Fmoc-D-Leu-OH CAS 114360-54-2 N-Fmoc-D-Leucine Puritas >99.0% (HPLC) Factory
Shanghai Ruifu Chemical Co., Ltd. est primarius fabrica N-Fmoc-D-Leucine (Fmoc-D-Leu-OH) (CAS: 114360-54-2) cum magna qualitate.Ruifu chemica seriem amino acida supplet.Praebere possumus terrarum traditionem, pretium competitive, quantitates parvas et parvas in promptu.Purchase Fmoc-D-Leu-OH,Please contact: alvin@ruifuchem.com
Nomen chemicum | N-Fmoc-D-Leucine |
Synonyma | Fmoc-D-Leu-OH;Fmoc-D-Leucine;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-Leucine;N-9-Fluorenylmethoxycarbonyl-D-Leucine;(R) -Fmoc-2-Amino-4-Methylpentanoic Acid |
Stock Status | In Stock, Productio Capacitas ad Tons per Month |
CAS Number | 114360-54-2 |
Formulae hypotheticae | C21H23NO4 |
M. Pondus | 353.42 g/mol |
Liquescens punctum | 153.0 ad 1600℃ |
Density | 1.207±0.06 g/cm3 |
Aqua Solubility | Insolubilis in aqua |
Repono Nativ. | Frigus & siccum (2~8℃) |
COA & MSDS | Praesto |
Categoria | Fmoc-Amino Acids |
Brand | Ruifu Chemical |
Salus Denunciationes | S22 — Pulverem ne respirare.S24/25 - contactus cum cute et oculis fuge. | ||
WGK Germania | 3 | HS Code* | 2922491990 |
F | 10 |
Items | Signa inspectionis | Proventus |
Aspectus | Alba pulveris | Alba pulveris |
Imprimis rotationis [α]20/D | +25.0°±2.0° (C=1 in DMF) | +25.9° |
Liquescens punctum | 153.0 ad 1600℃ | 154.2℃ |
TLC * | ≥98.0% | >98.0% |
Elementum Analysis (C、H、N) | ≤5.0% | 5.0% |
Optical Puritas | <0.50% L-Enantiomer | Obsequitur |
Solutio in claritate | 0.3 gram in 2ml DMF Solutio Serena | Obsequitur |
Kaiser Test | <0.05% | <0.05% |
Aquae Caroli Fischer | <1.00% | 0.103% |
Damnum in Siccatio | <1.00% (80℃, 2h) | 0.28% |
Puritas / Analysis Methodus | >99.0% (HPLC) | 99.64% |
Massa Imaginis | Secundum Latin | Obsequitur |
NMR Imaginum | Secundum Latin | Obsequitur |
conclusio | Productum probatum & obsequitur cum specificationibus |
sarcina: Fluorinated Utrem, aluminium ffoyle, 25kg/cardboard Drum, vel secundum exigentiam emptoris.
Repono Condition:Condite in vasis obsignatis apud frigus et siccum (2~8℃) horreum ab substantiis incompossibilibus.A luce et humore protege.
Quam mercari?Quaeso contactumDr. Alvin Huang: sales@ruifuchem.com or alvin@ruifuchem.com
15 Annorum Usus?Plus quam XV annos experientiae habemus in fabricando et exportando amplis intermediis pharmaceuticis vel alchimicis pharmaceuticis amplis.
Mercatus principalis?Vendere mercatum domesticum, Americam septentrionalem, Europam, Indiam, Coream, Iaponicam, Australiam etc.
Commodi?Superior qualitas, parabilis pretium, officia professionalia et subsidia technica, ieiunium partus.
Qualitasfides?Qualitas strictioris temperantiae ratio.Pro instrumento analysi professionali includuntur NMR, LC-MS, GC, HPLC, ICP-MS, UV, IR, OR, KF, ROI, LOD, MP, Claritas, Solubilitas, Microbialis limes test, etc.
Exempla?Pleraque producta praebent exempla gratuita pro qualitate aestimationis, sumptus naviculas a clientibus solvendos.
Factory Audit?Factory audit gratissimum.Quaeso ante constitutum.
MOQ?Nec MOQ.Parvus ordo placet.
Tempus adferendi? Si intus prosapia, tres dies partus praestatur.
Transportatio?Per Express (FedEx, DHL), ab Air, per Mare.
Documenta?Post servitium venditionis: COA, MOA, ROS, MSDS, etc. praeberi possunt.
Consuetudo Synthesis?Consuetudo synthesis officia praebere potest ad optimas investigationes tuas necessitates aptandas.
Pensio conditio?Proforma cautionis primum post confirmationem ordinis mittetur, informationes nostrae ripae inclusas.Payment by T/T (Telex Transfer), PayPal, Western Union, etc.
N-Fmoc-D-Leucine (Fmoc-D-Leu-OH) (CAS: 114360-54-2) est N-Fmoc forma D-Leucine tuta est.D-Leucine, innaturalis isomer de L-Leucine.Acida fmoc-amino, in synthesi peptide adhibita, adhibentur ut synthesis organica media, media pharmaceutica, reagens vel chemica reagens.
Synthesis convergens structurae propositae -pestalazini B consecuta est in 4 gradibus utens N-alkylatione diketopiperazini tryptophanae nudae cum 3a-bromopyrrolidinoindolino ubi condensatio inter L-Tryptophan methyl ester et N-Fmoc-D -Leucine coram EDC ut copulatio agentis praebuit respondentem L-Trp-D-Leu dipeptide.
Synthesis methodi Alcali 9-Fluorenomethoxycarbonyl coram chloride reagit cum leucine ad obtinendum Fmoc-D-Leucine.Haec methodus simplex est ad operandum, Methodus praeparandi Fmoc-D-Leucine cum conditionibus lenis reactionis, alta cede ac late applicabilitas.