N-Carbamoyl-DL-aspartic Acid - ≥98%(T) , CAS No.923-37-5

CAS: 923-37-5 Cat. No.: N159242 Peso molecular: 176.13
Disponible para pedir
GRADE & PURITY ≥98%(T)
Synonyms
AKOS003271980 | HLKXYZVTANABHZ-UHFFFAOYSA-N | Ureidosuccinic acid, 98.0-102.0% (T) | carbamyul-aspartate | O3Y2KY16L1 | 2-isoureidosuccinic acid | 2-Ureidobutanedioic acid | N-carbamoylaspartate | BBL003547 | carbamyul-L-aspartate | AS-57486 | Aspartic ac
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
N159242-1g
3
9,90US$
5g
N159242-5g
3
19,90US$
25g
N159242-25g
3
70,90US$
100g
N159242-100g
3
222,90US$
250g
N159242-250g
2
496,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

A useful biochemical for proteomics research

Specifications

Sinónimos
AKOS003271980 | HLKXYZVTANABHZ-UHFFFAOYSA-N | Ureidosuccinic acid, 98.0-102.0% (T) | carbamyul-aspartate | O3Y2KY16L1 | 2-isoureidosuccinic acid | 2-Ureidobutanedioic acid | N-carbamoylaspartate | BBL003547 | carbamyul-L-aspartate | AS-57486 | Aspartic ac
Especificaciones y pureza
≥98%(T)
Mecanismos bioquímicos y fisiológicos
Metabolite of pyrimidine biosynthesis, alanine, aspartate and glutamate metabolism.
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%(T)
Nombres e identificadores
Pubchem Sid504750373
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750373
Sonrisas canónicasC(C(C(=O)O)NC(=O)N)C(=O)O
IUPAC Name2-(carbamoylamino)butanedioic acid
InChIKeyHLKXYZVTANABHZ-UHFFFAOYSA-N
INCHI1S/C5H8N2O5/c6-5(12)7-2(4(10)11)1-3(8)9/h2H,1H2,(H,8,9)(H,10,11)(H3,6,7,12)
Isómeros SMILES C(C(C(=O)O)NC(=O)N)C(=O)O
Peso molecular 176.13
Reaxy-Rn 1726859
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1726859&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 Fatty acids and conjugates  Dicarboxylic acids and derivatives  Isoureas  Carboxylic acids  Carboximidamides  Organopnictogen compounds  Organic oxides  Imines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Aspartic acid or derivatives - Dicarboxylic acid or derivatives - Fatty acid - Isourea - Carboximidamide - Carboxylic acid - Carboximidic acid derivative - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Organonitrogen compound - Imine - Organopnictogen compound - Organic oxygen compound - 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 C4-dicarboxylic acid - aspartic acid derivative - N-carbamoyl-amino acid
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CAD Tchem Dihydroorotase (27 Activities)
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A498 (42825 Activities)
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ACHN (49357 Activities)
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CAKI-1 (44928 Activities)
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CCRF-CEM (65223 Activities)
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DU-145 (51482 Activities)
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HT-29 (80576 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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M14 (47487 Activities)
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MOLT-4 (49676 Activities)
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OVCAR-3 (48710 Activities)
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OVCAR-4 (44535 Activities)
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OVCAR-5 (45555 Activities)
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OVCAR-8 (47708 Activities)
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PC-3 (62116 Activities)
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RPMI-8226 (44974 Activities)
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RXF 393 (41971 Activities)
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SF-295 (48000 Activities)
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SK-MEL-2 (46422 Activities)
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SK-MEL-28 (48833 Activities)
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SK-MEL-5 (47095 Activities)
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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
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TK-10 (45540 Activities)
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U-251 (51189 Activities)
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UACC-257 (46019 Activities)
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UACC-62 (47335 Activities)
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UO-31 (46270 Activities)
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786-0 (47912 Activities)
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A549 (127892 Activities)
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NCI/ADR-RES (33767 Activities)
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T47D (39041 Activities)
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EKVX (44102 Activities)
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NCI-H322M (45589 Activities)
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HCC 2998 (41480 Activities)
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HCT-116 (91556 Activities)
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HOP-92 (41141 Activities)
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Hs-578T (29457 Activities)
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NCI-H460 (60772 Activities)
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SF-268 (49410 Activities)
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IGROV-1 (47897 Activities)
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LOX IMVI (44321 Activities)
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HOP-62 (47048 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-435 (38290 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-N (28205 Activities)
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Malme-3M (44254 Activities)
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MDA-MB-231 (73002 Activities)
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SNB-75 (44215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H226 (44470 Activities)
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Mecanismos de acción
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.

7 results found

Lot NumberCertificate TypeFechaArticulo
G1706070Certificate of AnalysisFeb 08, 2025 N159242
E2615165Certificate of AnalysisSep 02, 2022 N159242
J2226583Certificate of AnalysisSep 02, 2022 N159242
J2226584Certificate of AnalysisSep 02, 2022 N159242
J2226606Certificate of AnalysisSep 02, 2022 N159242
J2226609Certificate of AnalysisSep 02, 2022 N159242
K2421036Certificate of AnalysisSep 02, 2022 N159242
Propiedades químicas y físicas
SolubilidadSoluble in hot water.
SensibilidadHeat Sensitive
Punto de fusión (°C)174-175°C
Peso molecular176.130 g/mol
XLogP3-1.900
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass176.043 Da
Monoisotopic Mass176.043 Da
Topological Polar Surface Area130.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity214.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Xiao Gu, Jiaying Wu, Dekai Liu, Chuxin Wang, Peiqin Chen, Chunying Jin, Guangya Zhang, Wei Jiang.  (2025)  Multienzyme Complex System for Cascade Biotransformation of Ammonia and Carbon Dioxide.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.5c05160]
Calculadoras de soluciones
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