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 | |
|---|---|---|
| Homovanillic Acid-[d3] | Homovanillic Acid-[d3] is an isotopically-labeled version of Homovanillic Acid (HVA). This important dopamine metabolite is predominantly found in human urine and is a valuable biochemical research tool for investigating the mechanisms underlying neuropsychiatric and neurodegenerative disorders, such as Parkinson's disease, Alzheimer's disease, and schizophrenia. Its use in these studies is useful, given the marked alterations in dopamine metabolism and function that are observed in these conditions. Uses: A neuroendocrine tumor marker. a labelled metabolite of dihydroxyphenylacetic acid (dopac) by catechol o-methyltransferase. Synonyms: Homovanillic Acid D3. Grade: 95% atom D. CAS No. 74495-71-9. Molecular formula: C9H7D3O4. Mole weight: 185.19. |  |
| Homovanillic acid-d5 | Homovanillic acid-d5 is the deuterium labeled Homovanillic acid. Homovanillic acid is a dopamine metabolite found to be associated with aromatic L-amino acid decarboxylase deficiency, celiac disease, growth hormone deficiency, and sepiapterin reductase deficiency. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Vanilacetic acid-d5. CAS No. 53587-32-9. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N0384S2. |  |
| Homovanillic Acid-[d5] | Homovanillic Acid-[d5]. Synonyms: HVA-d5; 2-(4-hydroxy-3-methoxyphenyl-2,5,6-d3)acetic-2,2-d2 acid. Grade: 98% by CP; 98% atom D. CAS No. 53587-32-9. Molecular formula: C9H5D5O4. Mole weight: 187.21. | |
| Homovanillic Acid Propyl Ester | Homovanillic Acid Propyl Ester. Group: Biochemicals. Alternative Names: 4-Hydroxy-3-methoxybenzeneacetic Acid Propyl Ester; (4-Hydroxy-3-methoxyphenyl)acetic Acid; 3-Methoxy-4-hydroxyphenylacetic Acid Propyl Ester. Grades: Highly Purified. CAS No. 52744-26-0. Pack Sizes: 1g. Molecular Formula: C12H16O4, Molecular Weight: 224.25. US Biological Life Sciences. |  Worldwide |
| Homovanillic acid (Standard) | Homovanillic acid (Standard) is the analytical standard of Homovanillic acid. This product is intended for research and analytical applications. Homovanillic acid is a dopamine metabolite found to be associated with aromatic L-amino acid decarboxylase deficiency, celiac disease, growth hormone deficiency, and sepiapterin reductase deficiency. Uses: Scientific research. Group: Natural products. Alternative Names: Vanilacetic acid (Standard). CAS No. 306-08-1. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0384R. | |
| Homovanillic Acid Sulfate Sodium Salt | A metabolite of Dihydroxyphenylacetic Acid (DOPAC) by catechol O-methyltransferase. Group: Biochemicals. Alternative Names: 3-Methoxy-4-(sulfooxy)-benzeneacetic Acid Disodium Salt. Grades: Highly Purified. CAS No. 38339-06-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Homovanillic Acid Sulfate Sodium Salt-d3 | A labeled metabolite of Dihydroxyphenylacetic Acid (DOPAC) by catechol O-methyltransferase. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Homovanillyl Alcohol | Homovanillyl Alcohol. Uses: Designed for use in research and industrial production. Product Category: Alcohols. Appearance: Oil. CAS No. 2380-78-1. Molecular formula: C9H12O3. Mole weight: 168.19. Purity: 0.98. IUPACName: 4-(2-hydroxyethyl)-2-methoxyphenol. Canonical SMILES: COC1=C(C=CC(=C1)CCO)O. Product ID: ACM2380781. Alfa Chemistry ISO 9001:2015 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. Synonyms: 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. Grade: ≥98%. Molecular formula: C16H20O10. Mole weight: 372.32. | |
| Homoveratronitrile | An impurity of Verapamil. An intermediate in the preparation of the muscle relaxant Papverine. Group: Biochemicals. Alternative Names: (3, 4-Dimethoxyphenyl) acetonitrile; 2- (3, 4-Dimethoxyphenyl) acetonitrile; 3, 4-Dimethoxy Benzene acetonitrile; 3,4-Dimethoxybenzyl cyanide; NSC 6324; Veratryl Cyanide. Grades: Highly Purified. CAS No. 93-17-4. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| 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 |
| Homo-VK-II-36 | Homo-VK-II-36 is a novel carvedilol analog that inhibits store- overload- induced calcium release (SOICR) through the RyR2 channel. Synonyms: Homo VK II 36; HomoVKII36; 3-Morpholinone, 6-[2-(9H-carbazol-4-yloxy)ethyl]-4-[2-(2-methoxyphenoxy)ethyl]-; 6-(2-((9H-Carbazol-4-yl)oxy)ethyl)-4-(2-(2-methoxyphenoxy)ethyl)morpholin-3-one. Grade: >98%. CAS No. 1479049-35-8. Molecular formula: C27H28N2O5. Mole weight: 460.52. | |
| HONB | HONB is used in solution-phase peptide synthesis. Used in the synthesis of enkephalin analogs. Group: Biochemicals. Alternative Names: 3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dione; N-Hydroxy-5-norbornene-2,3-dicarboximide; 3, 5-Dioxo-4-azatricyclo[5. 2. 1. 02'6]dec-8-en-4-ol; HONB; N-Hydroxy-5-bicyclo[2.2.1]heptene-2,3-dicarboximide; N-Hydroxy-5-norbornene-2,3-dicarboximide; NSC 100740; NSC 12953. Grades: Highly Purified. CAS No. 21715-90-2. Pack Sizes: 25g. 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 Powder | Honey Powder. Group: Others. Purity: Purity: 100%. Appearance: Light yellow powder. Source: Natural honey. Honey Powder. Cat No: EXTC-123. |  |
| Honey Powder | Honey Powder. | CA, FL & NJ |
| 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. | |
| Honeysuckle Flower Extract | Honeysuckle Flower Extract. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Chlorogenic acid. Product Category: Material of health food. Appearance: liquid. CAS No. 327-97-9. Molecular formula: C16H18O9. Mole weight: 354.31. Purity: 95+%. Product ID: ACM327979. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. Uses: Designed for use in research and industrial production. CAS No. 35354-74-6. Purity: 0.98. Product ID: BBC35354746. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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 - Product ID: NST-10-111. Category: Polyphenols. Alternative Names: Honokiol. Purity: 98%. Test method: HPLC. CAS No. 35354-74-6. Pack Sizes: 25g, 50g, 125g, 250g. Appearance: White to beige coloured Powder. Molecular formula: C18H18O2. Mole weight: 266.33. Storage: +2 +8 °C. |  |
| 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. Group: Natural products. Alternative Names: NSC 293100. CAS No. 35354-74-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg. Product ID: HY-N0003. | |
| 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. Synonyms: 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. Grade: ≥98%. CAS No. 35354-74-6 | |
| 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. Group: Signaling pathways. Alternative Names: Honokiol dichloroacetate. CAS No. 1620160-42-0. Pack Sizes: 10 mM * 1 mL; 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 solution | 0.1 mg/mL in isooctane, analytical standard. Group: Chemical class. |  |
| HOPan | HoPan inhibits phosphopantotenoylcysteine synthetase activity. Uses: Scientific research. Group: Signaling pathways. CAS No. 18679-90-8. Pack Sizes: 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. | |
| Hopantenate Calcium | Hopantenate Calcium. Group: Biochemicals. Alternative Names: 4- [ [ (2R) -2, 4-Dihydroxy-3, 3-dimethyl-1-oxobutyl] amino] butanoic Acid Calcium Salt (2:1); 4- (2, 4-Dihydroxy-3, 3-dimethylbutyramido) butyric Acid Calcium Salt (2:1); Calcium D-(+)-Homopantothenate; Calcium Homopantothenate; Calcium Hopantenate; D-(+)-Homopantothenic Acid Calcium Salt; Pantocalcin; Pantogam; Vivant. Grades: Highly Purified. CAS No. 17097-76-6. Pack Sizes: 1mg, 10mg. Molecular Formula: C20H36CaN2O10, Molecular Weight: 504.59. US Biological Life Sciences. | Worldwide |
| Hopantenate Calcium-d6 | Hopantenate Calcium-d6. Group: Biochemicals. Alternative Names: 4- [ [ (2R) -2, 4-Dihydroxy-3, 3-dimethyl-1-oxobutyl] amino] butanoic Acid Calcium Salt (2:1)-d6; 4- (2, 4-Dihydroxy-3, 3-dimethylbutyramido) butyric Acid Calcium Salt (2:1)-d6; Calcium D-(+)-Homopantothenate-d6; Calcium Homopantothenate-d6; Calcium Hopantenate-d6; D-(+)-Homopantothenic Acid Calcium Salt-d6; Pantocalcin-d6; Pantogam-d6; Vivant-d6. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C20H24D12CaN2O10, Molecular Weight: 516.66. US Biological Life Sciences. | Worldwide |
| 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. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). |  |
| 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. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 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. Uses: S may include: bioconjugation, drug delivery, peg hydrogel, crosslinker, and surface functionalization. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Dodecaethylene glycol. Product ID: 2- [2- [2- [2- [2- [2- [2- [2- [2- [2- [2- (2-hydroxyethoxy) ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethanol. Molecular formula: 546.6g/mol. Mole weight: C24H50O13. [H]OCCO. 1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2. LYCAIKOWRPUZTN-UHFFFAOYSA-N. | |
| 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. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 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. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: hydroxyl-PEG-Amine, HO-PEG-NH2, HO-PEG-NH2. Molecular formula: average Mn 1000. | |
| HO-PEG1K-NH2 | HCl Salt, average Mn 1,000. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| HO-PEG20K-NH2 | HCl Salt, average Mn 20,000. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 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. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: hydroxyl-PEG-Amine, HO-PEG-NH2, HO-PEG-NH2. Molecular formula: average Mn 20000. | |
| 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. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 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. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and redu. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: HO-PEG4-PA. Product ID: 3-(2-hydroxyethoxy)propanoic acid. Molecular formula: 134.13g/mol. Mole weight: C5H10O4. OCCOCCC(O)=O. 1S/C5H10O4/c6-2-4-9-3-1-5(7)8/h6H, 1-4H2, (H, 7, 8). GTIFLSYPOXYYFG-UHFFFAOYSA-N. | |
| HO-PEG5K-NHS | average Mn 5,000. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 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. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Hydroxyl-PEG-NHS Ester, HO-PEG-NHS. Molecular formula: average Mn 5000. | |
| 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. Uses: 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. Group: Poly(ethylene glycol) and poly(ethylene oxide). ≥ 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. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and redu. Group: Poly(ethylene glycol) and poly(ethylene oxide). Product ID: 2- [2- [2- [2- [2- [2- [2- (2-hydroxyethoxy) ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethanol. Molecular formula: 370.44g/mol. Mole weight: C16H34O9. C(COCCOCCOCCOCCOCCOCCOCCO)O. 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. GLZWNFNQMJAZGY-UHFFFAOYSA-N. | |
| 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. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and redu. Group: Poly(ethylene glycol) and poly(ethylene oxide). Product ID: 3- [2- [2- [2- [2- [2- [2- [2- (2-hydroxyethoxy) ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] propanoic acid. Molecular formula: 442.5g/mol. Mole weight: C19H38O11. C(COCCOCCOCCOCCOCCOCCOCCOCCO)C(=O)O. InChI= 1S / C19H38O11 / c20-2-4-24-6-8-26-10-12-28-14-16-30-1 8-17-29-15-13-27-11-9-25-7-5-23-3-1-1 9 (21) 22 / h20H, 1-18H2, (H, 21, 22). BGBLNDCLYGWOKM-UHFFFAOYSA-N | |
| HOPG | HOPG. Group: Graphene series. >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. Synonyms: 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. Grade: ≥90%. Molecular formula: C83H123N21O22. Mole weight: 1767.02. | |
| Hop human | recombinant, expressed in E. coli, ?99% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| 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 |
| Hoquizil hydrochloride | Hoquizil hydrochloride is a new oral bronchodilator. Synonyms: (2-hydroxy-2-methylpropyl) 4-(6,7-dimethoxyquinazolin-4-yl)piperazine-1-carboxylate; hydrochloride; Hoquizil hydrochloride; Hoquizil HCl; CP-14,185-1; CP-14185-1. Grade: >98%. CAS No. 23256-28-2. Molecular formula: C19H27ClN4O5. Mole weight: 426.89. | |
| 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 | Hordenine, an alkaloid found in plants, inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Ordenina; Peyocactine. CAS No. 539-15-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 20 mg. Product ID: HY-N0113. | |
| Hordenine-[d6] | Hordenine-[d6] is the labelled analogue of Hordenine. Hordenine is an alkaloid that occurs naturally in a variety of plants. Synonyms: Hordenine D6; 4-[2-(Dimethyl-d6)aminoethyl]phenol; Eremursine; Anhalin-d6; Anhaline-d6; Cactine-d6; p-[2-[(Dimethyl-d6)amino]ethyl]phenol. Grade: 95% by HPLC; 98% atom D. CAS No. 1346598-66-0. Molecular formula: C10H9D6NO. Mole weight: 171.27. | |
| 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 |
| Hordenine hydrochloride | Hordenine (hydrochloride), an alkaloid found in plants, inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Ordenina hydrochloride; Peyocactine hydrochloride. CAS No. 6027-23-2. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-N0113B. | |
| 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. | |
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