Ácido N-Fmoc-L-aspártico - ≥98% , CAS No.119062-05-4

CAS: 119062-05-4 Cat. No.: F100801 Peso molecular: 355.35
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
ácido (S)-2-(9H-fluoren-9-ilmetoxicarbonil-amino)succínico | Ácido N-Fmoc-L-aspártico | HY-W013182 | Oprea1_790414 | SCHEMBL378041 | 3,4,4-trimetil-2,5-dioxoimidazolina | ÁCIDO FMOC-ASPÁRTICO | Ácido (S)-2-(((9H-fluoren-9-il)metoxi)carbonilamino)succínico
Storage
Conservar a 2-8°C
Shipped In
Hielo húmedo
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
F100801-1g
3
9,90US$
5g
F100801-5g
3
10,90US$
25g
F100801-25g
3

23,90US$

35,90US$
Guardar 12,00 US$ (33.43%)
100g
F100801-100g
3

74,90US$

112,90US$
Guardar 38,00 US$ (33.66%)
500g
F100801-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

275,90US$

413,90US$
Guardar 138,00 US$ (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Conservar a 2-8°C Ships Hielo húmedo Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Aplicación

El ácido N-Fmoc-L-aspártico se utiliza para biosintetizar otros aminoácidos en el cuerpo humano.

Specifications

Sinónimos
ácido (S)-2-(9H-fluoren-9-ilmetoxicarbonil-amino)succínico | Ácido N-Fmoc-L-aspártico | HY-W013182 | Oprea1_790414 | SCHEMBL378041 | 3, 4, 4-trimetil-2, 5-dioxoimidazolina | ÁCIDO FMOC-ASPÁRTICO | Ácido (S)-2-(((9H-fluoren-9-il)metoxi)carbonilamino)succínico
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Conservar a 2-8°C
Enviado en
Hielo húmedo
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504764591
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504764591
Sonrisas canónicasC1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC(=O)O)C(=O)O
IUPAC Name(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)butanedioic acid
InChIKeyKSDTXRUIZMTBNV-INIZCTEOSA-N
INCHI1S/C19H17NO6/c21-17(22)9-16(18(23)24)20-19(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H,20,25)(H,21,22)(H,23,24)/t16-/m0/s1
Isómeros SMILES C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@@H](CC(=O)O)C(=O)O
WGK Alemania 3
Peso molecular 355.35
Reaxy-Rn 5887212
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5887212&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentAspartic acid and derivatives
Alternative Parents Fluorenes  Dicarboxylic acids and derivatives  Carbamate esters  Carboxylic acids  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Aspartic acid or derivatives - Fluorene - Benzenoid - Dicarboxylic acid or derivatives - Carbamic acid ester - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as aspartic acid and derivatives. These are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot NumberCertificate TypeFechaArticulo
C1812005Certificate of AnalysisOct 14, 2025 F100801
G2518027Certificate of AnalysisJul 22, 2025 F100801
L2114329Certificate of AnalysisJul 10, 2025 F100801
L2114330Certificate of AnalysisJul 10, 2025 F100801
L2114336Certificate of AnalysisJul 10, 2025 F100801
L2115088Certificate of AnalysisJul 10, 2025 F100801
I1721060Certificate of AnalysisApr 09, 2025 F100801
F1921194Certificate of AnalysisApr 12, 2023 F100801
Propiedades químicas y físicas
SolubilidadSoluble in methanol, and water.
Rotación específica [α]-30° (C=1,DMF)
Punto de fusión (°C)195-200°C
Peso molecular355.300 g/mol
XLogP32.200
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count7
Exact Mass355.106 Da
Monoisotopic Mass355.106 Da
Topological Polar Surface Area113.000 Ų
Heavy Atom Count26
Formal Charge0
Complexity528.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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