Boc-L-proline methyl ester
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Boc-L-proline methyl ester

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Category
BOC-Amino Acids
Catalog number
BAT-004323
CAS number
59936-29-7
Molecular Formula
C11H19NO4
Molecular Weight
229.30
Boc-L-proline methyl ester
IUPAC Name
1-O-tert-butyl 2-O-methyl (2S)-pyrrolidine-1,2-dicarboxylate
Synonyms
Boc-L-Pro-Ome; (S)-Boc-pyrrolidine-2-carboxylic acid methyl ester; (S)-1-tert-Butyl 2-methyl pyrrolidine-1,2-dicarboxylate
Appearance
Colorless or slightly yellow liquid
Purity
≥ 98.5% (GC)
Density
1.12g/cm3
Boiling Point
288.6ºC at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C11H19NO4/c1-11(2,3)16-10(14)12-7-5-6-8(12)9(13)15-4/h8H,5-7H2,1-4H3/t8-/m0/s1
InChI Key
WVDGSSCWFMSRHN-QMMMGPOBSA-N
Canonical SMILES
CC(C)(C)OC(=O)N1CCCC1C(=O)OC
1.Transformation pathways and acute toxicity variation of 4-hydroxyl benzophenone in chlorination disinfection process.
Liu W1, Wei D2, Liu Q3, Du Y1. Chemosphere. 2016 Apr 13;154:491-498. doi: 10.1016/j.chemosphere.2016.04.005. [Epub ahead of print]
Benzophenones compounds (BPs) are widely used as UV filters, and have been frequently found in multiple environmental matrices. The residual of BPs in water would cause potential threats on ecological safety and human health. Chlorination disinfection is necessary in water treatment process, in which many chemicals remained in water would react with disinfectant chlorine and form toxic by-products. By using ultra performance liquid phase chromatography quadrupole time of flight mass spectrometer (UPLC-QTOF-MS), nuclear magnetic resonance (NMR), the transformation of 4-hydroxyl benezophenone (4HB) with free available chlorine (FAC) was characterized. Eight major products were detected and seven of them were identified. Transformation pathways of 4HB under acid, neutral, and alkaline conditions were proposed respectively. The transformation mechanisms involved electrophilic chlorine substitution of 4HB, Baeyer-Villiger oxidation of ketones, hydrolysis of esters and oxidative breakage of benzene ring.
2.Comparison and validation of 2 analytical methods for the determination of free fatty acids in dairy products by gas chromatography with flame ionization detection.
Mannion DT1, Furey A2, Kilcawley KN3. J Dairy Sci. 2016 Apr 13. pii: S0022-0302(16)30178-3. doi: 10.3168/jds.2015-10795. [Epub ahead of print]
Accurate quantification of free fatty acids (FFA) in dairy products is important for quality control, nutritional, antimicrobial, authenticity, legislative, and flavor purposes. In this study, the performance of 2 widely used gas chromatographic flame ionization detection methods for determination of FFA in dairy products differing in lipid content and degree of lipolysis were evaluated. We used a direct on-column approach where the isolated FFA extract was injected directly and a derivatization approach where the FFA were esterified in the injector to methyl esters using tetramethylammonium hydroxide as a catalyst. A comprehensive validation was undertaken to establish method linearity, limits of detection, limits of quantification, accuracy, and precision. Linear calibrations of 3 to 700 mg/L (R2 > 0.999) and 20 to 700 mg/L (R2 > 0.997), and limits of detection and limits of quantification of 0.7 and 3 mg/L and 5 and 20 mg/L were obtained for the direct injection on-column and the derivatization method, respectively.
3.Advantages of Pure Platelet-Rich Plasma Compared with Leukocyte- and Platelet-Rich Plasma in Treating Rabbit Knee Osteoarthritis.
Yin WJ1, Xu HT1, Sheng JG1, An ZQ1, Guo SC1, Xie XT1, Zhang CQ1. Med Sci Monit. 2016 Apr 17;22:1280-1290.
BACKGROUND Concentrated leukocytes in leukocyte- and platelet-rich plasma (L-PRP) may deliver increased levels of pro-inflammatory cytokines to activate the NF-κB signaling pathway, to counter the beneficial effects of growth factors on osteoarthritic cartilage. However, to date no relevant studies have substantiated that in vivo. MATERIAL AND METHODS Autologous L-PRP and pure platelet-rich plasma (P-PRP) were prepared, measured for componential composition, and injected intra-articularly after 4, 5, and 6 weeks post-anterior cruciate ligament transection. Caffeic acid phenethyl ester (CAPE) was injected intraperitoneally to inhibit NF-κB activation. All rabbits were sacrificed after 8 weeks postoperative. Enzyme-linked immunosorbent assays were performed to determine interleukin 1β (IL-1β) and prostaglandin E2 (PGE2) concentrations in the synovial fluid, Indian ink staining was performed for gross morphological assessment, and hematoxylin and eosin staining and toluidine blue staining were performed for histological assessment.
4.Biodegradable, elastomeric coatings with controlled anti-proliferative agent release for magnesium-based cardiovascular stents.
Gu X1, Mao Z2, Ye SH1, Koo Y3, Yun Y3, Tiasha TR4, Shanov V4, Wagner WR5. Colloids Surf B Biointerfaces. 2016 Apr 7;144:170-179. doi: 10.1016/j.colsurfb.2016.03.086. [Epub ahead of print]
Vascular stent design continues to evolve to further improve the efficacy and minimize the risks associated with these devices. Drug-eluting coatings have been widely adopted and, more recently, biodegradable stents have been the focus of extensive evaluation. In this report, biodegradable elastomeric polyurethanes were synthesized and applied as drug-eluting coatings for a relatively new class of degradable vascular stents based on Mg. The dynamic degradation behavior, hemocompatibility and drug release were investigated for poly(carbonate urethane) urea (PCUU) and poly(ester urethane) urea (PEUU) coated magnesium alloy (AZ31) stents. Poly(lactic-co-glycolic acid) (PLGA) coated and bare stents were employed as control groups. The PCUU coating effectively slowed the Mg alloy corrosion in dynamic degradation testing compared to PEUU-coated, PLGA-coated and bare Mg alloy stents. This was confirmed by electron microscopy, energy-dispersive x-ray spectroscopy and magnesium ion release experiments.
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