A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
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| Product | Description | |
|---|---|---|
| Homovanillyl alcohol | Homovanillyl alcohol. Alternative Names: 4-Hydroxy-3-methoxyphenylethyl alcohol. CAS No. 2380-78-1. Purity: >98.0%. Product ID: FFC-AR-2380781. Molecular formula: C9H12O3. Mole weight: 168.19. IUPAC Name: 4-(2-hydroxyethyl)-2-methoxyphenol. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Homoveratric Acid | Homoveratric Acid is a dopamine metabolite that inhibits brain mitochondrial respiration via monoamine oxidase/H2O2-dependent or non-dependent pathway. Group: Biochemicals. Alternative Names: 3,4-Dimethoxyphenylacetic Acid; 2- (3, 4-Dimethoxyphenyl) acetate; 2-(3,4-Dimethoxyphenyl)acetic Acid; 3,4-Dimethoxybenzeneacetic Acid; NSC 2753; NSC 27897. Grades: Highly Purified. CAS No. 93-40-3. Pack Sizes: 2.5g. US Biological Life Sciences. |  Worldwide |
| Homoveratric acid acyl-β-D-glucuronide | Homoveratric acid acyl-β-D-glucuronide is a metabolite of Homoveratric acid, which is a significant compound used as a pharmaceutical intermediate and has been implicated in neurotransmitter metabolism, neuroprotection, and the alleviation of depression. It is also associated with the gut microbiome, suggesting a role in mental health through its influence on neurotransmitter levels and synaptic integrity. Alternative Names: 1-(3,4-Dimethoxybenzeneacetate) β-D-glucopyranuronic acid, Homoveratrate β-D-glucopyranuronic acid; (2S,3S,4S,5R,6S)-6-[(3,4-Dimethoxyphenyl)acetoxy]-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid. Grades: ≥98%. Molecular formula: C16H20O10. Mole weight: 372.32. |  |
| Homoveratrylamine | A methylated metabolite of Dopamine; a potent inhibitor of brain mitochondrial respiration used in Parkinsons disease studies. Group: Biochemicals. Grades: Highly Purified. CAS No. 120-20-7. Pack Sizes: 10g, 50g, 100g, 250g, 500g. Molecular Formula: C??H??NO?. US Biological Life Sciences. | Worldwide |
| Honey | Honey. CAS No. 8028-66-8. Product ID: PE-0478. Category: Binder Excipients. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Honey; Binder Excipients; Binder Excipients; /; 8028-66-8; 8028-66-8. UNII: NA. Chemical Name: Honey. Grade: Pharmceutical Excipients. Administration route: Oral; Topical. Dosage Form: Pill. Applications: Honey itself belongs to the food category. In the production process of health products and medicines, honey raw materials also act as auxiliary materials, such as safe edible adhesives and flavoring agents in pharmaceuticals, used in pills, ointments, tablets, oral liquid etc. |  |
| Honeybush CO2 Extract | Honeybush CO2 Extract. CAS No. MIXTURE. Kosher: Y. VIGON Item # 504880. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. |  America & Internationally |
| Honeybush Milled Powder (Cyclopia Subtemata) | Honeybush Milled Powder (Cyclopia Subtemata). |  CA, FL & NJ |
| Honey Extract | Honey from organic apiculture, natural humectant and moisturizer for skin hydration. CAS No. 91052-92-5. Product ID: CI-HC-0135. Alfa Chemistry - ISO 9001:32057 Certified. | |
| HONEYFLOR | Honeyflor is a brand that specializes in organic and natural honey-based products, such as honey-infused skincare products, herbal remedies, and gourmet honey blends. Alternative Names: (* Alt. CAS #) CAS: 2396-78-3; Methyl 3-hexenoate, 3-Hexenoic acid, methyl ester, (3E)-, FEMA CAS: 2396-78-3, HONEYFLOR, Methyl (E)-3-hexenoate, methyl (E)-hex-3-enoate, Methyl 3-Hexenoate (trans), Methyl e-3-Hexenoate, Methyl trans-3-hexenoate. Grades: 99.0%. CAS No. 13894-61-6. Molecular formula: C7H1202. Mole weight: 128.17. | |
| Honey Powder | Honey Powder. | CA, FL & NJ |
| Honey Powder | Honey Powder. Group: Others. Purity: Purity: 100%. Appearance: Light yellow powder. Source: Natural honey. Honey Powder. Cat No: EXTC-123. |  |
| Honey Signature | Honey Signature. CAS No. MIXTURE. VIGON Item # 508005. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, Aromatherapy, Essetial Oils. | America & Internationally |
| HoneySuchle Flowers Extract (Standard) | HoneySuchle Flowers Extract (Standard). Applications: Antibacterial and enhanced immune function; inhibition of protein synthesis resistant. Group: Others. Synonyms: HoneySuchle Flowers Extract (Standard). Purity: 25%, 10:1, HPLC. Appearance: White fine powder. Storage: 24 months with original packing under 18°C. Store in cool dry place,avoid sunlight and high temperature. Source: Natural plant honeysuckle. HoneySuchle Flowers Extract (Standard); plant extract. Pack: 1kg, 5kg, 10kg aluminum foil vacuum bag; or 20kg, 25kg Fiber Drum. Cat No: EXTW-203. | |
| Honeysuckle Extract | Honeysuckle extract is prepared from the flower of honeysuckle, which are used as a kind of tea drink for more than 2000 years in Japan and China. Honeysuckle flowers extract is the important herbs for clearing heat and relieving toxicity and an important intermediate in lignin biosynthesis. Japanese honeysuckle flowers extract is also known as an antioxidant, may also slow the release of glucose into the bloodstream after a meal. Group: Others. Mole weight: 354.31. Honeysuckle Extract; Lonicera japonica Thunb. Cat No: EXTC-025. | |
| Hongoquercin A | Hongoquercin A is a sesquiterpene antibiotic produced by an unidentified fungus. It has moderate anti-Gram-positive bacteria activity with a MIC of 4-8 μg/mL. Molecular formula: C23H32O4. Mole weight: 372.50. | |
| Hongoquercin B | Hongoquercin B is a sesquiterpene antibiotic produced by an unidentified fungus. It is only resistant to vancomycin-resistant Enterococcus faecium at high concentrations. Molecular formula: C25H34O6. Mole weight: 430.53. | |
| Honokiol | Honokiol is a bioactive, biphenolic phytochemical that possesses potent antioxidative, anti-inflammatory, antiangiogenic, and anticancer activities by targeting a variety of signaling molecules. It inhibits the activation of Akt. Honokiol can readily cross the blood brain barrier[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NSC 293100. CAS No. 35354-74-6. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-N0003. |  |
| Honokiol | Honokiol is a small-molecule polyphenol isolated from the genus Magnolia. Recent studies show that Honokiol displays antiangiogenic, antiinflammatory, and antitumor properties in preclinical models, without appreciable toxicity. Honokiol has been shown to inhibit the bone metastatic growth of human prostate cancer cells. Group: Biochemicals. Alternative Names: 3',5-Di-2-propen-1-yl-[1,1'-biphenyl]-2,4'-diol; 3',5-Di-2-propenyl-[1,1'-biphenyl]-2,4'-diol; 3',5-Diallyl-2,4'-biphenyldiol; NSC 293100. Grades: Highly Purified. CAS No. 35354-74-6. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Honokiol | Honokiol is a polyphenol found in the genus Magnolia. Honokiol acts as an Akt inhibitor and also inhibits NF-κB, displaying anti-inflammatory, antiangiogenic and antitumor properties. It results in inhibition of bone metastatic growth of human prostate cancer cells. Honokiol has obvious antioxidant and anti-aging effects, thus can be used in cosmetic material. It is a plant polyphenol that can inhibit tyrosinase, block melanin synthesis, reduce skin pigment intensity, absorb UV, prevent photoaging, reduce sun damage and age spot formation, and whiten and lighten spots. It also has the anti-glycation effect, can effectively improve skin tone and skin texture, prevent the generation of age spots, remove red bloodlines, and improve skin blood microcirculation. It has the activity of antibacterial, anti-inflammatory, antioxidant, oil control, acne, promoting healing, and can be widely used in anti-acne, deodorization, acne and other products. Uses: Anti-inflammatory and anti-cancer agent. Alternative Names: Honokiol;35354-74-6;5,3'-Diallyl-2,4'-dihydroxybiphenyl;NSC 293100;3,5'-Diallyl-4,2'-dihydroxybiphenyl;3',5-Diallylbiphenyl-2,4'-diol;C18H18O2;3',5-diallyl-2,4'-biphenyldiol;CPD000387107;CHEMBL16901;2-(4-hydroxy-3-prop-2-enylphenyl)-4-prop-2-enylphenol;CHEBI:5759;4-allyl-2-(3-allyl-4-hydroxy-phenyl)phenol;11513CCO0N;2-[4-hydroxy-3-(prop-2-en-1-yl)phenyl]-4-(prop-2-en-1-yl)phenol;5,3'-Diallyl-biphe. Grades: ≥98%. CAS No. | |
| Honokiol DCA | Honokiol DCA (Honokiol dichloroacetate) is a dichloroacetate analog of Honokiol. Honokiol DCA can inhibit the growth of human prostate cancer cells in vitro and suppress the androgen receptor (AR) protein level[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Honokiol dichloroacetate. CAS No. 1620160-42-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-124292. | |
| Hoodia Cactus Extract | Hoodia Cactus Extract. Applications: Used for health care products, dietary supplements, weight loss, reduce blood sugar. Group: Others. Synonyms: Hoodia Cactus Extract; Opuntia dillenii Haw. Purity: 4-10:1 By TLC. Appearance: Light yellow fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Root&Stem. Species: Opuntia dillenii Haw. Hoodia Cactus Extract; Opuntia dillenii Haw; plant extract. Pack: 20KG-25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-102. | |
| Hoodia Gordonii(African) | Hoodia Gordonii(African). | CA, FL & NJ |
| HOP-22(29)-ENE | HOP-22(29)-ENE. Alternative Names: HOP-22(29)-ENE; Hop-22(29)-ene solution; diploptene; 18α-Methyl-22α-(1-methylethenyl)-20,28,29,30-tetranor-5α-lupane; 5α-Hop-22(29)-ene; Hopene. Grades: 95%. CAS No. 1615-91-4. Molecular formula: C30H50. Mole weight: 410.72. | |
| HOPan | HOPan is a PanK substrate and Pantothenate (HY-B0430) analog. HOPan inhibits CoA levels[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 18679-90-8. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-139729. | |
| Hopane-7beta,22-diol | Hopane-7beta,22-diol. CAS No. 13416-66-5. Molecular formula: C30H52O2. Mole weight: 444.73. | |
| Hopeaphenol | Hopeaphenol is a natural product found in Dipterocarpus grandiflorus and Dipterocarpus hasseltii. Alternative Names: [6,6'-Bibenzo[6,7]cyclohepta[1,2,3-cd]benzofuran]-4,4',8,8',10,10'-hexol, 1,1',6,6',7,7',11b,11'b-octahydro-1,1',7,7'-tetrakis(4-hydroxyphenyl)-, (1R,1'R,6S,6'S,7R,7'R,11bR,11'bR)-; (1R,1'R,6S,6'S,7R,7'R,11bR,11'bR)-1,1',6,6',7,7',11b,11'b-Octahydro-1,1',7,7'-tetrakis(4-hydroxyphenyl)[6,6'-bibenzo[6,7]cyclohepta[1,2,3-cd]benzofuran]-4,4',8,8',10,10'-hexol; [6,6'-Bibenzo[6,7]cyclohepta[1,2,3-cd]benzofuran]-4,4',8,8',10,10'-hexol, 1,1',6,6',7,7',11b,11'b-octahydro-1,1',7,7'-tetrakis(4-hydroxyphenyl)-, [1α,6β(1'R*,6'S*,7'R*,11'R*),7α,11bα]-(-)-; [6,6'-Bibenzo[6,7]cyclohepta[1,2,3-cd]benzofuran]-4,4',8,8',10,10'-hexol, 1,1',6α,6'α,7,7',11bβ,11'bβ-octahydro-1α,1'α,7α,7'α-tetrakis(p-hydroxyphenyl)-; Benzo[6,7]cyclohepta[1,2,3-cd]benzofuran, bimol. deriv.; (-)-Hopeaphenol. Grades: ≥95%. CAS No. 17912-85-5. Molecular formula: C56H42O12. Mole weight: 906.94. | |
| HO-PEG10-OH | HO-PEG10-OH is a polyethylene glycol (PEG)-based PROTAC linker that can be used in the synthesis of a series of PROTACs. Alternative Names: 3,6,9,12,15,18,21,24,27-Nonaoxanonacosane-1,29-diol; Decaethylene Glycol; 2,2'-[Oxybis[2,1-ethanediyloxy(2,1-ethanediyl)oxy(2,1-ethanediyl)oxy(2,1-ethanediyl)oxy]]bis(ethanol). Grades: >97%. CAS No. 5579-66-8. Molecular formula: C20H42O11. Mole weight: 458.54. | |
| HO-PEG11-OH | HO-PEG11-OH is a polyethylene glycol (PEG)-based PROTAC linker. HO-PEG11-OH can be used in the synthesis of a series of PROTACs. Alternative Names: Undecaethylene Glycol; Hydroxy-PEG11-alcohol; 3,6,9,12,15,18,21,24,27,30-Decaoxadotriacontane-1,32-diol. Grades: >97%. CAS No. 6809-70-7. Molecular formula: C22H46O12. Mole weight: 502.59. | |
| HO-PEG12-COOH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. |  |
| HO-PEG12-NH2 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. | |
| HO-PEG12-OH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: Dodecaethylene glycol. Molecular formula: C24H50O13. Mole weight: 546.6g/mol. IUPAC Name: 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol. SMILES: [H]OCCO. InChI: 1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2. | |
| HO-PEG12-Propionic acid | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. | |
| HO-PEG13-OH | HO-PEG13-OH is a polyethylene glycol (PEG)-based PROTAC linker. HO-PEG13-OH can be used in the synthesis of a series of PROTACs. Alternative Names: PEG14; 3,6,9,12,15,18,21,24,27,30,33,36-Dodecaoxaoctatriacontane-1,38-diol. Grades: 95%. CAS No. 17598-96-8. Molecular formula: C26H54O14. Mole weight: 590.699. | |
| HO-PEG14-OH | HO-PEG14-OH is a polyethylene glycol (PEG)-based PROTAC linker. HO-PEG14-OH can be used in the synthesis of a series of PROTACs. Alternative Names: PEG15. CAS No. 1189112-05-7. Molecular formula: C28H58O15. Mole weight: 634.75. | |
| HO-PEG15-OH | HO-PEG15-OH is a polyethylene glycol (PEG)-based PROTAC linker. HO-PEG15-OH can be used in the synthesis of a series of PROTACs. Alternative Names: 3,6,9,12,15,18,21,24,27,30,33,36,39,42-Tetradecaoxatetratetracontane-1,44-diol; 28821-35-4; EINECS249-258-8; AC1L3Q0B; AC1Q592O; SCHEMBL3359595. Grades: 95%. CAS No. 28821-35-4. Molecular formula: C30H62O16. Mole weight: 678.80368. | |
| HO-PEG16-OH | HO-PEG16-OH (CAS# 6812-36-8 ) is a useful research chemical. Alternative Names: 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol; 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol. CAS No. 6812-36-8. Molecular formula: C32H66O17. Mole weight: 722.86. | |
| HO-PEG1K-NH2 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: hydroxyl-PEG-Amine, HO-PEG-NH2, HO-PEG-NH2. Mole weight: average Mn 1000. | |
| HO-PEG20K-NH2 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: hydroxyl-PEG-Amine, HO-PEG-NH2, HO-PEG-NH2. Mole weight: average Mn 20000. | |
| HO-PEG24-OH | HO-PEG24-OH. Alternative Names: HO-PEG24-OH; 2243942-52-9; PEG25; OH-PEG24-OH; 3,6,9,12,15,18,21,24,27,30,33,36,39,42,45,48,51,54,57,60,63,66,69-TRICOSAOXAHENHEPTACONTANE-1,71-DIOL; MFCD28976705; SCHEMBL2582270; DTXSID501025080. Grades: >95%. Molecular formula: C48H98O25. Mole weight: 1075.28. | |
| HO-PEG4-NH2 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. | |
| HO-PEG4-Propionic acid | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: HO-PEG4-PA. Molecular formula: C5H10O4. Mole weight: 134.13g/mol. IUPAC Name: 3-(2-hydroxyethoxy)propanoic acid. SMILES: OCCOCCC(O)=O. InChI: 1S/C5H10O4/c6-2-4-9-3-1-5(7)8/h6H,1-4H2,(H,7,8). | |
| HO-PEG4-silane | HO-PEG4-silane. Alternative Names: Silane-PEG-Hydroxy; Silane-polyethylene glycol-hydroxyl; OH-PEG4-silane. Molecular formula: C20H44N2O9Si. Mole weight: 484.66. | |
| HO-PEG5K-NHS | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: Hydroxyl-PEG-NHS Ester, HO-PEG-NHS. Mole weight: average Mn 5000. | |
| HO-PEG5-OH | Pentaethylene Glycol (CAS# 4792-15-8) is part of a group of compounds called polyethylene glycols (PEGs), which are major byproducts of non-ionic surfactants biodegradation. Pentaethylene glycol is a useful synthetic intermediate, and is used as a reagent to synthesize macrocyclic oligoesters through lipase-catalysis. Alternative Names: 2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethanol; 2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethanol. Grades: >98%. CAS No. 4792-15-8. Molecular formula: C10H22O6. Mole weight: 238.28. | |
| HO-PEG7-OH | HO-PEG7-OH is a polyethylene glycol (PEG)-based PROTAC linker that can be used in the synthesis of a series of PROTACs. Alternative Names: Heptaethylene Glycol; 3,6,9,12,15,18-Hexaoxaeicosane-1,20-diol; NSC 97395; 2-{2-[2-(2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]ethoxy}ethan-1-ol. Grades: ≥95%. CAS No. 5617-32-3. Molecular formula: C14H30O8. Mole weight: 326.38. | |
| HO-PEG8-NH2 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Purity: ≥ 95% (1H-NMR). Product conforms to structure by 1H-NMR. | |
| HO-PEG8-OH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Molecular formula: C16H34O9. Mole weight: 370.44g/mol. IUPAC Name: 2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol. SMILES: C(COCCOCCOCCOCCOCCOCCOCCO)O. InChI: InChI=1S/C16H34O9/c17-1-3-19-5-7-21-9-11-23-13-15-25-16-14-24-12-10-22-8-6-20-4-2-18/h17-18H,1-16H2. | |
| HO-PEG8-OH | Octaethylene Glycol (CAS# 5117-19-1) is part of a leaf extract (Murdannia Bracteata) which was shown to exhibit antioxidant, antimicrobial and anti-cancer properties.Octaethylene Glycol also shows potential application as functional hydraulic fluids. Uses: Octaethylene glycol is part of a leaf extract (murdannia bracteata) which was shown to exhibit antioxidant, antimicrobial and anti-cancer properties.octaethylene glycol also shows potential application as functional hydraulic fluids. Alternative Names: Octaethylene Glycol; 3,6,9,12,15,18,21-Heptaoxatricosane-1,23-diol; Octanethyl glycol; HO-dPEG8-OH; 2-(2-{2-[2-(2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]ethoxy}ethoxy)ethan-1-ol; NSC 97395. Grades: ≥95%. CAS No. 5117-19-1. Molecular formula: C16H34O9. Mole weight: 370.44. | |
| HO-PEG8-Propionic acid | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Molecular formula: C19H38O11. Mole weight: 442.5g/mol. IUPAC Name: 3-[2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid. SMILES: C(COCCOCCOCCOCCOCCOCCOCCOCCO)C(=O)O. InChI: InChI=1S/C19H38O11/c20-2-4-24-6-8-26-10-12-28-14-16-30-18-17-29-15-13-27-11-9-25-7-5-23-3-1-19(21)22/h20H,1-18H2,(H,21,22). | |
| HO-PEG9-OH | HO-PEG9-OH is a polyethylene glycol (PEG)-based PROTAC linker that can be used in the synthesis of a series of PROTACs. Alternative Names: 3,6,9,12,15,18,21,24-Octaoxahexacosane-1,26-diol; Nonaethylene Glycol; NSC 97395. Grades: ≥95%. CAS No. 3386-18-3. Molecular formula: C18H38O10. Mole weight: 414.49. | |
| HO-PEG-OH | Augment your research on Biodegradable Polymers with the reliable HO-PEG-OH from CD Bioparticles Drug Delivery. Group: Poly(ethylene glycol). |  |
| HOPG | HOPG. Purity: >99.99%. | |
| HO-Phe-Val-Gln-Trp-Leu-Ile-Ala-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH2 | HO-Phe-Val-Gln-Trp-Leu-Ile-Ala-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH2 is an 18-amino-acid peptide with a free hydroxyl group (HO) at the N-terminus and an amide group (NH2) at the C-terminus. This peptide features a mix of hydrophobic residues (Phe, Val, Trp, Leu, Ile, Ala), polar residues (Gln, Ser), and glycine (Gly) which contributes to its flexibility. The multiple proline residues (Pro) suggest potential for forming specific structural motifs. This peptide could be of interest for studying protein folding, structural interactions, or in designing peptides with specific biological activities. Alternative Names: Phe-Val-Gln-Trp-Leu-Ile-Ala-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH2; (S)-N1-((8S,11S,14S,17S)-1-((S)-2-(((S)-1-(((S)-1-((2-(((S)-1-((S)-2-((S)-2-((S)-2-(((S)-1-Amino-3-hydroxy-1-oxopropan-2-yl)carbamoyl)pyrrolidine-1-carbonyl)pyrrolidine-1-carbonyl)pyrrolidin-1-yl)-1-oxopropan-2-yl)amino)-2-oxoethyl)amino)-3-hydroxy-1-oxopropan-2-yl)amino)-3-hydroxy-1-oxopropan-2-yl)carbamoyl)pyrrolidin-1-yl)-11-((S)-sec-butyl)-18-(1H-indol-3-yl)-14-isobutyl-8-methyl-1,4,7,10,13,16-hexaoxo-3,6,9,12,15-pentaazaoctadecan-17-yl)-2-((S)-2-((S)-2-amino-3-phenylpropanamido)-3-methylbutanamido)pentanediamide. Grades: ≥90%. Molecular formula: C83H123N21O22. Mole weight: 1767.02. | |
| HOPO | Can be used as an additive during peptide synthesis to reduce racemization and thereby increase chiral purity of the final product. Its solubility in water makes it especially useful during solution-phase peptide synthesis. HOPO has also shown to be useful in other applications, including the functionalization of self-assembled monolayers. Uses: Peptide Synthesis. Group: Coupling Reagents. Alternative Names: 2-Hydroxypyridine-N-oxide. CAS No. 13161-30-3. |  Luxembourg Bio Technologies |
| Hops Extract (Ratio) | Hops Extract (Ratio). Group: Others. Purity: 4:1~20:1. Hops Extract (Ratio). Cat No: EXTW-039. | |
| Hops Flower Extract (Standard) | Hops are the female flower cones, also known as strobiles, of the hop plant (Humulus lupulus). The hop is part of the family Cannabaceae, which also includes the genus Cannabis (hemp). They are used primarily as a flavoring and stability agent in beer, though hops are also used for various purposes in other beverages and herbal medicine. Applications: It can inhibit the growth of various bacteria. such as bacillus anthracis, bacillus, corynebacterium diphtheriae, diplococcus pneumoniae and staphylococcus aureusit can also help to stimulate appetite , dispel flatulence, and relieve intestinal cramps. Group: Others. CAS No. 6754-58-1. Purity: 4.0% Flavones UV. Mole weight: 354.14. Hops Flower Extract (Standard); 6754-58-1; C21H22O5. Cat No: EXTW-018. | |
| Hops P.E. Powder & 30% Alpha Acids UV | Hops P.E. Powder & 30% Alpha Acids UV. | CA, FL & NJ |
| Hops Strobile P.E. 4:1 | Hops Strobile P.E. 4:1. | CA, FL & NJ |
| HOR1-C59 | HOR1-C59 is a highly selective Or5v1/Olfr110 agonist with an EC50 of 7.12 nM. HOR1-C59 can improve glucose homeostasis, alleviate obesity and insulin resistance. HOR1-C59 is applicable for obesity-related research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 189574-20-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-186028. | |
| Hordenine | A phenethylamine alkaloid with antibacterial and antibiotic properties found mainly in plants from the cactaceae family. It showed effects similar to Cytosine and acted as a depressant on the central nervous system (CNS) during animal testing. Group: Biochemicals. Alternative Names: 4- (2-Dimethylaminoethyl) phenol; Eremursine; p-[2- (Dimethylamino) ethyl]phenol; Anhalin; Anhaline; Cactine; Hordenin; N,N-Dimethyl-4-hydroxy- β-phenethylamine; N,N-Dimethyl-p-hydroxyphenethylamine; N,N-Dimethyltyramine; Ordenina; Peyocactine; p-Hydroxy-N, N-di methyl phenethylamine; p-[2- (Dimethylamino) ethyl]phenol. Grades: Highly Purified. CAS No. 539-15-1. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| Hordenine HCL 98% | Hordenine HCL 98%. | CA, FL & NJ |
| Hordenine hydrochloride | Hordenine hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 6027-23-2. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C10H15NOCIH. US Biological Life Sciences. | Worldwide |
| Hordeum vulgare Extract (Ratio) | Hordeum vulgare Extract (Ratio). Group: Others. Purity: 4:1~20:1. Hordeum vulgare Extract (Ratio). Cat No: EXTW-040. | |
| Hormaomycin | Hormaomycin is an ester peptide antibiotic produced by Streptomyces griseoflavus. It is a signal transmitting substance between cells, which interferes with the formation of some streptomyces gas hyphae and the production of secondary metabolites. It also has anti-Gram-positive bacteria effect. CAS No. 121548-21-8. Molecular formula: C55H69ClN10O14. Mole weight: 1129.65. | |
| Hormaomycin B | Hormaomycin B is an cyclic depsipeptide antibiotic from a Marine Mudflat-Derived Streptomyces sp. It has a significant inhibitory effect on both Gram-positive and Gram-negative bacteria. Molecular formula: C54H67ClN10O14. Mole weight: 1115.62. | |
| Hormaomycin C | Hormaomycin C is an cyclic depsipeptide antibiotic from a Marine Mudflat-Derived Streptomyces sp. It has a significant inhibitory effect on both Gram-positive and Gram-negative bacteria. Molecular formula: C54H67ClN10O14. Mole weight: 1115.62. | |
| hormone-sensitive lipase | This enzyme is a serine hydrolase. Compared with other lipases, hormone-sensitive lipase has a uniquely broad substrate specificity. It hydrolyses all acylglycerols (triacylglycerol, diacylglycerol and monoacylglycerol) as well as cholesteryl esters, steroid fatty acid esters, retinyl esters and p-nitrophenyl esters. It exhibits a preference for the 1- or 3-ester bond of its acylglycerol substrate compared with the 2-ester bond. The enzyme shows little preference for the fatty acids in the triacylglycerol, although there is some increase in activity with decreasing chain length. The enzyme activity is increased in response to hormones that elevate intracellular levels of cAMP. Group: Enzymes. Synonyms: HSL. Enzyme Commission Number: EC 3.1.1.79. 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-3507; hormone-sensitive lipase; EC 3.1.1.79; HSL. Cat No: EXWM-3507. | |
| H-Orn-AMC HCl | H-Orn-AMC HCl. Alternative Names: H-Orn-AMC hydrochloride salt. CAS No. 98516-75-7. Molecular formula: C15H19N3O3·HCl. Mole weight: 325.8. | |
| H-Orn(Boc)-2-Chlorotrityl Resin | 2-Chlorotrityl-Chloride-Resin is less acid-labile than Trityl Resin, and is widely used for solid phase immobilization. It has been used with the Fmoc/tBu methodology in the microwave-assisted solid phase peptide synthesis. | |
| H-Orn(Boc)-OtBu HCl | H-Orn(Boc)-OtBu HCl. Molecular formula: C14H28N2O4·HCl. Mole weight: 324.8. | |
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