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Sumanirole maleate, also referred as PNU 95666E or U95666E, is a high affinity D2 receptor full agonist that shows >200-fold selectivity over dopamine receptor subtypes (Ki values are 9.0, 1940, >2190 and >7140 for D2, D3, D4 and D1 receptors respectively) with an ED50 of about 46 nM. Sumanirole was developed for the treatment of Parkinson's disease and restless leg syndrome. While it has never been approved for medical use. Sumanirole is a highly valuable tool compound for basic research to identify neurobiological mechanisms that are based on a dopamine D2-linked (vs. D1, D3, D4, and D5-linked) mechanism of action. Synonyms: 5,6-dihydro-5-(methylamino)-4H-imidazo(4,5,1ij)-quinolin-2(1H)-one (Z)-2-butenedioate; PNU-95666; PNU95666; PNU 95666; Sumanirole; U 95666E; U-95666E; U95666E. CAS No. 179386-44-8. Molecular formula: C15H17N3O5. Mole weight: 319.31.
Sumanirole maleate
Sumanirole maleate (U-95666E; PNU-95666E) is a highly selective D2 receptor full agonist with an ED 50 of about 46 nM. Sumanirole plays an important role in the research of Parkinson's disease and restless leg syndrome [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: U-95666E; PNU-95666. CAS No. 179386-44-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-70081A.
Sumanirole Maleate
Sumanirole is a high affinity D2 receptor agonist (EC50 values are between 17 and 75 nM in cell-based assays). Sumanirole displays >200-fold selectivity for the D2 receptor against other dopamine receptor subtypes (Ki values are 9.0, 1940, >2190 and >7140 for D2, D3, D4 and D1 receptors respectively). Sumanirole exhibits anti-Parkinsonian activity similar to Ropinirole. Group: Biochemicals. Alternative Names: (5R)-5,6-Dihydro-5-(methylamino)-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (2Z)-2-Butenedioate; (R)-5,6-Dihydro-5-(methylamino)-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (2Z)-2-Butenedioate. Grades: Highly Purified. CAS No. 179386-43-7. Pack Sizes: 10mg. US Biological Life Sciences.
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Sumatriptan
Sumatriptan (GR 43175) is an orally active 5-HT1 receptor agonist with IC 50 s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT 1D , 5-HT 1B and 5-HT 1F receptors, respectively. Sumatriptan can be used for migraine headache research [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GR 43175 free base. CAS No. 103628-46-2. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-B0121B.
Sumatriptan
Sumatriptan is a Serotonin-1b and Serotonin-1d Receptor Agonist that acts selectively at 5HT1 receptors. It is a sulfonamide triptan with vasoconstrictor activity. It selectively binds to and activates serotonin 5-HT1D receptors in the central nervous system, thus constricts cerebral blood vessels. It may also relieve vascular headaches by decreasing the release of vasoactive neuropeptides from perivascular trigeminal axons in the dura mater. It is a medication used for the treatment of migraine headaches. Uses: Sumatriptan is a medication used for the treatment of migraine headaches. Synonyms: Imitrex; Sumatran; Sumax; Sumatriptanum; 1-[3-[2-(Dimethylamino)ethyl]-1H-indol-5-yl]-N-methylmethanesulfonamide; (3-[2-(Dimethylamino)ethyl]-1H-indol-5-yl)-N-methylmethanesulfonamide; GR-43175; GR43175. Grades: 95%. CAS No. 103628-46-2. Molecular formula: C14H21N3O2S. Mole weight: 295.40.
A serotonin 5HT1-receptor agonist. Antimigraine. Group: Biochemicals. Alternative Names: 3-[2-(Dimethyl-d6-amino)-ethyl]-N-methyl-1H-indole-5-methanesulfonamide. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
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Sumatriptan-d6 succinate
Sumatriptan-d6 succinate is the deuterium labeled Sumatriptan succinate. Sumatriptan succinate is an orally active 5-HT1 receptor agonist with K i s of 17 nM, 27 nM and 100 nM for 5-HT1D , 5-HT1B and 5-HT1A receptors , respectively. Sumatriptan succinate can be used for migraine headache research [1] [2] [3]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: GR 43175C-d6. CAS No. 1215621-31-0. Pack Sizes: 1 mg. Product ID: HY-B0121BS.
Sumatriptan-d6 succinate
Sumatriptan-d6 succinate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3-[2-(Dimethyl-d6-amino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Succinate, Imigran, Imitrex. Product Category: Heterocyclic Organic Compound. CAS No. 1215621-31-0. Molecular formula: C18H21D6N3O6S. Mole weight: 419.53. Purity: 0.96. IUPACName: 1-[3-[2-[bis(trideuteriomethyl)amino]ethyl]-1H-indol-5-yl]-N-methylmethanesulfonamide;butanedioic acid. Canonical SMILES: CNS(=O)(=O)CC1=CC2=C(C=C1)NC=C2CCN(C)C.C(CC(=O)O)C(=O)O. Product ID: ACM1215621310. Alfa Chemistry ISO 9001:2015 Certified.
Labelled Sumatriptan, a serotonin 5HT1-receptor agonist. Group: Biochemicals. Alternative Names: 3-[2-(Dimethyl-d6-amino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Succinate, Imigran, Imitrex. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
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Sumatriptan Dimer Impurity-d4
Sumatriptan Dimer Impurity-d4. Group: Biochemicals. Alternative Names: 1-[[3-[2-(Dimethylamino)ethyl]-1H-indol-5-yl]methyl]-3-[2-(Dimethylamino)ethyl]-N-methyl-indole-5-methanesulfonamide-d4. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C27H33D4N5O2S, Molecular Weight: 499.7. US Biological Life Sciences.
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Sumatriptan EP Impurity A
Sumatriptan EP Impurity A. Uses: For analytical and research use. Group: Impurity standards. CAS No. 545338-89-4. Molecular Formula: C27H37N5O2S. Mole Weight: 495.69. Catalog: APB545338894.
Sumatriptan EP impurity B
One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Monodesmethyl sumatriptan; N-Desmethyl SumatriptanDiscontinued; 88919-51-1; Sumatriptan EP Impurity B; Sumatriptan succinate specified impurity B [EP]. Grades: > 95%. CAS No. 88919-51-1. Molecular formula: C13H19N3O2S. Mole weight: 281.38.
Sumatriptan EP Impurity B
Sumatriptan EP Impurity B. Uses: For analytical and research use. Group: Impurity standards. CAS No. 88919-51-1. Molecular Formula: C13H19N3O2S. Mole Weight: 281.37. Catalog: APB88919511.
Sumatriptan EP impurity C
One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan EP Impurity C; Sumatriptan USP Related Compound C; [3-[2-(Dimethylamino)ethyl]-1-(hydroxymethyl)-1H-indol-5-yl]- N-methylmethanesulphonamide. Grades: > 95%. Molecular formula: C15H23N3O3S. Mole weight: 325.43.
Sumatriptan EP Impurity C
Sumatriptan EP Impurity C. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1797905-62-4. Molecular Formula: C15H23N3O3S. Mole Weight: 325.43. Catalog: APB1797905624.
Sumatriptan EP Impurity D
Sumatriptan EP Impurity D. Uses: For analytical and research use. Group: Impurity standards. CAS No. 212069-94-8. Molecular Formula: C14H21N3O3S. Mole Weight: 311.4. Catalog: APB212069948.
Sumatriptan EP impurity E
One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: 3-(2-Aminoethyl)-N-methyl-1H-indole-5-methanesulfonamide; 1-(3-(2-Aminoethyl)-1H-indol-5-yl)-N-methylmethanesulfonamide; Didesmethyl sumatriptan; 1-[3-(2-aminoethyl)-1H-indol-5-yl]-N-methylmethanesulfonamide. Grades: > 95%. CAS No. 88919-22-6. Molecular formula: C12H17N3O2S. Mole weight: 267.35.
Sumatriptan EP Impurity E
Sumatriptan EP Impurity E. Uses: For analytical and research use. Group: Impurity standards. CAS No. 88919-22-6. Molecular Formula: C12H17N3O2S. Mole Weight: 267.35. Catalog: APB88919226.
Sumatriptan EP Impurity F
Sumatriptan EP Impurity F. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2074615-63-5. Molecular Formula: C13H17N3O2S. Mole Weight: 279.36. Catalog: APB2074615635.
Sumatriptan EP Impurity H
Sumatriptan EP Impurity H. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1391052-59-7. Molecular Formula: C27H37N5O2S. Mole Weight: 495.69. Catalog: APB1391052597.
Sumatriptan Hydroxy-Oxindole Impurity (Sumatriptan Impurity 1). Uses: For analytical and research use. Group: Impurity standards. Pack Sizes: 5MG. Catalog: APS013024. Format: Neat. Shipping: Room Temperature.
Sumatriptan Impurity 1
One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Impurity 1; Sumatriptan Hydroxy-Oxindole Impurity; 1-(3-(2-(Dimethylamino)ethyl)-3-hydroxy-2-oxoindolin-5-yl)-N-methylmethane. Grades: > 95%. Molecular formula: C14H21N3O4S. Mole weight: 327.41.
Sumatriptan Impurity 2
One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Impurity 2. Grades: > 95%. Molecular formula: C14H22N3O3S. Cl. Mole weight: 347.86.
Sumatriptan Impurity 2
Sumatriptan Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2250254-19-2. Molecular Formula: C14H21N3O4S. Mole Weight: 327.4. Catalog: APB2250254192.
Sumatriptan Impurity 3
One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Impurity 3; 1-(3-(2-(Dimethylamino)ethyl)-1-((5-((N-methylsulfamoyl)methyl)-1H-indol-3-yl)methyl)-1H-indol-5-yl)-N-methylmethanesulfonamide. Grades: > 95%. Molecular formula: C25H33N5O4S2. Mole weight: 531.70.
Sumatriptan Impurity 3
Sumatriptan Impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 4025-75-6. Molecular Formula: C7H6ClNO4S. Mole Weight: 235.64. Catalog: APB4025756.
Sumatriptan Impurity A
One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan succinate specified impurity A [EP]; Sumatriptan succinate related compound A free base; (3-(2-(Dimethylamino)ethyl)-2-((3-(2-(dimethylamino)ethyl)-1H-indol-5-yl)methyl)-1H-indol-5-yl)-N-methylmethanesulfonamide. Grades: > 95%. CAS No. 545338-89-4. Molecular formula: C27H37N5O2S. Mole weight: 495.69.
Sumatriptan Impurity F
One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Impurity F; N-Methyl-1-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-6-yl)methanesulfonamide Succinate. Grades: > 95%. Molecular formula: C13H17N3O2S. Mole weight: 279.36.
Sumatriptan Impurity G
One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Impurity G; N-Methyl-1-(2-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-6-yl)methanesulfonamide. Grades: > 95%. Molecular formula: C14H19N3O2S. Mole weight: 293.39.
Sumatriptan Impurity H
One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Related Compound H; Sumatriptan Dimer Impurity; Sumatriptan EP Impurity H; N-(3-(2-(dimethylamino)ethyl)-1-((3-(2-(dimethylamino)ethyl)-1H-indol-5-yl)methyl)-1H-indol-5-yl)-N-methylmethanesulfonamide. Grades: > 95%. CAS No. 1391052-59-7. Molecular formula: C27H37N5O2S. Mole weight: 495.69.
Sumatriptan N-oxide
Sumatriptan N-oxide. Group: Biochemicals. Alternative Names: 3-[2- (Dimethyloxidoamino) ethyl]-N-methyl-1H-indole-5-methanesulfonamide; GR 112504. Grades: Highly Purified. CAS No. 212069-94-8. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C14H21N3O3S. US Biological Life Sciences.
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Sumatriptan N-Oxide
Sumatriptan N-Oxide. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Ph Eur Sumatriptan Impurity Mixture, BP Sumatriptan Impurity D, Sumatriptan Test Mix for Impurity Identification Solution 2, GR 112504, Ph Eur Sumatriptan Impurity D, GR 112504X, Sumatriptan N-Oxide,3-[2-(Dimethyloxidoamino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Sumatriptan N-oxide (GR 112504X). CAS No. 212069-94-8. Pack Sizes: 10MG. IUPAC Name: N,N-dimethyl-2-[5-(methylsulfamoylmethyl)-1H-indol-3-yl]ethanamine oxide. Molecular Formula: C14H21N3O3S. Mole Weight: 311.40. Catalog: APS212069948. SMILES: CNS (=O) (=O)Cc1ccc2[nH]cc (CC[N+] (C) (C)[O-])c2c1. Format: Neat. Shipping: Room Temperature.
Sumatriptan succinate
Sumatriptan succinate (GR 43175) is an orally active 5-HT1 receptor agonist with IC 50 s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT 1D , 5-HT 1B and 5-HT 1F receptors, respectively. Sumatriptan succinate can be used for migraine headache research [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GR 43175 succinate. CAS No. 103628-48-4. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-B0121.
Sumatriptan succinate
Sumatriptan succinate. Group: Biochemicals. Grades: Purified. CAS No. 103628-48-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
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Sumatriptan succinate
Sumatriptan Succinate is a triptan sulfa drug containing a sulfonamide group for the treatment of migraine headaches. Uses: Vasoconstrictor agents. Synonyms: GR 43175; GR43175; GR-4317. Grades: >98%. CAS No. 103628-48-4. Molecular formula: C14H21N3O2S.C4H6O4. Mole weight: 413.49.
A serotonin 5HT1-receptor agonist. Group: Biochemicals. Alternative Names: 3-[2-(Dimethylamino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Succinate, Imigran, Imitrex. Grades: Highly Purified. Pack Sizes: 50mg. US Biological Life Sciences.
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Sumatriptan Succinate EP impurity D
One metabolite impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan N-Oxide; Sumatriptan Succinate EP Impurity D; N,N-dimethyl-2-[5-(methylsulfamoylmethyl)-1H-indol-3-yl]ethanamine oxide. Grades: > 95%. CAS No. 212069-94-8. Molecular formula: C14H21N3O3S. Mole weight: 311.41.
An antimigraine agent. A Sumatriptan intermediate. Group: Biochemicals. Alternative Names: Didesmethyl Sumatriptan. Grades: Highly Purified. Pack Sizes: 250mg. US Biological Life Sciences.
Semi-synthetic macrolide antibiotic; related to Erythromycin A. Antibacterial. Group: Biochemicals. Alternative Names: CP-62993-d3; XZ-450-d3; Azitrocin-d3; Ribotrex-d3; Sumamed-d3; Trozocina-d3; Zithromaz-d3; Zitromax-d3. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Semi-synthetic macrolide antibiotic; related to Erythromycin A. Antibacterial. Group: Biochemicals. Alternative Names: CP-62993; XZ-450; Azitrocin; Ribotrex; Sumamed; Trozocina; Zithromaz; Zitromax. Grades: Highly Purified. CAS No. 117772-70-0. Pack Sizes: 25mg. US Biological Life Sciences.
Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care, Fragrance Products. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-103. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia.
New Jersey
Patchouli Oil Sumatra Dark Min 32 PA
Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-102. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia.
New Jersey
Patchouli Oil Sumatra Dark Premium Min 34 PA
Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-101. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia.
New Jersey
Patchouli Oil Sumatra Iron Free Min 30 PA
Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-202. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia.
New Jersey
Patchouli Oil Sumatra Iron Free Min 32 PA
Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-201. Olfactive Profile: Earthy, grounding, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia.
New Jersey
Patchouli Oil Sumatra M.D. Min 30 PA
Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care, Essential Oils, Fragrances. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-302. Olfactive Profile: Earthy, grounding, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia.
New Jersey
Patchouli Oil Sumatra M.D. Min 32 PA
Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care, Fragrance Products. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-301. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia.
Degradation product of Sumatriptan Succinate. Group: Biochemicals. Alternative Names: 3-[2-(Dimethylamino)ethyl]-1H-Indole-5-methanol. Grades: Highly Purified. CAS No. 334981-08-7. Pack Sizes: 10mg. US Biological Life Sciences.
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5-Nonyloxytryptamine oxalate
5-Nonyloxytryptamine oxalate is a potent agonist of the serotonin (5-HT) receptor 5-HT1Dβ with an EC50 value of 68 nM for adenylate cyclase activity in CHOKM6 cells transfected with the human 5-HT1Dβ receptor. It is several times more potent than sumatriptan and inactive as a 5-HT1A agonist (Ki at 5-HT1B = 1 nM, selectivity over 5-HT1A > 300-fold). Synonyms: 5-(Nonyloxy)-1H-Indole-3-ethanamine ethanedioate; 5-(Nonyloxy)tryptamine oxalate; 5-Nonyloxytryptamine oxalate. Grades: ≥99% by HPLC. CAS No. 157798-13-5. Molecular formula: C19H30N2O.C2H2O4. Mole weight: 392.49.
Used in the preparation of Sumatriptan impurity. Group: Biochemicals. Alternative Names: 3-[2-(Dimethylamino)-2-oxoacetyl]-1H-indole-5-carboxylic Acid Methyl Ester. Grades: Highly Purified. CAS No. 1052181-84-6. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
Azithromycin
Azithromycin is produced by the strain of Erythromycin. The antibacterial activity and pharmacokinetic properties are better than erythromycin, and it is widely used in clinic. Synonyms: azithromycin; Zithromax; Sumamed. Grades: > 98%. CAS No. 83905-01-5. Molecular formula: C38H72N2O12. Mole weight: 748.98.
Azithromycin-13CD3
Azithromycin-13CD3. Group: Biochemicals. Alternative Names: CP-62993-13Cd3; XZ-450-13Cd3; Azitrocin-13Cd3; Ribotrex-13Cd3; Sumamed-Cd3; Trozocina-d3; Zithromaz-13Cd3; Zitromax-13Cd3. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C3713CH69D3N2O12, Molecular Weight: 753. US Biological Life Sciences.
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Benzalkonium Chloride
Benzalkonium Chloride is used as an antimicrobial agent in preservative nasal sprays. It has recently been examined where it appears to produce adverse clinical effects on the human nasal tissue. Group: Biochemicals. Alternative Names: Alkyldimethylbenzyl Ammonium Chloride; Arquad CB 30; BTC; BTC 2565; BTC 471; Benzalkon A; Benzalkonium chloride; Biowash; Cedium; Culversan LC 80; Dimanin A; Erional EL; Genamin KDS; Kemamine BAC; Konrapo; Leda benzalkonium chloride; Magna M 407; Major C 100; Mefarol; Morpan BC 50; Mycosan; Mycosan S; Neo germ-i-tol; Niccanon 50; Nika-ekstra M; Osvan; P 3-Triquart AP; Parvosol II RTU; Phagomucor; Preventol R 80; Quaternium 1; Quatramine 50; Rhodaquat RP 50; Rhodaquat RP 80; Rodalon; Romergal CB; Smeik; Suma Bac D 10; Topax DD; Torizon; Whisper V; Zephiran; Zephiran chloride. Grades: Highly Purified. CAS No. 8001-54,63449-41-2. Pack Sizes: 100g, 500g. Molecular Formula: C?H??NRCl, Molecular Weight: 288.3. US Biological Life Sciences.
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