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CAS NO.97-59-6
| Allantoin Basic information |
| Anti-inflammatory analgesic effects Chemical properties Application Production methods |
| Product Name: | Allantoin |
| Synonyms: | (2,5-dioxo-4-imidazolidinyl)urea;ALLANTOIN;ALL;5-UREIDOHYDANTOIN;CORDIANINE;glyoxylic diureide;GLYOXYLIDIUREIDE;GLYOXYLIC ACID DIUREIDE |
| CAS: | 97-59-6 |
| MF: | C4H6N4O3 |
| MW: | 158.12 |
| EINECS: | 202-592-8 |
| Product Categories: | Substrates;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals;ALDACTAZINE;Cosmetics;Inhibitors |
| Mol File: | 97-59-6.mol |
|
|
|
| Allantoin Chemical Properties |
| mp | 230 °C (dec.)(lit.) |
| Fp | 230-234°C |
| storage temp. | Refrigerator |
| Decomposition | 230-234 ºC |
| Merck | 14,258 |
| BRN | 102364 |
| Stability: | Stable. Incompatible with strong oxidizing agents. |
| CAS DataBase Reference | 97-59-6(CAS DataBase Reference) |
| NIST Chemistry Reference | Urea, (2,5-dioxo-4-imidazolidinyl)-(97-59-6) |
| EPA Substance Registry System | Urea, (2,5-dioxo-4-imidazolidinyl)- (97-59-6) |
| Safety Information |
| Hazard Codes | Xn,Xi |
| Risk Statements | 22-36/37/38 |
| Safety Statements | 22-24/25-36-26 |
| WGK Germany | 1 |
| RTECS | YT1600000 |
| HS Code | 29332100 |
| Hazardous Substances Data | 97-59-6(Hazardous Substances Data) |
| MSDS Information |
| Provider | Language |
|---|---|
| (2,5-Dioxo-4-imidazolidinyl)urea | English |
| ACROS | English |
| SigmaAldrich | English |
| ALFA | English |
| Allantoin Usage And Synthesis |
| Anti-inflammatory analgesic effects | Allantoin has anti-inflammatory analgesic effects, but it also has a weak partial paralysis effect, can effectively reduce stimuli of stimulus, can be used as a skin protectant and anti-irritant, can reduce skin irritation of cosmetic ingredients, China food and Drug Administration rank it as the first kind efficient active ingredient of skin care agent, now has been widely used in many products such as shampoo, sunscreen products, creams and lotions, shaving creams and oral care products. |
| Chemical properties |
Colorless crystalline powder. Melting point is 238-240 ℃ (decomposition). Can be dissolved in hot water, hot alcohol and dilute sodium hydroxide solution, slightly soluble in water and alcohol, almost insoluble in ether and chloroform. Odorless, tasteless. In dry air is stable, prolonged boiling in the water. or strong base will be destroyed. pH of saturated aqueous solution is 5.5. The above information is edited by the chemicalbook of Liu Yujie. |
| Application |
1. Allantoin can promote skin cell growth and rapid wound healing. Used as anti-ulcer drug, mixed with dry aluminum hydroxide gel, for gastrointestinal ulcers and inflammation. The product can soften keratin, making the skin retain moisture, moist and soft, is special effects of additive in cosmetic. Allantoin and its derivatives are the quality improver and additive of many household chemical products. Allantoin protein may be formulated anti-irritant, anti-dandruff, cleaning and wound healing scalp preparations, making hair soft, shiny and elastic. The product is an amphoteric compound, can bind to a variety of material form double salts, with dark, antiseptic, analgesic, deodorant, anti-oxidation effect, and therefore is household chemical products, additives of cosmetics such as freckle cream, acne solution, shampoo , soap, toothpaste, shaving lotion, convergence liquid and antiperspirant deodorant detergent. Allantoin also is a biochemical reagents. 2. For the roles such as skin care, oral products, anti-allergy, the treatment of skin ulcers promote wound healing. 3. Widely used in treatment of a variety of skin ulcers and trauma and additives of nutritional cosmetics. |
| Production methods |
Allantoin presents in the sheath cyst fluid, fetal urine and some of the plants. However, the cost extracted Allantoin from these substances is too high. Currently synthesis methods of Allantoin are: potassium permanganate oxidation uric acid method: dichloroacetic acid and urea heated to synthesize Allantoin; direct condensation method of glyoxylic acid and urea. 1. technological process of dichloroacetic acid and urea as raw materials is as follows: The sodium methoxide solution and methanol were added into the reaction tank, and heated to 40-50 ℃, slowly dropwise added dichloroacetic acid, after added and reflux reaction for 2 h. Cooled to room temperature, filtered, washed with methanol and the filtrate was combined, washed, added methanol solution of sodium dimethoxyethane. The solution was reduced to dryness under reduced pressure , 2.8 portion of hydrochloric acid was added,heated and stirred into a paste in a water bath. Then heated to 90 ℃, and then cooled to about 10 ℃, filtered, 0.25 portion of hydrochloric acid and urea was added into , dissolved by heated, reacted at 80 ℃ for 2 h. Cooled and crystallization, and then maintained at 0 ℃ for above 3 h, centrifugation, washed ,spin-dried, dried to crude product. After The crude product was used 15 times of the water to recrystallize, Allantoin was obtained. As for the dichloroacetic acid, the total yield was 30.3%. 2. The direct condensation of glyoxylic acid and urea (glyoxylate derived by oxidation of glyoxal) operation example: (1) oxidation was in 500 ml four-hole boiling flask equipped with mechanical stirrer, condenser, thermometer and dropping funnel, added 193 g (1 mol) 30% glyoxal aqueous solution, controlled the internal temperature at 40 ± 2 ℃ and stirred to dropwise add 135.5 g ( 1 mol) 45% nitric acid, After addition, continued to stir at this temperature and reacted for 2-3 h, until reddish brown oxidation no longer escaped, the reaction solution was blue-green and immediately disappeared. Replaced by simple distillation apparatus, at about 2.76 kPa, the outside temperature did not exceed 60 ℃ and about 125 g water was evaporated, concentrate solution was standing overnight at room temperature, oxalic acid crystals were precipitated (dried to get 19 g, together 0.21 mol), concentration was 39% ). Continue to stir and react for about 8h at an internal temperature of 40 ± 2 ℃, the oxidation reaction was completed. (2) condensation In 500 ml three-hole boiling flask equipped with mechanical stirrer, condenser and thermomete, above 150 g glyoxylic acid aqueous solution was added, added 170 g (2.83 mol) urea and 23.3 g of concentrated hydrochloric acid, heated to an internal temperature of 80 ℃ under stirring. After about 15min urea was dissolved, the reaction solution was transparent, approximately another 30-45 min, the reactant appeared white cloudy, white precipitate was gradually increased, stirred at an inner temperature of 80 ℃ for 1 h, heating was stopped and the reactant was cooled to room temperature, The white precipitate was collected on a Buchner funnel, precipitated with cold water several times, obtained crude product of Allantoin. Used 1000 ml distilled water to recrystallize. 60-63% white fine crystalline Allantoin was obtained, melting point was 236 ℃ (decomposition). Calculated by glyoxal, the theoretical yield of Allantoin was 38-40% (weight yield was 103-108%). |
| Chemical Properties | White Solid |
| Usage | wound healing agent |
| Usage | diuretic |
| Usage | Vulnerary; debriding agent. Purine metabolite via the uric acid pathway. |
| Allantoin Preparation Products And Raw materials |
| Raw materials | Urea-->Glyoxal-->Glyoxylic acid-->Dichloroacetic acid |
| Allantoin Basic information |
| Anti-inflammatory analgesic effects Chemical properties Application Production methods |
| Product Name: | Allantoin |
| Synonyms: | (2,5-dioxo-4-imidazolidinyl)urea;ALLANTOIN;ALL;5-UREIDOHYDANTOIN;CORDIANINE;glyoxylic diureide;GLYOXYLIDIUREIDE;GLYOXYLIC ACID DIUREIDE |
| CAS: | 97-59-6 |
| MF: | C4H6N4O3 |
| MW: | 158.12 |
| EINECS: | 202-592-8 |
| Product Categories: | Substrates;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals;ALDACTAZINE;Cosmetics;Inhibitors |
| Mol File: | 97-59-6.mol |
|
|
|
| Allantoin Chemical Properties |
| mp | 230 °C (dec.)(lit.) |
| Fp | 230-234°C |
| storage temp. | Refrigerator |
| Decomposition | 230-234 ºC |
| Merck | 14,258 |
| BRN | 102364 |
| Stability: | Stable. Incompatible with strong oxidizing agents. |
| CAS DataBase Reference | 97-59-6(CAS DataBase Reference) |
| NIST Chemistry Reference | Urea, (2,5-dioxo-4-imidazolidinyl)-(97-59-6) |
| EPA Substance Registry System | Urea, (2,5-dioxo-4-imidazolidinyl)- (97-59-6) |
| Safety Information |
| Hazard Codes | Xn,Xi |
| Risk Statements | 22-36/37/38 |
| Safety Statements | 22-24/25-36-26 |
| WGK Germany | 1 |
| RTECS | YT1600000 |
| HS Code | 29332100 |
| Hazardous Substances Data | 97-59-6(Hazardous Substances Data) |
| MSDS Information |
| Provider | Language |
|---|---|
| (2,5-Dioxo-4-imidazolidinyl)urea | English |
| ACROS | English |
| SigmaAldrich | English |
| ALFA | English |
| Allantoin Usage And Synthesis |
| Anti-inflammatory analgesic effects | Allantoin has anti-inflammatory analgesic effects, but it also has a weak partial paralysis effect, can effectively reduce stimuli of stimulus, can be used as a skin protectant and anti-irritant, can reduce skin irritation of cosmetic ingredients, China food and Drug Administration rank it as the first kind efficient active ingredient of skin care agent, now has been widely used in many products such as shampoo, sunscreen products, creams and lotions, shaving creams and oral care products. |
| Chemical properties |
Colorless crystalline powder. Melting point is 238-240 ℃ (decomposition). Can be dissolved in hot water, hot alcohol and dilute sodium hydroxide solution, slightly soluble in water and alcohol, almost insoluble in ether and chloroform. Odorless, tasteless. In dry air is stable, prolonged boiling in the water. or strong base will be destroyed. pH of saturated aqueous solution is 5.5. The above information is edited by the chemicalbook of Liu Yujie. |
| Application |
1. Allantoin can promote skin cell growth and rapid wound healing. Used as anti-ulcer drug, mixed with dry aluminum hydroxide gel, for gastrointestinal ulcers and inflammation. The product can soften keratin, making the skin retain moisture, moist and soft, is special effects of additive in cosmetic. Allantoin and its derivatives are the quality improver and additive of many household chemical products. Allantoin protein may be formulated anti-irritant, anti-dandruff, cleaning and wound healing scalp preparations, making hair soft, shiny and elastic. The product is an amphoteric compound, can bind to a variety of material form double salts, with dark, antiseptic, analgesic, deodorant, anti-oxidation effect, and therefore is household chemical products, additives of cosmetics such as freckle cream, acne solution, shampoo , soap, toothpaste, shaving lotion, convergence liquid and antiperspirant deodorant detergent. Allantoin also is a biochemical reagents. 2. For the roles such as skin care, oral products, anti-allergy, the treatment of skin ulcers promote wound healing. 3. Widely used in treatment of a variety of skin ulcers and trauma and additives of nutritional cosmetics. |
| Production methods |
Allantoin presents in the sheath cyst fluid, fetal urine and some of the plants. However, the cost extracted Allantoin from these substances is too high. Currently synthesis methods of Allantoin are: potassium permanganate oxidation uric acid method: dichloroacetic acid and urea heated to synthesize Allantoin; direct condensation method of glyoxylic acid and urea. 1. technological process of dichloroacetic acid and urea as raw materials is as follows: The sodium methoxide solution and methanol were added into the reaction tank, and heated to 40-50 ℃, slowly dropwise added dichloroacetic acid, after added and reflux reaction for 2 h. Cooled to room temperature, filtered, washed with methanol and the filtrate was combined, washed, added methanol solution of sodium dimethoxyethane. The solution was reduced to dryness under reduced pressure , 2.8 portion of hydrochloric acid was added,heated and stirred into a paste in a water bath. Then heated to 90 ℃, and then cooled to about 10 ℃, filtered, 0.25 portion of hydrochloric acid and urea was added into , dissolved by heated, reacted at 80 ℃ for 2 h. Cooled and crystallization, and then maintained at 0 ℃ for above 3 h, centrifugation, washed ,spin-dried, dried to crude product. After The crude product was used 15 times of the water to recrystallize, Allantoin was obtained. As for the dichloroacetic acid, the total yield was 30.3%. 2. The direct condensation of glyoxylic acid and urea (glyoxylate derived by oxidation of glyoxal) operation example: (1) oxidation was in 500 ml four-hole boiling flask equipped with mechanical stirrer, condenser, thermometer and dropping funnel, added 193 g (1 mol) 30% glyoxal aqueous solution, controlled the internal temperature at 40 ± 2 ℃ and stirred to dropwise add 135.5 g ( 1 mol) 45% nitric acid, After addition, continued to stir at this temperature and reacted for 2-3 h, until reddish brown oxidation no longer escaped, the reaction solution was blue-green and immediately disappeared. Replaced by simple distillation apparatus, at about 2.76 kPa, the outside temperature did not exceed 60 ℃ and about 125 g water was evaporated, concentrate solution was standing overnight at room temperature, oxalic acid crystals were precipitated (dried to get 19 g, together 0.21 mol), concentration was 39% ). Continue to stir and react for about 8h at an internal temperature of 40 ± 2 ℃, the oxidation reaction was completed. (2) condensation In 500 ml three-hole boiling flask equipped with mechanical stirrer, condenser and thermomete, above 150 g glyoxylic acid aqueous solution was added, added 170 g (2.83 mol) urea and 23.3 g of concentrated hydrochloric acid, heated to an internal temperature of 80 ℃ under stirring. After about 15min urea was dissolved, the reaction solution was transparent, approximately another 30-45 min, the reactant appeared white cloudy, white precipitate was gradually increased, stirred at an inner temperature of 80 ℃ for 1 h, heating was stopped and the reactant was cooled to room temperature, The white precipitate was collected on a Buchner funnel, precipitated with cold water several times, obtained crude product of Allantoin. Used 1000 ml distilled water to recrystallize. 60-63% white fine crystalline Allantoin was obtained, melting point was 236 ℃ (decomposition). Calculated by glyoxal, the theoretical yield of Allantoin was 38-40% (weight yield was 103-108%). |
| Chemical Properties | White Solid |
| Usage | wound healing agent |
| Usage | diuretic |
| Usage | Vulnerary; debriding agent. Purine metabolite via the uric acid pathway. |
| Allantoin Preparation Products And Raw materials |
| Raw materials | Urea-->Glyoxal-->Glyoxylic acid-->Dichloroacetic acid |