History of Cosmetics & Product Forms
History of Cosmetics & Product Forms
Chemi
Cosmetics
A substance or preparation intended for placement in contact with any external part of the human body (this
includes the mouth and teeth).
It is also used to cleanse, protect, and change the body’s appearance or alter its odors.
Cosmetics are limited on make-up and include creams, perfumes, talcum powder, shampoo deodorants, and
other toiletries.
History of Cosmetics
Cream
It contains medium to high viscosity emulsions.
It is suitable to be put in jars or small bottles with a wide mouth or bigger pump nozzles.
Examples: Anti-aging creams, skincare creams
Creams can be in the form of:
1. Oil in water emulsions (o/w)
droplets of oil in water continuous phase
Tends to have a light-after feel on the skin being waterbased
2. Water in oil emulsions (w/o)
droplets of water in a continuous oil phase
Has a greasier-after feel since it is oil-base
Powder Balm Mud
It is mostly or entirely oil-based It is often presented as a semi-
It is utilized readily in the color
with semi-solid consistency. solid product with the use of
cosmetics industry like eye
Examples: Hair and lip balm, lipstick different clay and with the
shadow, blushes, pressed, loose
presence of oils
powder, and mineral make-up.
Examples: Mud clay mask
Examples: baby powder, talc,
blusher, most of the make-up
produc
Scrub
It contains various sized particles
to exfoliate skin mechanically.
Examples: Salt or sugar
exfoliating body scrub
Greek
1800 1791 Europe
By the second
In the mid-1800s, In 1791, Nicholas Soap making was an century, a Greek
Ernest Solvay Leblanc patented established craft in Europe physician,
invented another making soda ash or in the 7th century. Italy, Galen,
soap technology, the sodium carbonate Spain, and France were the recommended soap
ammonia process, to from common salt. early centers for soap for medicinal and
make soda ash out Soda ash is manufacturing cleansing purposes.
of common table combined with fat due to their ready supply
salt. to form soap. of raw materials such as
This process further oils from olive trees. Soap
reduced the cost of was a luxury enjoyed
obtaining soda ash
and increased its Germany mainly by those who could
afford it. Manufactured
quantity and quality bar soaps were not
for soap available until the late 18th
In 1916, Germany created
manufacturing. century in Europe and the
the first synthetic
U.S. Widespread use of
detergent. It is in response
soap during this period can
to World War I soap
be attributed to
ingredient shortages. It
advertising campaigns
encouraged manufacturers
touting the relationship
to develop synthetic
between good personal
cleaners to meet demand.
hygiene and health.
By the 1950s, detergents
had overtaken traditional
soap products in homes
across America.
Chemistry of Soap & Detergent
Soap and detergent are two of the most common cleaning products used in a household. They are used in
laundering, dishwashing, bathing, hand washing, and other types of cleaning. As a consumer, it is a must for you to
understand the chemistry behind these commercial products. It will serve as a guide for you to understand their
performance, efficacy, and safety. It can also help you to be more productive and efficient in your cleaning
strategies.
Preparation of
Soap Ingredients:
Fatty acid from animal fats and vegetable oils
source of the hydrocarbon chain – hydrophobic
(water-hating end) but attracted to grease and
oils
Carboxylate end – hydrophilic (water-loving end)
Alkali
Chemical Structure of Soap; Sodium hydroxide (NaOH) or caustic soda –
produces hard soap- like bath and bar soap
Potassium hydroxide (KOH) or caustic potash –
Saponification produces soft soap like in liquid hand soap
Involves heating plant oils and animal fats,
reacting them with a liquid alkali to produce
soap plus water plus glycerine.
Preparation of Detergent
Ingredients:
Hydrolysis
Another way of soap making is the hydrolysis 1. Petrochemicals (derived from petroleum) and
of oils and fats in high-pressure steam to yield oleochemical (derived from fats and oils – the
crude fatty acids and glycerine – purification source of the hydrocarbon chain, the
of fatty acids through distillation and hydrophobic end of detergent but attracted to
neutralization of fatty acids with alkali to form grease and oils
soap and water 2. Other chemicals like sulfur trioxide, sulfuric acid,
or ethylene oxide - the source of hydrophilic
end of the detergent
3. Alkali – sodium or potassium hydroxide
Chemical Structure of Detergent;
Dye
An organic compounds that are widely used for imparting color to textiles. They are produced either
from natural or synthetic resources. Unlike paint (pigments), they do not build upon the material’s
surface but are absorbed in the fibers’ pores. It is possible because of the following reasons:
1. The dye molecules are smaller than the size of the pores of the fibers. The planar shape of its
molecules with a little thickness helps to slip into the fiber’s polymer system.
2. There is an affinity between the dye and the fiber due to the force of attraction.
Unique Property of Dye The chromophore must be a part of the conjugated system. Just
like the figure below:
The first example shows a colorless compound because the
1. Dyes absorb light in the visible spectrum chromophore – the azo group is attached in between two methyl
(400-700 nm) group (not conjugated system)
2. They have at least one chromophore (color- The second example obtained an orange color because the
bearing group) chromophore – the azo group is attached between two benzene
3. They have a conjugated system – a rings (a conjugates system)
structure with alternating double and single
bonds.
4. They exhibit resonance of electrons, the
stabilizing force in organic compounds.
Synthetic
Hydrophobic
Disperse Dye Water Good fastness Disperse Blue165
Substrates
Water withsodium
Vat and Sulfur Dye Cotton, linen, rayon hydrosulphite in Wet fast Natural dye Indigo
sodium hydroxide
Insect Repellants
Mosquitoes, flies, mites, ticks, and other insects can pose a severe risk to public health. In the Philippines, it is
prevalent that mosquitoes can transmit diseases like dengue and Japanese encephalitis. Flies can also transmit
diseases as they land on our skin, food, or clothing. When properly used, insect repellants can help to eradicate
this kind of problem with insect- carrying diseases.
Insect repellants are available in various forms and concentrations. Aerosol and pump-spray products are intended
for skin applications as well as treating clothing. Liquid, cream, lotion, spray, and stick products enable direct skin
application. The concentration of active ingredients may be useful in areas where there are either minimally
exposed or highly infested places where insects are difficult to repel.
Pyrethrum
It is a natural plant oil from two species of
pyrethrum daisy.
The insecticidal component – six esters
(pyrethrins) – is found in tiny oil- containing glands
on the surface of the seed case in the flower head.
Incorporated to mosquito coils – derived from the
incense used in religious activities of Hindus and
Buddhist
The powder was used by armies from Napoleon’s
time to World War II to combat head and body lice.
It affects the central nervous system of all types
of flying and crawling insects, blocking sodium-
gated nerve junctions, so that nerve impulses fail,
and the insect is knocked down and then
eventually dies.
The Development of Modern
Synthetic Insect Repellants
DMP
Chemical Name: dimethyl phthalate
Patented in 1929 as a fly repellant
Significant protection against scrub chiggers
Resulted in a hot and restricted vision on head nets of troops
Indalone
Chemical Name: butyl-3,3- dihydro-2,2-dimethyl-4-oxo-2H-pyran-6- carboxylate
Patented in 1937
Significant protection against scrub chiggers
Resulted in a hot and restricted vision on head nets of troops
Rutgers 612
Chemical Name: 2-ethyl-1,3-hexanediol
Available on 1939
Voluntarily removed in USA and Canada markets showing low lung expansion in the offspring of an exposed mammal
6-2-2 or M-250
Six parts DMP, two parts Indalone and two parts of Rutgers 612
Mild developmental toxicity after cutaneous administration to pregnant rats
Natural Citriodiol
Can be extracted from lemon eucalyptus oil – Because of the health risk imposed by the
from the leaves of the lemon eucalyptus tree chemicals present on the previous insect
Natural occurring substance – para-menthane- 3,8-diol repellants and even the environmental effect of
known as PMD the traditional way – smoke, the industry tried
20%-26% PMD may be useful as 15%-20% of DEET their best to formulate safer insect repellants.
against mosquitoes and ticks The following are chemical compositions of the
Most effective botanical insect repellant commercially-available insect repellants on the
Can cause allergic skin reactions market. They are far way safer compared to
Effective against as mosquitoes, fly, gnat repellant and those initially formulated insect repellants.
also as a miticide against insects and mites
DEET
Chemical Name: N, N-diethyl-3- methylbenzamide also listed as N, N-diethyl-m- toluamide
Principal and most effective repellant use today
“Gold-standard” repellant
It is a broad spectrum repellant that is highly
effective against all mosquitoes, sand flies, black flies, chiggers, hard and soft ticks, bedbugs, and fleas.
Proven to reduce malaria in areas greatly affected
Currently available to the public in the form of liquid, lotion, spray, and impregnated materials (wrist bands)
Designed to direct application to human skin to repel insects, rather than killing them
Use lower concentration (<6%) on children and not allowed to infants and pregnant women.
IR-3535 or MERCK 3535
Chemical Name: 3-(N-acetyl-N-butyl) amino propionic acid ethyl ester
Developed in 1975 by Merck
Low toxicity, irritating to the eyes and sometimes on the skin
Classified as a biopesticide, as it is a substituted B-amino acid
No recorded incidence of adverse reaction
Picaridin
Chemical Name: 1-piperidine carboxylic acid- 2(2-hydroxyethyl)-1-methylpropyl ester
Also known as Icaridin, Bayrepel (trademark name), KBR 3023
Developed by Bayer in 1980
Very low toxicity
Practically no dermal and eye irritation
Colorless, odorless, and has a pleasant feel on the skin
Evaporates slower rate than DEET (less repellant than DEET when freshly applied)
WHO designated it as a “repellant of choice for malaria prevention.”