Sulfate neutral

Where the supply water is of low hardness but high alkalinity (the major contributor to alkalinity is sodium rather than calcium), neutralization by a small addition of RW before the degasser adds back a small amount of calcium but no further alkalinity. Where the supply water is of high hardness and alkalinity but has lower levels of chlorides and sulfates, neutralization after the degasser, using caustic soda, is the preferred practice. 

Neutral tertiary and secondary amides react with very reactive alkylating agents, such as triethyloxonium tetrafluoroborate, to give O-alkylation.63 The same reaction occurs, but more slowly, with tosylates and dimethyl sulfate. Neutralization of the resulting salt provides iminoethers. 

Overdose may lead to bleeding complications ranging from local ecchymoses to major hemorrhage. Antidote Protamine sulfate (1% solution) equal to the dose of enoxaparin injected. One mgprotamine sulfate neutralizes 1 mg enoxaparin, A second dose of 0,5 mg protamine sulfate per 1 mg enoxaparin may be given if aPTT tested 2-4 hr after first injection remains prolonged. 

The agents like protamine sulfate react with the strongly acidic groups of heparin and can abolish its anticoagulant activity. Approximately 1 mg of protamine sulfate neutralizes 80 to 100 units of heparin. It is used only in severe bleeding or when heparin action needs to be terminated rapidly e.g. after cardiac or vascular surgery. 

Synonym Neatsfoot Oil Necatorina Nechexane Neutral Ahhonium Pluoride Neutral Anhydrous Calcium Hypochlorite Neutral Lead Acetate Neutral Nicotine Sulfate Neutral Potassium Chromate Neutral Sodium Chromatetanhydrous Neutral Verdigris Nickel Acetate Nickel Acetate Tetrahyorate Nickel Ammonium Sulfate Nickel Ammonium Sulfate Hexahydrate Nickel Bromide Nickel Bromide Trihydrate Nickel Carbonyl Nickel Chloride Nickel Chloride Nickel Cyanide Nickel Iiu Fluoborate Nickel Fluoroborate Solution Nickel Fluoroborate Nickel Formate Nickel Formate Dihyorate Nickel Nitrate Nickel Nitrate Hexahydrate Nickel Sulfate Nickel Tetracarbokyl Nickelous Acetate Nickelous Sulfate Nicotine Nicotine Sulfate Nifos Nitralin Nitram O-Nitraniline P-Nitraniline Nitric Acid Nitric Acid, Aluminum Salt Nitric Acid, Iron (111) Salt Compound Name Oil Neatsfoot Carbon Tetrachloride Neohexane Ammonium Fluoride Calcium Hypochlorite Lead Acetate Nicotine Sulfate Potassium Chromate Sodium Chromate Copper Acetate Nickel Acetate Nickel Acetate Nickel Ammonium Sulfate Nickel Ammonium Sulfate Nickel Bromide Nickel Bromide Nickel Carbonyl Nickel Chloride Nickel Chloride Nickel Cyanide Nickel Fluoroborate Nickel Fluoroborate Nickel Fluoroborate Nickel Formate Nickel Formate Nickel Nitrate Nickel Nitrate Nickel Sulfate Nickel Carbonyl Nickel Acetate Nickel Sulfate Nicotine Nicotine Sulfate Tetraethyl Pyrophosphate Nitralin Ammonium Nitrate 2-Nitroaniline 4-Nitroaniline Nitric Acid Aluminum Nitrate Ferric Nitrate... 

Magnesium sulfate Neutral High Medium Rapid General... 

Sodium sulfate Neutral High Low Medium General... 

Nitration 5 Pg Triton X-100, phenolic compounds. (Tris, SDS, urea, thiols, reducing agents, glycerol, ammonium sulfate, neutral detergents do not interfere)... 

Magnesium sulfate Magnesium sulfate neutralizing agent Firming agent ADI not specified ... 

If major bleeding occurs in a patient receiving an LMWH, it is recommended that protamine sulfate be administered intravenously. However, because of its limited binding to the shorter LMWH chains, protamine sulfate cannot neutralize their anticoagulant effects completely. When given in equimolar concentrations, protamine sulfate neutralizes an estimated 60% to 75% of the antithrombotic activity. The recommended dose of protamine sulfate is 1 mg/1 mg of enoxaparin or 1 mg/100 anti-factor Xa units of dalteparin or tinzaparin administered in the previous 8 hours. If the LMWH dose was given in the previous 8 to 12 hours, a 0.5-mg dose of protamine should be given for every 100 anti-factor Xa units. The use of protamine sulfate is not recommended if the LMWH was administered more than 12 hours earlier. 

Disodic Sulfate—Sodic sulfate—Neutral sodium sulfate—Glauber s salt—Sodii sulfas (TJ. S.)—Sodas sul a.s (Br.)—NaaSO, - -n Aq —142 -f- n 18—occurs in nature in solid deposits, and in solution in natural waters. It is obtained as a secondary product in the manufacture of HCl, by the. action of HaSOa on NaCl,... 

Ordinary metal sulfates have, initially, no surface acidity and become solid acids only after proper physical treatment. This is in sharp contrast to an intrinsically acidic hydrogen sulfate. Neutral salt needs some sort of activation for its surface to show any significant acidic property. This activation arises from a process involving either heat, compression, or irradiation to induce some imperfection on the otherwise regular crystal surface. 

Typical enulsifiers used in emulsion polymerization of VC are anirmic emulsifiers like sodium alkyl sulfonates, sodium diaUcyl sulfosucdnates, fatty acid soaps and sodium ethoxy sulfates. Neutral emulsifiers like alltyl phenol ethoxylates and fatty acid ethoxylates are often added during after polymerization in Oder b> increase latex stability. The emulsifiers are not only chosen for control of the particle formation and latex stability during polymerization, but for a number of other reasons like mechanical stability, reactor wall build-up, plastisol formation, heat and colour stability and water resistance of the final product [1]. 

Neutral Ahhonium Pluoride Neutral Anhydrous Calcium Hypochlcrite Neutral Lead Acetate Neutral Nicotine Sulfate Neutral Potassium Chromate Neutral Sodium Chromatetanhydrous Neutral Verdigris Nickel Acetate... 

The manufacture of fatty alcohol sulfate or ether sulfate can be divided into five stages process air preparation, sulfur trioxide generation, sulfation, neutralization, and exhaust gas treatment. 

Early studies on the metabolism of mercapturic acids involved determination of the sulfur distribution in the urine as sulfate, neutral sulfur, and ethereal sulfate. The procedures used were incapable of detecting minor metabolites. Changes in the neutral sulfur were assumed to arise from excretion of mercapturic acids particularly. 

Olefins, diolefins, and acetylenes are attacked by even 76 per cent acid. High temperatures and acid concentrations favor polymerization of olefins, and low temperatures and acid concentrations favor the formation of alkyl acid sulfates, neutral esters, and sec. and tert. alcohols. Higher alcohols, dipolymers, and to some extent acid alkyl sulfates dissolve in cracked distillate and upon redistillation the acid alkyl sulfates decompose, yielding alcohols, sulfur dioxide, and colored materials. These sul-... 

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