3,5-Dinitro salicylic acid(DNS) - ≥98% , CAS No.609-99-4

CAS: 609-99-4 Cat. No.: D109090 Peso molecular: 228.12 Beilstein Registry Number: 2220661 Número EC: 210-204-3
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
DNS | 3,5-Dinitrosalicylic acid, used in colorimetric determination of reducing sugars | SCHEMBL125292 | 2-Hydroxy-3,5-dinitrobenzoic acid | 2-hydroxy-3,5-dinitro-benzoic acid | 3,5-DinitrosalicylsA currencyure | 3,5-Dinitro-2-hydroxybenzoic acid | 3,5-Di
Storage
Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
D109090-1g
4
9,90US$
5g
D109090-5g
4
10,90US$
25g
D109090-25g
10
19,90US$
100g
D109090-100g
9
47,90US$
500g
D109090-500g
3
142,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

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

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Storage & shipping

Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 103 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

3,5-Dinitrosalicylic acid is a dinitrated derivative of salicylic acid. 3,5-Dinitrosalicylic acid is used in preparing DISAL glycosyl donors, as well as colorimeteric determination of reducing sugars and glycosidase activity. Proton-transfer compounds composed of 3,5-Dinitrosalicylic acid/Strychnine and 3,5-Dinitrosalicylic acid/benzidine have also been described.

Specifications

Sinónimos
DNS | 3, 5-Dinitrosalicylic acid, used in colorimetric determination of reducing sugars | SCHEMBL125292 | 2-Hydroxy-3, 5-dinitrobenzoic acid | 2-hydroxy-3, 5-dinitro-benzoic acid | 3, 5-DinitrosalicylsA currencyure | 3, 5-Dinitro-2-hydroxybenzoic acid | 3, 5-Di
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488181458
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181458
Sonrisas canónicasC1=C(C=C(C(=C1C(=O)O)O)[N+](=O)[O-])[N+](=O)[O-]
IUPAC Name2-hydroxy-3,5-dinitrobenzoic acid
InChIKeyLWFUFLREGJMOIZ-UHFFFAOYSA-N
INCHI1S/C7H4N2O7/c10-6-4(7(11)12)1-3(8(13)14)2-5(6)9(15)16/h1-2,10H,(H,11,12)
Isómeros SMILES C1=C(C=C(C(=C1C(=O)O)O)[N+](=O)[O-])[N+](=O)[O-]
WGK Alemania 3
RTECS VO2965000
Peso molecular 228.12
Beilstein 2220661
Reaxy-Rn 2220661
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2220661&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.

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📊 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
SuperclassBenzenoids
ClasePhenols
SubclassNitrophenols
Intermediate Tree Nodes Not available
Direct ParentDinitrophenols
Alternative Parents Nitrobenzoic acids and derivatives  Salicylic acids  Benzoic acids  Nitrobenzenes  Benzoyl derivatives  Nitroaromatic compounds  Vinylogous acids  Propargyl-type 1,3-dipolar organic compounds  Carboxylic acids  Organic oxoazanium compounds  Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  Organonitrogen compounds  Organooxygen compounds  Organopnictogen compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Dinitrophenol - Nitrobenzoate - Hydroxybenzoic acid - Salicylic acid or derivatives - Salicylic acid - Benzoic acid or derivatives - Benzoic acid - Nitrobenzene - Nitroaromatic compound - Benzoyl - Monocyclic benzene moiety - Vinylogous acid - C-nitro compound - Organic nitro compound - Organic oxoazanium - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as dinitrophenols. These are organic aromatic compounds containing a benzene that carries a single phenol group and exactly two nitro groups.
External Descriptors C-nitro compound - monohydroxybenzoic acid
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (no humanos)
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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.

30 results found

Lot NumberCertificate TypeFechaArticulo
A2628400Certificate of AnalysisJan 07, 2026 D109090
A2628401Certificate of AnalysisJan 07, 2026 D109090
A2628402Certificate of AnalysisJan 07, 2026 D109090
A2628514Certificate of AnalysisJan 07, 2026 D109090
H2515053Certificate of AnalysisAug 23, 2025 D109090
H2515054Certificate of AnalysisAug 22, 2025 D109090
D2129254Certificate of AnalysisFeb 07, 2025 D109090
D2527480Certificate of AnalysisJun 27, 2024 D109090
D2521076Certificate of AnalysisJun 27, 2024 D109090
D2521075Certificate of AnalysisJun 27, 2024 D109090
D2303738Certificate of AnalysisNov 22, 2022 D109090
H2402043Certificate of AnalysisNov 22, 2022 D109090
F2510127Certificate of AnalysisNov 22, 2022 D109090
D2518071Certificate of AnalysisNov 22, 2022 D109090
D2303762Certificate of AnalysisNov 22, 2022 D109090
A2304531Certificate of AnalysisNov 22, 2022 D109090
D2303737Certificate of AnalysisNov 22, 2022 D109090
A2304563Certificate of AnalysisNov 22, 2022 D109090
A2304560Certificate of AnalysisNov 22, 2022 D109090
A2304559Certificate of AnalysisNov 22, 2022 D109090
A2304543Certificate of AnalysisNov 22, 2022 D109090
A2304542Certificate of AnalysisNov 22, 2022 D109090
A2304541Certificate of AnalysisNov 22, 2022 D109090
A2304538Certificate of AnalysisNov 22, 2022 D109090
A2304532Certificate of AnalysisNov 22, 2022 D109090
G2226469Certificate of AnalysisJul 01, 2022 D109090
G2226470Certificate of AnalysisJul 01, 2022 D109090
G2226471Certificate of AnalysisJul 01, 2022 D109090
G2226472Certificate of AnalysisJul 01, 2022 D109090
G2226473Certificate of AnalysisJul 01, 2022 D109090

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Propiedades químicas y físicas
SolubilidadSoluble in water (Partly miscible), DMSO, methanol, ethanol, and benzene.
SensibilidadHeat sensitive &Hygroscopic
Punto de fusión (°C)173-174°C
Peso molecular228.120 g/mol
XLogP31.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count1
Exact Mass228.002 Da
Monoisotopic Mass228.002 Da
Topological Polar Surface Area149.000 Ų
Heavy Atom Count16
Formal Charge0
Complexity320.000
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
Preguntas frecuentes y artículos
Research Progress in Detection Technologies for Soluble Sugars in Plants
Trehalose: Physicochemical Characteristics, Manufacturing Processes, and Application Guidelines
Recent Advances in Methods for Measuring Starch-Related Indices in Plants and Their Application-Oriented Selection
Hemicellulases: A Review of Substrate Specificity, Catalytic Systems, and Research and Industrial Applications
Chitinases: Substrate-Specific Degradation Mechanisms, Enzymatic Properties, and Application Directions
Ferulic Acid: Structural Features, Preparation Routes, and Key Points for Research Applications
Functional Properties, Application Scenarios, and Manufacturing Processes of Maltotetraose (G4): A Review
Synergy of Enzymes in Plant Cell Wall Hemicellulose Degradation: Xylanase, β-Xylosidase, and Debranching Enzymes
Citations of This Product
Referencias
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2. Yu Yin, Chunhui Ma, Wei Li, Sha Luo, Zhanshuo Zhang, Shouxin Liu.  (2023)  High Lewis acidity catalyst for direct depolymerization of microcrystalline cellulose to 5- hydroxymethylfurfural: Reaction optimization by central composite design.  BIOMASS & BIOENERGY,      [PMID:] [10.1016/j.biombioe.2023.107009]
3. Zhang Xiaoling, Miao Qin, Tang Bingling, Mijakovic Ivan, Ji Xiao-Jun, Qu Lingbo, Wei Yongjun.  (2023)  Discovery of novel alkaline-tolerant xylanases from fecal microbiota of dairy cows.  Biotechnology for Biofuels and Bioproducts,  16  (1): (1-13).  [PMID:38012750] [10.1186/s13068-023-02435-8]
4. Chang Liu, Shuo Liu, Zengyuan Cao, Dajun He, Dongyu Gu, Jing Tian, Yi Yang.  (2023)  Immobilization of α-amylase on mesoporous silica nanoparticles as a target fishing tool for rapid affinity recognition of an active component from Schisandra chinensis (Turcz.) Baill.  PROCESS BIOCHEMISTRY,      [PMID:] [10.1016/j.procbio.2023.11.013]
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