Cas no 499-86-5 (Ac-lys(ac)-OH)
Ac-lys(ac)-OH Chemical and Physical Properties
Names and Identifiers
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- L-Lysine,N2,N6-diacetyl-
- AC-LYS (AC)-OH
- Ac-Lys(Ac)-OH?DCHA
- NA,E-BIS-ACETYL-L-LYSINE
- AC-LYSINE (AC)-OH
- N,N-diacetyl-L-lysine
- N,N'-Diacetyllysine
- S-diacetyllysine
- Diacetyl-L-lysine
- Nalpha,Nepsilon-Diacetyl-L-lysine
- alpha,epsilon-Diacetyl-L-lysine
- Ac-lys(ac)-OH
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- Inchi： 1S/C10H18N2O4/c1-7(13)11-6-4-3-5-9(10(15)16)12-8(2)14/h9H,3-6H2,1-2H3,(H,11,13)(H,12,14)(H,15,16)/t9-/m0/s1
- InChI Key： ZHZUEHHBTYJTKY-VIFPVBQESA-N
- SMILES： OC([C@H](CCCCNC(C)=O)NC(C)=O)=O
Computed Properties
- Exact Mass: 230.12700
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 16
- Rotatable Bond Count: 9
Experimental Properties
- Density: 1.148±0.06 g/cm3 (20 oC 760 Torr),
- Solubility: Soluble (220 g/l) (25 o C),
- PSA: 95.50000
- LogP: 0.66390
Ac-lys(ac)-OH Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | A169240-100mg |
Ac-lys(ac)-OH |
499-86-5 | 100mg |
$ 82.00 | 2023-09-09 | ||
| TRC | A169240-500mg |
Ac-lys(ac)-OH |
499-86-5 | 500mg |
$ 213.00 | 2023-09-09 | ||
| TRC | A169240-1g |
Ac-lys(ac)-OH |
499-86-5 | 1g |
$ 402.00 | 2023-09-09 | ||
| Apollo Scientific | OR36382-5g |
Ac-Lys(Ac)-OH |
499-86-5 | 5g |
￡1182.00 | 2025-02-20 | ||
| Apollo Scientific | OR36382-25g |
Ac-Lys(Ac)-OH |
499-86-5 | 25g |
￡1,306.00 | 2023-03-08 | ||
| eNovation Chemicals LLC | Y1249665-1g |
AC-LYS (AC)-OH |
499-86-5 | 95% | 1g |
$315 | 2023-09-04 | |
| eNovation Chemicals LLC | Y1249665-5g |
AC-LYS (AC)-OH |
499-86-5 | 95% | 5g |
$900 | 2023-09-04 | |
| TRC | A169240-1000mg |
Ac-lys(ac)-OH |
499-86-5 | 1g |
$ 402.00 | 2023-04-19 | ||
| SHENG KE LU SI SHENG WU JI SHU | sc-295898-1 g |
Nalpha,epsilon-Bis-acetyl-L-lysine, |
499-86-5 | ≥98% | 1g |
￥933.00 | 2023-07-10 | |
| SHENG KE LU SI SHENG WU JI SHU | sc-295898A-5 g |
Nalpha,epsilon-Bis-acetyl-L-lysine, |
499-86-5 | ≥98% | 5g |
￥3,911.00 | 2023-07-10 |
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Ac-lys(ac)-OH Related Literature
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S. Müller,S. Knapp Med. Chem. Commun. 2014 5 288
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2. Volumetric properties of mixtures of simple molecular fluidsAmalia Crespo Colín,Elena G. Lezcano,Aurora Compostizo,Ramón G. Rubio,Mateo Díaz Pe?a J. Chem. Soc. Faraday Trans. 1 1989 85 4295
Additional information on Ac-lys(ac)-OH
L-Lysine, N2,N6-diacetyl: A Comprehensive Overview
L-Lysine, N2,N6-diacetyl, also known by its CAS number 499-86-5, is a derivative of the essential amino acid L-lysine. This compound has gained significant attention in recent years due to its unique chemical properties and diverse applications in various fields. The diacetylation at the N2 and N6 positions of lysine introduces distinct functional groups that enhance its stability and bioavailability, making it a valuable compound in pharmaceuticals, nutraceuticals, and biotechnology.
The synthesis of N2,N6-diacetyl-L-lysine involves a multi-step process that typically includes acetylation of lysine using acetylating agents such as acetic anhydride. This reaction is carefully controlled to ensure selective acetylation at the specified positions. Recent advancements in catalytic methods have improved the yield and purity of this compound, making it more accessible for large-scale production. Researchers have also explored alternative methods, such as enzymatic acetylation, which offers a greener and more sustainable approach to synthesizing this compound.
In terms of applications, N2,N6-diacetyl-L-lysine has been extensively studied for its role in improving the bioavailability of lysine in dietary supplements. Lysine is an essential amino acid required for protein synthesis, immune function, and collagen production. However, its bioavailability can be limited due to poor absorption in the gastrointestinal tract. The diacetylation modification enhances its solubility and stability, allowing for better absorption and utilization by the body. This has led to its incorporation into various nutraceutical products aimed at improving muscle recovery, immune support, and overall nutritional balance.
Recent studies have also highlighted the potential of N2,N6-diacetyl-L-lysine in pharmaceutical formulations. Its improved stability makes it an ideal candidate for use in sustained-release drug delivery systems. Researchers have demonstrated that this compound can serve as a carrier for hydrophobic drugs, enhancing their solubility and bioavailability. Additionally, its biocompatibility and lack of toxicity make it a promising material for use in biomedical applications such as drug delivery vehicles and tissue engineering scaffolds.
The structural modifications introduced by diacetylation also confer unique properties to this compound in terms of its interaction with other molecules. For instance, the acetyl groups can act as protecting groups during chemical synthesis, preventing unwanted side reactions. This has made N2,N6-diacetyl-L-lysine a valuable intermediate in the synthesis of complex biomolecules such as peptides and proteins. Recent advancements in peptide chemistry have leveraged this property to develop more efficient synthesis routes for bioactive peptides with enhanced stability and functionality.
In conclusion, L-Lysine, N2,N6-diacetyl (CAS No 499-86-5) is a versatile compound with a wide range of applications across multiple industries. Its unique chemical properties, derived from the strategic acetylation of lysine, make it an invaluable tool in pharmaceuticals, nutraceuticals, and biotechnology. As research continues to uncover new potential uses for this compound, its role in advancing healthcare and nutrition is expected to grow significantly.
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