5-(tert-butoxycarbonylamino)valeric acid
5-(boc-amino)valeric acid
CAS: 27219-07-4
Molecular Formula: C10H19NO4
5-(tert-butoxycarbonylamino)valeric acid - Names and Identifiers
5-(tert-butoxycarbonylamino)valeric acid - Physico-chemical Properties
| Molecular Formula | C10H19NO4 |
| Molar Mass | 217.26 |
| Density | 1.1518 (rough estimate) |
| Melting Point | 48-52°C(lit.) |
| Boling Point | 160-168°C0.8mm Hg(lit.) |
| Flash Point | >230°F |
| Solubility | soluble in Methanol |
| Vapor Presure | 2.07E-06mmHg at 25°C |
| Appearance | Powder |
| Color | Off-white |
| BRN | 2048862 |
| pKa | 4.72±0.10(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Refractive Index | 1.4500 (estimate) |
| MDL | MFCD00076903 |
5-(tert-butoxycarbonylamino)valeric acid - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 10-21 |
| HS Code | 29241990 |
| Hazard Class | IRRITANT |
5-(tert-butoxycarbonylamino)valeric acid - Introduction
5-(boc-amino)valeric acid, also known as 5-(boc-amino)valeric acid, is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: 5-(boc-amino)valeric acid is a white crystalline solid.
-molecular formula: C10H19NO4.
-Molecular weight: 217.26g/mol.
-Melting point: About 60-65°C.
-Solubility: Soluble in some organic solvents, such as ethanol, dimethyl sulfoxide and formamide.
-Stability: Stable at room temperature.
Use:
- 5-(boc-amino)valeric acid is a commonly used reagent for protecting amino acid groups. It can protect the amino group by reacting with the tert-butoxycarbonyl group (BOC) on the amino group to prevent attack by other reagents during the synthesis.
-It can also be used as an intermediate in organic synthesis and used to synthesize other compounds, such as peptide compounds.
Method: The preparation method of
- 5-(boc-amino)valeric acid usually involves the alkylation reaction of pentanoic acid. A specific synthesis step may be: reacting pentanoic acid with N-tert-butoxycarbonylimine to synthesize the target product under alkaline conditions.
Safety Information:
- 5-(boc-amino)valeric acid has no public report of apparent toxicity or danger under normal conditions of use.
-When using, should follow the laboratory safety operation regulations.
-Need to store in a dry place, away from fire and oxidizing agents, and avoid contact with air.
-During the treatment, direct contact with skin and eyes should be avoided, and inhalation or intake should be avoided. In case of inadvertent contact, wash the affected area thoroughly and seek medical help if necessary.
Nature:
-Appearance: 5-(boc-amino)valeric acid is a white crystalline solid.
-molecular formula: C10H19NO4.
-Molecular weight: 217.26g/mol.
-Melting point: About 60-65°C.
-Solubility: Soluble in some organic solvents, such as ethanol, dimethyl sulfoxide and formamide.
-Stability: Stable at room temperature.
Use:
- 5-(boc-amino)valeric acid is a commonly used reagent for protecting amino acid groups. It can protect the amino group by reacting with the tert-butoxycarbonyl group (BOC) on the amino group to prevent attack by other reagents during the synthesis.
-It can also be used as an intermediate in organic synthesis and used to synthesize other compounds, such as peptide compounds.
Method: The preparation method of
- 5-(boc-amino)valeric acid usually involves the alkylation reaction of pentanoic acid. A specific synthesis step may be: reacting pentanoic acid with N-tert-butoxycarbonylimine to synthesize the target product under alkaline conditions.
Safety Information:
- 5-(boc-amino)valeric acid has no public report of apparent toxicity or danger under normal conditions of use.
-When using, should follow the laboratory safety operation regulations.
-Need to store in a dry place, away from fire and oxidizing agents, and avoid contact with air.
-During the treatment, direct contact with skin and eyes should be avoided, and inhalation or intake should be avoided. In case of inadvertent contact, wash the affected area thoroughly and seek medical help if necessary.
Last Update：2024-04-10 22:29:15
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Product Name: Boc-5-Aminopentanoic Acid Visit Supplier Webpage Request for quotationCAS: 27219-07-4
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QQ: 3008007409
Wechat: 18301782025
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