CAS Number923-27-3
Synonyms(R)-2,6-Diaminocaproic acid; (R)-lysine; EINECS 213-091-9; Benzonitrile,2,6-diamino; D-Lysine; Lysine; D-2,6-Diaminohexanoic acid; (2R)-2,6-diaminohexanoic acid; (R)-2,6-Diaminohexanoic acid; r-lysine; MFCD00008234
Molecular FormulaH2N(CH2)4CH(NH2)CO2H
Molecular Weight146.19
Purity≥98 (HPLC)%
Density1.1±0.1 g/cm3
Boiling Point311.5±32.0 °C at 760 mmHg
Melting Point218 °C (dec.) (lit.)
Appearancepowder
EINECS213-091-9
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 923-27-3 |
| Catalog No. | 2A-9025599 |
| Chinese Name | D-赖氨酸 |
| Synonyms | (R)-2,6-Diaminocaproic acid; (R)-lysine; EINECS 213-091-9; Benzonitrile,2,6-diamino; D-Lysine; Lysine; D-2,6-Diaminohexanoic acid; (2R)-2,6-diaminohexanoic acid; (R)-2,6-Diaminohexanoic acid; r-lysine; MFCD00008234 |
| Molecular Formula | H2N(CH2)4CH(NH2)CO2H |
| Molecular Weight | 146.19 |
| Purity | ≥98 (HPLC) |
| Density | 1.1±0.1 g/cm3 |
| Boiling Point | 311.5±32.0 °C at 760 mmHg |
| Melting Point | 218 °C (dec.) (lit.) |
| Appearance | powder |
| Storage Condition | -20℃, avoid light, ventilated and dry place, seale |
| Application | D-lysine is a useful raw material as an analogue of luteinizing hormone-releasing hormone and as a pharmaceutical carrier in the form of polylysine. D-lysine reduces renal radioactivity uptake during |
| EINECS | 213-091-9 |
| HTC | 2922499990 |
| PubChem ID | 24896491 |
| MDL Number | MFCD00008234 |
| SMILES | NCCCC[C@@H](N)C(O)=O |
| InChI | 1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)/t5-/m1/s1 |
| InChI Key | KDXKERNSBIXSRK-RXMQYKEDSA-N |
| Beilstein/REAXYS | 1722530 |
| NACRES Code | NA.26 |
| UNSPSC | 12352209 |
| Hazard Symbols | transportation |
| MSDS | msds/25599_1_923_27_3.pdf |
| Bioactivity | D-Lysine is a useful raw material employed as an analog of lutenizing-hormone-releasing hormone and as a drug carrier in the form of polylysine. D-Lysine decreases renal uptake of radioactivity during scintigraphy and PRRT with low toxicity. D-Lysine not interferes with the natural amino acid metabolic balance[1][2]. Related Catalog Research Areas >> Others Target Human Endogenous Metabolite In Vivo D-Lysine (400 mg/kg; i.v. or p.o.) dose not result in significantly greater inhibition of kidney uptake of '"In-DTPAOC, and Oral administration of D-lysine also reduces kidney uptake in rats[1]. References [1]. Bernard BF, et al. D-lysine reduction of indium-111 octreotide and yttrium-90 octreotide renal uptake. J Nucl Med. 1997 Dec;38(12):1929-33. [2]. Takahashi E, et al. D-lysine production from L-lysine by successive chemical racemization and microbial asymmetric degradation. Appl Microbiol Biotechnol. 1997 Apr;47(4):347-51. Chemical & Physical Properties Density 1.1±0.1 g/cm3 Boiling Point 311.5±32.0 °C at 760 mmHg Melting Point 218ºC (dec.) Molecular Formula C6H14N2O2 Molecular Weight 146.188 Flash Point 142.2±25.1 °C Exact Mass 146.105530 PSA 89.34000 LogP -1.04 Vapour Pressure 0.0±1.4 mmHg at 25°C Index of Refraction 1.503 InChIKey KDXKERNSBIXSRK-RXMQYKEDSA-N SMILES NCCCCC(N)C(=O)O Storage condition −20°C |
| Use of | D-Lysine is a useful raw material employed as an analog of lutenizing-hormone-releasing hormone and as a drug carrier in the form of polylysine. D-Lysine decreases renal uptake of radioactivity during scintigraphy and PRRT with low toxicity. D-Lysine not interferes with the natural amino acid metabolic balance[1][2]. Properties Articles42 Name D-lysine Synonym More Synonyms D-Lysine Biological Activity Description D-Lysine is a useful raw material employed as an analog of lutenizing-hormone-releasing hormone and as a drug carrier in the form of polylysine. D-Lysine decreases renal uptake of radioactivity during scintigraphy and PRRT with low toxicity. D-Lysine not interferes with the natural amino acid metabolic balance[1][2]. Related Catalog Research Areas >> Others Human Endogenous Metabolite References [1]. Bernard BF, et al. D-lysine reduction of indium-111 octreotide and yttrium-90 octreotide renal uptake. J Nucl Med. 1997 Dec;38(12):1929-33. [2]. Takahashi E, et al. D-lysine production from L-lysine by successive chemical racemization and microbial asymmetric degradation. Appl Microbiol Biotechnol. 1997 Apr;47(4):347-51. Chemical & Physical Properties Molecular Formula C6H14N2O2 Exact Mass 146.105530 PSA 89.34000 LogP -1.04 Index of Refraction 1.503 InChIKey KDXKERNSBIXSRK-RXMQYKEDSA-N SMILES NCCCCC(N)C(=O)O |
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| Transport Info | Shipping Name: UN |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available |
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