| Identification | Back Directory | [Name]
N-LAUROYL-L-GLUTAMIC ACID | [CAS]
3397-65-7 | [Synonyms]
SOFTAN LG-A
Lauryl glutamic acid
LAUROYL GLUTAMIC ACID
Hot sell High quality
Lauroyl Glutamate Acid
N-Dodecylglutamic acid
N-Lauroylglutamic acid
N-LAUROYL-L-GLUTAMIC ACID
Dodecanoyl-L-glutamic acid
N-(1-OXODODECYL)GLUTAMICACID
N-Dodecanoyl-L-glutamic acid
N-(1-oxododecyl)-L-glutamic acid
L-Glutamic acid, N-(1-oxododecyl)-
N-LAUROYL-L-GLUTAMIC ACID USP/EP/BP
(S)-2-dodecanamidopentanedioic acid
L-Glutamicacid,N-(1-oxododecyl)-(9CI)
n-lauroyl-l-glutamic acid CAS 3397-65-7 | [EINECS(EC#)]
222-261-1 | [Molecular Formula]
C17H31NO5 | [MDL Number]
MFCD06410798 | [MOL File]
3397-65-7.mol | [Molecular Weight]
329.43 |
| Chemical Properties | Back Directory | [Melting point ]
95-96 °C | [Boiling point ]
543.6±40.0 °C(Predicted) | [density ]
1.081±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Aqueous Base (Slightly), Chloroform (Slightly) | [form ]
Solid | [pka]
3.46±0.10(Predicted) | [color ]
White to Off-White | [InChI]
InChI=1S/C17H31NO5/c1-2-3-4-5-6-7-8-9-10-11-15(19)18-14(17(22)23)12-13-16(20)21/h14H,2-13H2,1H3,(H,18,19)(H,20,21)(H,22,23)/t14-/m0/s1 | [InChIKey]
AVBJHQDHVYGQLS-AWEZNQCLSA-N | [SMILES]
C(O)(=O)[C@H](CCC(O)=O)NC(=O)CCCCCCCCCCC | [LogP]
2.964 (est) | [EPA Substance Registry System]
L-Glutamic acid, N-(1-oxododecyl)- (3397-65-7) |
| Hazard Information | Back Directory | [Uses]
N-Lauroyl-L-glutamic Acid is used in preparation method thereof and application in degrdation of formaldehyde. | [Synthesis]
Methyl laurate and monosodium glutamate were used as raw materials and mixed in a molar ratio of 1.8:0.7. Potassium oxide and magnesium oxide were added as metal oxide catalysts, and the amount of catalyst added was 0.05% of the total weight of the reactants. The reaction was carried out according to the one-step synthesis method of Example 1. In the primary mixer, the reaction temperature is controlled at 20 to 30°C, in particular, the mixer inlet temperature is controlled at 25°C, and the mixer outlet temperature is controlled at 25°C; the pH of the reaction system is maintained at 10. In the secondary mixer, the reaction temperature is controlled at 30 to 40°C, in particular, the secondary mixing inlet temperature is controlled at 35°C, and the outlet temperature of both mixers is controlled at 35°C ; the pH of the reaction system was maintained at 13. Upon completion of the reaction, 0.069% of the methanol by-product was obtained by separation, resulting in lauroyl glutamic acid with 88.67% active sodium content and 98% purity. | [References]
[1] Patent: CN107353223, 2017, A. Location in patent: Paragraph 0028; 0029; 0030 |
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