Fenugreek Saponins Extract Manufacturers

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Hot Products

  • Nicotinamide

    Nicotinamide

    China H&Z® Nicotinamide (Niacinamide), also known as nicotinamide, is an amide compound of nicotinic acid. White crystalline powder; odorless or almost odorless, bitter taste; slightly hygroscopic. Soluble in water or ethanol, soluble in glycerol. It is mainly used in the prevention and treatment of pellagra, stomatitis, glossitis, sick sinus syndrome.
  • D(+)-Xylose

    D(+)-Xylose

    China H&Z® D(+)-Xylose is a colorless to white crystals or white crystalline powder, slightly sweet odor and refreshing. D-Xylose Sweetness of sucrose 40%. Relative density 1.525, melting point of 114 degrees, were right-handed light and variable optical activity, soluble in water and hot ethanol, insoluble in alcohol and ether. The body can not digest, D-Xylose E967 can not use. Natural crystal exists in a variety of mature fruit.
  • Ketoconazole

    Ketoconazole

    Ketoconazole, white or almost white crystalline powder, is a synthetic imidazole antifungal drug used primarily to treat fungal infections.China H&Z® Ketoconazole is sold commercially as a tablet for oral administration (although this use has been discontinued in a number of countries), and in a variety of formulations for topical administration, such as creams (used to treat tinea; cutaneous candidiasis, including candidal paronychia; and pityriasis versicolor) and shampoos (used primarily to treat dandruff-seborrhoeic dermatitis of the scalp).
  • Sodium Bromide

    Sodium Bromide

    Sodium bromide/NaBr CAS:7647-15-6
  • Sodium Alginate

    Sodium Alginate

    China H&Z® Sodium alginate is used to replace starch, gelatin as the stabilizer of ice cream, controlling the formation of ice crystals and improving the flavor of ice cream. It can also stabilize mixed beverages like sugar ice cream, sherbet, frozen milk etc.
  • Serrapeptase

    Serrapeptase

    China H&Z® Serrapeptase has anti-inflammatory, swelling effect: thermal burns in rats as a model of inflammation after oral administration of visible vascular permeability was inhibited.

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