Fmoc-Leu-OH CAS 35661-60-0 N-Fmoc-L-Leucine Puritas >99.0% (HPLC) Factory

Description:

Nomen chemicum: N-Fmoc-L-Leucine

Synonyma: Fmoc-Leu-OH

CAS: 35661-60-0

Puritas: >99.0% (HPLC)

Aspectus: pulveris albi

Fmoc-Amino Acids, High Quality

Contactus: Dr

Mobile/Wechat/Whatsapp: +86-15026746401

E-Mail: alvin@ruifuchem.com


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Descriptio:

Shanghai Ruifu Chemical Co., Ltd. est primarium fabrica N-Fmoc-L-Leucine (Fmoc-Leu-OH) (CAS: 35661-60-0) magna qualitate.Ruifu chemica seriem amino acida supplet.Praebere possumus terrarum traditionem, pretium competitive, quantitates parvas et parvas in promptu.Purchase Fmoc-Leu-OH,Please e-mail: alvin@ruifuchem.com

Chemical Properties:

Nomen chemicum N-Fmoc-L-Leucine
Synonyma Fmoc-Leu-OH;Fmoc-L-Leu-OH;Fmoc-L-Leucine;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-Leucine;N-(9-Fluorenylmethoxycarbonyl)-L-Leucine
Stock Status In Stock, Productio Capacitas ad Tons per Month
CAS Number 35661-60-0
Formulae hypotheticae C21H23NO4
M. Pondus 353.42 g/mol
Liquescens punctum 153.0 ad 1600℃
Density 1.207±0.06 g/cm3
Sensitiva Hygroscopic
Solubilitas in Methanol Prope diaphanum
Repono Nativ. Frigus & siccum (2~8℃)
COA & MSDS Praesto
Categoria Fmoc-Amino Acids
Brand Ruifu Chemical

Specifications:

Items Signa inspectionis Proventus
Aspectus Alba pulveris Alba pulveris
Imprimis rotationis [α]20/D -25.0°±2.0° (C=1 in DMF)
-24.6°
Liquescens punctum 153.0 ad 1600℃ 155.1℃
TLC * ≥98.0% >98.0%
Optical Puritas <0.30% D-Enantiomer Obsequitur
Solutio in claritate 0.3 gram in 2ml DMF Solutio Serena Obsequitur
Kaiser Test <0.05% <0.05%
Aquae Caroli Fischer <0.50% 0.12%
Damnum in Siccatio <0.50% (60℃, 2h) 0.15%
Fmoc-β-Ala-OH <0.20% (HPLC) Obsequitur
Fmoc-β-Ala-Leu-OH <0.10% (HPLC) Obsequitur
Fmoc-Leu-Leu-OH <0.10% (HPLC) Obsequitur
Fmoc-Ile-OH <0.10% (HPLC) Obsequitur
Amino acid <0.20% (GC) Obsequitur
Ethyl Acetate <0.50% (GC) Obsequitur
Puritas / Analysis Methodus >99.0% (HPLC) 99.85%
Massa Imaginis Secundum Latin Obsequitur
NMR Imaginum Secundum Latin Obsequitur
conclusio Productum probatum & obsequitur cum specificationibus

Sarcina & Repono:

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.

Methodus Analysis:

Inspection procedure
1. Aspectus
-- Visual inspectionem
2. Munditia (HPLC)
2.1 Instrument
Altus effectus liquidi chromatographiae, PDA detector.
Statera analytica electronica
2.2 Reagent
Acidum acetonitrile (chromatographicum), acidum trifluoroaceticum (gradus chromatographicus)
2.3 chromatographicae conditiones
2.3.1 Column: YMC-ODS-AM, 5μL, 250x4.6 mm
2.3.2 Deprehensio necem: INC220nm
Fluunt rate: 1.0mL/min
Magnitudo: 10μL (reference)
Diluent: acetonitrile
Data collection time: 25.00min
2.4 Mobilis tempus praeparationis
Acum mobile A (aquam acidum trifluoroaceticum 0,1%): accurate hauriunt 2.0ml acidum trifluoroaceticum, aqua dilutum ad 2000ml, bene misce et decassing;
Mobile tempus B (acidi trifluoroaceticum 0,1% acetonitrile): accurate hauriunt 2.0ml acidum trifluoroaceticum, 2000ml cum acetonitrili dilutum, mixtum et degassing;
Tempus (min) A% B%
0.00 90 10
13.00 10 90
18.00 10 90
18.01 90 10
23.00 90 10
2.6 Praeparatio specimen solution
Expende et dissolve specimen 0.1g cum acetonitrile et diluto ad 100ml, bene quate ad usum vel eandem intentionem.Para duo exemplaria in parallela.
2.7 Sample Determinatio
Sampling Analyze secundum haec ratio sampling:
Plus quam I iniectio solutionis blank
I acus transire sample solution I #
I acus sample solution II #
2.8 Ex Calculation
2.8.1 Vertex area ordinationem methodi usus est ad puritatem HPC deducendo spatium vacuum computare.
2.8.2 Medium relativum deviatio puritatis duarum acuum non erit maior quam 1%
2.8.3 Si exitus utriusque injectiones in acceptatione criteria occurrant, mediocris puritas tamquam effectus finalis accipitur.
3, punctum liquescens -- RY-1 punctum instrumenti liquescens
4. Damnum exarescat test modum
4.1 Instrumenta:
Electrica thermostatica clibano siccat, 1/10,000 trutina.
4.2 De modo procedendi:
In utre plano appensis constanti pondere et operculo oris humus nimis siccitatis, appende 1 gram (accurate ad 0.0001 gram) exempli.Specimen aequaliter spargi debet in fundo uter pondo crassitudine non plus quam 10mm, in clibano thermostatico electrica siccando, ad 105~ 110℃ per 3 horas siccendo, ac deinde in siccitate ad refrigerandum movendum est. locus temperatus ad appensionem.
Calculus: Loss de siccitate %= (M1-M2) ÷M×100
Ubi: M1: pondus specimen et utrem metiendi ante in siccationem, P
M2: pondus sample et utrem metiendi exsiccato, in P.*
M: Pondus Sample, P
5. Imprimis gyrationis
-- Imprimis gyratio mensuratur secundum GB/T613-1988 .
Sample praeparatio: 0.5000g specimen accurate appensum et ad utrem volutricam puram et aridam 50ml voluminetricam, 20ml DMF addita est, utre capped et ad dissolvendum agitatus est, et postea ad libram cum DMF dilutus est.
Test: gyroscopi nullam ante probationem accommodes, deinde tubo testante solutione specimen oneratis, angulum rotationis note, et certam rotationem exempli cum hac formula computa.
[а]D20=(r×50) (L×W)
[а]D20: Imprimis rotationis opticae solutionis 25℃ sample
r: Optical rotationis observandae XX, pro sample solutione
50: Volumen solutionis exempli paratae (ml)
w: Sample pondus (g)
L: Tubus gyrationis longitudo optica (dm)

commoda:

Satis capacitas: sufficientes facilities et technici

Professional Service: One stop acquireing service

Altera Package: Custom sarcina ac titulus praesto

Ieiunium Delivery: Si intra stirpem, tres dies partus praestatur

Supple firmum: Esse rationabile stirpe

Technical Support: Technology solution praesto

Custom Synthesis Service: Range from P. to kilos

High Quality: Qualitas certa ratio completa constituti

FAQ:

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.

35661-60-0 — Periculum et Salus;

Periculosam symbola Xi - Irritant
Periculum Codes 36/37/38 - Irritando ad oculos, systema respiratorium et cutem.
Safety Description S22 - Pulverem ne respirare.
S24/25 - contactus cum cute et oculis fuge.
S36/37/39 - Indumentum tutelae idoneum, caestus et oculi/facies tutelam gerunt.
S27 - Exue illico omnem vestem contaminatam.
S26 - In contactu cum oculis, statim cum aqua multa ablue et consilium medicinae quaeras.
WGK Germania 3
HS CIC 2922491990

Applicatio:

N-Fmoc-L-Leucine (Fmoc-Leu-OH) (CAS: 35661-60-0) est acidum derivativum amino, quod praeparari potest per reactionem L-Leucine et 9-Fluorenomethoxycarbonyl Chloride.
Acida fmoc-amino, in synthesi peptide adhibita, adhibentur ut synthesis organica media, media pharmaceutica, reagens vel chemica reagens.
Fmoc-L-Leu-OH est acidum derivativum amino, in chemia peptide adhibitum.Latin aedificium obstructionum pro usu solidi periodi peptidis synthesis sequens Fmoc-tactica.Est etiam unum e ligandis novis PPARγ quae diversimode PPARγ movere possunt, differentiationem osteoclastis reducens, et sic meliores sunt scuta therapeutica in diabete quam traditionales antidiabeticas medicinae.
Praeparatio 1.05g (0.008 mol) Solidum L-Leucinum in solutione 10% sodium carbonatis dissolutum, excitatum ad solidum glycinum plene solvendum, et 9-fluorene methoxycarbonyl chloridi (2.10g, 0.008 mol) solutione toluene dissolutae (2~ 205 ml) additur dropwise ad 20~30℃, addita gutta pro 30~60 minuta, addita guttatim, excita ad 20~30℃ pro 1~8 horis, adde 30-200 ml aquae ad dilutum, et extrahe cum n-butyl. acetas (80 ml) ad excessum chloridi 9-fluoreni methoxycarbonylis detrahendum, Acidum aqueum nactus cum acido hydrochlorico coacto ad PH = 0,5~3.5, ac deinde cum acetate n-butylo extractum (80 ml), et Phase oleum consecutum est. aqua lota ad acidum hydrochloricum removendum, Phase oleum coactum ad acetatem n-butylam solvendam, crystallis albis praecipitati, percolantur et exsiccati ad obtinendum 2.46g ex Nα-9-fluorene methoxycarbonyl-L-leucinum cum fructu 87.0 %.

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