:4,5-Di-O-isopropylidene-D-mannitol, an indispensable chemical compound prevalent in the biomedical realm, possesses exceptional versatility for diverse drug synthesis and specialized disease treatments. Its eminent role encompasses the creation of antiviral and anticancer medications, along with remedies targeting diabetes and cardiovascular afflictions. Synonyms: 1,2:4,5-Di-O-isopropylidene-D-mannitol; 3969-61-7; 1,2:4,5-Di-O-isopropylidene-a-D-mannitol; NSC 93066; 1,2:4,5-Di-O-isopropylidene-alpha-D-mannitol; 1,2:4,5-Bis-O-(1-methylethylidene)-D-mannitol; SCHEMBL9204270; MFCD00198003; 1,2:4,5-Diisopropylidene-D-mannitol; AKOS040768243; W-202632; (2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-(5-HYDROXYMETHYL-2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-METHANOL; (R)-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)((4S,5R)-5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methanol; (R)-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-[(4S,5R)-5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]methanol. CAS No. 3969-61-7. Molecular formula: C12H22O6. Mole weight: 262.3.
1,2:5,6-Di-O-cyclohexylidene-D-mannitol
1,2:5,6-Di-O-cyclohexylidene-D-mannitol, also known as a chemical compound extensively employed in the field of biomedicine, showcases remarkable antiviral and antimicrobial traits. This renders it a propitious contender for addressing diverse viral and bacterial infections. Moreover, owing to its distinctive properties, this compound demonstrates immense potential in the arena of pharmaceutical exploration and progression, particularly in combating drug-resistant strains and enhancing prevailing therapeutic methodologies. Synonyms: (1S,2S)-1,2-Di((R)-1,4-dioxaspiro[4.5]decan-2-yl)ethane-1,2-diol; (1S,2S)-1,2-bis[(3R)-1,4-dioxaspiro[4.5]decan-3-yl]ethane-1,2-diol;(1S,2S)-1,2-bis[(2R)-1,4-dioxaspiro[4.5]decan-2-yl]ethane-1,2-diol;1,2:5,6-Di-O-cyclohexylidene-D-mannitol, 98%. CAS No. 76779-67-4. Molecular formula: C18H30O6. Mole weight: 342.4.
1,2:5,6-Di-O-isopropylidene-D-mannitol
Cas No. 1707-77-3.
1,2:5,6-Di-O-isopropylidene-D-mannitol
Nebivolol intermediate. Group: Biochemicals. Alternative Names: 1,2:5,6-Bis-O-(1-methylethylidene)-D-mannitol; D- ( + ) -1, 2: 5, 6-Di-O-isopropyl idenemannitol; D-Mannitol 1,2:5,6-Bis-acetonide; Mannitol Diacetonide; NSC 47987; NSC 67545; NSC 89874. Grades: Highly Purified. CAS No. 1707-77-3. Pack Sizes: 10g. US Biological Life Sciences.
Worldwide
1,2,5,6-Tetramethanesulfonyl-D-mannitol
1,2,5,6-Tetramethanesulfonyl-D-mannitol is a reagent used in the preparation of pharmaceutical compounds for tumor diagnosis and treatment. Group: Biochemicals. Grades: Highly Purified. CAS No. 7518-35-6. Pack Sizes: 50mg, 100mg. Molecular Formula: C10H22O14S4, Molecular Weight: 494.53. US Biological Life Sciences.
Worldwide
1,2-O-Isopropylidene-D-mannitol
1,2-O-Isopropylidene-D-mannitol, a revolutionary biomedical product, stands at the forefront of cutting-edge research and treatment for a myriad of conditions, notably diabetes, hypertension, and cancer. With its awe-inspiring attributes encompassing anti-diabetic, anti-hypertensive, and anti-tumor properties, this compound has captivated the attention of scientific experts worldwide. Synonyms: 1-(2,2-dimethyl-1,3-dioxolan-4-yl)butane-1,2,3,4-tetrol; 4306-35-8; 1,2-O-Isopropylidene-D-mannitol; NSC226057; DTXSID90310347; NSC-226057; FT-0635217; A826132. CAS No. 4306-35-8. Molecular formula: C9H18O6. Mole weight: 222.24.
1,3:4,6-Di-O-benzylidene-D-mannitol
1,3:4,6-Di-O-benzylidene-D-mannitol is a biomedically compound, showing good performance in the research of effective cerebrovascular disease medication. It is also commonly used in treatment and prevention studies of ischemic stroke. Synonyms: 1,3:4,6-Di-O-benzylidene-D-mannitol; 28224-73-9; (4R,4'R,5R,5'R)-2,2'-Diphenyl-[4,4'-bi(1,3-dioxane)]-5,5'-diol; (4R,5R)-4-[(4R,5R)-5-HYDROXY-2-PHENYL-1,3-DIOXAN-4-YL]-2-PHENYL-1,3-DIOXAN-5-OL; SCHEMBL1038804; NVEGGHPETXMRSV-NIJYPJQDSA-N; DTXSID401292783; AKOS027320438; 1,3:4,6-Di-O-benzyliden-D-mannitol; CS-W009793; 1,3:4,6-di-O-ben-zylidene-d-mannitol; BS-42545; 1,3:4,6-bis-O-(phenylmethylene)-D-Mannitol; E84509; W-202181; 1,3:4,6-Di-O-benzylidene-D-mannitol, >=98.0% (sum of enantiomers, HPLC). CAS No. 28224-73-9. Molecular formula: C20H22O6. Mole weight: 358.39.
1,4:3,6-Dianhydro-2,5-di-O-methyl-L-mannitol
1,4:3,6-Dianhydro-2,5-di-O-methyl-L-mannitol, a derivative of sugar alcohol, is known to serve as an essential cryoprotectant in the biopharmaceutical industry owing to its potential to enhance cell viability and maintain optimal functionality during the process of freezing and thawing. Its utility in preserving tissues and cells for research and transplantation purposes cannot be ignored due to its demonstrated utility and efficiency in this regard. Molecular formula: C8H14O4. Mole weight: 174.19.
1,4:3,6-Dianhydro-D-mannitol
1,4:3,6-Dianhydro-D-mannitol is a reagent used in the synthesis of new isomannide-based peptidomimetic as human tissue kallikrein 1 inhibitor using Ugi multicomponent reaction. It also functions as a chiral ligand for stereoselective synthesis. Group: Biochemicals. Grades: Highly Purified. CAS No. 641-74-7. Pack Sizes: 1g, 5g. Molecular Formula: C6H10O4, Molecular Weight: 146.139999999999. US Biological Life Sciences.
Worldwide
1,4:3,6-Dianhydro-L-mannitol
1,4:3,6-Dianhydro-L-mannitol is colloquially referred to as Isosorbide, functioning predominantly as a nitrate-induced vasodilator. CAS No. 1394295-11-4. Molecular formula: C6H10O4. Mole weight: 146.14.
1,4-Anhydro-D-mannitol
1,4-Anhydro-D-mannitol, an esteemed biomedicine, is widely employed in the efficacious treatment of distinct pharmaceuticals and ailments. This exceptional compound holds immense promise in the realm of pharmacology, functioning as a pivotal excipient in drug compositions, thereby imparting robustness and augmenting therapeutic conveyance. Furthermore, its multifarious utilization extends to the realm of diagnosing and remedying an assortment of maladies, encompassing cancer, cardiovascular disorders, and metabolic anomalies. CAS No. 7726-97-8. Molecular formula: C6H12O5. Mole weight: 164.16.
1,4-Dideoxy-1,4-imino-D-mannitol HCI
1,4-Dideoxy-1,4-imino-D-mannitol HCl
It is a competitive glycosidase inhibitor. Synonyms: (2R,3S,4R)-2-[(1S)-1,2-Dihydroxyethyl]-3,4-pyrrolidinediol hydrochloride; 1,4-Dideoxy-1,4-imino-D-mannitol Hydrochloride; (2R,3S,4R)-2-((S)-1,2-Dihydroxyethyl)pyrrolidine-3,4-diol hydrochloride; 3,4-Pyrrolidinediol, 2-[(1S)-1,2-dihydroxyethyl]-, (2R,3S,4R)-, hydrochloride (1:1). Grades: ≥90%. CAS No. 114976-76-0. Molecular formula: C6H13NO4.HCl. Mole weight: 199.63.
A competitive glycosidase inhibitor. It is also a glycoprotein mannosidase inhibitor-inhibiting jack bean, and to a lesser extent lysosomal alpha-mannosidase. It is an azofuranose analog of mannose, and is structurally related to swainsonine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences.
This enzyme is present in some but not all Rhizobium species and belongs in the GFO/IDH/MocA protein family. This enzyme differs from hepatic 1,5-anhydro-D-fructose reductase, which yields 1,5-anhydro-D-glucitol as the product (see EC 1.1.1.263). In Sinorhizobium morelense, the product of the reaction, 1,5-anhydro-D-mannitol, can be further metabolized to D-mannose. The enzyme also reduces 1,5-anhydro-D-erythro-hexo-2,3-diulose and 2-ketoaldoses (called osones), such as D-glucosone (D-arabino-hexos-2-ulose) and 6-deoxy-D-glucosone. It does not reduce common aldoses and ketoses, or non-sugar aldehydes and ketones. Group: Enzymes. Synonyms: 1,5-anhydro-D-fructose reductase (ambiguous); AFR. Enzyme Commission Number: EC 1.1.1.292. 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-0201; 1,5-anhydro-D-fructose reductase (1,5-anhydro-D-mannitol-forming); EC 1.1.1.292; 1,5-anhydro-D-fructose reductase (ambiguous); AFR. Cat No: EXWM-0201.
1,5-Anhydro-D-mannitol
1,5-Anhydro-D-mannitol, an esteemed compound extensively employed in the realm of biomedicine, necessitates heed. Within this realm, its potential as a curative agent against an array of ailments, such as diabetes, inflammation, and cancer, is distinctly conspicuous. By virtue of its amplified constancy and singular structural attributes, 1,5-Anhydro-D-mannitol engenders an optimistic outlook for pioneering pharmaceuticals and therapeutic approaches within the domain of biomedicine. Synonyms: 1,5-Anhydro-d-mannitol; 492-93-3; Styracitol; 1,5-Anhydromannitol; 1,5-Anhydro-mannitol; Styracit; (2R,3S,4R,5R)-2-(hydroxymethyl)oxane-3,4,5-triol; 2,6-Anhydro-D-mannitol; D-Mannitol, 1,5-anhydro-; 1-deoxy-alpha-D-mannopyranose; 6V415COZ8I; 1-5-ANHYDRO-D-MANNITOLCRYSTALLINE; UNII-6V415COZ8I; AH2; D-1,5-anhydro-Mannitol; STYRACITOL, (-)-; SCHEMBL2282745; CHEMBL3800290; CHEBI:49182; MPCAJMNYNOGXPB-KVTDHHQDSA-N; DTXSID701314215; HY-N9911; MFCD00067387; AKOS006274375; CS-0204027; F87624; W-202872; Q27121518; (-)-(2R,3S,4R,5R)-2-hydroxymethyl-tetrahydro-pyran-3,4,5-triol; 1,5-Anhydromannitol; 1-deoxy-alpha-D-mannose; 1-deoxy-D-mannose; 1-deoxy-mannose. CAS No. 492-93-3. Molecular formula: C6H12O5. Mole weight: 164.16.
1,5-Dideoxy-1,5-imino-D-mannitol
It is produced by the strain of Streptomyces lavendulae GC-148. Synonyms: (-)-1-Deoxynojirimycin. CAS No. 146747-37-7. Molecular formula: C6H13NO4. Mole weight: 163.17.
1,6-Dibromo-1,6-dideoxy-D-mannitol
1,6-Dibromo-1,6-dideoxy-D-mannitol. CAS No: 488-41-5
Sarchem Laboratories New Jersey NJ
1,6-Dimethanesulfonate-D-mannitol
1,6-Dimethanesulfonate-D-mannitol is a reagent used in the preparation of pharmaceutical compounds for tumor diagnosis and treatment. Group: Biochemicals. Grades: Highly Purified. CAS No. 1187-00-4. Pack Sizes: 100mg, 250mg. Molecular Formula: C8H18O10S2, Molecular Weight: 338.35. US Biological Life Sciences.
Worldwide
1-Amino-1-deoxy-D-mannitol
1-Amino-1-deoxy-D-mannitol is a glycosidase inhibitor with functions of diminishing glycemic concentration. CAS No. 57027-74-4.
1-Amino-2,5-anhydro-1-deoxy-D-mannitol
1-Amino-2,5-anhydro-1-deoxy-D-mannitol is an amino sugar serving as a tool for studying diseases related to carbohydrate metabolism. Synonyms: 1-Amino-2,5-anhydro-1-deoxy-D-mannitol; 228862-97-3; D-Mannitol, 1-amino-2,5-anhydro-1-deoxy-; (2R,3S,4S,5R)-2-(AMINOMETHYL)-5-(HYDROXYMETHYL)OXOLANE-3,4-DIOL; AKOS006279638; W-201954. CAS No. 228862-97-3. Molecular formula: C6H13NO4. Mole weight: 163.17.
1-Deoxy-1-nitro-D-mannitol
1-Deoxy-1-nitro-D-mannitol is a potent pharmaceutical compound used in the treatment of certain bacterial infections. It exhibits excellent antibiotic properties against various drug-resistant strains due to its unique chemical structure. This product plays a crucial role in biomedical research, contributing to the development of new antibacterial drugs for combating infections caused by specific pathogens. Synonyms: 1-Deoxy-1-nitro-D-mannitol; 14199-83-8; (2R,3R,4R,5R)-6-nitrohexane-1,2,3,4,5-pentol; 6-nitrohexane-1,2,3,4,5-pentol; SCHEMBL5518124; DTXSID201311230; GEO-04693; W-201226; (2R,3R,4R,5R)-6-nitrohexane-1,2,3,4,5-pentaol. CAS No. 14199-83-8. Molecular formula: C6H13NO7. Mole weight: 211.17.
1-Deoxy-1-nitro-L-mannitol
1-Deoxy-1-nitro-L-mannitol is a potent antibacterial agent, primarily used in biomedical research involving diseases caused by gram-positive bacteria. The product is also used in the study of multi-drug resistant infections. Synonyms: 1-Deoxy-1-nitro-L-mannitol; 6027-42-5; (2S,3S,4S,5S)-6-nitrohexane-1,2,3,4,5-pentol; EINECS 227-894-7; SCHEMBL9809656; HOFCJTOUEGMYBT-BXKVDMCESA-N; DTXSID701311285; GEO-04695; NSC 25292; 3- (TERT-BUTYLAMINOCARBONYL) PHENYLBORONICACID; J-200018; (2S,3S,4S,5S)-6-nitrohexane-1,2,3,4,5-pentaol. CAS No. 6027-42-5. Molecular formula: C6H13NO7. Mole weight: 211.2.
1-Deoxy-L-mannitol
1-Deoxy-L-mannitol is a hexitol derivative, serving principally in the exploration pertinent to the biogenetic mechanism of mannitol. This compound stands a promising candidate for prospective research and development in treatments including diabetic retinopathy and post-stroke injury. Synonyms: 6-Deoxy-L-mannitol. Molecular formula: C6H14O5. Mole weight: 166.17.
(1R)-1,5-Anhydro-1-C-1H-indol-2-yl-2,3,4-tris-O-(phenylmethyl)-D-Mannitol 6-Acetate is an intermediate in the synthesis of 2-(α-D-Mannopyranosyl)-L-tryptophan (M166450), a tryptophan glycoconjugate being tested as a diagnostic tool for the accurate measure of renal function. Group: Biochemicals. Grades: Highly Purified. CAS No. 358620-68-5. Pack Sizes: 1mg, 5mg. Molecular Formula: C37H37NO6. US Biological Life Sciences.
(1R)-1,5-Anhydro-1-C-1H-indol-2-yl-2,3,4-tris-O-(phenylmethyl)-D-Mannitol 6-Acetate-d4 is an isotope labelled intermediate in the synthesis of 2-(α-D-Mannopyranosyl)-L-tryptophan (M166450), a tryptophan glycoconjugate being tested as a diagnostic tool for the accurate measure of renal function. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 5mg. Molecular Formula: C37H33D4NO6. US Biological Life Sciences.
2,3,4,5-Tetra-O-acetyl-1,6-dibromo-1,6-dideoxy-D-mannitol, a fascinating biomedical substance, holds immense potential for combating diseases. Through its remarkable efficacy in inhibiting microbial infections, it emerges as a compelling solution against drug-resistant pathogens. Harnessing its distinctive structure and properties, this compound paves the way for groundbreaking therapeutic approaches in the realm of infectious diseases. Synonyms: 1,6-Dibromo-1,6-dideoxy-D-mannitol 2,3,4,5-tetraacetate. CAS No. 15410-49-8. Molecular formula: C14H20Br2O8. Mole weight: 476.11.
2,3,4,6-Tetra-O-acetyl-1,5-anhydro-D-mannitol
2,3,4,6-Tetra-O-acetyl-1,5-anhydro-D-mannitol is a compound of immense versatility within the esteemed biomedical realm. Its multifaceted nature illuminates a myriad of possibilities in pharmaceutical formulations, catering to a plethora of applications. Meticulous research has showcased its remarkable prowess in combating insidious maladies, including the formidable adversaries of cancer and diabetes. Synonyms: 1,5-Anhydro-D-mannitol tetraacetate; NSC 231899. CAS No. 13121-61-4. Molecular formula: C14H20O9. Mole weight: 332.30.
2,5-Anhydro-1-O-trityl-D-mannitol
2,5-Anhydro-1-O-trityl-D-mannitol, a pivotal transitional compound, stands as an eminent agent in the pharmaceutical domain, particularly for combatting cancer. Various forms of this relentless disease, including breast cancer, colon cancer, lymphoma, and leukemia, have been thwarted by the employment of this potent ingredient. Additionally, the formulation of drugs designed to treat heart issues and diabetes utilizes this paramount substance. CAS No. 68774-48-1. Molecular formula: C25H26O5. Mole weight: 406.48.
2,5-Anhydro-D-mannitol
2,5-Anhydro-D-mannitol is a remarkable and multifunctional entity, serving as an eminent stabilizer and excipient. Through its profound influence, it elevates the stability and solubility of a diverse array of pharmaceutical agents. Synonyms: 2,5-Anhydro-D-mannitol; 41107-82-8; D-Mannitol, 2,5-anhydro-; 2,5-Anhydromannitol; W5DLZ1WC4B; (2R,3S,4S,5R)-2,5-Bis(hydroxymethyl)tetrahydrofuran-3,4-diol; NSC-129241; EINECS 255-221-7; NSC 129241; UNII-W5DLZ1WC4B; SCHEMBL389614; (2R,3S,4S,5R)-2,5-bis(hydroxymethyl)oxolane-3,4-diol; MCHWWJLLPNDHGL-KVTDHHQDSA-N; MFCD00012443; F76911; W-202693. CAS No. 41107-82-8. Molecular formula: C6H12O5. Mole weight: 164.16.
2,5-Anhydro-D-mannitol-1,6-diphosphate dibarium salt dihydrate
2,5-Anhydro-D-mannitol-1,6-diphosphate dibarium salt dihydrate is a biomedical product with widely applications in the research of targeting specific enzymes or biochemical pathways related to drug-resistant infections and metabolic disorders. Synonyms: 2,5-Anhydro-D-mannitol-1,6-diphosphate Dibarium Salt; 2,5-Anhydro-D-mannitol-1,6-diphosphate dibarium salt dihydrate; barium(2+); [(2R,3S,4S,5R)-3,4-dihydroxy-5-(phosphonatooxymethyl)oxolan-2-yl]methyl phosphate; dihydrate; MFCD09750695; J-019996; 2,5-Anhydro-D-mannitol-1,6-diphosphate,dibarium salt dihydrate. CAS No. 352000-03-4. Molecular formula: C6H10Ba2O11P2.2H2O. Mole weight: 630.77.
2,5-Anhydro-D-mannitol-1-phosphate barium salt hydrate
2,5-Anhydro-D-mannitol-1-phosphate barium salt hydrate, renowned in the biomedical sector as an efficient biochemical reagent, has been recognized for its exceptional ability to impede cell growth in specific cancer types by disrupting energy metabolism. Additionally, this compound has been identified as a potential treatment for diabetes and metabolic abnormalities, as evidenced by extensive research conducted within the field. Synonyms: 2,5-Anhydro-D-mannitol-6-phosphate, barium salt hydrate. CAS No. 52011-52-6. Molecular formula: C6H11BaO8P.H2O. Mole weight: 397.46.
2,5-Anhydro-D-mannitol-1-phosphate, Barium Salt Hydrate
Inhibits gluconeogenesis in isolated hepatcytes as well as preventing hormonal stimulation of gluconeogenesis and the corresponding decrease in lactate production from dihydroxyacetone. Uses: Inhibits gluconeogenesis in isolated hepatcytes as well as preventing hormonal stimulation of gluconeogenesis and the corresponding decrease in lactate production from dihydroxyacetone. Synonyms: 2,5-Anhydro-D-Mannitol-6-Phosphate, Barium Salt Hydrate. Grades: 95%. CAS No. 352000-02-3. Molecular formula: C6H15BaO10P. Mole weight: 415.48.
2,5-Anhydro-D-mannitol tetraacetate
2,5-Anhydro-D-mannitol tetraacetate, a biomedical marvel, reigns as a formidable weapon in combating diverse maladies. Hailing from Mother Nature's bounty, this enigmatic compound manifests noteworthy antiviral and anti-inflammatory attributes. Prized as a cornerstone in pioneering pharmaceutical concoctions that thwart viral invasions and assuage autoimmune afflictions, its distinctive molecular framework enables precision-guided therapeutic administration. Synonyms: 2,5-Anhydro-D-mannitol peracetate. CAS No. 65729-88-6. Molecular formula: C14H20O9. Mole weight: 332.30.
2,5-Dideoxy-2,5-imino-D-mannitol
A glucosidase inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
2,5-Dideoxy-2,5-imino-D-mannitol HCl
2,5-Dideoxy-2,5-imino-D-mannitol HCl, a highly efficacious pharmaceutical compound, occupies a prominent position in the biomedical landscape owing to its profound therapeutic value in tackling Fabry disease. This exceptionally intricate and infrequent genetic anomaly manifests itself as an aberrant accumulation of globotriaosylceramide (GL-3). The remarkable inhibitory action of this medication on the alpha-galactosidase A enzyme effectively restricts the accrual of GL-3, thereby thwarting the relentless advancement of this incapacitating ailment. Synonyms: 2,5-Anhydro-2,5-imino-D-mannitol HCl. CAS No. 210115-92-7. Molecular formula: C6H13NO4.HCl. Mole weight: 199.63.
2,5-Dideoxy-2,5-imino-L-mannitol
2,5-Dideoxy-2,5-imino-L-mannitol is a compound used in the research of type 2 diabetes. It acts as an alpha-glucosidase inhibitor, reducing the breakdown and absorption of carbohydrates. This compound, derived from L-mannitol, interacts with specific enzymes involved in glucose metabolism. Synonyms: DMDP; 2R,5R-Bis(hydroxylmethyl)-(3R,4R)-dihydroxypyrrolidine,; (2R,3R,4R,5R)-2,5-β(hydroxymethyl)pyrrolidine-3,4-diol; L-DMDP; (2R,3R,4R,5R)-3,4-Dihydroxy-2,5-pyrrolidinedimethanol; NSC613239; D-Mannitol, 2,5-dideoxy-2,5-imino-, (6R-(6alpha,7alpha,7(R*)))-. Grades: ≥98%. CAS No. 59920-31-9. Molecular formula: C6H13NO4. Mole weight: 163.17.
2-Chloro-2-deoxy-D-mannitol
2-Chloro-2-deoxy-D-mannitol, a promising glycosidase inhibitor, exhibits potential in therapeutic strategies for lysosomal storage disorders, including Gaucher and Fabry diseases. Moreover, it may have antiviral properties, rendering it a possible intervention for viral infections. Synonyms: 2-Chloro-2-deoxy-D-mannitol; 127530-02-3; SCHEMBL16897682. Molecular formula: C6H13ClO5. Mole weight: 200.62.
2-Deoxy-1,3:4,5-di-O-isopropylidene-2-oxamoylamino-D-mannitol, an extensively employed compound within the biomedical field, showcases remarkable efficacy in combating a multitude of bacterial and viral pathogens. This exceptional versatility renders it an invaluable asset towards the progression of pharmaceutical advancements. CAS No. 128741-75-3. Molecular formula: C14H24N2O7. Mole weight: 332.35.
3,4-O-Isopropylidene-D-mannitol, a pivotal compound widely utilized in the biomedical sector, assumes an invaluable role in pharmaceutical drug synthesis for diverse ailments. Demonstrating exceptional attributes, it is prominently leveraged to fabricate medications targeting cardiovascular anomalies, diabetes, as well as neurodegenerative disorders. Such multifaceted compound imparts stability and augments the therapeutic potency of medicinal formulations, thus assuming an indispensable position within the pharmaceutical realm. Synonyms: 3,4-O-Isopropylidene-D-mannitol; 3969-84-4; (1R,1'R)-1,1'-((4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-diyl)bis(ethane-1,2-diol); MFCD00075122; IsopropylideneDmannitol; (1R)-1-[(4R,5R)-5-[(1R)-1,2-dihydroxyethyl]-2,2-dimethyl-1,3-dioxolan-4-yl]ethane-1,2-diol; SCHEMBL1301822; YCOMFYACDCWMMD-WCTZXXKLSA-N; AKOS016010553; 3,4-O-Isopropylidene-D-mannitol, 97%; AS-73644; I0489; T72427; A873589; W-202633; (1R,1'R)-1,1'-((4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-diyl)diethane-1,2-diol. CAS No. 3969-84-4. Molecular formula: C9H18O6. Mole weight: 222.24.
3,6-Dideoxy-3,6-imino-4,5-O-isopropylidene-D-mannitol, a remarkable biomedical agent, showcases its prowess as a therapeutic marvel in combating microbial infections. By impeding the proliferation and vitality of drug-resistant bacteria, it emerges as a potent remedy. Behold its profound antimicrobial attributes, noxious pathogens stand no chance as it wages a relentless war, offering a beacon of hope in the realm of infectious disease management. Molecular formula: C9H17NO4. Mole weight: 203.24.