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| Product | Description | |
|---|---|---|
| PARP Inhibitor III, DPQ - CAS 129075-73-6 | The PARP Inhibitor III, DPQ, also referenced under CAS 129075-73-6, controls the biological activity of PARP. This small molecule/inhibitor is primarily used for Cell Structure applications. Group: Fluorescence/luminescence spectroscopy. |  |
| PARP Inhibitor IV, IQD - CAS 1188540 | The PARP Inhibitor IV, IQD, also referenced under CAS 1188540, controls the biological activity of PARP. This small molecule/inhibitor is primarily used for Cell Structure applications. Group: Fluorescence/luminescence spectroscopy. | |
| PARP Inhibitor IX, EB-47 | The PARP Inhibitor IX, EB-47 controls the biological activity of PARP. This small molecule/inhibitor is primarily used for Cell Structure applications. Group: Fluorescence/luminescence spectroscopy. | |
| PARP Inhibitor VIII, PJ34 - CAS 344458-15-7 | The PARP Inhibitor VIII, PJ34, also referenced under CAS 344458-15-7, controls the biological activity of PARP. This small molecule/inhibitor is primarily used for Cell Structure applications. Group: Fluorescence/luminescence spectroscopy. | |
| PARP Inhibitor VI, NU1025 - CAS 90417-38-2 | The PARP Inhibitor VI, NU1025, also referenced under CAS 90417-38-2, controls the biological activity of PARP. This small molecule/inhibitor is primarily used for Cell Structure applications. Group: Fluorescence/luminescence spectroscopy. | |
| PARP Inhibitor XII - CAS 489457-67-2 | The PARP Inhibitor XII, also referenced under CAS 489457-67-2, controls the biological activity of PARP. This small molecule/inhibitor is primarily used for Cell Structure applications. Group: Fluorescence/luminescence spectroscopy. | |
| PARP Inhibitor XIV - CAS 1104546-89-5 | The PARP Inhibitor XIV, also referenced under CAS 1104546-89-5, controls the biological activity of PARP. This small molecule/inhibitor is primarily used for Cell Structure applications. Group: Fluorescence/luminescence spectroscopy. | |
| PARP Inhibitor XV, UPF-1035 - CAS 370872-09-6 | The PARP Inhibitor XV, UPF-1035, also referenced under CAS 370872-09-6, controls the biological activity of PARP. This small molecule/inhibitor is primarily used for Cell Structure applications. Group: Fluorescence/luminescence spectroscopy. | |
| PARP (Poly ADP-Ribose Polymerase). Positive Control A | PARP (Poly ADP-Ribose Polymerase) Positive Control A. Group: Molecular Biology. Pack Sizes: 60ul. US Biological Life Sciences. |  Worldwide |
| PARP (Poly ADP-Ribose Polymerase). Positive Control B | PARP (Poly ADP-Ribose Polymerase) Positive Control B. Group: Molecular Biology. Pack Sizes: 60 ul. US Biological Life Sciences. | Worldwide |
| Parsaclisib | Parsaclisib (INCB050465) is a potent, selective and orally active inhibitor of PI3Kδ , with an IC 50 of 1 nM at 1 mM ATP. Parsaclisib shows approximately 20000-fold selectivity over other PI3K class I isoforms. Parsaclisib can be used for the research of relapsed or refractory B-cell malignancies [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: INCB050465; IBI-376. CAS No. 1426698-88-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109068. |  |
| Parsaclisib hydrochloride | Parsaclisib hydrochloride (INCB050465 hydrochloride) is a potent, selective and orally active inhibitor of PI3Kδ , with an IC 50 of 1 nM at 1 mM ATP. Parsaclisib hydrochloride shows approximately 20000-fold selectivity over other PI3K class I isoforms. Parsaclisib hydrochloride can be used for the research of relapsed or refractory B-cell malignancies [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: INCB050465 hydrochloride; IBI-376 hydrochloride. CAS No. 1995889-48-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109068A. | |
| p-Arsanilic acid | 100g Pack Size. Group: Building Blocks, Organics. Formula: C6H8AsNO3. CAS No. 98-50-0. Prepack ID 31968396-100g. Molecular Weight 217.05. See USA prepack pricing. |  |
| p-Arsanilic acid | p-Arsanilic acid. CAS No: 98-50-0 |  Sarchem Laboratories New Jersey NJ |
| Parsatuzumab | Parsatuzumab (Anti-EGFL7; RG 7414) is a humanized monoclonal antibody, acts as an immunomodulator and binds to EGFL7. Parsatuzumab selectively blocks the interaction between EGFL7 and endothelial cells, potentially inhibiting vascular regrowth and reducing vascular endothelial growth factor ( VEGF ) inhibition [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Anti-EGFL7; RG 7414. CAS No. 1312797-14-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99215. | |
| Parsley Leaf Powder | Parsley Leaf Powder. |  CA, FL & NJ |
| Parsley Seed Oil | Parsley Seed Oil. CAS No. 8000-68-8. FEMA No. 2836. Kosher: Y. VIGON Item # 500783. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Parstatin (human) | Parstatin is a 41-amino acid peptide, formed by proteolytic cleavage on activation of the protease activated receptor-1, with antiangiogenic properties. Parstatin (human) attenuates endothelial cell migration and proliferation (IC50 ~ 3 μM), and induces cell cycle arrest. It promotes activation of caspase-3 and exhibits pro-apoptotic activity in vitro. Synonyms: H-Met-Gly-Pro-Arg-Arg-Leu-Leu-Leu-Val-Ala-Ala-Cys-Phe-Ser-Leu-Cys-Gly-Pro-Leu-Leu-Ser-Ala-Arg-Thr-Arg-Ala-Arg-Arg-Pro-Glu-Ser-Lys-Ala-Thr-Asn-Ala-Thr-Leu-Asp-Pro-Arg-OH; L-methionyl-glycyl-L-prolyl-L-arginyl-L-arginyl-L-leucyl-L-leucyl-L-leucyl-L-valyl-L-alanyl-L-alanyl-L-cysteinyl-L-phenylalanyl-L-seryl-L-leucyl-L-cysteinyl-glycyl-L-prolyl-L-leucyl-L-leucyl-L-seryl-L-alanyl-L-arginyl-L-threonyl-L-arginyl-L-alanyl-L-arginyl-L-arginyl-L-prolyl-L-alpha-glutamyl-L-seryl-L-lysyl-L-alanyl-L-threonyl-L-asparagyl-L-alanyl-L-threonyl-L-leucyl-L-alpha-aspartyl-L-prolyl-L-arginine. Grades: ≥98%. CAS No. 1065755-99-8. Molecular formula: C191H330N64O53S3. Mole weight: 4467.29. |  |
| Parstatin (mouse) | Parstatin, a 41-mer peptide which is cleaved upon activation of Proteinase-Activated Receptor 1, attenuates endothelial cell migration and proliferation (IC50 ~ 20 μM), and induces cell cycle arrest. It promotes activation of caspase-3 and exhibits pro-apoptotic activity in vitro. Synonyms: H-Met-Gly-Pro-Arg-Arg-Leu-Leu-Ile-Val-Ala-Leu-Gly-Leu-Ser-Leu-Cys-Gly-Pro-Leu-Leu-Ser-Ser-Arg-Val-Pro-Met-Ser-Gln-Pro-Glu-Ser-Glu-Arg-Thr-Asp-Ala-Thr-Val-Asn-Pro-Arg-OH; L-methionyl-glycyl-L-prolyl-L-arginyl-L-arginyl-L-leucyl-L-leucyl-L-isoleucyl-L-valyl-L-alanyl-L-leucyl-glycyl-L-leucyl-L-seryl-L-leucyl-L-cysteinyl-glycyl-L-prolyl-L-leucyl-L-leucyl-L-seryl-L-seryl-L-arginyl-L-valyl-L-prolyl-L-methionyl-L-seryl-L-glutaminyl-L-prolyl-L-alpha-glutamyl-L-seryl-L-alpha-glutamyl-L-arginyl-L-threonyl-L-alpha-aspartyl-L-alanyl-L-threonyl-L-valyl-L-asparagyl-L-prolyl-L-arginine. Grades: ≥98%. CAS No. 1065756-01-5. Molecular formula: C189H326N58O57S3. Mole weight: 4419.19. | |
| Parthenolide | 500mg Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C15H20O3. CAS No. 20554-84-1. Prepack ID 73041456-500mg. Molecular Weight 248.32. See USA prepack pricing. | |
| Parthenolide | Parthenolide. Group: Biochemicals. Grades: Purified. CAS No. 20554-84-1. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Parthenolide | Parthenolide - Product ID: NST-10-182. Category: Terpenes. Alternative Names: (-)-Parthenolide. Purity: 98%. Test method: HPLC. CAS No. 20554-84-1. Pack Sizes: 0,05g, 0,1g, 0,25g, 0,5g. Appearance: White powder. Molecular formula: C15H20O3. Mole weight: 248.32. Storage: +2 +8 °C. |  |
| Parthenolide | (-)-Parthenolide is a sesquiterpene lactone which occurs naturally in the plant feverfew (Tanacetum parthenium) and also promotes the ubiquitination of MDM2 and activates p53 cellular functions. Uses: 5-ht antagonist; anti-tumor; anti-cancer; antimycobacterial; anti-inflammatory. Synonyms: NSC-157035; NSC 157035; NSC157035. Grades: >98%. CAS No. 20554-84-1. Molecular formula: C15H20O3. Mole weight: 248.32. | |
| Parthenolide | Parthenolide is a sesquiterpene lactone found in the medicinal herb Feverfew. Parthenolide exhibits anti-inflammatory activity by inhibiting NF-?B activation; also inhibits HDAC1 protein without affecting other class I/II HDACs. Uses: Scientific research. Group: Natural products. Alternative Names: (-)-Parthenolide. CAS No. 20554-84-1. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-N0141. | |
| Parthenolide ((1aR-[1aR*, 4E, 7aS*, -10aS*, -10bR*])-2, 3-6, 7, 7a, 8, 10a, 10b-octahydro-1a, 5-dimethyl-8-methyleneoxireno[9, 10]cyclo deca[1,2-b]furan-9(1aH)-one) | An anti-inflammatory agent. Specifically inhibits activation of NF-kB by preventing the degradation of IkBa and IkBb. Inhibits activation of MAP kinase (MAPK/ERK) and generation of leukotriene B4 and thromboxane B2. Potent anticancer agent. Induces apoptosis in various cancer cell lines. Specifically inhibits histone deacetylase 1 (HDAC1) without affecting other class I/II HDACs. Group: Biochemicals. Grades: Highly Purified. CAS No. 20554-84-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Partially-neutralized methacrylic acid and ethyl acrylate copolymer (1:1) | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Particulate Matter in Impinger Solution | Proficiency Testing Material. Group: Atomic absorption spectroscopy (aas). | |
| Particulate Matter on Filter Paper | Proficiency Testing Material. Group: Atomic absorption spectroscopy (aas). | |
| Parvisporin | It is a neuritogenic agent produced by the strain of Stachyborrys parvispora F4708. It promotes the enlargement of the neural sinus of P12 cells, and the effect of Stachybotrin C is obvious, but the effect of Parvisporin is weak. Molecular formula: C23H34O5. Mole weight: 390.51. | |
| Parvodicin A | It is produced by the strain of Actinomadura paroosalo. It's a glycopeptide antibiotic. It has inhibitory effect on Staphylococcus aureus, Staphylococcus furfur, Staphylococcus hemolyticus and enterococcus faecalis. Synonyms: Ristomycin A aglycone, 5,31-dichloro-7-demethyl-64-O-demethyl-19-deoxy-56-O-(2-deoxy-2-((1-oxodecyl)amino)-beta-D-glucopyranuronosyl)-42-O-alpha-D-mannopyranosyl-N15-methyl-. CAS No. 110882-81-0. Molecular formula: C81H84N8O29Cl2. Mole weight: 1704.48. | |
| Parvodicin B1 | It is produced by the strain of Actinomadura paroosalo. It's a glycopeptide antibiotic. It has inhibitory effect on Staphylococcus aureus, Staphylococcus furfur, Staphylococcus hemolyticus and enterococcus faecalis. The terminal branching activity of lipid chains is greater than straight chains (C1>C2>C3>C4, B1>B2), and the chain length is greater than short chains (C2>B). It acts by inhibiting the synthesis of bacterial cell wall. Synonyms: Antibiotic A-40926 A0; Ristomycin A aglycone, 5,31-dichloro-7-demethyl-64-O-demethyl-19-deoxy-56-O-(2-deoxy-2-((9-methyl-1-oxodecyl)amino)-beta-D-glucopyranuronosyl)-42-o-alpha-D-mannopyranosyl-N15-methyl-. CAS No. 110882-82-1. Molecular formula: C82H86N8O29Cl2. Mole weight: 1718.50. | |
| Parvodicin B2 | It is produced by the strain of Actinomadura paroosalo. It's a glycopeptide antibiotic. It has inhibitory effect on Staphylococcus aureus, Staphylococcus furfur, Staphylococcus hemolyticus and enterococcus faecalis. The terminal branching activity of lipid chains is greater than straight chains (C1>C2>C3>C4, B1>B2), and the chain length is greater than short chains (C2>B). It acts by inhibiting the synthesis of bacterial cell wall. Synonyms: Antibiotic A-40926 A1; Antibiotic A 40926 factor A; Antibiotic A 40926A; Ristomycin A aglycone, 5,31-dichloro-7-demethyl-64-O-demethyl-19-deoxy-56-O-(2-deoxy-2-((1-oxoundecyl)amino)-beta-D-glucopyranuronosyl)-42-o-alpha-D-mannopyranosyl-N15-methyl-. CAS No. 110882-83-2. Molecular formula: C82H86N8O29Cl2. Mole weight: 1718.50. | |
| Parvodicin C1 | It is produced by the strain of Actinomadura paroosalo. It's a glycopeptide antibiotic. It has inhibitory effect on Staphylococcus aureus, Staphylococcus furfur, Staphylococcus hemolyticus and enterococcus faecalis. Parvodicin C1 and C2 have stronger antibacterial effects than Parvodicin C3 and C4. The antibacterial activity of Parvodicin C is 1-4 times stronger than Tecomycin and 2-4 times stronger than vancomycin. The terminal branching activity of lipid chains is greater than straight chains (C1>C2>C3>C4, B1>B2), and the chain length is greater than short chains (C2>B). The half-life of Parvodicin C1 is longer in vivo than vancomycin and Archeomycin. Synonyms: Ristomycin A aglycone, 5,31-dichloro-7-demethyl-64-O-demethyl-19-deoxy-56-O-[2-deoxy-2-[(10-methyl-1-oxoundecyl)amino]-b-D-glucopyranuronosyl]-42-O-a-D-mannopyranosyl-N15-methyl-; A 40926B; A 40926 B0; Antibiotic A 40926 factor B0; Antibiotic A 40926B. CAS No. 110882-84-3. Molecular formula: C83H88N8O29Cl2. Mole weight: 1732.53. | |
| Parvodicin C2 | It is produced by the strain of Actinomadura paroosalo. It's a glycopeptide antibiotic. It has inhibitory effect on Staphylococcus aureus, Staphylococcus furfur, Staphylococcus hemolyticus and enterococcus faecalis. Parvodicin C1 and C2 have stronger antibacterial effects than Parvodicin C3 and C4. The antibacterial activity of Parvodicin C is 1-4 times stronger than Tecomycin and 2-4 times stronger than vancomycin. The terminal branching activity of lipid chains is greater than straight chains (C1>C2>C3>C4, B1>B2), and the chain length is greater than short chains (C2>B). The half-life of Parvodicin C1 is longer in vivo than vancomycin and Archeomycin. Synonyms: Antibiotic A-40926 B1; Ristomycin A aglycone, 5,31-dichloro-7-demethyl-64-O-demethyl-19-deoxy-56-O-(2-deoxy-2-((1-oxododecyl)amino)-beta-D-glucopyranuronosyl)-42-o-alpha-D-mannopyranosyl-N15-methyl-. CAS No. 110882-85-4. Molecular formula: C83H88N8O29Cl2. Mole weight: 1732.53. | |
| Parvodicin complex | It is produced by the strain of Actinomadura paroosalo. It's a glycopeptide antibiotic. It has inhibitory effect on Staphylococcus aureus, Staphylococcus furfur, Staphylococcus hemolyticus and enterococcus faecalis. Parvodicin C1 and C2 have stronger antibacterial effects than Parvodicin C3 and C4. The antibacterial activity of Parvodicin C is 1-4 times stronger than Tecomycin and 2-4 times stronger than vancomycin. The terminal branching activity of lipid chains is greater than straight chains (C1>C2>C3>C4, B1>B2), and the chain length is greater than short chains (C2>B). The half-life of Parvodicin C1 is longer in vivo than vancomycin and Archeomycin. Synonyms: A 40926 complex. Grades: >95% by HPLC. CAS No. 187888-13-7. Molecular formula: C83H88Cl2N8O29 (for C1). Mole weight: 1732.53. | |
| Parylene f | Parylene f. Group: Supramolecular host materials. Alternative Names: Dimer,Parylene F; 5, 6, 11, 12, 13, 14, 15, 16-Octafluorotricyclo[8.2.2.24, 7]hexadeca-4, 6, 10, 12, 13, 15-hexaene; Parylene F Dimer. CAS No. 1785-64-4. Product ID: 5, 6, 11, 12, 13, 14, 15, 16-octafluorotricyclo[8.2.2.24, 7]hexadeca-1(12), 4(16), 5, 7(15), 10, 13-hexaene. Molecular formula: 352.22g/mol. Mole weight: C16H8F8. C1CC2=C (C (=C (CCC3=C (C (=C1C (=C3F)F)F)F)C (=C2F)F)F)F. InChI=1S/C16H8F8/c17-9-5-1-2-6-11 (19)15 (23)8 (16 (24)12 (6)20)4-3-7 (13 (9)21)14 (22)10 (5)18/h1-4H2. GUHKMHMGKKRFDT-UHFFFAOYSA-N. |  |
| Pasaconazole | Pasaconazole. CAS No. 171228-49-2. Product ID: 8-04399. Molecular formula: C37H42F2N8O4. Mole weight: 700.79. Categories: Posaconazole. |  |
| Pascolizumab | Pascolizumab (SB-240683) is a humanized anti-IL-4 monoclonal antibody. Pascolizumab has the potential for the research of asthma [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: SB-240683. CAS No. 331243-22-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99801. | |
| Pashanone | Formula: Group: Biochemicals. Grades: Plant Grade. CAS No. 42438-78-8. Pack Sizes: 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Pasireotide | Pasireotide pamoate, also known as SOM230, is an orphan drug approved for the treatment of Cushing's disease in patients who fail or are ineligible for surgical therapy. It was developed by Novartis. Pasireotide is a somatostatin analog with a 40-fold increased affinity to somatostatin receptor 5 compared to other somatostatin analogs. Synonyms: Pasireotide; SOM230; SOM-203; SOM 203; Signifor. Grades: >98%. CAS No. 396091-73-9. Molecular formula: C58H66N10O9. Mole weight: 1047.227. | |
| Pasireotide | Pasireotide (SOM230), a long-acting cyclohexapeptide somatostatin analogue, can improve agonist activity at somatostatin receptors (subtypes sst1/2/3/4/5 , pK i =8.2/9.0/9.1/<7.0/9.9, respectively). Pasireotide can suppress GH, IGF-I and ACTH secretion, indicating potential efficacy in acromegaly and Cushing's disease. Pasireotide also exhibits antisecretory, antiproliferative, and proapoptotic activity [1] [2] [3]. Uses: Scientific research. Group: Peptides. Alternative Names: SOM230. CAS No. 396091-73-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-16381. | |
| Pasireotide acetate | Pasireotide (SOM230) acetate, a long-acting cyclohexapeptide somatostatin analogue, can improve agonist activity at somatostatin receptors (subtypes sst1/2/3/4/5 , pK i =8.2/9.0/9.1/<7.0/9.9, respectively). Pasireotide acetate can suppress GH, IGF-I and ACTH secretion, indicating potential efficacy in acromegaly and Cushing's disease. Pasireotide acetate also exhibits antisecretory, antiproliferative, and proapoptotic activity [1] [2] [3]. Uses: Scientific research. Group: Peptides. Alternative Names: SOM230 acetate. CAS No. 396091-76-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-16381A. | |
| Pasireotide Diaspartate | Pasireotide is an orphan drug approved for the treatment of Cushing's disease in patients who fail or are ineligible for surgical therapy. It is a somatostatin receptor (SSTR) agonist with selectively for SST1, SST2, SST3, and SST5 over SST4 (IC50s = 9.3, 1, 1.5, 0.16, and >100 nM, respectively, for human recombinant receptors). Uses: Hormones. Synonyms: SOM230. Grades: ≥95%. CAS No. 820232-50-6. Molecular formula: C58H66N10O9·2C4H7NO4. Mole weight: 1313.41. | |
| Pasireotide L-aspartate salt | Pasireotide is a synthetic long-acting cyclic hexapeptide exhibits unique high-affinity binding to human somatostatin receptors. Uses: High-affinity binding to human somatostatin receptors. Synonyms: cyclo((4R)-4-(2-Aminoethylcarbamoyloxy)-L-prolyl-L-phenylglycyl-D-tryptophyl-L-lysyl-4-O-benzyl-L-tyrosyl-L- phenylalanyl-) L-aspartate salt. Grades: ≥98%. CAS No. 396091-77-3. Molecular formula: C62H73N11O13. Mole weight: 1180.31. | |
| Pasotuxizumab | Pasotuxizumab (BAY 2010112) is a PSMA and CD3 bispecific T-cell engager (BiTE). Pasotuxizumab binds to CD3 and PSMA with K D s of 9.4 nM and 47.0 nM for human CD3 and PSMA. Pasotuxizumab can be used for research of metastatic castration-resistant prostate cancer (mCRPC) [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BAY 2010112; AMG 212. CAS No. 1442657-12-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99802. | |
| Paspalinine | Paspalinine is a tremorgenic mycotoxin extracted from the fermentation broth of Aspergillus flavus OUCMDZ-2205. It can inhibit the combination of [125I]charybdotoxin (ChTX) to maxi-K channels in bovine aortic smooth muscle sarcolemmal membranes. It displays tremorgenic action due in part to their inhibition of GABAA receptor function. It shows insecticidal properties. Synonyms: 4H-3,15a-Epoxy-1-benzoxepino(6',7':6,7)indeno(1,2-b)indol-4-one, 2,3,5b,6,7,7a,8,13,13b,13c,14,15-dodecahydro-5b-hydroxy-2,2,13b,13c-tetramethyl-, (3R-(3alpha, 5balpha, 7abeta, 13balpha, 13cbeta, 15aalpha))-; 4H-3,15a-Epoxy-1-benzoxepino[6',7':6,7]indeno[1,2-b]indol-4-one, 2,3,5b,6,7,7a,8,13,13b,13c,14,15-dodecahydro-5b-hydroxy-2,2,13b,13c-tetramethyl-, (3R,5bS,7aS,13bS,13cR,15aS)-. Grades: ≥98%. CAS No. 63722-91-8. Molecular formula: C27H31NO4. Mole weight: 433.54. | |
| Passifloran | Passifloran. CAS No. 136954-25-1. FEMA No. 3816. Kosher: Y. VIGON Item # 504783. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, passiflora acetate. | America & Internationally |
| Passion Flower Extract | Passion flower extract is prepared from passiflora caerulea, a species of flowering plant native to South America. Passion flower extract targets the central nervous system and works to ease tension and prevent twitching in the muscles. This calming effect of passion flower extract flavon does not affect brain function or respiratory rate, which is therefore much safer than medications with sedative effects. Group: Others. Passion Flower Extract; Passiflora Coerulea Linn. Cat No: EXTC-008. |  |
| Passion Flower Powder | Passion Flower Powder. | CA, FL & NJ |
| Passion Fruit Water Phase | Water Phase Aroma. Uses: Flavors. Group: Essences. Grade: Food. Pack Sizes: Pails to Drums. |  Bradenton, FL |
| Paste PVC Resin ALFA01 | The resin product is a white powder. It has good compatibility with plasticizers, organic solvents and fillers. It can form plastisols or organosols to make a variety of products. Uses: Non-foaming and microfoaming artificial leather for spray-dyed metal coatings, fiberglass, impregnation and general purpose products. Group: Pvc resins. Alternative Names: Paste poly(vinyl chloride) resins. | |
| Paste PVC Resin ALFA02 | The resin product is a white powder. It has good compatibility with plasticizers, organic solvents and fillers. It can form plastisols or organosols to make a variety of products. Uses: Resilient floor foam layer, foam artificial leather, wallpaper. Group: Pvc resins. Alternative Names: Paste poly(vinyl chloride) resins. | |
| Paste PVC Resin ALFA03 | Emulsion PVC is a homopolymer of polyvinyl chloride, which is a light white microfine powder. Uses: It is mixed with plasticizers and other additives and can be used for coating, rotational molding, impregnation, spraying and foaming. Group: Pvc resins. Alternative Names: Paste poly(vinyl chloride) resins. | |
| Paste PVC Resin ALFA04 | Emulsion PVC is a homopolymer of polyvinyl chloride, which is a light white microfine powder. Uses: It is mixed with plasticizers and other additives and can be used for coating, rotational molding, impregnation, spraying and foaming. Group: Pvc resins. Alternative Names: Paste poly(vinyl chloride) resins. | |
| Patagonic acid | Patagonic acid is a dibenzofuran compound obtained from lichen bunodophoron patagonicum. Synonyms: Benzoic acid, 2-hydroxy-4-[(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-6-(2-oxononyl)-; 2-Hydroxy-4-[(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-6-(2-oxononyl)benzoic acid. CAS No. 158202-35-8. Molecular formula: C25H30O8. Mole weight: 458.5. | |
| Patamostat | Patamostat (E-3123) is a potent protease inhibitor. Patamostat potently inhibits trypsin, plasmin and thrombin with IC 50 s of 39 nM, 950 nM and 1.9 μM, respectively. Patamostat may possess suppressing effects on pathogenesis and development of acute pancreatitis [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: E-3123. CAS No. 114568-26-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114080. | |
| Patchouli alcohol | Purity (HPLC): Group: Biochemicals. Alternative Names: Patchoulol. Grades: Highly Purified. CAS No. 5986-55-0. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. US Biological Life Sciences. | Worldwide |
| Patchouli alcohol | Patchouli alcohol is a natural tricyclic sesquiterpene, exhibits anti- Helicobacter pylori , anti-inflammatory and antioxidant properties [1]. Uses: Scientific research. Group: Natural products. CAS No. 5986-55-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-N0207. | |
| Patchouli Alcohol | Patchouli alcohol is a natural tricyclic sesquiterpene extracted from Pogostemon cablin (Blanco) Benth, and exhibits anti-Helicobacter pylori and anti-inflammatory properties. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Patchoulanol. Product Category: Inhibitors. Appearance: Powder. CAS No. 5986-55-0. Molecular formula: C15H26O. Mole weight: 222.37. Purity: 0.98. IUPACName: (1R,3R,6S,7S,8S)-2,2,6,8-tetramethyltricyclo[5.3.1.03,8]undecan-3-ol. Canonical SMILES: C[C@H]1CC[C@@]2([C@@]3([C@H]1C[C@H](C2(C)C)CC3)C)O. Density: 1.028 g/ml. Product ID: ACM5986550. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Patchouli Oil Dark | Patchouli Oil Dark. CAS No. MIXTURE. Kosher: Y. VIGON Item # 507476. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Patchouli Oil Dark 100% Pure | Patchouli Oil Dark 100% Pure. CAS No. 8014-09-3. FEMA No. 2838. Kosher: Y. VIGON Item # 508264. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Cosmetics, Aromatherapy, Essetial Oils. | America & Internationally |
| Patchouli Oil Heart 55 PA | "Clove trees are indigenous to the Maluku islands of Indonesia. Indonesia has been the dominant producer off clove buds and clove oil globally for decades. Indonesia is also the largest consumer of clove buds as a spice, which is primarily used in the kretek cigarette industry. It is due to this high demand for Clove Buds in the cigarette industry that farmers are using the remaining components (dry leaves, and stems/ claws) of the clove tree to produce clove oil its derivatives thereafter.". Uses: Personal care, Fragrance products, Aromatherapy. 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-306. Olfactive Profile: Woody, balsamic, earthy, camphor. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. |  New Jersey |
| Patchouli Oil Heart 65 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-305. Olfactive Profile: Woody, balsamic, earthy, camphor. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Light | Patchouli Oil Light. CAS No. MIXTURE. Kosher: Y. VIGON Item # 507475. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Patchouli Oil Molecular Distilled | Patchouli Oil Molecular Distilled. CAS No. MIXTURE. Kosher: Y. VIGON Item # 507477. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Patchouli Oil Sulawesi Dark Min 28 PA Acid < 15 | 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-109. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi Dark Min 29 PA Acid < 15 | 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-107. Olfactive Profile: Earthy, grounding, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi Dark Min 29 PA Acid < 8 | 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-106. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi Dark Min 30 PA Acid < 5 | 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. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-105. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi Dark Min 30 PA Acid < 8 | 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. 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-104. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
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