A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Degradation product of Venlafaxine. Venlafaxine impurity. Group: Biochemicals. Alternative Names: β -1-Cyclohexen-1-yl-4-methoxy-N, N-dimethyl Benzene ethanamine. Grades: Highly Purified. CAS No. 93413-57-1. Pack Sizes: 1mg. US Biological Life Sciences.
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Dehydro Warfarin
One of the impurities of Warfarin, which is a kind of Coumarin anticoagulant. Synonyms: Dehydrowarfarin; 4-Hydroxy-3-(3-oxo-1-phenyl-1-buten-1-yl)-2H-1-benzopyran-2-one; NSC 289346. CAS No. 67588-18-5. Molecular formula: C19H14O4. Mole weight: 306.32.
Dehydroxy- (2-methyl-4- (2-methylbenzamido) benzoate) Tolvaptan is the impurity of the drug Tolvaptan (T536650), which is a selective, competitive arginine vasopressin V2 receptor antagonist used to treat hyponatremia (low blood sodium levels) associated with congestive heart failure, cirrhosis, and the syndrome of inappropriate antidiuretic hormone (SIADH). Group: Biochemicals. Grades: Highly Purified. CAS No. 1580889-36-6. Pack Sizes: 1mg, 5mg. Molecular Formula: C42H36ClN3O5, Molecular Weight: 698.21. US Biological Life Sciences.
Worldwide
Dehydroxyamino Oxamflatin Acid
Intermediate in the synthesis of Oxamflatin. Group: Biochemicals. Alternative Names: (2E) -5-[3-[ (Phenylsulfonyl) amino]phenyl]-2-penten-4-ynoic Acid. Grades: Highly Purified. CAS No. 151720-90-0. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Dehydroxy bisoprolol
Dehydroxy bisoprolol. Group: Biochemicals. Alternative Names: 3-[4-[[2- (1-Methylethoxy) ethoxy]methyl]phenoxy]-N- (1-methylethyl) -2-propen-1-amine. Grades: Highly Purified. CAS No. 1217245-60-7. Pack Sizes: 500ug, 1mg, 2mg, 5mg, 10mg. Molecular Formula: C18H29NO3. US Biological Life Sciences.
Worldwide
Dehydroxy Bromocelecoxib
Dehydroxy Bromocelecoxib is an intermediate in the synthesis of Celecoxib (C251000), a selective cyclooxygenase-2 (COX-2) inhibitor with known anti-inflammatory properties. Group: Biochemicals. Alternative Names: 4-[5-[4-(Bromomethyl)phenyl]-3-(trifluoromethyl)-1H-pyrazol-1-yl]-benzenesulfonamide. Grades: Highly Purified. CAS No. 170570-75-9. Pack Sizes: 50mg. US Biological Life Sciences.
Dehydroxydehydro Terfenadine. Group: Biochemicals. Alternative Names: 1-[4-[4-(1,1-Dimethylethyl)phenyl]-3-buten-1-yl]-α,α-diphenyl-4-piperidinemethanol. Grades: Highly Purified. Pack Sizes: 100mg. Molecular Formula: C32H39NO, Molecular Weight: 453.66. US Biological Life Sciences.
Worldwide
Dehydroxy Idarubicin
Dehydroxy mirabegron
Dehydroxy mirabegron is an impurity of mirabegron, a medication used to treat overactive bladder. Synonyms: 2-Amino-N-[4-[2-[(2-phenylethyl)amino]ethyl]phenyl]-4-Thiazoleacetamide. CAS No. 1581284-82-3. Molecular formula: C21H24N4OS. Mole weight: 380.5.
Dehydroxy Mirabegron Hydrochloride Salt
Dehydroxy Mirabegron is an impurity of Mirabegron, a potent bladder relaxant and reagent for diabetes remedy. Synonyms: 2-Amino-N-[4-[2-[(2-phenylethyl)amino]ethyl]phenyl]-4-Thiazoleacetamide Hydrochloride Salt. Grades: > 95%. CAS No. 1581284-79-8. Molecular formula: C21H24N4OS HCl. Mole weight: 416.975.
Dehydroxy ractopamine
Dehydroxy ractopamine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Dehydroxy Optaflexx; Dehydroxy Paylean; Dehydroxy Topmax 9. Product Category: Heterocyclic Organic Compound. Appearance: Off-White Solid. CAS No. 1246816-72-7. Molecular formula: C18H23NO2. Mole weight: 285.38. Purity: 0.96. IUPACName: 4-[3-[2-(4-hydroxyphenyl)ethylamino]butyl]phenol. Canonical SMILES: CC(CCC1=CC=C(C=C1)O)NCCC2=CC=C(C=C2)O. Product ID: ACM1246816727. Alfa Chemistry ISO 9001:2015 Certified.
Dehydroxy Ractopamine
Ractopamine derivative. Ractopamine is a veterinary drug, now considered illegal. A beta-adrenoceptor agonist, binding to muscle cell membrane receptors, resulting in increased protein synthesis and increased muscle fibers. Group: Biochemicals. Alternative Names: Dehydroxy Optaflexx; Dehydroxy Paylean; Dehydroxy Topmax 9. Grades: Highly Purified. CAS No. 1246816-72-7. Pack Sizes: 10mg. US Biological Life Sciences.
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Dehydroxy Ractopamine-d6 (Major) Hydrochloride Salt
Labeled Dehydroxy Ractopamine. Monoclonal antibody hybridoma immunoassay Ractopamine. Ractopamine is a veterinary drug, now considered illegal. A beta-adrenoceptor agonist, binding to muscle cell membrane receptors, resulting in increased protein synthesis and increased muscle fibers. Group: Biochemicals. Alternative Names: 4- [3- [ [2- (4-Hydroxyphenyl) ethyl] amino] butyl] phenol-d6 Hydrochloride Salt. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Dehydroxy Terfenadine
Dehydroxy Terfenadine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg. Molecular Formula: C32H41NO, Molecular Weight: 455.67. US Biological Life Sciences.
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Dehydroxytramadol Hydrochloride
Dehydroxytramadol Hydrochloride is an impurity of Tramadol Hydrochloride (T712500), an analgesic. Group: Biochemicals. Grades: Highly Purified. CAS No. 66170-32-9. Pack Sizes: 10mg, 100mg. Molecular Formula: C16H23NO; (HCl), Molecular Weight: 245.363645999999. US Biological Life Sciences.
Worldwide
Dehydrozingerone
Dehydrozingerone (Compound 10), a structural half analogue of Curcumin (HY-N0005), is a phenolic compound with antibacterial, anticancer, antioxidant, anti-Alzheimers and antifungal activity, which is isolated from ginger ( Zingiber officinale ) rhizomes. Dehydrozingerone shows moderate inhibitory activities on the secretion of HBsAg in HepG 2 cells with an IC 50 value of 0.50 mM [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1080-12-2. Pack Sizes: 5 g; 10 g; 25 g. Product ID: HY-134635.
Deiodo Amiodarone. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Amiodarone Hydrochloride Imp. C (EP), Amiodarone Hydrochloride Imp. C (EP) as Hydrochloride, Amiodarone Imp. C (EP), (2-Butylbenzofuran-3-yl)[4-[2-(diethylamino)ethoxy]-3-iodo-phenyl]methanone Hydrochloride. Pack Sizes: 10MG. IUPAC Name: (2-butyl-1-benzofuran-3-yl)-[4-[2-(diethylamino)ethoxy]-3-iodophenyl]methanone;hydrochloride. Molecular formula: C25H30INO3.ClH. Mole weight: 555.88. Catalog: APS007355. SMILES: Cl.CCCCc1oc2ccccc2c1C(=O)c3ccc(OCCN(CC)CC)c(I)c3. Format: Neat. Shipping: Room Temperature.
De-Ionised Distilled Water
5lt Pack Size. Group: Analytical Reagents, Solvents, Water Analysis. Formula: H_{2}O. CAS No. 7732-18-5. Prepack ID 34750941-5lt. Molecular Weight 18.0153. See USA prepack pricing.
Deisovalerylblastmycin
Deisovalerylblastmycin is an antimycin antibiotic produced by Streptomyces sp. 5140-A. It has a strong resistance to the rice pear (Magnae grisea) activity, with a MIC of 0.8 μg/mL. Synonyms: Deisovalerylblastmycin; Blastmycin, deisovalery-; N-(7-Butyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-3-formamidosalicylamide; Salicylamide, N-(7-butyl-4,9-dimethyl-2,6-dioxo-8-hydroxy-1,5-dioxonan-3-yl)-3-formamido-. Grades: >98%. CAS No. 60504-95-2. Molecular formula: C21H28N2O8. Mole weight: 436.45.
DEL22379
DEL22379, also known as NPX800, is ERK dimerization inhibitor. DEL-22379 has been reported to inhibit ERK dimerization which was unaffected by drug-resistant mechanism reactivating the ERK signaling. Uses: Designed for use in research and industrial production. Additional or Alternative Names: DEL22379; DEL-22379; DEL 22379; NPX800; NPX 800; NPX-800. Product Category: Inhibitors. Appearance: To be determined. CAS No. 1693734-80-3. Molecular formula: C26H28N4O3. Mole weight: 444.53. Purity: >98%. IUPACName: N-[2,3-Dihydro-3-[(5-methoxy-1H-indol-3-yl)methylene]-2-oxo-1H-indol-5-yl]-1-piperidinepropanamide. Canonical SMILES: O=C(NC1=CC2=C(NC(/C2=C/C3=CNC4=C3C=C(OC)C=C4)=O)C=C1)CCN5CCCCC5. Product ID: ACM1693734803. Alfa Chemistry ISO 9001:2015 Certified.
DEL-22379 is a water-soluble ERK dimerization inhibitor with IC50 of ?0.5 μM. Synonyms: DEL-22379; DEL 22379; DEL22379. Grades: 98%. CAS No. 181223-80-3. Molecular formula: C26H28N4O3. Mole weight: 444.53.
Delactamimipenem Monosodium (Mixture of Diastereomers)
Delactamimipenem Monosodium (Mixture of Diastereomers). Group: Biochemicals. Alternative Names: 5-Carboxysodium-3, 4-dihydro-α - (1-hydroxyethyl) -4-[[2-[ (iminomethyl) amino]ethyl]thio]-2H-Pyrrole-2-acetic Acid; Imipenem Amino Acid. Grades: Highly Purified. Pack Sizes: 10mg. Molecular Formula: C12H18N3NaO5S, Molecular Weight: 339.34. US Biological Life Sciences.
Worldwide
Delafloxacin
Delafloxacin is a fluoroquinolone antibiotic that demonstrates extremely high potency against a wide range of bacteria in vitro, including levofloxacin-resistant strains of S. pneumoniae and methicillin-resistant S. aureus. It has an anionic structure, which enhances its potency in acidic environments and in skin and soft tissue infections. Uses: Anti-infective agents. Synonyms: ABT-492; RX-3341; WQ-3034; Abt 492. Grades: 98%. CAS No. 189279-58-1. Molecular formula: C18H12ClF3N4O4. Mole weight: 440.8.
Delafloxacin (RX-3341; WQ-3034; ABT492) is a broad-spectrum fluoroquinolone antibiotic. Delafloxacin has a broad spectrum of activity that includes drug-resistant Staphylococcus aureus , Streptococcus pneumoniae , and Klebsiella pneumonia [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RX-3341; WQ-3034; ABT492. CAS No. 189279-58-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-14814.
delafloxacin meglumine
Delafloxacin meglumine is a fluoroquinolone that can be used to treat acute bacterial skin and skin structure infections (ABSSSI) in adult patients. Studies indicated that it has excellent tolerance and low toxicity to liver and kidney. Uses: The treatment of cute bacterial skin and skin structure infections (absssi). Synonyms: Baxdela; 1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-7-(3-hydroxyazetidin-1-yl)-4-oxoquinoline-3-carboxylic acid;(2R,3R,4R,5S)-6-(methylamino)hexane-1,2,3,4,5-pentol. CAS No. 352458-37-8. Molecular formula: C25H29ClF3N5O9. Mole weight: 635.978.
Delafloxacin meglumine
Delafloxacin meglumine (ABT492 meglumine; RX-3341 meglumine; WQ-3034 meglumine) is a broad-spectrum fluoroquinolone antibiotic. Delafloxacin has a broad spectrum of activity that includes drug-resistant Staphylococcus aureus , Streptococcus pneumoniae , and Klebsiella pneumonia [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT492 meglumine; RX-3341 meglumine; WQ-3034 meglumine. CAS No. 352458-37-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14814A.
Delamanid
Delamanid is used for the treatment of multi-drug-resistant tuberculosis. It functions by blocking the synthesis of mycolic acids in Mycobacterium tuberculosis, the organism which causes tuberculosis, thus destabilising its cell wall. Uses: The treatment of multi-drug-resistant tuberculosis. Synonyms: OPC-67683; OPC 67683; OPC67683; Deltyba; (2R)-2-methyl-6-nitro-2-[[4-[4-[4-(trifluoromethoxy)phenoxy]piperidin-1-yl]phenoxy]methyl]-3H-imidazo[2,1-b][1,3]oxazole. Grades: ≥98%. CAS No. 681492-22-8. Molecular formula: C25H25F3N4O6. Mole weight: 534.492.
Delamanid
25mg Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C25H25F3N4O5. CAS No. 681492-22-8. Prepack ID 90026659-25mg. Molecular Weight 534.48. See USA prepack pricing.
Delamanid
Delamanid, a newer mycobacterial cell wall synthesis inhibitor, inhibits the synthesisi of mucolic acids [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: OPC-67683. CAS No. 681492-22-8. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10846.
Delaminomycin A
Delaminomycin A is an extracellular Matrix receptor antagonist and immunomodulator produced by Streptomyces albulus MJ202-72F3. It inhibits cell adhesion ECM (Extracellular matrix), reduces immune response activity, and inhibits Gram-positive bacteria. Synonyms: 2H-Imidazol-2-one, 3-((2-(2,8-dihydroxy-7-methyl-3,5-decadienyl)-1,2,4a,5,6,7,8,8a-octahydro-1,6,8-trimethyl-1-naphthalenyl)carbonyl)-1,5-dihydro-4,5-dihydroxy-5-methoxy-; 2H-Pyrrol-2-one, 1,5-dihydro-4,5-dihydroxy-3-((2-(2,8-dihydroxy-7-methyl-3,5-decadienyl)-1,2,4a,5,6,7,8,8a-octahydrox-1,6,8-trimethyl-1-naphthalenyl)carbonyl)-. CAS No. 149779-38-4. Molecular formula: C29H43NO6. Mole weight: 501.65.
Delaminomycin B
Delaminomycin B is an extracellular Matrix receptor antagonist and immunomodulator produced by Streptomyces albulus MJ202-72F3. It inhibits cell adhesion ECM (Extracellular matrix), reduces immune response activity, and inhibits Gram-positive bacteria. CAS No. 149779-39-5. Molecular formula: C30H45NO6. Mole weight: 515.68.
Delaminomycin C
Delaminomycin C is an extracellular Matrix receptor antagonist and immunomodulator produced by Streptomyces albulus MJ202-72F3. It inhibits cell adhesion ECM (Extracellular matrix), reduces immune response activity, and inhibits Gram-positive bacteria. Synonyms: (3Z)-3-[[2-[(3E,5E)-2,8-dihydroxy-7-methyldeca-3,5-dienyl]-1,6,8-trimethyl-4a,5,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-hydroxymethylidene]pyrrolidine-2,4-dione; 2H-Imidazol-2-one, 3-((2-(2,8-dihydroxy-7-methyl-3,5-decadienyl)-1,2,4a,5,6,7,8,8a-octahydro-1,6,8-trimethyl-1-naphthalenyl)carbonyl)-1,5-dihydro-4-hydroxy-. CAS No. 149779-40-8. Molecular formula: C29H43NO5. Mole weight: 485.65.
Delanzomib
Delanzomib is an orally active proteasome inhibitor. Delanzomib has been shown to down-modulate NF-κB, induce apoptosis, inhibit angiogenesis and M-CSF-RANKL-induced osteoclastogenesis. Group: Biochemicals. Alternative Names: [ (1R) -1- [ [ (2S, 3R) -3-Hydroxy-1-oxo-2- [ [ (6-phenyl-2-pyridinyl) carbonyl] amino] butyl] amino] -3-methylbutyl] boronic Acid; CEP 18770; CIP 18770; CT 47098; NPH 007098; [(1R)-1-[[(2S,3R)-3-Hydroxy-2-[[(6-phenylpyridin-2-yl)carbonyl]amino]-1-oxobutyl]amino]-3-methylbutyl]boronic Acid. Grades: Highly Purified. CAS No. 847499-27-8. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
Delanzomib
Delanzomib, also known as CEP-18770, is An orally bioavailable synthetic P2 threonine boronic acid inhibitor of the chymotrypsin-like activity of the proteasome, with potential antineoplastic activity. Proteasome inhibitor CEP 18770 represses the proteasomal degradation of a variety of proteins, including inhibitory kappaBalpha (IkappaBalpha), resulting in the cytoplasmic sequestration of the transcription factor NF-kappaB; inhibition of NF-kappaB nuclear translocation and transcriptional up-regulation of a variety of cell growth-promoting factors; and apoptotic cell death in susceptible tumor cell populations. In vitro studies indicate that this agent exhibits a favorable cytotoxicity profile toward normal human epithelial cells, bone marrow progenitors, and bone marrow-derived stromal cells relative to the proteasome inhibitor bortezomib. The intracellular protein IkappaBalpha functions as a primary inhibitor of the proinflammatory transcription factor NF-kappaB. Uses: Proteasome inhibitors. Synonyms: CEP18770; CEP 18770; CEP-18770; Delanzomib. CAS No. 847499-27-8. Molecular formula: C21H28BN3O5. Mole weight: 413.27.
Delapril
Delapril. Uses: Designed for use in research and industrial production. Additional or Alternative Names: DELAPRIL;Alindapril;Glycine, N-(2,3-dihydro-1H-inden-2-yl)-N-[N-[1-(ethoxycarbonyl)-3-phenylpropyl]-L-alanyl]-, (S)-;Glycine, N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]-L-alanyl-N-(2,3-dihydro-1H-inden-2-yl)-;Indalapril;N-[N-[(S)-1-(Ethoxycarbonyl)-3-phe. Product Category: Heterocyclic Organic Compound. CAS No. 83435-66-9. Molecular formula: C26H32N2O5. Mole weight: 452.548. Product ID: ACM83435669. Alfa Chemistry ISO 9001:2015 Certified.
DelapRil HCl
DelapRil HCl. Group: Biochemicals. Grades: Highly Purified. CAS No. 83435-67-0. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences.
Worldwide
Delapril hydrochloride
Delapril Hydrochloride is the hydrochloride salt form of delapril, which is a lipophilic, non-sulfhydryl angiotensin-converting enzyme (ACE) inhibitor with antihypertensive effect. Synonyms: Alindapril hydrochloride; Delapril HCl; CV 3317; UNII-2SMM3M5ZMH. CAS No. 83435-67-0. Molecular formula: C26H33ClN2O5. Mole weight: 489.
Delapril hydrochloride
Delapril hydrochloride is an angiotensin-converting enzyme ( ACE ) inhibitor for the treatment of cardiovascular diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 83435-67-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107337.
De-(L-Asn)-L-Gln Vancomycin B
An impurity of Vancomycin. Vancomycin is a glycopeptide antibiotic for the treatment of gram-positive bacteria. Vancomycin exhibits an antibacterial effect by inhibiting bacterial cell wall synthesis. Molecular formula: C67H77Cl2N9O24 HCl. Mole weight: 1499.77.
Delavinone
Delavinone is an alkaloid isolated from the bulbs of Fritillaria yuminensis. Synonyms: Puqiedinone; Sinpeinine A; 3-Hydroxycevan-6-one. Grades: >98%. CAS No. 96997-98-7. Molecular formula: C27H43NO2. Mole weight: 413.646.
Delavirdine
Delavirdine. Group: Biochemicals. Alternative Names: N-[2-[[4-[3-[(1-Methylethyl)amino]-2-pyridinyl]-1-piperazinyl]carbonyl]-1H-indol-5-yl]methanesulfonamide; BHAP-U 90152; U-90152. Grades: Highly Purified. CAS No. 136817-59-9. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C22H28N6O3S. US Biological Life Sciences.
Worldwide
Delavirdine
Delavirdine is a non-nucleoside reverse transcriptase inhibitor (NNRTI). It is used as part of highly active antiretroviral therapy (HAART) for the treatment of human immunodeficiency virus (HIV) type 1. Synonyms: U 90152; U90152; U-90152; BHAP-U 90152. Grades: >98%. CAS No. 136817-59-9. Molecular formula: C22H28N6O3S. Mole weight: 456.56.
Delavirdine
Delavirdine (U 90152) is a potent, highly specific and orally active non-nucleoside reverse transcriptase inhibitor (NNRTI). Delavirdine selectively inhibits HIV-1 reverse transcriptase (RT) ( IC 50=0.26 μM) over DNA polymerase α (IC 50=440 μM) and polymerase δ (IC 50 >550 μM). Delavirdine is an inhibitor of HIV-1 replication and can can be used for the study of AIDs [1]. Uses: Scientific research. Group: Natural products. Alternative Names: U 90152; BHAP-U 90152. CAS No. 136817-59-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10571.
Delavirdine mesylate
Delavirdine (U 90152) mesylate is a potent, highly specific and orally active non-nucleoside reverse transcriptase inhibitor (NNRTI). Delavirdine mesylate selectively inhibits HIV-1 reverse transcriptase (RT) ( IC 50=0.26 μM) over DNA polymerase α (IC 50=440 μM) and polymerase δ (IC 50 >550 μM). Delavirdine mesylate is an inhibitor of HIV-1 replication and can can be used for the study of AIDs [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: U 90152 mesylate; BHAP-U 90152 mesylate. CAS No. 147221-93-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10571A.
Delavirdine is a non-nucleoside reverse transcriptase inhibitor (NNRTI). It is used as part of highly active antiretroviral therapy (HAART) for the treatment of human immunodeficiency virus (HIV) type 1. Uses: Anti-hiv agents. Synonyms: Delavirdine mesylate; Rescriptor; U-90152S; U 90152S; U90152S; U 90152T U-90152T; U90152T; U 90152E; U-90152E; U90152E. Grades: >98%. CAS No. 147221-93-0. Molecular formula: C23H32N6O6S2. Mole weight: 552.67.
Delavirdine mesylate
Delavirdine mesylate. Group: Biochemicals. Alternative Names: N-[2-[[4-[3-[(1-Methylethyl)amino]-2-pyridinyl]-1-piperazinyl]carbonyl]-1H-indol-5-yl]methanesulfonamide methanesulfonate; U-90152S. Grades: Highly Purified. CAS No. 147221-93-0. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C23H32N6O6S2. US Biological Life Sciences.