Name | L-Asparagine |
Synonyms | ASN H-ASN-OH H-Asn-OH ASPARAGINE Asparagine L-Asparagine L-ASPARAGINE ASPARTIC ACID L-(+)-ASPARAGINE ASPARAGINIC ACID (S)-(+)-ASPARAGINE L-ASPARTIC ACID 4-AMIDE L-2-Aminosuccinamic acid L-2-AMINOSUCCINAMIC ACID L-2-AMINOBUTANEDIOIC ACID (S)-(+)-2-Aminosuccinamic acid 4-AMIDE-2-aminosuccinamic acid 2-amino-3-carbamoylpropanoic acid (2S)-2-amino-3-(aminomethoxy)propanoic acid (S)-2-AMINOSUCCINIC ACID 4-AMIDEl-aspargine |
CAS | 70-47-3 |
EINECS | 200-735-9 |
InChI | InChI=1/C4H10N2O3/c5-2-9-1-3(6)4(7)8/h3H,1-2,5-6H2,(H,7,8)/t3-/m0/s1 |
Molecular Formula | C4H8N2O3 |
Molar Mass | 132.12 |
Density | 1,543g/cm |
Melting Point | 235 °C (dec.) (lit.) |
Boling Point | 244.01°C (rough estimate) |
Specific Rotation(α) | 34.5 º (c=10, 2N HCl) |
Flash Point | 147.7°C |
Water Solubility | H2O: 20 g/L (20 oC) , clear, colorless |
Solubility | Soluble in water (3g/100L,25°C), almost insoluble in ethanol and ether. The aqueous solution is acidic. |
Vapor Presure | 6.51E-05mmHg at 25°C |
Appearance | White crystal or crystalline powder |
Color | White |
Odor | sltly sweet taste |
Merck | 14,837 |
BRN | 1723527 |
pKa | 2.17(at 20℃) |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Stability | Stable, but may be moisture-sensitive. Incompatible with strong oxidizing agents. |
Sensitive | Hygroscopic |
Refractive Index | 1.4880 (estimate) |
MDL | MFCD00064401 |
Physical and Chemical Properties | White orthorhombic crystal or crystalline powder. Slightly Sweet. The melting point was about 234 °c. Recrystallization method with water is the best, followed by ethanol. In case of alkaline water, it was hydrolyzed to aspartic acid. Heating of the aqueous solution also decomposes. Soluble in water (3G/100L,25 ° C), almost insoluble in ethanol and ether. The aqueous solution was acidic. Non-essential amino acids. If the lack of influence development, can regulate the metabolic function of brain and nerve cells. Natural products are present in various legumes and the like. |
Use | Used as a Biochemical reagent |
Hazard Symbols | Xn - Harmful |
Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S24/25 - Avoid contact with skin and eyes. S36 - Wear suitable protective clothing. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
UN IDs | UN 2811 6.1 / PGIII |
WGK Germany | 3 |
FLUKA BRAND F CODES | 3-10 |
TSCA | Y |
HS Code | 29241900 |
Hazard Class | IRRITANT |
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orthorhombic half-plane crystal. Acidic to litmus. Insoluble in methanol, ethanol, ether benzene, soluble in acid, alkali.
aspartic acid was prepared by acetylation.
biochemical reagents.
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
trait | white powder |
properties | L-aspartic acid is a white crystal or crystalline powder with a slightly sour taste. Slightly soluble in water, insoluble in ethanol and ether, often in the presence of monohydrate, orthorhombic half-plane-shaped crystals. Melting point of 234~235 °, and sugar heat amino carbonyl reaction, can form a special flavor substances. |
uses | nutritional supplements have a wide range of uses in medicine, food and chemical industry. 1. In medicine, can be used for the treatment of heart disease, liver disease, hypertension, with the prevention and recovery of fatigue, and a variety of amino acids together, made of amino acid infusion, used as ammonia antidote, liver function promoter, fatigue recovery agent. In the food industry, is a good nutritional supplements, added to a variety of cool drinks; Also Sweet (aspartame)-aspartame-the main raw material of methyl aspartate. In the chemical industry, can be used as a raw material for the manufacture of synthetic resin. It can also be used as a nutritional additive for cosmetics. nutritional supplements. Co-heating with sugar for amino-carbonyl reaction, can form a special flavor substances. For cool drinks. used in biochemical research, used to treat myocardial infarction, myocardial metabolic disorders, heart failure, heart block, fatigue and other symptoms. amino acid drugs. used as biochemical reagents used in the synthesis of organic raw materials or pharmaceutical intermediates biological culture, peptide synthesis, detection of chlorine enzyme substrate, tuberculosis culture, treatment of acrylonitrile wastewater, preparation of biological medium. |
production method | White Lupine as raw material, after germination, slurry, heat treatment, under the condition of pH less than 6, the crude product is obtained by diatomite filtration and centrifugation, and then concentrated and crystallized to obtain the finished product. isolated from an aqueous extract of bean sprouts of Lupin and soybean having a high L-asparagine content. Obtained by amidation of L-aspartic acid with ammonium hydroxide. |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |