Dichloromethane Physical & Chemical Properties:
Density, Boiling Point, Polarity & Full Technical Data
Complete property reference for formulators, engineers & procurement teams
🔗 View DCM Product Page📋 Table of Contents
- Quick-Reference Property Summary
- Thermal Properties: Boiling Point, Melting Point & Vapor Pressure
- Density & Specific Gravity
- Polarity, Dipole Moment & Dielectric Constant
- Solvency Power: KB Value, Hansen Parameters & Solubility
- Transport Properties: Viscosity, Surface Tension & Diffusivity
- Spectroscopic & Optical Properties
- Safety-Relevant Properties: Flash Point, Flammability & Reactivity
- Frequently Asked Questions
💡 How to use this reference: All values are for pure dichloromethane (CAS 75-09-2) at standard conditions (20 °C, 1 atm) unless otherwise stated. For commercial-grade DCM specifications (purity, acidity, water content), please refer to the DCM product page or request a Certificate of Analysis.
📊 1. Quick-Reference Property Summary
The table below condenses the most-referenced DCM properties into a single lookup. Detailed discussion and engineering context for each parameter follows in subsequent sections.
| Property | Value | Conditions / Notes |
|---|---|---|
| Molecular Formula | CH₂Cl₂ | MW = 84.93 g/mol |
| Boiling Point | 39.6 °C (103.3 °F) | At 1 atm (101.3 kPa) |
| Melting Point | −96.7 °C (−142.1 °F) | Remains liquid over vast temperature range |
| Density | 1.325 g/cm³ | At 20 °C; denser than water |
| Vapor Pressure | 47.4 kPa (355 mmHg) | At 20 °C; very high - evaporates rapidly |
| Flash Point | None (closed cup) | Not a flammable liquid per GHS / DOT criteria |
| Autoignition Temperature | 556 °C (1033 °F) | Very high - further reduces fire risk |
| Explosive Limits (LEL/UEL) | 13 – 23 vol% in air | Flammable range exists at elevated temps |
| Dipole Moment | 1.60 D | Tetrahedral geometry; net polar molecule |
| Dielectric Constant (ε) | 8.93 | At 25 °C; intermediate polarity |
| Refractive Index (nD²⁰) | 1.4242 | At 20 °C; useful purity check |
| Viscosity | 0.44 mPa·s (cP) | At 20 °C; very low - excellent wetting |
| Surface Tension | 27.2 mN/m | At 20 °C |
| Water Solubility | 20 g/L | At 20 °C; slight - two-phase system forms |
| Kauri-Butanol (KB) Value | 136 | Very high solvency (toluene = 105) |
| Log P (octanol/water) | 1.25 | Moderate lipophilicity |
| Critical Temperature | 237 °C (510 K) | |
| Critical Pressure | 6.08 MPa | Relevant for supercritical applications |
🌡️ 2. Thermal Properties: Boiling Point, Melting Point & Vapor Pressure
DCM's thermal profile is one of its most defining commercial characteristics. Its boiling point of 39.6 °C is the lowest of all common chlorinated solvents, sitting just above room temperature. This single fact underpins several of DCM's most valued process advantages.
DCM evaporates completely at mild temperatures (40–60 °C), enabling simple distillation or evaporation-based recovery without degrading heat-sensitive substrates. This is critical in pharmaceutical API drying and food-grade decaffeination.
With a melting point of −96.7 °C, DCM remains fully liquid at all realistic process temperatures, including cryogenic reaction conditions used in asymmetric synthesis and low-temperature extractions.
Vapor pressure of 47.4 kPa at 20 °C means rapid evaporation in open systems. This creates significant inhalation exposure risk if local exhaust ventilation is not installed. Closed-system handling is strongly preferred for large volumes.
| Temperature (°C) | Vapor Pressure (kPa) | Vapor Pressure (mmHg) | Engineering Note |
|---|---|---|---|
| 0 °C | 19.3 | 145 | Storage in cool warehouse; significant headspace pressure |
| 10 °C | 30.1 | 226 | Typical cool-day ambient; accelerated evaporation |
| 20 °C | 47.4 | 355 | Reference condition - very high evaporation rate |
| 30 °C | 71.9 | 539 | Warm ambient; drums must be vented-and-sealed properly |
| 39.6 °C | 101.3 | 760 | Boiling point at 1 atm |
💡 Heat of vaporization: DCM has a ΔHvap of approximately 28.6 kJ/mol at its boiling point - relatively low, confirming the ease of evaporation. For comparison, water's ΔHvap is 40.7 kJ/mol. This low value means DCM-based processes consume less energy in evaporation/recovery steps.
⚖️ 3. Density & Specific Gravity
At 1.325 g/cm³ (20 °C), DCM is significantly denser than water (1.000 g/cm³) and denser than most organic solvents. This property is exploited in liquid–liquid extraction: when DCM and an aqueous layer are mixed and allowed to separate, DCM consistently settles to the bottom of the separatory funnel, making layer separation straightforward and predictable.
| Solvent | Density (g/cm³, 20 °C) | Position vs Water |
|---|---|---|
| Hexane | 0.659 | Floats (upper layer) |
| Ethyl acetate | 0.902 | Floats (upper layer) |
| Toluene | 0.867 | Floats (upper layer) |
| Water | 1.000 | Reference |
| Dichloromethane (DCM) | 1.325 | Sinks (lower layer) ✅ |
| Chloroform | 1.489 | Sinks (lower layer) |
| Carbon tetrachloride | 1.594 | Sinks (lower layer) |
Density varies with temperature. The table below provides values across the liquid range relevant to process design:
| Temperature (°C) | Density (g/cm³) | Specific Gravity |
|---|---|---|
| −10 | 1.366 | 1.366 |
| 0 | 1.351 | 1.351 |
| 20 | 1.325 | 1.325 |
| 25 | 1.318 | 1.318 |
| 35 | 1.302 | 1.302 |
⚠️ Practical packaging note: A 200 L steel drum filled with DCM at 20 °C contains approximately 265 kg net weight (200 L × 1.325 g/cm³). This is substantially heavier than a comparable drum of most organic solvents. Always verify forklift and racking load limits before handling full DCM drums.
🧲 4. Polarity, Dipole Moment & Dielectric Constant
DCM's polarity profile is one of the most frequently misunderstood aspects of its chemistry. The molecule is polar - it has a net dipole moment of 1.60 D - yet it is miscible with nonpolar solvents like hexane and only slightly soluble in water. This apparent paradox is what makes DCM so uniquely versatile as a solvent.
🔬 Why DCM is Polar but Not Water-Miscible
DCM has a tetrahedral-like geometry (C₂ᵥ symmetry). The two C–Cl bond dipoles do not cancel - they point in the same direction due to the H–C–H angle - resulting in a net dipole of 1.60 D. However, DCM lacks the ability to form hydrogen bonds as a donor (no O–H or N–H groups), which is the primary interaction holding water molecules together. As a result:
- ✅ DCM dissolves well in nonpolar solvents (hexane, heptane, petroleum ether)
- ✅ DCM dissolves well in moderately polar solvents (ethyl acetate, acetone, diethyl ether)
- ✅ DCM solvates both polar and nonpolar solutes simultaneously
- ⚠️ DCM is only slightly soluble in water (20 g/L) - two-phase system forms
| Solvent | Dipole Moment (D) | Dielectric Constant (ε) | Polarity Classification |
|---|---|---|---|
| Hexane | 0.09 | 1.88 | Nonpolar |
| Toluene | 0.36 | 2.38 | Slightly polar |
| Ethyl acetate | 1.78 | 6.02 | Moderately polar |
| Dichloromethane | 1.60 | 8.93 | Moderately polar ← unique range |
| Chloroform | 1.04 | 4.81 | Slightly polar |
| Acetone | 2.88 | 20.7 | Polar (miscible with water) |
| Water | 1.85 | 80.1 | Highly polar |
💡 TLC and chromatography note: In thin-layer chromatography (TLC) and column chromatography, DCM is placed between ethyl acetate and hexane on the eluent polarity scale. A DCM/hexane gradient provides excellent resolution for many intermediate-polarity natural products and pharmaceutical intermediates.
🧪 5. Solvency Power: KB Value, Hansen Parameters & Solubility
DCM's solvency power - its ability to dissolve a wide range of organic compounds - is exceptional among common laboratory and industrial solvents. The Kauri-Butanol (KB) value of 136 places DCM significantly above toluene (105) and xylene (98), reflecting its ability to solvate resins, polymers, waxes, oils, and chlorinated compounds that resist dissolution in weaker solvents.
| Hansen Parameter | Symbol | DCM Value (MPa½) | Physical Meaning |
|---|---|---|---|
| Dispersion component | δd | 18.2 | Van der Waals / nonpolar interactions |
| Polar component | δp | 6.3 | Dipole–dipole interactions |
| Hydrogen bonding component | δh | 7.1 | H-bond acceptor capacity (weak donor) |
| Total (Hildebrand) | δt | 20.3 | Total cohesion energy |
Key materials that DCM dissolves readily include: cellulose acetate, polycarbonate (surface dissolution), PVC, natural and synthetic rubbers, alkyd resins, acrylic polymers, epoxy resins, waxes, fats, and most pharmaceutical active ingredients. The table below summarizes solubility of common substrates:
| Material / Substrate | Solubility in DCM | Application Relevance |
|---|---|---|
| Alkyd & epoxy coatings | ✅ Excellent | Paint stripping |
| Polyurethane coatings | ✅ Excellent | Coating removal, reaction solvent |
| PVC & polycarbonate | ✅ Good (surface swell) | Solvent welding, adhesives |
| Fats, oils & waxes | ✅ Excellent | Food-grade extraction, degreasing |
| Most pharmaceutical APIs | ✅ Good to excellent | Synthesis, recrystallization, extraction |
| PTFE, polyethylene | ❌ Insoluble | DCM-safe material for containers |
| Water, inorganic salts | ❌ Immiscible / insoluble | Enables aqueous/organic extraction |
💧 6. Transport Properties: Viscosity, Surface Tension & Diffusivity
DCM's transport properties - primarily its very low viscosity and moderate surface tension - directly influence its behavior in wetting, penetration, and mass-transfer applications such as paint stripping and liquid–liquid extraction.
Extremely low viscosity at 20 °C - roughly half that of ethanol (1.1 mPa·s). This enables rapid penetration into porous substrates, coating films, and weld seam capillaries. In paint stripping, this means DCM reaches the substrate/coating interface quickly, enabling fast blistering and lift.
Lower than water (72 mN/m) but moderate among organic solvents. DCM wets most industrial surfaces readily. Its spreading coefficient on metal surfaces is favorable, making it effective for degreasing applications where complete surface contact is required.
Gas-phase diffusion coefficient ≈ 1.01 × 10⁻⁵ m²/s at 25 °C, 1 atm. Combined with its high vapor pressure, DCM vapors disperse rapidly in air. In poorly ventilated spaces, concentrations can build to occupational exposure limits within minutes - underlining the need for local exhaust ventilation.
🔬 7. Spectroscopic & Optical Properties
Spectroscopic data for DCM is relevant both for purity verification and for its use as an NMR and IR reference solvent. The table below summarizes key spectroscopic identifiers.
| Technique | Key Data | Application / Note |
|---|---|---|
| ¹H NMR | δ 5.30 ppm (s, 2H, residual CHDCl₂ in CD₂Cl₂) | CD₂Cl₂ is a common NMR deuterated solvent; residual peak at 5.32 ppm |
| ¹³C NMR | δ 53.8 ppm (septet in CD₂Cl₂) | Characteristic single carbon signal |
| IR (key bands) | 2985, 1424, 1265, 898, 738 cm⁻¹ | C–H stretch, CH₂ scissor, C–Cl stretch. 738 cm⁻¹ band is diagnostic |
| UV cutoff | 235 nm | Transparent above 235 nm; suitable HPLC mobile phase for UV detection |
| Refractive Index (nD²⁰) | 1.4242 | Precise purity verification by refractometry; ±0.0005 tolerance common in specs |
| Mass Spectrum (EI) | m/z 84/86/88 (M⁺ isotope cluster); base peak m/z 49 (CH₂Cl⁺) | Characteristic 3:2:1 chlorine isotope pattern confirms identity |
🦺 8. Safety-Relevant Properties: Flash Point, Flammability & Reactivity
Understanding DCM's safety-relevant properties is essential for proper classification, storage, and risk assessment. DCM occupies an unusual safety category: it does not meet the standard definition of a flammable liquid yet presents real fire and health risks under certain conditions.
| Safety Property | Value | Regulatory / Engineering Implication |
|---|---|---|
| Flash point (c.c.) | None | Not classified as flammable liquid (GHS Cat. 1–4); not subject to flammable storage rules |
| Autoignition temp. | 556 °C | Very high - ignition from hot surfaces is extremely unlikely under normal conditions |
| LEL / UEL | 13% / 23% (vol in air) | Flammable range is narrow and high - requires concentrated vapor to ignite |
| GHS health hazard | Acute Tox. 4 (inhal.); Carc. 1A; STOT RE 1 | Carcinogen classification drives the most stringent workplace controls |
| Stability | Stable under normal conditions | Reacts with strong bases/alkalis to form phosgene or CO; incompatible with strong oxidizers |
| Reactivity risk | Phosgene formation possible | DCM can oxidize to phosgene (COCl₂) in UV light or fire conditions - do not use near open flames |
| Ozone depletion (ODP) | ≈ 0 (not regulated under Montreal Protocol) | No ODP restriction; however increasing atmospheric monitoring due to rising emissions |
⚠️ Phosgene Formation Warning
When DCM is exposed to UV radiation, high temperatures, or open flames in the presence of oxygen, it can decompose to form phosgene (COCl₂) - a highly toxic gas (IDLH: 2 ppm). This risk is particularly relevant in welding areas near DCM degreasing operations or fire suppression scenarios. Never use halogenated solvent degreasers near open welding arcs.
❓ 9. Frequently Asked Questions
Q1: Is dichloromethane more dense than water?
Yes - DCM has a density of 1.325 g/cm³ at 20 °C, making it approximately 32.5% denser than water (1.000 g/cm³). This means when DCM is mixed with an aqueous solution and the layers are allowed to separate, DCM consistently settles to the bottom. This property is fundamental to liquid–liquid extraction technique in organic chemistry and pharmaceutical manufacturing.
Q2: What is the boiling point of DCM and why does it matter?
DCM boils at 39.6 °C at atmospheric pressure - just above room temperature. This low boiling point means DCM can be removed from a product or reaction mixture by simple evaporation at mild temperatures (40–60 °C), without requiring vacuum or heat that would degrade sensitive compounds. For pharmaceutical manufacturers, this allows complete solvent removal from APIs using gentle drying. The downside is rapid evaporation in open systems, requiring ventilation controls.
Q3: Is DCM polar or nonpolar?
DCM is a polar molecule with a dipole moment of 1.60 D and a dielectric constant of 8.93 - placing it in the "moderately polar" category. However, it is NOT miscible with water because it lacks hydrogen bond donor capability (no O–H or N–H groups). This unusual combination - polar but not water-miscible - is what makes DCM an exceptionally broad-spectrum solvent, capable of dissolving both polar organic compounds and nonpolar waxes and oils.
Q4: What does "Kauri-Butanol value of 136" mean for DCM?
The Kauri-Butanol (KB) value measures a solvent's ability to dissolve kauri resin in a standardized test - essentially a practical measure of solvency power. DCM's KB value of 136 is exceptionally high: toluene scores 105, xylene around 98, and heptane just 27. A higher KB value means DCM can dissolve tougher coatings, resins, and polymers that weaker solvents cannot penetrate - which is why it is uniquely effective in paint stripping applications.
Q5: How do I verify DCM purity using physical properties?
The most practical on-site checks are: (1) Refractive index - pure DCM should read 1.4242 ± 0.0005 at 20 °C by refractometer; (2) Density - should be 1.323–1.328 g/cm³ at 20 °C; (3) Appearance - water-white, essentially colorless (APHA ≤10 for technical grade). For precise purity and impurity profiling (chloroform, methanol, water content), gas chromatography (GC) analysis per the COA is required.
Q6: Why does DCM have no flash point but still has explosive limits?
Flash point measures whether a liquid can sustain a flame at a given temperature under standard test conditions. DCM cannot sustain combustion below its LEL of 13 vol% in air under standard test conditions, so it has no flash point by definition. However, its LEL (13%) and UEL (23%) define a concentration range where a spark CAN ignite the vapor-air mixture. In practice, reaching 13% DCM in air requires substantial accumulation - equivalent to roughly 570 g/m³ - which is far above any occupational exposure limit and would require a confined, poorly ventilated space with significant DCM release.
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