N-ACETYL-DL-2-AMINO CAPROIC ACID
N-acetyl-D-norleucine
CAS: 7682-16-8
Molecular Formula: C8H15NO3
N-ACETYL-DL-2-AMINO CAPROIC ACID - Names and Identifiers
| Name | N-acetyl-D-norleucine |
| Synonyms | AC-DL-NLE-OH AC-DL-AHX(2)-OH AC-DL-ACPO(2)-OH ACETYL-DL-NORLEUCINE N-acetyl-D-norleucine N-ACETYL-DL-NORLEUCINE AC-DL-NHCH[CH3(CH2)3]-COOH ACETYL-DL-2-AMINOHEXANOIC ACID N-ACETYL-DL-2-AMINO CAPROIC ACID |
| CAS | 7682-16-8 |
| InChI | InChI=1/C8H15NO3/c1-3-4-5-7(8(11)12)9-6(2)10/h7H,3-5H2,1-2H3,(H,9,10)(H,11,12)/t7-/m1/s1 |
N-ACETYL-DL-2-AMINO CAPROIC ACID - Physico-chemical Properties
| Molecular Formula | C8H15NO3 |
| Molar Mass | 173.21 |
| Density | 1.072g/cm3 |
| Melting Point | 108 °C |
| Boling Point | 378.3°C at 760 mmHg |
| Flash Point | 182.6°C |
| Vapor Presure | 9.05E-07mmHg at 25°C |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.46 |
| MDL | MFCD00037272 |
N-ACETYL-DL-2-AMINO CAPROIC ACID - Introduction
N-acetyl-D-norleucine, whose chemical name is N-acetyl-D-norleucine, is an amino acid. It is an N-acetyl derivative of D-hexanoic acid with one carbon atom removed from the structure. Its molecular formula is C9H17NO3 and its relative molecular mass is 187.24g/mol.
N-acetyl-D-norleucine is a white solid that can be dissolved in water and organic solvents. It is stable under acidic and neutral conditions, but undergoes hydrolysis under alkaline conditions. It is a non-polar molecule and does not have significant polarity and charge properties.
The main use of N-acetyl-D-norleucine is as a reagent for laboratory research. It can be used for the synthesis of peptide compounds, protein research and preparation of related compounds in the field of medicine.
There are two main methods for the preparation of N-acetyl-D-norleucine: one is the reaction of hexanoic acid with acid chloride to obtain an intermediate, which is then reacted with acetic anhydride to obtain the final product; the other is synthesized by acylation of hexyloxy alcohol.
Regarding safety information, the N-acetyl-D-norleucine is relatively safe under normal circumstances. However, if there is misuse or long-term exposure, there may be a certain risk to health. Therefore, it is necessary to pay attention to personal protection during handling and storage to avoid inhalation, intake or skin contact. Wear chemical protective gloves, protective goggles and protective masks when necessary. Discontinue use immediately when any discomfort or irritation occurs and seek medical help. Before use, it is recommended to refer to the relevant safety data sheets and operating manuals.
N-acetyl-D-norleucine is a white solid that can be dissolved in water and organic solvents. It is stable under acidic and neutral conditions, but undergoes hydrolysis under alkaline conditions. It is a non-polar molecule and does not have significant polarity and charge properties.
The main use of N-acetyl-D-norleucine is as a reagent for laboratory research. It can be used for the synthesis of peptide compounds, protein research and preparation of related compounds in the field of medicine.
There are two main methods for the preparation of N-acetyl-D-norleucine: one is the reaction of hexanoic acid with acid chloride to obtain an intermediate, which is then reacted with acetic anhydride to obtain the final product; the other is synthesized by acylation of hexyloxy alcohol.
Regarding safety information, the N-acetyl-D-norleucine is relatively safe under normal circumstances. However, if there is misuse or long-term exposure, there may be a certain risk to health. Therefore, it is necessary to pay attention to personal protection during handling and storage to avoid inhalation, intake or skin contact. Wear chemical protective gloves, protective goggles and protective masks when necessary. Discontinue use immediately when any discomfort or irritation occurs and seek medical help. Before use, it is recommended to refer to the relevant safety data sheets and operating manuals.
Last Update：2024-04-09 20:02:46
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