Potassium phosphate dibasic - PharmPure™, USP , CAS No.7758-11-4

CAS: 7758-11-4 Cat. No.: P433942 Fórmula: K2HPO4 Peso molecular: 174.18 Número EC: 231-834-5
Disponible para pedir
GRADE & PURITY PharmPure™ ? PharmPure™ — Aladdin's line of biopharmaceutical raw and starting materials. Use for pharma manufacturing inputs needing high purity and documentation. USP ? United States Pharmacopeia grade — meets USP monograph specs for pharmaceutical use. Use for drug manufacturing, QC, and applications requiring US compendial compliance.
Synonyms
Dipotassium hydrogen orthophosphate | DI-POTASSIUM HYDROGEN ORTHOPHOSPHATE | dipotassium;hydrogen phosphate | EC 231-834-5 | POTASSIUM PHOSPHATE DIBASIC [WHO-DD] | CHEBI:131527 | DIBASIC POTASSIUM PHOSPHATE COMPONENT OF POTASSIUM PHOSPHATES | Potassium ph
Storage
Room temperature
★
Size
USA
Alemania (EU)*
Price
Qty
100g
P433942-100g
2 Disponible
—

103,90US$

121,90US$
Guardar 18,00 US$ (14.77%)
500g
P433942-500g
3 Disponible
—

412,90US$

499,90US$
Guardar 87,00 US$ (17.40%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

PharmPure™, USP PharmPure™,USP for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships 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 327 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Dipotassium hydrogen orthophosphate | DI-POTASSIUM HYDROGEN ORTHOPHOSPHATE | dipotassium;hydrogen phosphate | EC 231-834-5 | POTASSIUM PHOSPHATE DIBASIC [WHO-DD] | CHEBI:131527 | DIBASIC POTASSIUM PHOSPHATE COMPONENT OF POTASSIUM PHOSPHATES | Potassium ph
Especificaciones y pureza
PharmPure™, USP
Condiciones de almacenamiento de almacenamiento
Room temperature
Grado
PharmPure™, USP
Nombres e identificadores
Pubchem Sid504753203
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504753203
Sonrisas canónicasOP(=O)([O-])[O-].[K+].[K+]
IUPAC Namedipotassium;hydrogen phosphate
InChIKeyZPWVASYFFYYZEW-UHFFFAOYSA-L
INCHI1S/2K.H3O4P/c;;1-5(2,3)4/h;;(H3,1,2,3,4)/q2*+1;/p-2
Isómeros SMILES OP(=O)([O-])[O-].[K+].[K+]
Peso molecular 174.18
Reaxy-Rn 11343458
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11343458&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

KingdomInorganic compounds
SuperclassMixed metal/non-metal compounds
ClaseAlkali metal oxoanionic compounds
SubclassAlkali metal phosphates
Intermediate Tree Nodes Not available
Direct ParentAlkali metal phosphates
Alternative Parents Inorganic salts  Inorganic oxides  
Molecular FrameworkNot available
Substituents Alkali metal phosphate - Inorganic oxide - Inorganic salt
DescripciónThis compound belongs to the class of inorganic compounds known as alkali metal phosphates. These are inorganic compounds in which the largest oxoanion is phosphate, and in which the heaviest atom not in an oxoanion is an alkali metal.
External Descriptors organic molecular entity
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.

9 results found

Lot NumberCertificate TypeFechaArticulo
G2620106Certificate of AnalysisOct 12, 2024 P433942
I2425583Certificate of AnalysisOct 12, 2024 P433942
I2425584Certificate of AnalysisOct 12, 2024 P433942
I2425598Certificate of AnalysisOct 12, 2024 P433942
B2429469Certificate of AnalysisJan 22, 2024 P433942
B2429470Certificate of AnalysisJan 22, 2024 P433942
B2429471Certificate of AnalysisJan 22, 2024 P433942
B2429472Certificate of AnalysisJan 22, 2024 P433942
B2429473Certificate of AnalysisJan 22, 2024 P433942
Propiedades químicas y físicas
SensibilidadHygroscopic;Moisture sensitive
Punto de fusión (°C)340℃
Peso molecular174.176 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass173.889 Da
Monoisotopic Mass173.889 Da
Topological Polar Surface Area83.400 Ų
Heavy Atom Count7
Formal Charge0
Complexity46.500
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 Count3
Preguntas frecuentes y artículos
Fura-2 AM Staining Protocol
From Spec to Bench: Understanding and Using USP Grade Reagents
How should laboratory strains be preserved?
Operational Guide for Fluorescent Labeling of Antibodies Using AF594 NHS Ester
General Principles of Antibody Labeling with NHS-Activated Esters, F/P Calculation, and Troubleshooting Guide
How to Choose a Hydrogen Evolution (HER) Catalyst: Kinetic Barriers in Water Electrolysis, AWE/PEM/AEM Pathways, and a Materials-Family Roadmap (with a Product Map)
Installing a Redox Switch on Biomolecules: Principles, Conjugation Essentials, and an Application Guide for ATTO MB2 NHS ester
A Review of Ten Commonly Used Techniques for Detection, Quantification, and Interaction Analysis in Nucleic Acid Research
Selection of Common Research Salts: A Task Map for Alkali Metal Salts & Alkaline Earth Metal Salts (with Product Tables 1–6)
From “Reduction First, Then Acylation” to “Direct Amidation”: An Unconventional Route to Amide Bond Formation from Nitro and Nitroso Substrates with α-Keto Carboxylic Acids
The Methodological Value of TCFH: Advantages in Challenging Amidation and the Switching Logic of Carboxylic Acid Activation Pathways
What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications
Design Logic of Fluorinated 3,3-Disubstituted Oxetane Building Blocks: Structural Construction and Modulation of Amine Basicity, Lipophilicity, and Metabolic Stability
Citations of This Product
Calculadoras de soluciones
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