L-Prolinamide
L-Prolinamide structure
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Common Name | L-Prolinamide | ||
|---|---|---|---|---|
| CAS Number | 7531-52-4 | Molecular Weight | 114.146 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 303.6±31.0 °C at 760 mmHg | |
| Molecular Formula | C5H10N2O | Melting Point | 95-97 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 137.4±24.8 °C | |
Use of L-ProlinamideL-Prolinamide is a proline derivative[1]. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | L-prolinamide |
|---|---|
| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| Description | L-Prolinamide is a proline derivative[1]. |
|---|---|
| Related Catalog | |
| In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
| References |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| Density | 1.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 303.6±31.0 °C at 760 mmHg |
| Melting Point | 95-97 °C(lit.) |
| Molecular Formula | C5H10N2O |
| Molecular Weight | 114.146 |
| Flash Point | 137.4±24.8 °C |
| Exact Mass | 114.079315 |
| PSA | 55.12000 |
| LogP | -1.51 |
| Vapour Pressure | 0.0±0.6 mmHg at 25°C |
| Index of Refraction | 1.491 |
| InChIKey | VLJNHYLEOZPXFW-BYPYZUCNSA-N |
| SMILES | NC(=O)C1CCCN1 |
This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.
This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xn: Harmful; |
| Risk Phrases | R22 |
| Safety Phrases | S22-S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2933990090 |
This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.
This table lists upstream starting materials and downstream derivative products related to this chemical.
| Precursor 9 | |
|---|---|
| DownStream 10 | |
CAS#:34079-31-7
CAS#:35150-07-3
CAS#:2577-48-2
CAS#:147-85-3
CAS#:2133-40-6
CAS#:115134-39-9
CAS#:71989-31-6
CAS#:7732-18-5
CAS#:17460-56-9
CAS#:59936-29-7
CAS#:214398-99-9
CAS#:29133-55-9
CAS#:274901-16-5
CAS#:24305-27-9
CAS#:207557-35-5
CAS#:66411-54-9This table shows customs‑related data including HS‑code, tariff and regulatory conditions for import and export.
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
This table lists relevant public references with title, journal and publication metadata for this compound.
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Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.
Nat. Chem. Biol. 5 , 45-52, (2009) Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr... |
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Enantioseparation of amino acids and alpha-hydroxy acids on ligand-exchange continuous beds by capillary electrochromatography.
Electrophoresis 31 , 1517-1520, (2010) A new chiral stationary phase based on continuous bed (CB) technology using L-prolinamide as a chiral selector was prepared. Its ability for enantioseparation of amino acids and alpha-hydroxy acids by... |
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d-Glucosamine in a chimeric prolinamide organocatalyst for direct asymmetric aldol addition
Carbohydr. Res. 356 , 273-7, (2012) O-TBDPS D-glucosamine coupled with l-proline is reported to act as an efficient organocatalyst in the accomplishment of direct aldol reactions. Excellent results, in terms of chemical yields, as well ... |
This table contains target information, in‑vitro & in‑vivo assay data for this compound.
This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| (S)-Prolinamide |
| (2S)-2-Pyrrolidinecarboxamide |
| h-pro-nh2 |
| (S)-Pyrrolidine-2-carboxylic acid amide |
| MFCD00005253 |
| (2S)-2-Pyrrolidinecarboximidic acid |
| EINECS 231-397-0 |
| (S)-pyrrolidine-2-carboxamide |
| L-Prolinamide |
| (2S)-pyrrolidine-2-carboxamide |
| Prolinamide |
| L-proline amide |
| L-Prolineamide |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What are the downstream products of L-prolinamide? |
| A: Related downstream products(CAS) of L-prolinamide: 34079-31-7;35150-07-3;59936-29-7;214398-99-9;29133-55-9;274901-16-5;24305-27-9;147-85-3;207557-35-5;66411-54-9. |
| Q: What is the safety information for L-prolinamide? |
| A: Safety information for L-prolinamide: S22-S24/25. |
| Q: What is the CAS number of L-prolinamide? |
| A: CAS number of L-prolinamide is 7531-52-4. |
| Q: What is the boiling point of L-prolinamide? |
| A: Boiling point of L-prolinamide is 303.6±31.0 °C at 760 mmHg. |
| Q: What are the uses of L-prolinamide? |
| A: Main uses of L-prolinamide: L-Prolinamide is a proline derivative[1]. |
| Q: What is the SMILES notation of L-prolinamide? |
| A: SMILES notation of L-prolinamide is NC(=O)C1CCCN1. |
| Q: What is the LogP of L-prolinamide? |
| A: LogP of L-prolinamide is -1.51. |
| Q: What is the molecular formula of L-prolinamide? |
| A: Molecular formula of L-prolinamide is C5H10N2O. |
| Q: What is the molecular weight of L-prolinamide? |
| A: Molecular weight of L-prolinamide is 114.146. |
| Q: What is the melting point of L-prolinamide? |
| A: Melting point of L-prolinamide is 95-97 °C(lit.). |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |
| Dayang Chem (Hangzhou) Co., Ltd. |
| Henan Tianfu Chemical Co., Ltd. |