Potassium phosphate dibasic - UltraPureChrom™, for HPLC, ≥99%(T) , CAS No.7758-11-4

CAS: 7758-11-4 Cat. No.: P433944 Formula: K2HPO4 Molecular Weight: 174.18 EC Number: 231-834-5
AVAILABLE TO ORDER
GRADE & PURITY UltraPureChrom™ ? UltraPureChrom™ — Aladdin's ultra-pure line for chromatography and spectroscopy. Use as a premium solvent/reagent where the lowest impurity background is required. for HPLC ? Suitable for HPLC — meets purity needs for liquid-chromatography use. Use for routine HPLC mobile phases and sample prep. ≥99%(T)
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
Germany (EU)*
Price
Qty
50g
P433944-50g
3 In stock
—
$79.90
250g
P433944-250g
2 In stock
1 In stock
$309.90
Enter a quantity for the sizes you want to add.
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Why this grade

UltraPureChrom™, for HPLC, ≥99%(T) for HPLC,UltraPureChrom™ 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

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
Specifications & Purity
UltraPureChrom™, for HPLC, ≥99%(T)
Storage
Room temperature
Grade
for HPLC, UltraPureChrom™
Purity
≥99%(T)
Names and Identifiers
Pubchem Sid528774346
Canonical SmilesOP(=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
Isomeric SMILES OP(=O)([O-])[O-].[K+].[K+]
Molecular Weight 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
ClassAlkali 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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 TypeDateItem
G2627013Certificate of AnalysisAug 05, 2026 P433944
G2627012Certificate of AnalysisJul 31, 2026 P433944
F2611723Certificate of AnalysisJun 16, 2026 P433944
G2602027Certificate of AnalysisJun 16, 2026 P433944
E2629457Certificate of AnalysisAug 05, 2024 P433944
G2426046Certificate of AnalysisAug 05, 2024 P433944
G2426048Certificate of AnalysisAug 02, 2024 P433944
Chemical and Physical Properties
SolubilityH2O: 5%, clear, colorless
SensitivityMoisture sensitive
Melt Point(°C)340℃
Molecular Weight174.176 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
Documents & Articles
UltraPureChrom™: The Pinnacle of Purity for Chromatography
Introduction: “Suitable for HPLC” (HPLC Grade)
HPLC-Grade Solvents for High-Performance Liquid Chromatography: From Concept to Practice
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
Solution Calculators
Reviews

Customer Reviews

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