Zinc standard - 1000ug/ml Zn in 1% HNO3 , CAS No.7440-66-6

CAS: 7440-66-6 Cat. No.: Z117293 Summenformel: Zn Molekulargewicht: 65.39 EG-Nummer: 231-175-3
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GRADE & PURITY 1000ug/ml Zn in 1% HNO3
Storage
Protected from light,Room temperature
Shipped In
Normal
★
Size
Deutschland (EU)
USA*
Price
Qty
20ml
Z117293-20ml
Auf Bestellung · 8–12 Wochen

22,47€

25,95€
Speichern 3,47 € (13.38%)
50ml
Z117293-50ml
—
2 Auf Lager

30,28€

36,36€
Speichern 6,07 € (16.71%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

1000ug/ml Zn in 1% HNO3 for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,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 216 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Spezifikationen & Reinheit
1000ug/ml Zn in 1% HNO3
Storage
Protected from light,Room temperature
Verschickt in
Normal
Namen und Kennungen
Isomere SMILES
[Zn]
UN-Nummer
UN 1789
Verpackungsgruppe
II
Molekulargewicht
65.39

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

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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 TypeDatumArtikel
D2622483Certificate of AnalysisMay 14, 2026 Z117293
D2622457Certificate of AnalysisMay 14, 2026 Z117293
G2523473Certificate of AnalysisAug 06, 2025 Z117293
D2527419Certificate of AnalysisMay 08, 2025 Z117293
G2405528Certificate of AnalysisJul 17, 2024 Z117293
A2423326Certificate of AnalysisFeb 23, 2024 Z117293
A2423327Certificate of AnalysisFeb 23, 2024 Z117293
Chemische und physikalische Eigenschaften
Siedepunkt (°C)907°C
Schmelzpunkt (°C)419.6°C
FAQs und Artikel
A Practical Guide to Organozinc Reagents for Synthesis (Organozinc Reagents): Structural Features, Key Reactions, and a Practical Selection Navigation (Including Aladdin Product Tables)
Make “Aryl Chlorides + Low Pd Loading + Scale-Up Reproducibility” Reliable: The Initiation and Durability Logic of Pd–NHC (Palladium–N-Heterocyclic Carbene) Cross-Coupling (with Selection Navigation and Product Tables)
Flavones: Structural Features, Physicochemical Properties, and Key Points for Research and Applications
Fluorocarbon Resin Coating Formulation Design: Resin Selection, Supporting Systems, and Key Application Control Points
Formulation Design of Chlorinated Rubber Coatings: Component Synergy and Performance Control
Types of Inorganic Salts That Can Undergo Reduction Reactions: Nitrates, Sulfur-Containing Salts, Halogen Oxyanion Salts, and Metal Salts
Thietanes: Promising Small-Ring Building Blocks with Tunable Physicochemical Properties through Sulfur Oxidation-State Control
Reactions and Applications of 3,3-Difluoroallyl Sulfonium Salts (DFASs): Small-Molecule gem-Difluoroallylation, Selective Peptide Modification, and Subsequent Functionalization
Construction and Transformation of Aziridines in Drug Synthesis: Ring Strain, N-Substituent Control, Selective Ring Opening, and Scaffold Expansion
Regioselective Deprotonative Metalation of Pyridines: C–H Acidity, Coordination Effects, and Metal Systems
Regioselectivity of Pyridine-Diimine (PDI)–Cobalt-Catalyzed Simmons–Smith-Type Cyclopropanation: Alkene Substitution Patterns and the Methylene-Transfer Mechanism
From Temporary Covalent Assembly to Intramolecular Smiles Aryl Migration: DCPDC-Mediated Phenol–Primary Amine C–N Cross-Coupling
Citations of This Product
Lösungsrechner
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