495-69-2 Hippuric acid BENZAMINOACETIC ACID
Product Name: Hippuric acid
Synonyms: BENZAMINOACETIC ACID;BENZOYLAMINOACETIC ACID;BENZOYLGLYCINE;BZ-GLY-OH;BZO-GLY-OH;HIPPURIC ACID;AKOS B029712;TIMTEC-BB SBB003759
CAS: 495-69-2
MF: C9H9NO3
MW: 179.17
EINECS: 207-806-3
Product Categories: Intermediates of Dyes and Pigments;Aromatic Cinnamic Acids, Esters and Derivatives;Aromatics;amino
Mol File: 495-69-2.mol
Hippuric acid Structure
Hippuric acid Chemical Properties
Melting point 187-191 °C(lit.)
density 1,371 g/cm3
storage temp. Store at RT.
Water Solubility Soluble in water.
Merck 14,4716
BRN 1073987
Stability: Stable. Incompatible with oxidizing agents.
CAS DataBase Reference 495-69-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-37/38-41-36/37/38
Safety Statements 26-39-36/37-22
WGK Germany 3
RTECS MR8150000
F 3-10
TSCA Yes
HazardClass IRRITANT
Physical and Chemical Properties Hippuric acid is also known as "Benzoylaminoethanoic acid",its molecular formula is C9H9NO3. The molecular weight is 179.18. As colorless crystals. Melting point 187~188 ℃. It's soluble in cold water, chloroform, ether, cold ethanol, slightly soluble in amyl alcohol, soluble in hot water, hot ethanol, sodium phosphate solution, almost insoluble in benzene, carbon disulfide, petroleum ether. Naturally it occurs in herbivores (such as horses) of urine, it is also present in small amounts in human urine,it is easily hydrolyzed to benzoic acid and glycine. Hippuric acid can reduce urine pH within a certain range,which makes the bacteria living environment change, and then plays a synergistic bactericidal effect. Urinary hippuric acid is measured using pyridine-benzene chloride colorimetry. The principle is that hippuric acid reacts with benzene sulfonyl chloride in pyridine solution, and the product in ethanol solution is yellow compound, according to the color depth, quantitative analysis is processed by colorimetry. Normal urine hippuric acid content varies widely because of different varieties of diet and intake (from 0.3 to 2.5 grams per day), and there are individual differences. After Toluene goes into the body, through metabolic transformation, most of it becomes to hippuric acid and is excreted through urine. Determination of horse urine hippuric acid content can be used as exposure indicators to reflect the body's absorption of toluene, but it can not serve as indicators of the diagnosis.
Hippuric acid can be made by reaction of benzoyl chloride with glycine in sodium hydroxide solution . It can be used for biochemical reagents and organic synthesis. Hippuric acid ammonium salt is crystal, soluble in water, soluble in ethanol; potassium salt is crystal, containing single molecule of crystal water, soluble in water, soluble in ethanol.
Properties, uses, methods of synthesis of hippuric acid Information compiled by Andy of ChemicalBook (2016-11-19).
Hippuric acid excretion test The use of the principles of sodium benzoate going into the human body and binding glycine in the liver to be non-toxic hippuric acid and being excreted with the urine,can be used to exam liver detoxification function, which is called hippuric acid excretion test. The kidneys can not only excrete hippuric acid, it can also synthesize a small amount of hippuric acid .It is only in normal renal function that hippuric acid test can truly reflect the liver's detoxification function using hippuric acid excretion test . A little after the subjects take breakfast, oral 6g sodium benzoate is taken. 4h after taking the drug, collect the urine, measure the urine excretion, the normal amount ofhippuric acid after 4h discharge should be> 3.0g. To avoid nausea and vomiting induced often by oral sodium benzoate , intravenous injection 1.77g sodium benzoate can be slowly done ,urine is collected 1h after injection, discharge amount is measured , the normal discharge amount should be 1h> 0.7g. When there is liver parenchymal disease, such as hepatitis, cirrhosis and liver necrosis, the liver synthesis of hippuric acid dysfunctions, which decreases production of hippuric acid . Obstructive jaundice causes small changes. Reduced renal blood flow and renal excretion dysfunction also lead to the reducing of the amount of hippuric acid discharge . Some fruits contain benzoic acid such as apples, bananas, etc., they should be banned when testing. Hippuric acid test has many factors and sodium benzoate can cause adverse reactions in patients, and the valuation of liver detoxification function is less precise, it has been less clinical.
Reference: China Medical Encyclopedia twenty-seven DIAGNOSIS [author:Sun Rongwu]
Uses The product is used for medicine, dyes intermediates and it is used for the production of fluorescent yellow H8GL, disperse fluorescent FFL and so on.
production method Benzoyl chloride reacts with the amino acid in sodium hydroxide solution, amido sodium benzene is obtained, then it is acidized with hydrochloric acid. The amino acid is dissolved in sodium hydroxide solution, at the same time drop benzoyl chloride and sodium hydroxide solution below 30 ℃ , the reaction solution is always alkaline. After finishing adding, stir for 30min. Then add hydrochloric acid to pH 2, filter crude, use water to recrystallize , hippuric acid is obtained. Consumption of raw materials fixed: amino acid (90%) 610kg/t, benzoyl chloride (60%) 1520kg/t, caustic soda (30%) 1960kg/t, hydrochloric acid (30%) 900kg/t.
Chemical Properties White crystalline powder
Uses N-Benzoylglycine also known as Hippuric Acid is the glycine conjugate of benzoic acid commonly found in ruminant urine. It is synthesized in the liver and its production is greatly increased following consuption of benzoic acid. In itself it does not have a direct biological function, however p-hydroxy-hippurica acid can be used as an inhibitor of Ca2+ ATPase.
Uses N-Benzoylglycine also known as Hippuric Acid is the glycine conjugate of benzoic acid commonly found in ruminant urine. Hippuric acid is synthesized in the liver and its production is greatly increase d following consumption of benzoic acid. In itself it does not have a direct biological function, however p-hydroxy-hippurica acid can be used as an inhibitor of Ca2+ ATPase.
Definition ChEBI: An N-acylglycine in which the acyl group is specified as benzoyl.
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