Company Name: |
Aithaca Chemical Corp.
|
Tel: |
(516) 229-2330 |
Email: |
sales@aithaca.com |
Products Intro: |
Cas:
ProductName:COBALT ASPARTATE
|
Company Name: |
Sichuan Jisheng Biopharmaceutical Co.,Ltd.
|
Tel: |
+86-0833-2598983 +86-18086877136 |
Email: |
Nyx-peptide@jsjpharm.cn |
Products Intro: |
Cas:21059-46-1
ProductName:Calcium Aspartate
Purity: 98 | Package: 25KG/
|
Company Name: |
SPECGX LLC
|
Tel: |
?1-314-654-2720 |
Email: |
shane.hoover@mnk.com |
Products Intro: |
Cas:25333-81-7
ProductName:AMPHETAMINE ASPARTATE
|
- ETHYL ASPARTATE
-
- $1.10 / 1g
-
2024-04-17
- CAS:21860-85-5
- Min. Order: 1g
- Purity: 99.0% min
- Supply Ability: 100 tons min
- ASPARTATE CALCIUM
-
- $7.00 / 1KG
-
2019-09-02
- CAS: 10389-09-0
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 1000KG
|
| Aspartate Chemical Properties |
Melting point | >300 °C (dec.)(lit.) | alpha | 25 º (c=8, 6N HCl) | Boiling point | 245.59°C (rough estimate) | density | 1.66 | refractive index | 1.4540 (estimate) | FEMA | 3656 | L-ASPARTIC ACID | storage temp. | Store below +30°C. | solubility | H2O: 5 mg/mL | form | powder | pka | 1.99(at 25℃) | color | White | PH | 2.5-3.5 (4g/l, H2O, 20℃) | Odor | acid taste | Odor Type | odorless | optical activity | [α]20/D +24.7±1°, c = 5% in 5 M HCl | Water Solubility | 5 g/L (25 ºC) | λmax | λ: 260 nm Amax: 0.20 λ: 280 nm Amax: 0.10 | JECFA Number | 1429 | Merck | 14,840 | BRN | 1723530 | Stability: | Stable. Combustible. Incompatible with strong oxidising agents. | InChIKey | CKLJMWTZIZZHCS-REOHCLBHSA-N | LogP | -0.67 | CAS DataBase Reference | 56-84-8(CAS DataBase Reference) | NIST Chemistry Reference | Aspartic acid(56-84-8) | EPA Substance Registry System | Aspartic acid (56-84-8) |
| Aspartate Usage And Synthesis |
Description | Aspartate is a non-essential amino acid, meaning that it is readily and naturally synthesized by mammals. It is one of the 20 building-block amino acids of proteins, 3-letter code is ASP, one letter code is D. The DNA codons encoding aspartic acid are GAC and GAU.
| Chemical Properties | In proteins aspartate sidechains are often hydrogen bonded to form asx turns or asx motifs, which frequently occur at the N-termini of alpha helices.Aspartate, like glutamic acid, is classified as an acidic amino acid, with a pKa of 3.9; however, in a peptide this is highly dependent on the local environment, and could be as high as 14.
| Uses | Aspartate is used as an electrolyte supplement for aminophenol transfusion, inorganic ion supplement (K+, Ca+, etc.) and fatigue restorer. Potassium magnesium aspartate injection or oral solution can be used for arrhythmia, premature beat, tachycardia, hypokalemia, hypomagnesemia, heart failure, myocardial infarction, angina pectoris, hepatitis, cirrhosis and other diseases caused by cardiac glycoside poisoning. | Hazard |
Low toxicity
| Synthesis | Industrially, aspartate is produced by amination of fumarate catalyzed by L-aspartate ammonia-lyase.Racemic aspartic acid can be synthesized from diethyl sodium phthalimidomalonate, (C6H4(CO)2NC(CO2Et)2).
| Forms and nomenclature | There are two forms or enantiomers of aspartic acid. Of these two forms, only one, "L-aspartic acid", is directly incorporated into proteins. The biological roles of its counterpart, "D-aspartic acid" are more limited. Where enzymatic synthesis will produce one or the other, most chemical syntheses will produce both forms, "DL-aspartic acid", known as a racemic mixture. |
| Aspartate Preparation Products And Raw materials |
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