A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the suppliers website for prices or more information.
| Product | Description | |
|---|---|---|
| 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 Blend | Plant based liquid concentrate that has antimicrobial properties. Active components are isolated from herbs, namely Lonicera Japonica (Japanese Honeysuckle) and Lonicera Caprifolium. The concentrate is suitable for the antimicrobial protection of cosmetic and pharmaceutical applications. Uses: All kinds of emulsions, surfactant systems (cleansers), and other products that contain water. Group: Skin actives. CAS No. 84603-62-3/223749-79-9/773218-5. Appearance: Light clear yellow liquid, moderate characteristic odor. Catalog: CI-SC-0993. |  |
| Honeysuckle Extract | Extract obtained from Lonicera Caprifolum (Honeysuckle) flowers. Contains 20% extract dissolved in water and glycerin. Has antimicrobial, aromatic and cleansing properties. Uses: Creams and lotions, soaps, and cleansers. Group: Skin actives. CAS No. 7732-18-5 / 56-81-5 / 84603-62-3 / 122-99-6. Appearance: Light to medium amber liquid, characteristic odor. Catalog: CI-SC-0831. | |
| 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 - 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. Group: Inhibitors. Alternative Names: 3',5-Diallyl-2,4'-biphenyldiol. CAS No. 35354-74-6. Molecular formula: C18H18O2. Mole weight: 266.33. Appearance: White powder. Purity: 0.98. IUPACName: 2-(4-Hydroxy-3-prop-2-enylphenyl)-4-prop-2-enylphenol. Canonical SMILES: C=CCC1=CC (=C (C=C1)O)C2=CC (=C (C=C2)O)CC=C. Density: 1.107±0.06 g/ml. Catalog: ACM35354746. | |
| 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 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 Standard | Heterocyclic Organic Compound. CAS No. 035354-74-6. Purity: N/A. Catalog: ACM035354746. | |
| Honyucitrin | Flavonoids. CAS No. 114542-44-8. Molecular formula: C25H26O5. Mole weight: 406.48. Appearance: Yellow powder. Purity: 0.98. IUPACName: 5,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]chromen-4-one. Canonical SMILES: CC (=CCC1=CC (=CC (=C1O)CC=C (C)C)C2=CC (=O)C3=C (C=C (C=C3O2)O)O)C. Catalog: ACM114542448. | |
| HOOBT | HOOBt is a STAT5-SUMO protein-protein interaction inhibitor that suppresses SUMOylation of phosphorylated STAT5. Synonyms: 3-Hydroxy-1,2,3-benzotriazin-4(3H)-one; 3-hydroxy-3H-benzo[d][1,2,3]triazin-4-one; DHBT; oxohydroxybenzotriazole; 4-oxo-3,4-dihydro-3-hydroxy-1,2,3-benzotriazine; 3-Hydroxy-4-ketobenzotriazine; 3,4-Dihydro-3-hydroxy-4-oxo-1,2,3-benzotriazine; 1,2,3-Benzotriazin-4(3H)-one,3-hydroxy; 3,4-dihydro-3-hydroxy-4-keto-1,2,3-benzotriazine; 3-Hydroxy-3,4-dihydro-4-oxo-1,2,3-benzotriazine. Grades: 98% (HPLC). CAS No. 28230-32-2. Molecular formula: C7H5N3O2. Mole weight: 163.13. | |
| 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 |
| 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 |
| Hopeachinol B | Phenols. CAS No. 1238083-45-8. Molecular formula: C35H24O9. Mole weight: 588.6. Appearance: Powder. Purity: 0.98. Canonical SMILES: C1=CC (=CC=C1C2C3C4=CC (=CC5=C4C (C (O5)C6=CC=C (C=C6)O)C7=CC (=CC (=C7C (=O)C8=CC (=CC (=C38)O2)O)O)O)O)O. Catalog: ACM1238083458. | |
| 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-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 | 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%. | |
| 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 | Extract obtained from dried Humulus Lupulus (Hops) strobiles. Contains 20% extract dissolved in water and glycerin. Has anti-irritating, soothing and calming properties. Uses: Creams and lotions, bath preparations. Group: Skin actives. CAS No. 7732-18-5 / 56-81-5 / 8016-25-9 / 8060-28-4 / 122-99-6. Appearance: Light to medium golden amber liquid, characteristic odor. Catalog: CI-SC-0793. | |
| 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. Grades: >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 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. | |
| 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 | Synonyms: H-Orn-AMC hydrochloride salt. CAS No. 98516-75-7. Molecular formula: C15H19N3O3·HCl. Mole weight: 325.8. | |
| H-Orn(Boc)-OtBu HCl | Molecular formula: C14H28N2O4·HCl. Mole weight: 324.8. | |
| Horny goat weed extract | Horny goat weed extract. Applications: Functional food, health care products and pharmaceuticals. Group: Others. Purity: Icariin 10% - 98%. Appearance: Brown to yellow powder. Source: Epimedium, also called horny goat weed, grows as an ornamental herb in Asia and the Mediterranean. In Asia, its leaves have been used for treating fatigue and boosting sex drive for a long history since 16th century. Nowadays, the plant is a traditional Chinese medicine and is widely used as dietary supplement in western countries. It is also sometimes referred to by its active ingredient, Icariin. Icariin is known as a prenylated flavonoid compound and has been shown to exert much of the aphrodisiac effects of Horny Goat Weed. It has also been shown in one rat study to increase Testosterone levels at a rather high dose, and moderate dosages are shown to be beneficial for bone health. Horny goat weed extract. Cat No: EXTC-131. | |
| Horny Goat Weed P.E. 10% Icariins HPLC | Horny Goat Weed P.E. 10% Icariins HPLC. | CA, FL & NJ |
| horrilysin | A 56 kDa hemorrhagic endopeptidase from the venom of the timber rattlesnake (Crotalus horridus horridus) that cleaves basement membrane, hide powder and fibrinogen. Group: Enzymes. Synonyms: Crotalus horridus metalloendopeptidase; hemorrhagic proteinase IV; Crotalus horridus horridus venom hemorrhagic proteinase. Enzyme Commission Number: EC 3.4.24.47. CAS No. 84056-81-5. 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-4329; horrilysin; EC 3.4.24.47; 84056-81-5; Crotalus horridus metalloendopeptidase; hemorrhagic proteinase IV; Crotalus horridus horridus venom hemorrhagic proteinase. Cat No: EXWM-4329. | |
| Horse Chestnut Extract | Natural Horse Chestnut extract made from whole plant. Other parts, for example, the bark have been used as a yellow dye. Contains 20% of extract dissolved in water and glycerin. Uses: Creams & lotions, shampoos & conditioners, hair mask, body wraps, face cleansers, toners and moisturizers, masks and gels. Group: Skin actives. CAS No. 56-81-5/7732-18-5/8053-39-2/122-99-6. Appearance: Light yellow liquid, characteristic odor. Catalog: CI-SC-0665. | |
| Horse Chestnut Extract (Ratio) | Horse Chestnut Extract (Ratio). Group: Others. Purity: 4:1~20:1. Horse Chestnut Extract (Ratio). Cat No: EXTW-041. | |
| Horse Chestnut Extract (Standard) | Horse Chestnut (Aesculus hippocastanum) is native to a small area in the Pindus Mountains mixed forests and Balkan mixed forests of South East Europe. It is widely cultivated in streets and parks throughout the temperate world. Applications: It has anti-inflammatory health effects.buckeye makes veins strong and flexible, improves blood flow through veins.diminish varicose veins.heal hemorrhoids.reduce edema. Group: Others. CAS No. 6805-41-0. Purity: 20.0% Aescins UV/HPLC. Mole weight: 1131.26. Horse Chestnut Extract (Standard); 6805-41-0; C55H86O24. Cat No: EXTW-009. | |
| Horse Chestnut Liquid Extract | Horse Chestnut Liquid Extract. | CA, FL & NJ |
| Horse Chestnut Seed Extract | Horse chestnut extract is extracted from the seeds of horse chestnut tree (Aesculus hippocastanum). Horse chestnut is native to areas of Europe, but is now grow in many areas around the world. Esicin (also spelt as aescin) is the most abundant active compound of horse chestnut extract and exhibits a range of actions. Group: Others. Mole weight: 1131.26. Horse Chestnut Seed Extract; Aesculus Chinensis Bunge. Cat No: EXTC-056. | |
| Horse Placenta P.E. 25:1 (New Zealand) | Horse Placenta P.E. 25:1 (New Zealand). | CA, FL & NJ |
| Horseradish Extract | Extract obtained from Cochlearia Armoracia (Horseradish) roots. Contains 20% extract dissolved in water and glycerin. Has purifying, anti-blemish and stimulating properties. Uses: Creams and lotions for skin lightening, cleaners and shampoos. Group: Skin actives. CAS No. 7732-18-5 / 56-81-5 / 84775-62-2 / 122-99-6. Appearance: Light to pale yellow liquid, characteristic odor. Catalog: CI-SC-0859. | |
| Horseradish peroxidase | Peroxidase is a heme-containing enzyme, and it can be used to oxidize a wide variety of substrates. Synonyms: HRP; Peroxidase. CAS No. 9003-99-0. Molecular formula: H2O3. | |
| Horsetail | Heterocyclic Organic Compound. Alternative Names: Horsetail;Equisetum arvense, tincture;Horsetail rush (equisetum arvense). CAS No. 129677-90-3. Catalog: ACM129677903. | |
| Horsetail Extract | Horsetail Extract. Group: Others. Purity: 7% Organic Silica Test by UV. Source: Horsetail (Equistum Arvense L.) an herbal remedy dating back to at least ancient Roman and Greek medicine, was used traditionally to stop bleeding, heal ulcers and wounds, and treat tuberculosis and kidney problems. The name Equisetum is derived from the Latin roots equus, meaning "horse," and seta, meaning "bristle.". Horsetail Extract. Cat No: EXTC-188. | |
| Horsetail Extract | Extract obtained from Equisetum Arvense L. (Horsetail) plants. Contains 20% extract dissolved in water and glycerin. Natural emulsifying and mattifying properties; creates a matte finish while maintaining good moisturizing features. Used for centuries as anti-irritant and soothing agent. Also used in deodorants. Uses: All kinds of skin and hair care products. also useful in makeup products. Group: Skin actives. CAS No. 7732-18-5 / 56-81-5 / 71011-23-9 / 122-99-6. Appearance: Colorless to light brown liquid, characteristic odor. Catalog: CI-SC-0785. | |
| Horsetail P.E. 10:1 & 7% Silica HPLC | Horsetail P.E. 10:1 & 7% Silica HPLC. | CA, FL & NJ |
| Hortein | Hortein is a polyketide fungal metabolite isolated from H. werneckii. Grades: >95% by HPLC. CAS No. 346610-88-6. Molecular formula: C20H12O6. Mole weight: 348.31. | |
| Hortiamide | Other Alkaloids. CAS No. 106055-13-4. Molecular formula: C20H23NO2. Mole weight: 309.4. Purity: 98%+ (HPLC). IUPACName: N-[2-[4-(3-Methylbut-2-enoxy)phenyl]ethyl]benzamide. Canonical SMILES: CC (=CCOC1=CC=C (C=C1)CCNC (=O)C2=CC=CC=C2)C. Catalog: ACM106055134. | |
| Hosenkoside A | Hosenkoside A. Group: Biochemicals. Grades: Plant Grade. CAS No. 156791-82-1. Pack Sizes: 10mg. Molecular Formula: C48H82O20, Molecular Weight: 979.16. US Biological Life Sciences. | Worldwide |
Our database is helping our users find suppliers everyday.
