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| Product | Description | |
|---|---|---|
| 1,3-O-Benzylidene-4-O-DMT-D-threitol | 1,3-O-Benzylidene-4-O-DMT-D-threitol, a chemical compound widely employed in the synthesis of numerous pharmaceuticals and medicinal agents, exhibits promising therapeutic potential in addressing ailments like Alzheimer's and Parkinson's disease. Remarkably distinctive in structure, it functions as an invaluable intermediate in building various biologically active compounds. Its scientific significance warrants further investigation towards novel therapeutic avenues and drug development. |  |
| 1,3-O-Benzylidene-4-O-t-butyl-dimethylsilyl-D-threitol | 1,3-O-Benzylidene-4-O-t-butyl-dimethylsilyl-D-threitol, a versatile compound with chiral structures, holds significant potential in the realm of carbohydrate-based drugs and therapies. This compound's distinctive molecular composition allows it to serve as a valuable chiral building block for synthesizing complex carbohydrates and glycoconjugates, which exhibit an array of potential biomedical applications. From targeting drug delivery to personalized immunotherapy, this compound's multifaceted nature offers a vital tool in biomedicine research. As such, it has garnered significant attention for its unique properties in diverse fields, including cancer, diabetes, and viral infections. CAS No. 652979-92-5. Molecular formula: C17H28O4Si. Mole weight: 324.49. | |
| 1,3-O-Benzylidene-4-O-trityl-D-threitol | 1,3-O-Benzylidene-4-O-trityl-D-threitol, a synthetic derivative, holds a great promise in biomedical research due to its multifaceted properties as a potential therapeutic agent. Its dynamic antioxidant and anti-inflammatory traits received extensive attention in studying oxidative-stress-related illnesses including cancer, diabetes, and neurodegenerative ailments. Evidently, this compound could provide a crucial intervention for future treatments of these diseases. Molecular formula: C30H28O4. Mole weight: 452.54. | |
| (+)-1,4-Di-O-benzyl-D-threitol | (+)-1,4-Di-O-benzyl-D-threitol, a highly prized compound within the biomedical industry, constitutes a vital component for the creation of groundbreaking pharmaceuticals. Unveiling its indispensability, this compound triumphs as an integral player in combating various ailments such as cancer and diabetes. Prudently procured from reputed suppliers, it guarantees unparalleled purity and efficacy. Synonyms: (+)-(2R,3R)-1,4-Bis(benzyloxy)-2,3-butanediol. CAS No. 91604-41-0. Molecular formula: C18H22O4. Mole weight: 302.36. | |
| (-)-1,4-Di-O-benzyl-L-threitol | (-)-1,4-Di-O-benzyl-L-threitol is a chiral building block involved in the synthesis of antiviral drugs, specifically for treating HIV. It's also applied in the preparation of other therapeutically significant compounds in the biomedical industry. Synonyms: (-)-(2S,3S)-1,4-Bis(benzyloxy)-2,3-butanediol. CAS No. 17401-06-8. Molecular formula: C18H22O4. Mole weight: 302.36. | |
| 1,4-Di-O-tosyl-2,3-O-isopropylidene-L-threitol | 1,4-Di-O-tosyl-2,3-O-isopropylidene-L-threitol has been used in coordination chemistry of (R,R)-DIPPOP. Group: Biochemicals. Grades: Highly Purified. CAS No. 37002-45-2. Pack Sizes: 1g, 2.5 g. Molecular Formula: C21H26O8S2. US Biological Life Sciences. |  Worldwide |
| 1,4-Dithio-DL-threitol | Reagent for the quantitative reduction of disulfide group. Prevents the oxidation of cholecystokinin during its extraction from brain and duodenal tissues. Cleavage of disulfide bonds in proteins. Uses: Used as a reagent in biochemistry to prevent oxidation of thiol groups and to reduce disulfides to dithiols; has been used as a radioprotectant; dithiothreitol (dtt) is the common name for a small-molecule redox reagent known as cleland's reagent. Synonyms: DL-1,4-Dithiothreitol; DTT; Cleland's reagent; threo-1,4-Dimercapto-2,3-butanediol; Dithiothreitol; dl-Dithiothreitol; 1,4-Dithiothreitol; D-Dtt; 1,4-Dithio-dl-threitol; DL-Dithiothreitol; threo-1,4-Dimercapto-2,3-butanediol. Grades: ≥ 99 % (Assay by titration). CAS No. 3483-12-3. Molecular formula: C4H10O2S2. Mole weight: 154.25. | |
| 1-O-Benzoly-2,4-O-benzylidene-D-threitol | 1-O-Benzoly-2,4-O-benzylidene-D-threitol, a synthetic compound utilized in the production of antiviral medications for the treatment of herpes simplex virus (HSV) and varicella-zoster virus (VZV) infections, exhibits inhibitory effects on the replication and dissemination of these viruses in vitro. Thus, it presents a promising foundation for the development of new antiviral drugs. | |
| 2,3-Di-O-isopropylidene-D-threitol | 2,3-Di-O-isopropylidene-D-threitol. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| 2,3-O-Isopropylidene-1,1,4,4-tetraphenyl-L-threitol | 2,3-O-Isopropylidene-1,1,4,4-tetraphenyl-L-threitol is a chiral oxygen ligand for enantioselective synthesis with high yield and high enantioselective results. Synonyms: (4R5R)-2,2,-Dimethyl-a,a,a,a-tetraphenyldioxolane-4,5-dimethanol (-)-Taddol (-)-trans-a,a-(Dimethyl-1,3-dioxalane-4,5-diyl)bis(diphenylmethanol). Grades: 98%. CAS No. 93379-48-7. Molecular formula: C31H30O4. Mole weight: 466.57. | |
| 2,3-O-Isopropylidene-1,4-di-O-tosyl-D-threitol | 2,3-O-Isopropylidene-1,4-di-O-tosyl-D-threitol, a highly versatile compound, holds significant importance in the field of biomedical research due to its diverse applications. Acting as a safeguarding agent, it proves essential in the synthesis of numerous drugs and pharmaceutical intermediates. Synonyms: (+)-1,4-Di-O-tosyl-2,3-O-isopropylidene-D-threitol; 1,4-Di-O-tosyl-2,3-O-isopropylidene-D-threitol; (4R-trans)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethyl bis(toluene-p-sulphonate); ((4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-diyl)bis(methylene) bis(4-methylbenzenesulfonate); (+)-2,3-O-Isopropylidene-1,4-di-O-tosyl-D-threitol; [(4R,5R)-2,2-dimethyl-5-[(4-methylphenyl)sulfonyloxymethyl]-1,3-dioxolan-4-yl]methyl 4-methylbenzenesulfonate; (4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol 4,5-Bis(4-methylbenzenesulfonate)1111. CAS No. 51064-65-4. Molecular formula: C21H26O8S2. Mole weight: 470.56. | |
| 2,3-O-Isopropylidene-1,4-di-O-tosyl-L-threitol | 2,3-O-Isopropylidene-1,4-di-O-tosyl-L-threitol, a highly significant compound extensively utilized in the field of biomedicine, demonstrates exceptional prowess as a precursor for the synthesis of a plethora of therapeutic drugs and molecules. This indispensable substance effortlessly contributes to the development of cardiovascular medications, anti-inflammatory marvels, and potent antiviral remedies. Synonyms: (-)-1,4-di-O-Tosyl-2,3-O-isopropylidene-L-threitol; ((4S,5S)-2,2-Dimethyl-1,3-dioxolane-4,5-diyl)bis(methylene) bis(4-methylbenzenesulfonate); [(4S,5S)-2,2-dimethyl-5-[(4-methylphenyl)sulfonyloxymethyl]-1,3-dioxolan-4-yl]methyl 4-methylbenzenesulfonate; 1,4-di-o-tosyl-2,3-o-isopropylidene-l-threitol; MFCD00003212; (-)-1,4-Di-o-tosyl-2,3-o-isopropylidenethreitol; [(4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]bis(methylene) bis(4-methylbenzenesulfonate); C21H26O8S21111. CAS No. 37002-45-2. Molecular formula: C21H26O8S2. Mole weight: 470.56. | |
| (-)-2,3-O-Isopropylidene-D-threitol | (-)-2,3-O-Isopropylidene-D-threitol, an indispensable compound in the biomedical realm, stands at the forefront of scientific innovation and therapeutic breakthroughs. By serving as a pivotal chiral building block, it assumes a vital role in the intricate synthesis of a myriad of life-saving drugs and pharmaceuticals. Its remarkable versatility extends even further, finding eminence in the treatment of afflictions such as cancer, propelling the advancements of targeted therapies and drug delivery systems. With its profound impact on medical progress, (-)-2,3-O-Isopropylidene-D-threitol emerges as an unsurpassable cornerstone within the realm of biomedicine. Synonyms: 2,3-O-Isopropylidene-D-threitol; (4R,5R)-(-)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol; (4R,5R)-4,5-Bis(hydroxymethyl)-2,2-dimethyl-1,3-dioxolane. CAS No. 73346-74-4. Molecular formula: C7H14O4. Mole weight: 162.18. | |
| (+)-2,3-O-ISOPROPYLIDENE-D-THREITOL 1,4-DIMETHANE SULFONATE | Heterocyclic Organic Compound. Alternative Names: (+)-2,3-O-ISOPROPYLIDENE-D-THREITOL 1,4-DIMETHANE SULFONATE;(+)-2,3-O-Isopropylidene-D-threitol-2,3-dimethanesulfonate;(+)-2,3-O-Isopropylidene-D-threitol2,3-dimethanesulfonate. CAS No. 109281-59-6. Molecular formula: C9H18O8S2. Mole weight: 318.36442. Purity: 0.96. IUPACName: [(4R,5R)-2,2-dimethyl-5-(methylsulfonyloxymethyl)-1,3-dioxolan-4-yl]methyl methanesulfonate. Canonical SMILES: CC1 (OC (C (O1)COS (=O) (=O)C)COS (=O) (=O)C)C. Catalog: ACM109281596. |  |
| 2,3-O-Isopropylidene-L-threitol | 2,3-O-Isopropylidene-L-threitol, a highly significant reagent in the realm of pharmaceuticals and therapeutics, unfolds as a pivotal player in the manufacture of medicinal drugs. Its indisputable significance lies in its indispensable involvement in the synthesis of anti-diabetic medications, striving to counteract the ravages of elevated blood sugar levels. Synonyms: (+)-2,3-O-Isopropylidene-L-threitol; ((4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-diyl)dimethanol; 2,3-o-isopropylidene-l-threitol; [(4S,5S)-5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]methanol; MFCD00063761; (+)-2,3,O-Isopropylidene-L-threitol; (4S,5S)-(+)-4,5-Bis(hydroxymethyl)-2,2-dimethyl-1,3-dioxolane; 86992-57-6; 1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-, (4S,5S)-; SCHEMBL292538; (4S,5S)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol; 2,3-O-Isoproylidene-L-threitol; DTXSID40964859; INVRLGIKFANLFP-WDSKDSINSA-N; AKOS015899228; AS-69880; CS-0097523; I0376; T72536; A854539; Q63408895; 1,3-Dioxolane-4,5-dimethanol,2,2-dimethyl-, (4S,5S)-; (4S,5S)-(+)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol; (4S,5S)-4,5-BIS-(HYDROXYMETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE; (4S,5S)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol, >=97.0% (sum of enantiomers, GC). CAS No. 50622-09-8. Molecular formula: C7H14O4. Mole weight: 162.18. | |
| 2,3-O-Isopropylidene-L-threitol | 2,3-O-Isopropylidene-L-threitol is an intermediate in the synthesis of versicolactone compounds. Group: Biochemicals. Grades: Highly Purified. CAS No. 50622-09-8. Pack Sizes: 2.5g, 10g. Molecular Formula: C7H14O4. US Biological Life Sciences. | Worldwide |
| (-)-2,3-O-Isopropylidene-L-threitol-1,4-dimethane sulfonate | (-)-2,3-O-Isopropylidene-L-threitol-1,4-dimethane sulfonate stands as a cornerstone in the biomedical realm. It exerts its significance in the synthesis of an array of medicinal agents and pharmaceutics. Synonyms: [(4s,5s)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]dimethanediyl dimethanesulfonate; [(4S,5S)-2,2-dimethyl-5-(methylsulfonyloxymethyl)-1,3-dioxolan-4-yl]methyl methanesulfonate; (-)-2,3-O-Isopropylidene-L-threitol-1,4-dimethane sulfonate; (-)-2,3-O-ISOPROPYLIDENE-L-THREITOL 1,4-DIMETHANE SULFONATE; NSC60499; 1,3-Dioxolane-4,5-dimethanol,2,2-dimethyl-, 4,5-dimethanesulfonate, (4S,5S)-1111. CAS No. 4248-74-2. Molecular formula: C9H18O8S2. Mole weight: 318.37. | |
| 2,4-O-Benzylidene-1-O-tosyl-D-threitol | 2,4-O-Benzylidene-1-O-tosyl-D-threitol, a chemical entity, finds application in the realm of neurodegenerative disorders, such as Alzheimer's and Parkinson's. It manifests its potential through inhibition of certain enzymes, catalyzing beta-amyloid plaque formation, which is known to augment disease pathogenesis. This compound, hence, displays prospective therapeutic benefits in the management of aforementioned neurological maladies. | |
| 2,4-O-Benzylidene-D-threitol | 2,4-O-Benzylidene-D-threitol, a chemical entity of significant interest, has been shown to display potential antiviral activities. Its effectiveness in attenuating respiratory viruses, including Influenza virus and SARS-CoV, highlights its potency as a tool for potential treatments. The mechanism of function of this agent involves thwarting the virus replication process and effectively curtailing the viral infection's gravity. | |
| Dithiothreitol (DTT) | Dithiothreitol (DTT) is the common name for a small-molecule redox reagent known as Cleland's reagent. DTT's oxidized form is a disulfide-bonded 6-membered ring. Its name derives from the four-carbon sugar, threose. DTT has an epimeric ('sister') compound, dithioerythritol (DTE).DTT is an unusually strong reducing agent, owing to its high conformational propensity to form a six-membered ring with an internal disulfide bond. It has a redox potential of -0.33 V at pH 7. The reduction of a typical disulfide bond proceeds by two sequential thiol-disulfide exchange reactions and is illustrated below. The intermediate mixed-disulfide state is unstable (i.e., poorly populated) because the...ting."DTT is frequently used to reduce the disulfide bonds of proteins and, more generally, T... Group: Biochemicals. Alternative Names: Cleland's reagent;; (2R,3R)-rel-1,4-Dimercapto-2,3-butanediol; (±)-1,4-Dimercapto-2,3-butanediol; (±)-Dithiothreitol; 1,4-Dithio-DL-threitol; 1,4-Dithiothreitol; DL-1,4-Dimercapto-2,3-dihydroxybutane; DL-1,4-Dithiothreitol; DL-Dithiothreitol; Sputolysin; WR 34678; threo-1,4-Dimercapto-2,3-butanediol; threo-2,3-Dihydroxy-1,4-butanedithiol; threo-2,3-Dihydroxy-1,4-dithiolbutane. Grades: Molecular Biology Grade. CAS No. 3483-12-3. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C4H10O2S2, Molecular Weight: 154.24. US Biological Life Sciences. | Worldwide |
| D-Threitol | D-threitol serves as a antifreeze agent in the Alaskan beetle Upis ceramboides. Uses: Scientific research. Group: Natural products. CAS No. 2418-52-2. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-W012846. |  |
| D-(+)-Threitol | D-(+)-Threitol is a multifaceted commodity extensively adopted realm, used for studying diverse afflictions such as diabetes, cardiovascular maladies and neurodegenerative states. Synonyms: (2R,3R)-1,2,3,4-Butanetetrol. Grades: ≥98%, ≥95%e.e. CAS No. 2418-52-2. Molecular formula: C4H10O4. Mole weight: 122.12. | |
| D-threitol dehydrogenase (NAD+) | The enzyme, characterized from the bacterium Mycobacterium smegmatis, participates in the degradation of D-threitol. Group: Enzymes. Synonyms: dthD (gene name). Enzyme Commission Number: EC 1.1.1.403. 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-0325; D-threitol dehydrogenase (NAD+); EC 1.1.1.403; dthD (gene name). Cat No: EXWM-0325. |  |
| L-Threitol | L-Threitol is a useful synthetic intermediate. It was used to synthesize novel aza-sugar-based metalloproteinase MMP/ADAM inhibitors. It is also a diastereomer of Erythritol which is a food additive. Synonyms: 1,3,5-orthoformate-myo-inositol; meso-D-myo-inositol-1,3,5-O-orthoformate; L-1,2,3,4-Butanetetrol; myo-inositol 1,3,5-monoorthoformate; (2s,3s)-butane-1,2,3,4-tetraol. Grades: ≥ 95%. CAS No. 2319-57-5. Molecular formula: C4H10O4. Mole weight: 122.12. | |
| 1,4-Anhydro-D-erythritol | 1,4-Anhydro-D-erythritol, a versatile sugar alcohol, is employed in the synthesis of a plethora of compounds, from biodegradable plastics to pharmaceuticals. The potential scope of its applications extends towards the therapeutic treatment of diabetes, owing to its hypoglycemic effects. Its antimicrobial properties have been extensively scrutinized, with studies targeting its potential employment in countering streptococcal bacteria responsible for dental caries. Synonyms: 1,4-Anhydroerythritol; cis-Tetrahydrofuran-3,4-diol; (3R,4S)-tetrahydrofuran-3,4-diol; (3R,4S)-oxolane-3,4-diol; 1,4-Anhydro-D-erythritol; Erythritan; (-)-1,4-ANHYDRO-L-THREITOL; (3~{S},4~{R})-oxolane-3,4-diol; 3,4-Furandiol, tetrahydro-, (3R,4S)-rel-; cis-3,4-Dihydroxytetrahydrofuran; MFCD00075210; cis-3,4-Tetrahydrofurandiol; SCHEMBL196429; 1 pound not4-Anhydroerythritol; 1,4-Anhydroerythritol, 95%; SSYDTHANSGMJTP-ZXZARUISSA-N; DTXSID401318325; AMY16786; (3R, 4S)-tetrahydrofuran-3,4-diol; AKOS016011113; AS-33974; CS-0049648; EN300-195706; P15622; A872684; IJ8. CAS No. 4358-64-9. Molecular formula: C4H8O3. Mole weight: 104.10. | |
| alditol oxidase | The enzyme from Streptomyces sp. IKD472 and from Streptomyces coelicolor is a monomeric oxidase containing one molecule of FAD per molecule of protein. While xylitol (five carbons) and sorbitol (6 carbons) are the preferred substrates, other alditols, including L-threitol (four carbons), D-arabitol (five carbons), D-galactitol (six carbons) and D-mannitol (six carbons) can also act as substrates, but more slowly. Belongs in the vanillyl-alcohol-oxidase family of enzymes. Group: Enzymes. Synonyms: xylitol oxidase; xylitol:oxygen oxidoreductase; AldO. Enzyme Commission Number: EC 1.1.3.41. CAS No. 177322-52-0. 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-0414; alditol oxidase; EC 1.1.3.41; 177322-52-0; xylitol oxidase; xylitol:oxygen oxidoreductase; AldO. Cat No: EXWM-0414. | |
| D-erythrulose 4-kinase | The enzyme, characterized from the bacterium Mycobacterium smegmatis, participates in the degradation of erythritol and D-threitol. Group: Enzymes. Synonyms: derK (gene name). Enzyme Commission Number: EC 2.7.1.210. 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-3046; D-erythrulose 4-kinase; EC 2.7.1.210; derK (gene name). Cat No: EXWM-3046. | |
| L-erythrulose 4-kinase | The enzyme, characterized from the bacterium Mycobacterium smegmatis, participates in the degradation of L-threitol. Group: Enzymes. Synonyms: lerK (gene name). Enzyme Commission Number: EC 2.7.1.209. 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-3044; L-erythrulose 4-kinase; EC 2.7.1.209; lerK (gene name). Cat No: EXWM-3044. | |
| L-erythrulose 4-phosphate epimerase | The enzyme, characterized from the bacterium Mycobacterium smegmatis, participates in the degradation of L-threitol. Group: Enzymes. Synonyms: lerI (gene name). Enzyme Commission Number: EC 5.1.3.39. 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-5426; L-erythrulose 4-phosphate epimerase; EC 5.1.3.39; lerI (gene name). Cat No: EXWM-5426. | |
| (S,S)-(-)-1,4-Dimethoxy-2,3-butanediol | (S,S)-(-)-1,4-Dimethoxy-2,3-butanediol, an intriguing chemical compound renowned for its multifaceted biomedical potential, assumes a pivotal role in synthesizing an extensive range of formidable pharmaceutical intermediates. Synonyms: (-)-1,4-Di-O-methyl-L-threitol. CAS No. 50622-10-1. Molecular formula: C6H14O4. Mole weight: 150.17. | |
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