magnesium aluminosilicat CAS# 71205-22-6
magnesium aluminosilicat , Promotion Season Now in Store and Free Sample for Testing with Factory Price
Chemical Name: magnesium aluminosilicat
CAS No.: 71205-22-6
Molecular Fomula: C11H14O
magnesium aluminosilicat : The Complete Guide
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Description of magnesium aluminosilicat
Almasilate is an antacid.
Basic Info of magnesium aluminosilicat
Almasilato [INN-Spanish];Malinal;Almasilate;Almasilatum [INN-Latin];Almasilatum;Expand
Appearance & Physical State
273.9ºC at 760 mmHg
What is magnesium aluminosilicat?
With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is Ambroxan which has developed particularly rapidly in recent years. Do you know about Ambroxan?
The official answer: White compound gelatinous substance. Water content is less than 8%. Non-toxic. Odorless. Insoluble in water. Dispersible in water. pH 7.5~9.5. Good rheology and thixotropy.
What’s the application of magnesium aluminosilicat?
- UsesReduced glutathione is a small molecule peptide, which exists in large quantities in living organisms, especially in liver cells, and has the function of protecting liver cell membranes and promoting liver enzyme activity, and plays the role of detoxification by combining with many toxic chemicals. It has good effect on drug poisoning, alcohol poisoning and other diseases caused by various reasons such as liver injury and cirrhosis of the liver. Uses: Antioxidant, free radical scavenging, detoxification, immunity enhancement, aging delay, anti-cancer, anti-radiation hazard, etc.
- Uses: Biochemical reagent, detoxification Chemicalbook medicine, mainly used for heavy metal, acrylonitrile, fluoride, carbon monoxide and organic solvents and other poisoning
- Use biochemical research use endogenous antioxidant that plays an important role in the reduction of reactive oxygen species formed during cell metabolism and sudden respiration. Glutathione-S-transferase catalyzes the formation of glutathione sulfide with xenobiotics, leukotrienes and other molecules with electrophilic centers. Glutathione also forms disulfide bonds with cysteine residues in proteins. Through these mechanisms, it may have the singular effect of reducing the potency of anticancer agents.
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