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Raloxifene (Keoxifene) is a benzothiophene-derived selective estrogen receptor modulator (SERM). Raloxifene has estrogen-agonistic effects on bone and lipids and estrogen-antagonistic effects on the breast and uterus. Raloxifene is used for breast cancer and osteoporosis research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Keoxifene; LY156758 free base; LY139481. CAS No. 84449-90-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-13738.
Raloxifene 4-Monomethyl Ether
Raloxifene 4-Monomethyl Ether. Group: Biochemicals. Alternative Names: [6-Hydroxy-2- (4-methoxyphenyl) benzo [b] thien-3-yl] [4- [2- (1-piperidinyl) ethoxy] phenyl] methanone. Grades: Highly Purified. CAS No. 185415-07-0. Pack Sizes: 10mg. Molecular Formula: C29H29NO4S, Molecular Weight: 487.61. US Biological Life Sciences.
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Raloxifene 6-Monomethyl Ether
Raloxifene 6-Monomethyl Ether. Group: Biochemicals. Alternative Names: [2- (4-Hydroxyphenyl) -6-methoxybenzo [b] thien-3-yl] [4- [2- (1-piperidinyl) ethoxy] phenyl] methanone. Grades: Highly Purified. CAS No. 178451-13-3. Pack Sizes: 10mg. Molecular Formula: C29H29NO4S, Molecular Weight: 487.61. US Biological Life Sciences.
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Raloxifene bismethyl ether
Raloxifene bismethyl ether. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 6-Methoxy-2-(4-methoxyphenyl)benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]-methanone; [6-Methoxy-2-(4-methoxyphenyl)benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]methanone. Product Category: Heterocyclic Organic Compound. Appearance: Yellow Solid. CAS No. 84541-38-8. Molecular formula: C30H31NO4S. Mole weight: 501.64. Purity: 0.96. IUPACName: [6-methoxy-2-(4-methoxyphenyl)-1-benzothiophen-3-yl]-[4-(2-piperidin-1-ylethoxy)phenyl]methanone. Product ID: ACM84541388. Alfa Chemistry ISO 9001:2015 Certified.
Raloxifene Bismethyl Ether
An intermediate in the synthesis of Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences.
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Raloxifene-d4
Deuterated Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
An intermediate in the production of labeled Raloxifene metabolites. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
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Raloxifene-d4 6,4-Bis- β-D-glucuronide
A labeled metabolite of Raloxifene. Group: Biochemicals. Alternative Names: 2-[4-( β -D-Glucopyranuronosyloxy) phenyl]-3- [4- [2- (1-piperidinyl) ethoxy-d4]benzoyl]benzo [b]thien-6-yl β-D-Glucopyranosiduronic Acid. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
A labeled metabolite of Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Alternative Names: 2-(4-Hydroxyphenyl)-3-[4-[2-(1-piperidinyl)ethoxy-d4-benzoyl]benzo[b]thien-6-yl]-ß-D-glucopyranosiduronic acid. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences.
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Raloxifene-d4 Bismethyl Ether
An intermediate in the synthesis of deuterated Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
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Raloxifene-d4, Hydrochloride
Deuterated Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
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Raloxifene EP IMpurity E
Raloxifene EP IMpurity E. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1700655-64-6. Molecular formula: C28H27NO4S. Mole weight: 473.59. Catalog: APB1700655646.
Raloxifene hydrochloride
Raloxifene hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 82640-04-8. Pack Sizes: 50mg. US Biological Life Sciences.
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Raloxifene hydrochloride
Raloxifene hydrochloride (Keoxifene hydrochloride) is a second generation selective and orally active estrogen receptor modulator. Raloxifene hydrochloride produces estrogen-agonistic effects on bone and lipid metabolism and estrogen-antagonistic effects on uterine endometrium and breast tissue [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Keoxifene hydrochloride; LY156758; LY139481 hydrochloride. CAS No. 82640-04-8. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-13738A.
A nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Alternative Names: [6-Hydroxy-2- (4-hydroxyphenyl) -benzo [b] thien-3-yl] [4- [2- (1-piperidinyl) ethoxy] phenyl] methanone, Keoxifene, LY-139481. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences.
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Raloxifene (hydrochloride) (Standard)
Raloxifene (hydrochloride) (Standard) is the analytical standard of Raloxifene (hydrochloride). This product is intended for research and analytical applications. Raloxifene hydrochloride (Keoxifene hydrochloride) is a second generation selective and orally active estrogen receptor modulator. Raloxifene hydrochloride produces estrogen-agonistic effects on bone and lipid metabolism and estrogen-antagonistic effects on uterine endometrium and breast tissue [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Keoxifene (hydrochloride)(Standard); LY156758(Standard); LY139481 (hydrochloride) (Standard). CAS No. 82640-04-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13738AR.
Raloxifene Impurity 11
Raloxifene Impurity 11. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1677681-02-5. Molecular formula: C18H22N2O4S. Mole weight: 362.44. Catalog: APB1677681025.
Raloxifene impurity D
Raloxifene impurity D. Group: Biochemicals. Grades: Highly Purified. CAS No. 177744-96-6. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C21H14O4S. US Biological Life Sciences.
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Raloxifene N-oxide
Raloxifene N-oxide. Group: Biochemicals. Alternative Names: [6-Hydroxy-2- (4-hydroxyphenyl) benzo [b] thien-3-yl] [4- [2- (1-oxido-1-piperidinyl) ethoxy] phenyl] methanone; Raloxifene impurity C. Grades: Highly Purified. CAS No. 195454-31-0. Pack Sizes: 500mg. Molecular Formula: C28H27NO5S. US Biological Life Sciences.
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Raloxifene N-Oxide
Raloxifene N-Oxide. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Raloxifene Imp. C (EP), Raloxifene USP RC C, Raloxifene N-Oxide,Raloxifene Hydrochloride Imp. C (EP), Raloxifene USP Related Compound C, [6-Hydroxy-2-(4-hydroxyphenyl)-1-benzothiophen-3-yl][4-[2-(piperidin-1-yl)ethoxy]phenyl]methanone N-Oxide. CAS No. 195454-31-0. IUPAC Name: [6-hydroxy-2-(4-hydroxyphenyl)-1-benzothiophen-3-yl]-[4-[2-(1-oxidopiperidin-1-ium-1-yl)ethoxy]phenyl]methanone. Molecular formula: C28H27NO5S. Mole weight: 489.58. Catalog: APS195454310. SMILES: Oc1ccc(cc1)c2sc3cc(O)ccc3c2C(=O)c4ccc(OCC[N+]5([O-])CCCCC5)cc4. Format: Neat.
Raloxifene Related Compound C
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
An intermediate in the synthesis for the metabolite of Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
An intermediate in the synthesis for the metabolite of Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
An intermediate in the synthesis for the metabolite of Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences.
An intermediate in the synthesis for the metabolite of Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
An intermediate in the synthesis for the metabolite of Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences.
Labeled protected Raloxifene metabolite. Group: Biochemicals. Alternative Names: 2-(4-Hydroxyphenyl)-3-[4-[2-(1-piperidinyl)ethoxy-d4-benzoyl]benzo[b]thien-6-yl]-2,3,4-tri-O-acetyl- β-D-glucopyranosiduronic Acid Methyl Ester. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
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2- (4-Hydroxyphenyl) benzo[b]thiophen-6-ol
2- (4-Hydroxyphenyl) benzo[b]thiophen-6-ol is used in the synthesis of Raloxifene (R100000) an estrogen receptor modulator. Group: Biochemicals. Grades: Highly Purified. CAS No. 63676-22-2. Pack Sizes: 100mg, 250mg. Molecular Formula: C14H10O2S. US Biological Life Sciences.
2- (4-Hydroxyphenyl) benzo[b]thiophen-6-ol Bimesylate is a Raloxifene (R100000) impurity, a nonsteroidal, selective estrogen receptor modulator (SERM). Antiosteoporotic. Group: Biochemicals. Grades: Highly Purified. CAS No. 84449-65-0. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C16H14O6S3, Molecular Weight: 398.47. US Biological Life Sciences.
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2-Ethylbenzo[b]thiophene
2-Ethylbenzo[b]thiophene is derived from Benzo[b]thiophene (B206870), which has application in organic as well as pharmaceutical industry as a component in the synthesis of Raloxifene, a breast cancer therapeutic, or hydrodesulfurization reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 1196-81-2. Pack Sizes: 2.5mg, 10mg. Molecular Formula: C10H10S, Molecular Weight: 162.25. US Biological Life Sciences.
3-Bromo-6-methoxy-2- (4-methoxyphenyl) benzo[b]thiophene is an intermediate in the synthesis of nonsteroidal, selective estrogen receptor modulator (SERM), Raloxifene (R100000). Group: Biochemicals. Grades: Highly Purified. CAS No. 176672-06-3. Pack Sizes: 1g, 10g. Molecular Formula: C16H13BrO2S. US Biological Life Sciences.
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Acolbifene
Acolbifene, also known as EM-652, or SCH-57068, is a selective estrogen receptor modulator (SERM). Acolbifene is currently being studied in the prevention of breast cancer in women at high risk of breast cancer. EM-652 is the compound having the highest affinity for the estrogen receptor, including estradiol. It has higher affinity for the ER than ICI 182780, hydroxytamoxifen, raloxifene, droloxifene and hydroxytoremifene. EM-652 was also the most potent inhibitor of the percentage of cycling cancer cells. Synonyms: EM-652; SCH 57068; (2S)-3-(4-Hydroxyphenyl)-4-methyl-2-[4-[2-(1-piperidinyl)ethoxy]phenyl]-2H-1-benzopyran-7-ol; (S)-3-(4-Hydroxyphenyl)-4-methyl-2-[4-[2-(1-piperidinyl)ethoxy]phenyl]-2H-1-benzopyran-7-ol; (S)-3-(4-hydroxyphenyl)-4-methyl-2-(4-(2-(piperidin-1-yl)ethoxy)phenyl)-2H-chromen-7-ol. Grade: ≥98%. CAS No. 182167-02-8. Molecular formula: C29H31NO4. Mole weight: 457.57.
Arzoxifene
Arzoxifene, also known as LY353381, a synthetic aromatic derivative with anti-estrogenic properties, displays greater bioavailability and higher anti-estrogenic potency in the breast than another selective estrogen receptor modulators (SERMs),raloxifene. Synonyms: 2-(4-methoxyphenyl)-3-[4-(2-piperidin-1-ylethoxy)phenoxy]-1-benzothiophen-6-ol; 4'F-DMA; 182133-27-3 (hydrochloride salt); arzoxifene; LY 353381; LY-353381; LY353381. Grade: >98%. CAS No. 182133-25-1. Molecular formula: C28H29NO4S. Mole weight: 475.60.
Benzo[b]thiophene
Benzo[b]thiophene has application in organic as well as pharmaceutical industry as a component in the synthesis of Raloxifene, a breast cancer therapeutic, or hydrodesulfurization reactions. Group: Biochemicals. Alternative Names: 1-Benzothiophene; 1-Benzothiophene; 1-Thiaindene; 2,3-Benzothiophene; Benzothiofuran; Benzothiophen; Benzothiophene; NSC 47196; Thianaphthen; Thianaphthene; Thionaphthene. Grades: Highly Purified. CAS No. 95-15-8. Pack Sizes: 25g. US Biological Life Sciences.
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