Dichloromethane - electronic grade, UPS grade, ≥99.5% , CAS No.75-09-2

CAS: 75-09-2 Cat. No.: D1523634 Formula: CH2Cl2 Molecular Weight: 84.93 Beilstein Registry Number: 1730800 EC Number: 200-838-9 PubChem CID: 6344
Out of stock
GRADE & PURITY Electronic grade ? Electronic grade — ultra-low metallic and particulate impurities for microelectronics. Use in semiconductor and electronics processes intolerant of contamination. UPS grade ? Ultra-pure-special (UPS) grade — purity above UP for stringent semiconductor steps. Use where UP grade is insufficient for contamination control. ≥99.5%
Storage
Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice,FedEx DG Service
No options of this product are available.
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Why this grade

electronic grade, UPS grade, ≥99.5% Electronic grade,UPS grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Protected from light,Argon charged Ships Wet ice,FedEx DG Service 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 2362 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Specifications & Purity
electronic grade, UPS grade, ≥99.5%
Storage
Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice,FedEx DG Service
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Electronic grade, UPS grade
Purity
≥99.5%
Names and Identifiers
Canonical Smiles
C(Cl)Cl
IUPAC Name
dichloromethane
InChIKey
YMWUJEATGCHHMB-UHFFFAOYSA-N
INCHI
1S/CH2Cl2/c2-1-3/h1H2
Isomeric SMILES
C(Cl)Cl
WGK Germany
1
RTECS
PA8050000
PubChem CID
6344
UN Number
1593
Packing Group
III
Molecular Weight
84.93
Beilstein
1730800

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
SuperclassOrganohalogen compounds
ClassAlkyl halides
SubclassHalomethanes
Intermediate Tree Nodes Not available
Direct ParentHalomethanes
Alternative Parents Organochlorides  Hydrocarbon derivatives  Alkyl chlorides  
Molecular FrameworkAliphatic acyclic compounds
Substituents Halomethane - Hydrocarbon derivative - Organochloride - Alkyl chloride - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as halomethanes. These are organic compounds in which at least one of the four hydrogen atoms of methane (CH4) are replaced by halogen atoms.
External Descriptors a small molecule
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.

3 results found

Lot NumberCertificate TypeDateItem
I2608766Certificate of AnalysisAug 26, 2026 D1523634
I2608767Certificate of AnalysisAug 26, 2026 D1523634
I2608769Certificate of AnalysisAug 26, 2026 D1523634
Chemical and Physical Properties
SolubilitySlightly soluble in water; Degree of Solubility in water: 13 g/l 20 °C; Miscible with Acetone,Alcohol,Ether,Chloroform
Sensitivityheat sensitive,light sensitive
Refractive Index1.424
Boil Point(°C)40°C
Melt Point(°C)-95.1°C
Molecular Weight84.930 g/mol
XLogP31.500
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count0
Exact Mass83.9534 Da
Monoisotopic Mass83.9534 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count3
Formal Charge0
Complexity2.800
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
Documents & Articles
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
From Nitroarenes to Pharmaceutically Relevant Pyridines: A Photochemically Induced Aryl Nitrene-Mediated Skeletal Editing Strategy
Direct O-Alkylation of Bicyclo[1.1.1]pentan-1-ol: Avoiding Alkoxide-Mediated Skeletal Fragmentation through Electrophile Activation
How Cyclization Changes Peptide Behavior: Conformational Preorganization, Skin Delivery, and Integrin Binding, Using Cyclopeptide-5 as an Example
1,8-Naphthyridine-Based Aldose Reductase Inhibitors: Scaffold Construction, In Vitro Inhibitory Activity, and Directions for Structural Optimization
Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination
Solid Supports in Packed Gas Chromatography Columns: Definition, Mechanisms of Action, Classification, and Selection
Selectivity Mechanism of the Triple Aryne–Tetrazine Cascade Reaction: Reaction-Pathway Switching and Intermediate Transformations
Reaction Mechanism of Pyrrole Skeletal Recasting: Reconstruction of Intraring Atomic Connectivity during Dearomatization—Skeletal Reorganization—Rearomatization
Construction of the Key α-Bromoketone Intermediate for LY3509754: A β-Keto Ester Strategy and Concomitant Decarboxylation Following Enzymatic Ester Hydrolysis
Tether Effects in Intramolecular [2+2] Photocycloadditions: Straight and Crossed Regioselectivity and Stepwise C–C Bond Formation
Regioselectivity of Pyridine-Diimine (PDI)–Cobalt-Catalyzed Simmons–Smith-Type Cyclopropanation: Alkene Substitution Patterns and the Methylene-Transfer Mechanism
ACT-1014-6470 Kilogram-Scale Synthesis: N7-Selective Reductive Amination of an Unprotected Pyrazole, Subsequent N2 Alkylation, and Intramolecular Urea Formation
How to Evaluate Reaction Generality through Substrate Scope: From the Number of Examples to Standardized Substrate Selection
Citations of This Product
Solution Calculators
Reviews

Customer Reviews

Frequently Asked Questions

What is the purity of this product?
This product is supplied at ≥99.5% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
What does electronic grade mean?
electronic grade indicates that the material has been processed and tested for semiconductor and electronics manufacturing. Specifications focus on the impurities that affect performance in that application — for example, metal content for electronics, particle size for batteries, refractive index for optics, or moisture content for moisture-sensitive processes.
What does UPS grade mean?
UPS grade indicates that the material has been processed and tested for semiconductor and electronics manufacturing. Specifications focus on the impurities that affect performance in that application — for example, metal content for electronics, particle size for batteries, refractive index for optics, or moisture content for moisture-sensitive processes.
How should this product be stored?
Store at 2–8 °C, protected from light, under argon. It is supplied under an argon blanket; reseal under inert gas after each use.
How is this product shipped?
This product ships chilled on wet ice. Unpack on arrival and transfer it to the storage condition stated above.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 75-09-2, the molecular formula is CH2Cl2, and the molecular weight is 84.93 g/mol. InChIKey YMWUJEATGCHHMB-UHFFFAOYSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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