Skip to main content

Benzalkonium chloride

Structure of Benzalkonium chloride, source: Wikipedia

Properties

White to white-yellow powder or gelatinous yellowwhite fragments, the compound is hygroscopic, which means it easily attracts water (from f.e. the air).
When the compound gets heated, it will form a clear molten mass.
It is soluble in water and alcohol. When it is resolved in water, the H2O solution will form excessive foam.


How to identify the compound
It
- UV spectrophotometry: maxima at 257 nm, 263 nm and 269 nm.
- Using liquid chromatography
- Adding Na-tetraphenylborate and acetic acid will form a sediment of benzalkoniumtetraphenylborate. Which has a characteristic melting point of 127-133 °C.
- Bringing the compound in a NaOH solution together with BFB (bromephenol blue) and dimethylchloride will form a blue colour in the CH2Cl2 layer. This is caused by the ionpair forming with the anionic pigment (BFB) and extraction of the ionpair in the organic layer.
- Identification of Cl- ions: + AgNO3 will form a white precipitate which is soluble in NH3.
Or if you add dichromate -> chromylchloride will be formed + phenylcarbazide -> white precipitate.



Determining the content

Adding KI in an alkaline environment -> forms benzalkoniumiodide which will be extracted to CH2Cl2 (organic layer).
The excess of the I- ions (in the water layer) will be determined using KIO3 in strong acid (H+ milieu). This is also called the method of Andrews


I- + IO3- -> I+ (jodoxyl)
Intermediate = I2


Use of benzalkonium chloride

It's used as a disinfectant in concentrations of about 0,1% for hands (used in surgery), small wounds, eat and drinking disinfectant, bed sheets, etc.

Comments

Popular posts from this blog

Coca-Cola: Life - myth or truth?

"Coca-Cola Life" Recently the Coca-Cola company released a new beverage: the Coca-Cola Life drink. It should contain less sugar than the normal Coca-Cola drink; a part of the sugar is replaced with the recently approved sweetener from the Stevia plant (stevioglycosides). It's being sold as a 'natural' drink, but those stevioglycosides are as natural as the chemical sweetener aspartame found in Light and Zero drinks. However it is true that the amount of sugar is much lower (being reported as 33%, some say it's around 20%); yet approximately still 3-4 sugar cubes / 33 cl can (5-6 in a normal can). I bought it myself and found that the flavor has not really changed from the original Coca-Cola, however it does taste more "flat" - but definitely true it yourself. The outside of the can has the colour green. I personally do not associate this "healthy - natural" colour with Coca-Cola, but it's growing on me. In sum...

Painkillers: brand names for paracetamol (= acetaminophen) in foreign countries

Do you ever need a medication when in a foreign country, but in this country the medication you need is not available under a certain name? It's useful to know the active compound of the medication! In this case, I will present to you a list of brand names which contain paracetamol (= acetaminophen) throughout the world. When you are in the local pharmacy, ask about the active compound ("paracetamol" or "acetaminophen") and they will know immediately what you mean! If you talk about a brand from your own country it can take a while until the pharmacist knows what you mean. Useful : in almost all countries, generic brands are available, usually under the name of the active compound, so just ask for "paracetamol" or "acetaminophen" if you would like the cheapest product. Paracetamol = Acetaminophen EUROPE Austria: Ben-u-ron, Mexalen Belgium: Algostase, Dafalgan Croatia: Daleron, Lekadol, Plicet Czech Republic/Czechia: Paralen ...

Alkylhalides: Introduction

Alkylhalides: an initiation Background information Alkylhalides are compounds (in this case salts ) that consist of an alkyl group and an halogen (seventh row in the table of Mendeljev).  Alkylhalides have good leaving groups , these groups are the atoms (or the atom) that will be substituted or eliminated during elimination or substitution reactions on the molecule. This fenomenon is caused by the polar bond formed between the halogen and the alkyl group, making the halogen more afferent to be attacked (substituated / eliminated) by a nucleophile. Nucleophile substitution reaction ( SN2 reaction) A nucleophile 'attacks' the alkylhalide, the leaving group - in this case the halogen - will be taken of the compound and will be replaced (SUBSTITUTED) by the nucleophile (hense the reaction its name). This reaction however is characterized and depended by several factors including: the solvent in which the reaction is taking place the reactivity or acti...