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Molality Calculator

Chemistry

b = n_solute / m_solvent n_solute = m_solute / M

Examples:

Solute

Quick picks (fill the formula and an ideal van 't Hoff factor):

NaCl · M = 58.440 g/mol · Molar Mass Calculator
Default 1. Only affects the particle molality and the colligative preview.

Solvent

H2O · M = 18.015 g/mol (for mole fractions)
Molality (b)
0.6845mol/kg
= 0.6845 molal (m)
Moles of solute
0.1711 mol
Solvent mass (what b divides by)
0.2500 kg
Solute mass
10.00 g
Total solution mass
260.0 g
Particle molality i·b
1.369 mol/kg

Same solution in other units

Molality (b)

0.6845 mol/kg

Mass percent (w/w)

3.846 %

Mole fractions

x_solute = 0.01218 · x_solvent = 0.9878

Binary solution (one solute plus the solvent), counted in formula units rather than ions.

Molarity (c)

Add the solution density to see molarity.

Density of the finished solution, not the pure solvent.

Composition of the solution

By mass

solute 10.00 g · 3.846 % · n = 0.1711 mol

solvent 250.0 g · 96.15 %

molality divides by this: 0.2500 kg solvent

solute 10.00 g · 3.846 % · n = 0.1711 mol

solvent 250.0 g · 96.15 %

By amount (moles)

solute 0.1711 mol · x = 0.01218

solvent 13.88 mol · x = 0.9878

solute 0.1711 mol · x = 0.01218

solvent 13.88 mol · x = 0.9878

Colligative preview (ideal)

ΔTf = i·Kf·b = 2 × 1.860 × 0.6845 = 2.546 °C → freezes near -2.546 °C. Freezing Point Depression

ΔTb = i·Kb·b = 2 × 0.5120 × 0.6845 = 0.7009 °C → boils near 100.7 °C. Boiling Point Elevation

Ideal estimates with the factor i you entered; real electrolytes dissociate less as concentration rises.

Step-by-step derivation

Step 1

n = m_solute / Mn = 10.00 g / 58.44 g/moln = 0.1711 mol

Step 2

m_solvent in kgm_solvent = 250.0 gm_solvent = 0.2500 kg

Step 3

b = n / m_solventb = 0.1711 mol / 0.2500 kgb = 0.6845 mol/kg

Step 4

b_particles = i × bb_particles = 2 × 0.6845 mol/kgb_particles = 1.369 mol/kg

Ideal dissociation; real electrolytes dissociate less as concentration rises.

Step 5

w = 100·b·M / (1000 + b·M)w = 100 × 0.6845 × 58.44 / (1000 + 0.6845 × 58.44)w = 3.846 % (w/w)

1 kg of solvent holds b mol = b·M g of solute, so the solution weighs 1000 + b·M g.

Step 6

x = b / (b + 1000 / M_solvent)x = 0.6845 / (0.6845 + 1000 / 18.02)x_solute = 0.01218, x_solvent = 0.9878

1 kg of solvent is 1000 / M_solvent mol, next to b mol of solute (formula units, not ions).

About This Tool

Molality Calculator – Concentration per Kilogram of Solvent

Molality tells you how many moles of solute are dissolved in each kilogram of solvent. This calculator works it out from what you actually measured in the lab, tells you how much solute or solvent to weigh out for a target molality, and converts molality to and from molarity, mass percent and mole fraction. Every result comes with a step-by-step derivation and a picture of how the solution splits by mass and by amount.

The molality formula

b = n_solute / m_solvent        [mol/kg]
n_solute = m_solute / M_solute

IUPAC uses the symbol b; many textbooks write m and call the unit "molal". Both mean the same number, so 0.500 mol/kg is a 0.500 molal solution. As a worked example, 10.0 g of sodium chloride (M = 58.44 g/mol) is 0.1711 mol. Dissolved in 250 g of water, that gives b = 0.1711 / 0.2500 = 0.6845 mol/kg.

Divide by the solvent, not the solution

The most common molality mistake is dividing by the mass of the whole solution. The denominator is the solvent alone. If you weighed the finished solution, subtract the solute first: m_solvent = m_solution − m_solute. The calculator does this for you when you choose "Total solution mass", and the composition bar draws a bracket under the solvent segment only, so you can see what the formula divides by.

Solution mass is not solvent mass
Using 260 g of solution instead of 250 g of water in the example above gives 0.6581 mol/kg, about 4 % too low. The error grows as the solution gets more concentrated.

Molality vs molarity

Molarity (mol/L) divides by the volume of solution. Volumes expand and contract with temperature, so molarity drifts slightly when a solution warms up or cools down. Masses do not change, which makes molality temperature independent. That is why the colligative property equations, such as freezing point depression (ΔTf = i·Kf·b) and boiling point elevation (ΔTb = i·Kb·b), are written in terms of molality.

To convert between the two you need the solution's density ρ and the solute's molar mass M:

c = 1000·ρ·b / (1000 + b·M)
b = 1000·c / (1000·ρ − c·M)

For dilute aqueous solutions the two numbers are almost identical, because a litre of dilute solution is close to one kilogram of water. They separate for concentrated solutions. Concentrated hydrochloric acid at 37 % w/w and 1.18 g/mL is about 12.0 mol/L but 16.1 mol/kg.

Mass percent and mole fraction

Both conversions use a basis of one kilogram of solvent, which holds b mol of solute weighing b·M grams:

w = 100·b·M / (1000 + b·M)          mass percent
x = b / (b + 1000 / M_solvent)       solute mole fraction

The mole fraction assumes a binary solution, one solute in one solvent, and counts formula units rather than separate ions.

Preparing a solution of known molality

To make a solution in the lab, weigh the solute and the solvent separately. You don't need a volumetric flask, which is one practical advantage of molality. For a target b, the solute needed for a given solvent mass is n = b × m_solvent. If you want a fixed total mass T of solution instead, the solute mass is T·b·M / (1000 + b·M). For example, 500 g of 1.00 mol/kg NaCl needs 27.61 g of salt and 472.4 g of water.

Particle molality and the van 't Hoff factor

Colligative effects depend on the number of dissolved particles, not on the number of formula units. Multiplying by the van 't Hoff factor i gives the particle molality i·b. An ideal NaCl solution has i = 2 and CaCl₂ has i = 3, while non-electrolytes such as glucose and urea have i = 1.

Ideal values only
Real electrolytes dissociate less as concentration rises, so measured freezing-point and boiling-point changes are usually a little smaller than the ideal preview.

Frequently Asked Questions

Is the Molality Calculator free?

Yes, Molality Calculator is totally free :)

Can I use the Molality Calculator offline?

Yes, you can install the webapp as PWA.

Is it safe to use Molality Calculator?

Yes, any data related to Molality Calculator only stored in your browser (if storage required). You can simply clear browser cache to clear all the stored data. We do not store any data on server.

How does this molality calculator work?

It divides the moles of solute by the mass of solvent in kilograms (b = n / m_solvent). You can enter the solute as moles or as a mass with a formula or molar mass, and the solvent as a mass, a volume with its density, or the total solution mass. The same inputs also let you work out how much to weigh out for a target molality, or convert between molality, molarity, mass percent and mole fraction.

What is the difference between molality and molarity?

Molality (mol/kg) divides the moles of solute by the mass of the solvent alone, while molarity (mol/L) divides by the volume of the whole solution. Because masses do not change with temperature but volumes do, molality stays constant when a solution is heated or cooled, and molarity drifts slightly.

Can I enter the mass of the whole solution instead of the solvent?

Yes. Choose "Total solution mass" and the calculator subtracts the solute mass first, because molality is defined per kilogram of solvent. Putting the solution mass where the solvent mass belongs is the most common molality mistake, and it gives a value that is too low.

What does the van 't Hoff factor change?

Only the particle (colligative) molality i·b and the freezing- and boiling-point previews. The quick-pick values, such as 2 for NaCl or 3 for CaCl2, assume complete dissociation; real electrolytes dissociate less as concentration rises, so measured effects are usually a little smaller.

How accurate are the conversions to molarity and mole fraction?

The formulas are exact, so the results are as good as your inputs. Molarity needs the density of the solution itself, not the pure solvent, and the preset solvent densities apply only at the stated temperature. Mole fractions assume one solute in one solvent and count formula units rather than ions.

Why are molality and molarity almost equal for dilute water solutions?

A litre of dilute aqueous solution is very close to one kilogram of water, so dividing by litres of solution or kilograms of water gives nearly the same number. The two values separate as the solution gets more concentrated, or when the solvent density is far from 1 g/mL.