- InChI
- InChI=1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1
- InChI Key
- CKLJMWTZIZZHCS-REOHCLBHSA-N
- Formula
- C4H7NO4
- SMILES
- NC(CC(=O)O)C(=O)O
- Molecular Weight1
- 133.10
- CAS
- 1783-96-6
- Other Names
-
- (-)-Aspartic acid
- (R)-aspartic acid
- Asp
- Aspartic acid D-form
- D-(-)-Aspartic acid
- D-aminosuccinic acid
- L-aminosuccinic acid
- L-aspartic acid
- NSC 97922
- PAff : Proton affinity (kJ/mol).
- Cp,gas : Ideal gas heat capacity (J/mol×K).
- ΔfG° : Standard Gibbs free energy of formation (kJ/mol).
- ΔfH°gas : Enthalpy of formation at standard conditions (kJ/mol).
- ΔfusH° : Enthalpy of fusion at standard conditions (kJ/mol).
- ΔvapH° : Enthalpy of vaporization at standard conditions (kJ/mol).
- log10WS : Log10 of Water solubility in mol/l.
- logPoct/wat : Octanol/Water partition coefficient.
- McVol : McGowan's characteristic volume (ml/mol).
- Pc : Critical Pressure (kPa).
- Tboil : Normal Boiling Point Temperature (K).
- Tc : Critical Temperature (K).
- Tfus : Normal melting (fusion) point (K).
- Vc : Critical Volume (m3/kmol).
- 1: Molecular weight from the IUPAC atomic weights tables.
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Physical Properties
| Property | Value | Unit | Source |
|---|---|---|---|
| PAff | 916.30 | kJ/mol | NIST |
| ΔfG° | -484.67 | kJ/mol | Joback Calculated Property |
| ΔfH°gas | -627.00 | kJ/mol | Joback Calculated Property |
| ΔfusH° | 19.16 | kJ/mol | Joback Calculated Property |
| ΔvapH° | 81.60 | kJ/mol | Joback Calculated Property |
| log10WS | 0.76 | Crippen Calculated Property | |
| logPoct/wat | -1.127 | Crippen Calculated Property | |
| McVol | 92.080 | ml/mol | McGowan Calculated Property |
| Pc | 6642.18 | kPa | Joback Calculated Property |
| Tboil | 655.11 | K | Joback Calculated Property |
| Tc | 842.78 | K | Joback Calculated Property |
| Tfus | 424.60 | K | Joback Calculated Property |
| Vc | 0.333 | m3/kmol | Joback Calculated Property |
Temperature Dependent Properties
| Property | Value | Unit | Temperature (K) | Source |
|---|---|---|---|---|
| Cp,gas | [233.47; 261.69] | J/mol×K | [655.11; 842.78] | 
|
| Cp,gas | 233.47 | J/mol×K | 655.11 | Joback Calculated Property |
| Cp,gas | 238.94 | J/mol×K | 686.39 | Joback Calculated Property |
| Cp,gas | 244.10 | J/mol×K | 717.67 | Joback Calculated Property |
| Cp,gas | 248.94 | J/mol×K | 748.94 | Joback Calculated Property |
| Cp,gas | 253.48 | J/mol×K | 780.22 | Joback Calculated Property |
| Cp,gas | 257.73 | J/mol×K | 811.50 | Joback Calculated Property |
| Cp,gas | 261.69 | J/mol×K | 842.78 | Joback Calculated Property |
Similar Compounds
Find more compounds similar to D-Aspartic acid.
Mixtures
- sodium chloride + D-Aspartic acid + Water
- D-Aspartic acid + Tetramethylammonium chloride + Water
- D-Aspartic acid + Water
- D-Aspartic acid + Hydrogen chloride + Water
- sodium hydroxide + D-Aspartic acid + Water
- 2-Pyrrolidinone, 1-methyl- + D-Aspartic acid + Water
- Formamide, N,N-dimethyl- + D-Aspartic acid + Water
- D-Aspartic acid + Dimethyl Sulfoxide + Water
- D-Aspartic acid + 1,4-Dioxane + Water
- Ethanol + D-Aspartic acid + Water
- Ethanol + D-Aspartic acid
- D-Aspartic acid + Methyl Alcohol
- 1-Propanol + D-Aspartic acid
- D-Aspartic acid + 1-Butanol
- Isopropyl Alcohol + D-Aspartic acid
- D-Aspartic acid + Dimethyl Sulfoxide
- Formamide, N,N-dimethyl- + D-Aspartic acid
- 2-Pyrrolidinone, 1-methyl- + D-Aspartic acid
- 1,2-Ethanediol + D-Aspartic acid
- D-Aspartic acid + 1,4-Dioxane
Find more mixtures with D-Aspartic acid.
Sources
- Crippen Method
- Crippen Method
- Modeling solubility and acid-base properties of some polar side chain amino acids in NaCl and (CH3)4NCl aqueous solutions at different ionic strengths and temperatures
- Thermodynamics of the first and second proton dissociations from aqueous L-aspartic acid and L-glutamic acid at temperatures from (278.15 to 393.15) K and at the pressure 0.35 MPa: Apparent molar heat capacities and apparent molar volumes of zwitterionic, protonated cationic, and deprotonated anionic forms at molalities from (0.002 to 1.0) mol Ae kg 1
- Solubilities of magnesium-L-ascorbate, calcium-L-ascorbate, magnesium-L-glutamate, magnesium-D-gluconate, calcium-D-gluconate, calcium-D-heptagluconate, L-aspartic acid, and 3-nitrobenzoic acid in water
- Solubility modelling and thermodynamic aspect of d-aspartic acid in aqueous co-solvent mixtures of N-methyl-2-pyrrolidone, N,N-dimethylformamide, dimethyl sulfoxide and 1.4-dioxane
- Solubility of the Proteinogenic a-Amino Acids in Water, Ethanol, and Ethanol-Water Mixtures
- Solubility of d-Aspartic Acid in Several Neat Solvents: Determination, Modeling, and Solvent Effect Analysis
- Solubility of d-Aspartic Acid and l-Aspartic Acid in Aqueous Salt Solutions from (293 to 343) K
- Joback Method
- McGowan Method
- NIST Webbook
Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.