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| Other Sizes |
| Targets |
This compound does not possess a specific biological target; its primary function is as a chemical building block for peptide synthesis and as a research tool. As a phenylalanine derivative, it is used to introduce 4-nitrophenylalanine residues into peptides. The nitro group is a strong electron-withdrawing group that can modulate the electronic properties of the phenyl ring, affecting receptor binding and biological activity. Amino acids and amino acid derivatives have been commercially used as ergogenic supplements.
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| ln Vitro |
Commercial ergot supplements have been made from amino acids and their derivatives. They affect the release of anabolic hormones, the availability of fuel for activity, the ability to think clearly under pressure, and the prevention of muscular damage brought on by exertion. They are regarded as advantageous synergistic food ingredients [1].
This compound is not a biological agent and does not exhibit direct in vitro biological activity in a pharmacological sense. Its value lies in its chemical utility as a protected amino acid building block. Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. Any biological activity would reside in the final deprotected peptide product or drug candidate synthesized using this building block, not in the intermediate itself. |
| ln Vivo |
(S)-2-Amino-3-(4-nitrophenyl)propanoic acid hydrate is not administered in vivo as a therapeutic agent. It is a research chemical utilized as a building block in peptide synthesis and as a research tool. The final deprotected product, not this intermediate, would be the subject of in vivo pharmacological testing for therapeutic efficacy and safety. The compound is for research use only and is not intended for human or veterinary therapeutic applications.
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| Enzyme Assay |
Non-cellular enzyme/receptor binding assays are not applicable to this compound as it is not biologically active. Its use is in organic synthesis and peptide chemistry. A typical protocol involves its use as a building block in peptide synthesis, where it can be incorporated into peptide chains using standard coupling chemistry after appropriate protection strategies. The nitro group can serve as a chromophore for detection or as a handle for further functionalization (e.g., reduction to an amine).
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| Cell Assay |
This compound is not used in cell-based assays as a therapeutic agent. Its applications are in synthetic chemistry and peptide synthesis. It should be stored as a powder at -20°C for up to 3 years or at 4°C for up to 2 years; in solvent, it can be stored at -80°C for 6 months or at -20°C for 1 month. It is a solid. Purity is typically ≥97%. The compound is soluble in water and common organic solvents.
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| Animal Protocol |
In vivo animal experiments do not involve this compound as a test article. It is a chemical intermediate used in the synthesis of peptide-based drug candidates. If a researcher synthesizes a therapeutic peptide using this building block, that final deprotected and purified peptide product would be subjected to animal testing. The amino acid itself is never administered to animals as a test compound.
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| ADME/Pharmacokinetics |
Pharmacokinetic properties are not applicable to this compound as it is not a drug. It is a small molecule (MW 228.20 g/mol) with the formula C9H12N2O5. Its properties are relevant for chemical handling and storage rather than for systemic exposure or ADME studies. The compound is not designed to be bioavailable.
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| Toxicity/Toxicokinetics |
The toxicity of this compound is not extensively documented, as it is a research chemical not intended for human or veterinary use. As with all nitro-containing compounds, standard laboratory safety precautions should be followed, including handling in a well-ventilated area with appropriate personal protective equipment (gloves, lab coat, safety glasses). The compound should be stored as a powder at -20°C or below and protected from light and moisture. It is not intended for diagnostic, therapeutic, or other medical applications.
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| References | |
| Additional Infomation |
(S)-2-Amino-3-(4-nitrophenyl)propanoic acid hydrate (4-Nitro-L-phenylalanine monohydrate) is a phenylalanine analogue used as a building block in peptide synthesis and as a research tool. The nitro group is a strong electron-withdrawing group that can modulate the properties of the resulting peptides. This compound is not a pharmaceutical and has no clinical trials or approved therapeutic status.
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| Molecular Formula |
C9H12N2O5
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|---|---|
| Molecular Weight |
228.20
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| Exact Mass |
228.074
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| CAS # |
207591-86-4
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| PubChem CID |
2734751
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| Appearance |
White to off-white solid powder
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| Density |
1.408 g/cm3
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| Boiling Point |
495.6ºC at 760 mmHg
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| Melting Point |
245-251 °C (dec.)(lit.)
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| Flash Point |
253.5ºC
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| Vapour Pressure |
1.22E-10mmHg at 25°C
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| LogP |
1.708
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| Hydrogen Bond Donor Count |
3
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| Hydrogen Bond Acceptor Count |
6
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| Rotatable Bond Count |
3
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| Heavy Atom Count |
16
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| Complexity |
243
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| Defined Atom Stereocenter Count |
1
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| SMILES |
C1=CC(=CC=C1C[C@@H](C(=O)O)N)[N+](=O)[O-].O
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| InChi Key |
OLZDHJRNUIXKLU-QRPNPIFTSA-N
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| InChi Code |
InChI=1S/C9H10N2O4.H2O/c10-8(9(12)13)5-6-1-3-7(4-2-6)11(14)15;/h1-4,8H,5,10H2,(H,12,13);1H2/t8-;/m0./s1
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| Chemical Name |
(2S)-2-amino-3-(4-nitrophenyl)propanoic acid;hydrate
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| HS Tariff Code |
2934.99.9001
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| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
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| Solubility (In Vitro) |
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
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| Solubility (In Vivo) |
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.
Injection Formulations
Injection Formulation 1: DMSO : Tween 80： Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution → 50 μL Tween 80 → 850 μL Saline)(e.g. IP/IV/IM/SC) *Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution. Injection Formulation 2: DMSO : PEG300 ：Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO → 400 μLPEG300 → 50 μL Tween 80 → 450 μL Saline) Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO → 900 μL Corn oil) Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals). View More
Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO → 900 μL (20% SBE-β-CD in saline)] Oral Formulations
Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium) Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals). View More
Oral Formulation 3: Dissolved in PEG400 (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 4.3821 mL | 21.9106 mL | 43.8212 mL | |
| 5 mM | 0.8764 mL | 4.3821 mL | 8.7642 mL | |
| 10 mM | 0.4382 mL | 2.1911 mL | 4.3821 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:：Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
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