- L-(+)-Abrine
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- $42.00 / 100mg
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2024-11-19
- CAS:526-31-8
- Min. Order:
- Purity: ≥95%
- Supply Ability: 10g
- L-(+)-Abrine
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- $2800.00 / 1g
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2024-04-02
- CAS:526-31-8
- Min. Order: 1g
- Purity: 97
- Supply Ability: 500 Kg
- Abrine
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- $0.00 / 20mg
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2023-02-24
- CAS:526-31-8
- Min. Order: 5mg
- Purity: ≥98%(HPLC)
- Supply Ability: 10 g
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| L-Abrine Basic information |
| L-Abrine Chemical Properties |
Melting point | >300 °C (dec.)(lit.) | alpha | D21 +44° (0.28 g in 10 ml 0.5N HCl) | Boiling point | 358.94°C (rough estimate) | density | 1.272±0.06 g/cm3 (20 ºC 760 Torr) | refractive index | 65 ° (C=1, 0.5mol/L NaOH) | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | solubility | H2O : 2 mg/mL (9.16 mM; ultrasonic and adjust pH to 10 with NaOH) | form | Cryst. | pKa | 2.32±0.10(Predicted) | color | Off-white to light yellow | optical activity | [α]20/D +65°, c = 1 in 0.5 M NaOH | Merck | 14,10 | BRN | 86638 | CAS DataBase Reference | 526-31-8(CAS DataBase Reference) |
Hazard Codes | Xn | Risk Statements | 20/21/22 | Safety Statements | 36 | WGK Germany | 3 | HS Code | 29339900 |
| L-Abrine Usage And Synthesis |
Chemical Properties | white to light grey crystalline powder or crystals | Uses | L-Abrine is an indoleamino acid that displays radical scavenging and antioxidant properties. | Definition | ChEBI: A N-methyl-L-alpha-amino acid that is the Nalpha-methyl derivative of L-tryptophan. | reaction suitability | reaction type: solution phase peptide synthesis | Biochem/physiol Actions | An indoleamino acid that shows radical scavenging and antioxidant properties in vitro. | Purification Methods | Crystallise L-abrine from H2O or EtOH/H2O mixture and dry it for 2days at 60o in high vacuum; it has m 275-290o(dec with browning at 230o) and [] D +47.2o (c 2, 0.5N HCl) [Peter et al. Helv Chim Acta 46 577 1963]. [Gregory & Morley J Chem Soc 913 1968, Beilstein 22/14 V 40.] |
| L-Abrine Preparation Products And Raw materials |
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