L-Aspartic acid β-methyl ester hydrochloride - ≥98% , CAS No.16856-13-6

CAS: 16856-13-6 Cat. No.: A100440 Peso molecular: 183.59 Beilstein Registry Number: 4(4)3001 Número EC: 240-880-5
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
H-Asp(OMe)-OH | Glutamate Glycine dipeptide | HY-Y1801 | J-300066 | L-Aspartic acid beta-methyl ester, HCl | AC-9150 | H-Asp(OMe)-OH HCl | SCHEMBL37048 | ASPARTIC ACID(OME)-OH HCL | L-Aspartic Acid 4-Methyl Ester Hydrochloride | MFCD00038972 | (S)-2-Amino
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
A100440-1g
5
9,90US$
5g
A100440-5g
5
10,90US$
25g
A100440-25g
1
28,90US$
100g
A100440-100g
1
61,90US$
500g
A100440-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
306,90US$
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

Store at -20°C Ships Ice chest + Ice pads 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.

Specifications

Sinónimos
H-Asp(OMe)-OH | Glutamate Glycine dipeptide | HY-Y1801 | J-300066 | L-Aspartic acid beta-methyl ester, HCl | AC-9150 | H-Asp(OMe)-OH HCl | SCHEMBL37048 | ASPARTIC ACID(OME)-OH HCL | L-Aspartic Acid 4-Methyl Ester Hydrochloride | MFCD00038972 | (S)-2-Amino
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504767243
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504767243
Sonrisas canónicasCOC(=O)CC(C(=O)O)N.Cl
IUPAC Name(2S)-2-amino-4-methoxy-4-oxobutanoic acid;hydrochloride
InChIKeyQRBMPUYOGOCYDJ-DFWYDOINSA-N
INCHI1S/C5H9NO4.ClH/c1-10-4(7)2-3(6)5(8)9;/h3H,2,6H2,1H3,(H,8,9);1H/t3-;/m0./s1
Isómeros SMILES COC(=O)C[C@@H](C(=O)O)N.Cl
WGK Alemania 3
Peso molecular 183.59
Beilstein 4(4)3001
Reaxy-Rn 4715992
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4715992&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 L-alpha-amino acids  Fatty acid methyl esters  Dicarboxylic acids and derivatives  Quaternary ammonium salts  Methyl esters  Amino acids  Carboxylic acids  Organic zwitterions  Organic oxides  Organic chloride salts  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Aspartic acid or derivatives - Alpha-amino acid - L-alpha-amino acid - Fatty acid ester - Fatty acid methyl ester - Dicarboxylic acid or derivatives - Fatty acyl - Quaternary ammonium salt - Methyl ester - Amino acid - Carboxylic acid ester - Carboxylic acid - Organic oxide - Organic nitrogen compound - Organic chloride salt - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Amine - Organic zwitterion - Organic salt - Aliphatic acyclic 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
A1816010Certificate of AnalysisAug 18, 2025 A100440
A1816001Certificate of AnalysisAug 18, 2025 A100440
F1228026Certificate of AnalysisJan 08, 2025 A100440
J2330084Certificate of AnalysisOct 12, 2023 A100440
J2330085Certificate of AnalysisOct 12, 2023 A100440
J2330086Certificate of AnalysisOct 12, 2023 A100440
B2321235Certificate of AnalysisFeb 28, 2023 A100440
B2321238Certificate of AnalysisFeb 27, 2023 A100440
Propiedades químicas y físicas
SensibilidadHeat Sensitive
Rotación específica [α]11 ° (C=1, H2O)
Punto de fusión (°C)191-193°C
Peso molecular183.590 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass183.03 Da
Monoisotopic Mass183.03 Da
Topological Polar Surface Area89.600 Ų
Heavy Atom Count11
Formal Charge0
Complexity145.000
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 Count2
Calculadoras de soluciones
Reseñas

Reseñas de cliente

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.