5-Nitrobarbituric acid - ≥95% , CAS No.480-68-2

CAS: 480-68-2 Cat. No.: N159876 Peso molecular: 173.08 Número EC: 207-557-0
Disponible para pedir
GRADE & PURITY ≥95%
Synonyms
5-Nitrohexahydropyrimidine-2,4,6-trione | 5-24-09-00105 (Beilstein Handbook Reference) | Q-102035 | 5-Nitro barbituric acid | 5-nitro-1,3-diazinane-2,4,6-trione | 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-nitro- | 8WZ923176V | Maybridge1_005997 | MFCD00006667 |
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
N159876-1g
2
9,90US$
5g
N159876-5g
1
29,90US$
25g
N159876-25g
1
99,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal 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

Used as a microreagent for potassium with which it forms a characteristic precipitate.

Specifications

Sinónimos
5-Nitrohexahydropyrimidine-2, 4, 6-trione | 5-24-09-00105 (Beilstein Handbook Reference) | Q-102035 | 5-Nitro barbituric acid | 5-nitro-1, 3-diazinane-2, 4, 6-trione | 2, 4, 6(1H, 3H, 5H)-Pyrimidinetrione, 5-nitro- | 8WZ923176V | Maybridge1_005997 | MFCD00006667 |
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Tipo de acción
INHIBITOR
Pureza
≥95%
Nombres e identificadores
Pubchem Sid488181087
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181087
Sonrisas canónicasC1(C(=O)NC(=O)NC1=O)[N+](=O)[O-]
IUPAC Name5-nitro-1,3-diazinane-2,4,6-trione
InChIKeyABICJYZKIYUWEE-UHFFFAOYSA-N
INCHI1S/C4H3N3O5/c8-2-1(7(11)12)3(9)6-4(10)5-2/h1H,(H2,5,6,8,9,10)
Isómeros SMILES C1(C(=O)NC(=O)NC1=O)[N+](=O)[O-]
CAS alternativo 209529-81-7
Peso molecular 173.08
Reaxy-Rn 180758
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=180758&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
Direct ParentAlpha amino acids and derivatives
Alternative Parents Nitropyrimidines  Barbituric acid derivatives  N-acyl ureas  Diazinanes  1,3-dicarbonyl compounds  Dicarboximides  C-nitro compounds  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Alpha-amino acid or derivatives - Barbiturate - Nitropyrimidine - N-acyl urea - Pyrimidone - Ureide - 1,3-diazinane - Pyrimidine - 1,3-dicarbonyl compound - Dicarboximide - C-nitro compound - Carbonic acid derivative - Organic nitro compound - Urea - Organoheterocyclic compound - Organic oxoazanium - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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.

12 results found

Lot NumberCertificate TypeFechaArticulo
C2211065Certificate of AnalysisDec 10, 2025 N159876
H2416392Certificate of AnalysisJul 17, 2024 N159876
H2416393Certificate of AnalysisJul 17, 2024 N159876
H2416442Certificate of AnalysisJul 17, 2024 N159876
H2416443Certificate of AnalysisJul 17, 2024 N159876
H2416444Certificate of AnalysisJul 17, 2024 N159876
J2516344Certificate of AnalysisApr 15, 2024 N159876
J2516639Certificate of AnalysisApr 15, 2024 N159876
C2211045Certificate of AnalysisNov 08, 2021 N159876
C2211068Certificate of AnalysisNov 08, 2021 N159876
C2211545Certificate of AnalysisNov 08, 2021 N159876
C2211547Certificate of AnalysisNov 08, 2021 N159876

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Propiedades químicas y físicas
Peso molecular173.080 g/mol
XLogP3-1.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count0
Exact Mass173.007 Da
Monoisotopic Mass173.007 Da
Topological Polar Surface Area121.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity259.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
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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