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Chemistry of Hair By: Marlene Simas, Tavis Cano, and Kathleen Good
Hair Structure Made up of 3 layers Cuticle Outer covering Cortex  Elasticity  Curl  Medulla Body temperature regulation
Hair Composition 88% is made up of proteins  Mainly Keratin Many polypeptide chains Broken down = individual amino acids Right combo = specific protein Natural Hair pH is 5
A Helix Coil 1 hair = 3 “alpha helices”  protofibril 9 protofibrils bundled in a cirle  11 stranded cable microfibril 100s of microfibrils in a bundle  macrofibril Cortex of hair fiber
Natural Hair
Keratin Alpha helix polypeptide chain in human hair  3.6 amino acids per turn in the helix Peptide bond Between the Carbon and Nitrogen
Bonding in Keratin Protein
Bonding	 Hydrogen bond: Is between the coils of the alpha helix  Can change the shape of hair Elasticity  Salt bond: An ionic bond between side chain of the basic to the side chain of an acidic amino acid Happens parallel to the hair  Strength and elasticity
Bonding cont. Cystine Bond: Formed by the crosslinks between cystine residues (amino acids) of the main polypeptide chains  perpendicular to the hair & between polypedptide chains Strength 1 Cystine bond every 4 turns of the alpha helix Sugar Bond: Is between side chain of an amino     acid with OH group and acid amino group Perpendicular to the hair Toughness and some strength
How Shampoo Works
Shampoo Surfactants: Essential cleaning substances  Determines cleansing and lathering characteristics  cleansing, foam, condition, viscosity and aesthetic appeal combined with safety and mildness in use.
Surfactants	 Are divided based on the hydrophilic head Anionic: negative charge Cationic: positive charge Amphototeric – positive and negative charge Nonionic – no charge
Sodium Lareth Sulfate
Conditioners Are cationic Do not rinse out completely Leave hair coated with thin film Hydrophobic head is what gives hair conditioning ability; smoothing the hair and giving it weight  6 categories: Moisturizers Reconstructors Acidifiers  Detanglers Thermal Protection Glossers  Oils
Hexadecyltrimethylammoniumchloride Are usually quaternary ammonium compounds  4 R groups to 1 N Can also be tertiary  Form the thin coating on the hair shafts  Hexadecyltrimethylammonium chloride PEG-12 DIMETHICONE
CG Method!  Lorraine Massey  NO SHAMPOO  All products used – conditions, gels, creams, sprays, etc – are all free of Sulfates Silicones: -cone, -conel, -xane Can have any hair type to try
Wet hair stretches as the temporary hydrogen bonds are broken  When blow dried will return to the alpha keratin shape
Brazilian Blow Out
What’s In It? Formaldehyde Methylene Glycol Glutaraldehyde
Formaldehyde; What is it? Organic compound CH2O Simplest Aldehyde IUPAC name: Methanal Systematic name: Formaldehyde Colorless gas with a pungent odor Important in polymers Used as disinfectants Used for preservation of biological specimens  Widespread use: toxicity, volatility, carcinogenic  Other names: Formal, Methlyaldehyde, Methylenegylcol, Methylene Oxide
Formaldehyde Russian chemist AleksandrButlerov & August Wilhelm von Hofmann Produced by catalytic oxidation of methanol Most common catalysts: Silver, iron, 2 CH3OH + O2 -> 2 CH2O + 2 H2O CH3OH -> H2CO + H2 (dehydrogenation)
Cont.  Building block Highly reactive Tissue fixative “My eyes were irritated for a week or so after the treatment & my hair burned my boyfriends nose...”
Properties Of Formaldehyde Molecular formula: CH2O  Molar mass: 30.03 g mol−1 Exact mass: 30.010564686 g mol-1 Appearance Colorless gas  Density: 1.38 g cm-3 Melting point: -92 °C, 181 K, -134 °F Boiling point: -21 °C, 252 K, -6 °F Solubility: in water 400 g dm-3 log P: 0.350  Acidity: (pKa) 13.3  Basicity: (pKb) 0.7  Dipole moment: 2.33 D Structure  Molecular shape: Trigonal planar
Health Effects of Formaldehyde Runny nose Sore throat Cough Sleeping difficulties Headache Fatigue Breathing difficulties Sinus irritation; nose bleed Chest pain Decreased lung capacity Bronchitis Nausea  Abdominal pain Anxiety Coma Convulsions Diarrhea Respiratory problems (pneumonia) Dizziness Drowsiness Low Level Exposure Acute Exposure
Methylene Glycol Also known as Formaldehyde monohydrate or methylene glycol Chemical formula: CH4O2, or H2C(OH)2
Cont. Is a product of the hydration of formaldehyde  Predominates in water solution Methanediol is listed as one of the main ingredients of the Brazilian Blowout, even though the California-based manufacturer claims that the product contains no formaldehyde
Glutaraldehyde…What is it? Pungent & oily liquid at room temperature IUPAC name: Pentene-1,5-dial Other names: Pentanedial, Glutardialdehyde, Glutaricdialdehyde Used to disinfect medical and dental equipment  Organic compound Formula: CH2(CH2CHO)2
Cont. Produced by oxidation of cyclopentene Used in biological electron microscopy as fixative
Health Effects Sever eye, nose, throat and lung irritation  Headaches Drowsiness Dizziness Main source of occupational asthma
    Perm     Perm
Ammonium thioglycolate A solution containing ammonium thioglycolate contains a lot of free ammonia, which swells hair In the perm solution reduces the disulfide cystine bonds in the hair.  It removes crosslinks. After washing, the hair is treated with a mild solution of hydrogen peroxide, which oxidizes the cysteines back to cystine.  New bonds instruct the structural rigidity necessary for a successful perm. The rigidification process is akin to the vulcanization of rubber, where commonly polysulfide linkages are used to crosslink the polymer chains.  Not all disulfides are reformed Result: the hair is weaker than before the permanent was applied and repeated applications over the same spot may eventually cause strand breakage
Permanent Hair Wave Disulfide bond formation can produce curls in hair by the permanent wave process Hair keratine=many protein alpha helices 3 alpha-helices interwoven in coil=protofibril 11 protofibrils bonded and coiled together=microfibril Hundreds of microfilbrils cemented into buncle=macrofibril
Disuldife Bonds in Hair Formed by oxidation of sulfhydrl groups on cysteine Different protein chains loop within a single chain & help by strong covalent disulfide bonds
Reducing Agent Perming requires a basic reducing substance: Ammonium Thioglycolate Added to reduce/rupture some disulfide cross-links
The Results Since the alpha-helices are ruptured and no longer tightly cross-linked, the alpha helices can shift positions Rollers or curlers or inserted Oxidizing agent is added to reform bonds into new positions
Structure of Hair  ,[object Object]
consists of many microscopic scales
when they are aligned they give the appearance of shiny hair,[object Object]
The ratio and quantities of 
Eumalinen and Phaeomelanine
These two make up only 1% of hair structure
Phaeomelanine is resposible for red to blonde colors 
Eumalinen make brown to black shades of hair
While you can have one or both, the absence of both results in white/grey hair,[object Object]
Highlighting is a cosmetic effect of lightening streaks or sections of hair
Blonding is a process that strips away original color and adds color to hair to achieve blonde appearance
Usually achieved by a mixture of bleach and a coloring agent 
Precoloring makes hair a blank canvas which makes hair color applied after words brighter,[object Object]

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Presentation1

  • 1. Chemistry of Hair By: Marlene Simas, Tavis Cano, and Kathleen Good
  • 2. Hair Structure Made up of 3 layers Cuticle Outer covering Cortex Elasticity Curl Medulla Body temperature regulation
  • 3. Hair Composition 88% is made up of proteins Mainly Keratin Many polypeptide chains Broken down = individual amino acids Right combo = specific protein Natural Hair pH is 5
  • 4. A Helix Coil 1 hair = 3 “alpha helices”  protofibril 9 protofibrils bundled in a cirle  11 stranded cable microfibril 100s of microfibrils in a bundle  macrofibril Cortex of hair fiber
  • 6. Keratin Alpha helix polypeptide chain in human hair 3.6 amino acids per turn in the helix Peptide bond Between the Carbon and Nitrogen
  • 8. Bonding Hydrogen bond: Is between the coils of the alpha helix Can change the shape of hair Elasticity Salt bond: An ionic bond between side chain of the basic to the side chain of an acidic amino acid Happens parallel to the hair Strength and elasticity
  • 9. Bonding cont. Cystine Bond: Formed by the crosslinks between cystine residues (amino acids) of the main polypeptide chains perpendicular to the hair & between polypedptide chains Strength 1 Cystine bond every 4 turns of the alpha helix Sugar Bond: Is between side chain of an amino acid with OH group and acid amino group Perpendicular to the hair Toughness and some strength
  • 11. Shampoo Surfactants: Essential cleaning substances Determines cleansing and lathering characteristics cleansing, foam, condition, viscosity and aesthetic appeal combined with safety and mildness in use.
  • 12. Surfactants Are divided based on the hydrophilic head Anionic: negative charge Cationic: positive charge Amphototeric – positive and negative charge Nonionic – no charge
  • 14. Conditioners Are cationic Do not rinse out completely Leave hair coated with thin film Hydrophobic head is what gives hair conditioning ability; smoothing the hair and giving it weight 6 categories: Moisturizers Reconstructors Acidifiers Detanglers Thermal Protection Glossers Oils
  • 15. Hexadecyltrimethylammoniumchloride Are usually quaternary ammonium compounds 4 R groups to 1 N Can also be tertiary Form the thin coating on the hair shafts Hexadecyltrimethylammonium chloride PEG-12 DIMETHICONE
  • 16. CG Method!  Lorraine Massey NO SHAMPOO All products used – conditions, gels, creams, sprays, etc – are all free of Sulfates Silicones: -cone, -conel, -xane Can have any hair type to try
  • 17.
  • 18. Wet hair stretches as the temporary hydrogen bonds are broken When blow dried will return to the alpha keratin shape
  • 20.
  • 21. What’s In It? Formaldehyde Methylene Glycol Glutaraldehyde
  • 22. Formaldehyde; What is it? Organic compound CH2O Simplest Aldehyde IUPAC name: Methanal Systematic name: Formaldehyde Colorless gas with a pungent odor Important in polymers Used as disinfectants Used for preservation of biological specimens Widespread use: toxicity, volatility, carcinogenic Other names: Formal, Methlyaldehyde, Methylenegylcol, Methylene Oxide
  • 23. Formaldehyde Russian chemist AleksandrButlerov & August Wilhelm von Hofmann Produced by catalytic oxidation of methanol Most common catalysts: Silver, iron, 2 CH3OH + O2 -> 2 CH2O + 2 H2O CH3OH -> H2CO + H2 (dehydrogenation)
  • 24. Cont. Building block Highly reactive Tissue fixative “My eyes were irritated for a week or so after the treatment & my hair burned my boyfriends nose...”
  • 25. Properties Of Formaldehyde Molecular formula: CH2O Molar mass: 30.03 g mol−1 Exact mass: 30.010564686 g mol-1 Appearance Colorless gas Density: 1.38 g cm-3 Melting point: -92 °C, 181 K, -134 °F Boiling point: -21 °C, 252 K, -6 °F Solubility: in water 400 g dm-3 log P: 0.350 Acidity: (pKa) 13.3 Basicity: (pKb) 0.7 Dipole moment: 2.33 D Structure Molecular shape: Trigonal planar
  • 26. Health Effects of Formaldehyde Runny nose Sore throat Cough Sleeping difficulties Headache Fatigue Breathing difficulties Sinus irritation; nose bleed Chest pain Decreased lung capacity Bronchitis Nausea Abdominal pain Anxiety Coma Convulsions Diarrhea Respiratory problems (pneumonia) Dizziness Drowsiness Low Level Exposure Acute Exposure
  • 27.
  • 28. Methylene Glycol Also known as Formaldehyde monohydrate or methylene glycol Chemical formula: CH4O2, or H2C(OH)2
  • 29. Cont. Is a product of the hydration of formaldehyde Predominates in water solution Methanediol is listed as one of the main ingredients of the Brazilian Blowout, even though the California-based manufacturer claims that the product contains no formaldehyde
  • 30. Glutaraldehyde…What is it? Pungent & oily liquid at room temperature IUPAC name: Pentene-1,5-dial Other names: Pentanedial, Glutardialdehyde, Glutaricdialdehyde Used to disinfect medical and dental equipment Organic compound Formula: CH2(CH2CHO)2
  • 31. Cont. Produced by oxidation of cyclopentene Used in biological electron microscopy as fixative
  • 32. Health Effects Sever eye, nose, throat and lung irritation Headaches Drowsiness Dizziness Main source of occupational asthma
  • 33. Perm Perm
  • 34. Ammonium thioglycolate A solution containing ammonium thioglycolate contains a lot of free ammonia, which swells hair In the perm solution reduces the disulfide cystine bonds in the hair. It removes crosslinks. After washing, the hair is treated with a mild solution of hydrogen peroxide, which oxidizes the cysteines back to cystine. New bonds instruct the structural rigidity necessary for a successful perm. The rigidification process is akin to the vulcanization of rubber, where commonly polysulfide linkages are used to crosslink the polymer chains. Not all disulfides are reformed Result: the hair is weaker than before the permanent was applied and repeated applications over the same spot may eventually cause strand breakage
  • 35. Permanent Hair Wave Disulfide bond formation can produce curls in hair by the permanent wave process Hair keratine=many protein alpha helices 3 alpha-helices interwoven in coil=protofibril 11 protofibrils bonded and coiled together=microfibril Hundreds of microfilbrils cemented into buncle=macrofibril
  • 36. Disuldife Bonds in Hair Formed by oxidation of sulfhydrl groups on cysteine Different protein chains loop within a single chain & help by strong covalent disulfide bonds
  • 37. Reducing Agent Perming requires a basic reducing substance: Ammonium Thioglycolate Added to reduce/rupture some disulfide cross-links
  • 38. The Results Since the alpha-helices are ruptured and no longer tightly cross-linked, the alpha helices can shift positions Rollers or curlers or inserted Oxidizing agent is added to reform bonds into new positions
  • 39.
  • 40.
  • 41. consists of many microscopic scales
  • 42.
  • 43. The ratio and quantities of 
  • 45. These two make up only 1% of hair structure
  • 46. Phaeomelanine is resposible for red to blonde colors 
  • 47. Eumalinen make brown to black shades of hair
  • 48.
  • 49. Highlighting is a cosmetic effect of lightening streaks or sections of hair
  • 50. Blonding is a process that strips away original color and adds color to hair to achieve blonde appearance
  • 51. Usually achieved by a mixture of bleach and a coloring agent 
  • 52.
  • 53. A low volume of peroxide (5-30%) in a cream form combined with powder bleach creates a blue paste
  • 54. this is applied and left until desired amount of color is stripped from hair then rinsed out
  • 55.
  • 56. Usually done by mixing bleach component with a alkaline solution (often ammonia)
  • 57.
  • 58.
  • 59. Hydrogen peroxide breaks the sulfur bonds which releases larger amounts of sulfur
  • 60. This causes hardening, loss of mass, and produces smell
  • 61. minimized by using low levels of peroxide in cosmetic bleach
  • 62.
  • 63.
  • 64. Temporary - lasts 1-3 washes and involves no chemical reactions with the hair 
  • 65. Pigments are applied to surface without penetrating further
  • 66. Semi-permanent - stays in 5-15 washes usually made from vegetable dyes, mainly designed to adhere tightly to cuticle surface
  • 67.
  • 68. Permanent  - lasts indefinitely until hair grows out or chemically treated to remove color 
  • 69. First safe permanent hair dye created in 1907 by Eugene Schueller
  • 70. Main ingredient was paraphenylenediamine
  • 71. Often combines bleaching and coloring agent
  • 72. Dye molecules enter the hair cortex where they react and become trapped as the cuticles close
  • 73.
  • 74. 2-[(4-aminophenyI)azo] -1,3- dimethyl - 1H-               Imidazolium Chloride
  • 77. 8-[(4-Amino - 1 Phenyl)azo] -7 - hydroxy N,N,N Trimethyl - 2 - Naphthalenaminium Chloride
  • 78.
  • 79.
  • 83. And unexpected hair color results

Notas do Editor

  1. Dimethicone