Organic Chemistry for Cosmetic Chemists

Authors::
Anthony J. O'Lenick, Jr. and Thomas O'Lenick
Format::
Hardcover
 
$179.00
Qty:
 

Format Details

  • Hardcover
  • 304 Pages
  • Published 2008
  • ISBN-10: 1-932633-32-4
  • ISBN-13: 978-1-932633-32-0

For customers in Austria, Germany, Poland and Switzerland, please place your order through our distributor, Wissenschaftliche Verlagsgesellschaft (WVG)

Contact Marie Kuta for school volume discounts

  • Description
  • Table of Contents
  • Author Information
  • Expert Review

To be an effective cosmetic chemist, the cosmetic formulator must understand the basic components involved in the creation of products and raw materials used to make them. To be successful, the language of chemistry must be understood.

Organic Chemistry for Cosmetic Chemists focuses on refreshing the chemist with fundamentals of chemistry used to make raw materials used in our industry. Both theory and practice are presented. Many chapters contain problems at the end that allow the chemist to practice what they have learned. Topics include:

  • Structure of organic compounds
  • Raw materials
  • Synthesis approach
  • Nucleophilic substitution
  • Sulfation/sulfonation
  • Oxidation
  • Reduction
  • Polymers
  • Aldol condensation
  • Diels alder reactions
  • Ring ppening and closing

Packed with exercises, examples and patent references, this book is a must-have for the cosmetic chemist interested in staying on top of their game!

  • About the Authors
  • Acknowledgements and Dedication
  • Introduction
  • Chapter 1: Structure of Organic Compounds
    • Theory
      • Hydrocarbons
      • Alcohols
      • Amines
      • Quarternary Ammonium Compounds
      • Aldehydes
      • Ketones
      • Esters
      • Fatty Carboxylic Acids
      • Anhydrides
      • Ethers
      • Epoxides
      • Alkyl Halides
      • Acyl Halides
      • Aromatics
      • Mercaptans
      • Lactones
      • Lactams
      • Amides
    • Practice
      • Exercises
      • Exercise Solutions
  • Chapter 2: Raw Materials
    • Background
      • Triglycerides
      • Methyl Esters
    • Fatty Acids
      • Natural Acids
      • Synthetic Linear Acids
      • Synthetic Branched Acids
      • Ozone Acids
    • Fatty Alcohols
      • Oxo Alcohols
      • Ziegler Alcohols
      • Natural Alcohols
    • Reppe Chemistry
      • Acetylene Chemistry
      • Reactions of Alcohols and Acetylene-Vinyl Ethers
      • Phenol-Acetylene Reaction
      • Mercaptan Reactions
      • Reactions of Aldehydes with Acetylene
      • Tetrahydrofuran
      • Lactams
      • Propargyl Alcohol and Derivatives
      • Acrylic Acid
    • Alkanolamines
      • Ethanolamines
      • Isopropanolamines
      • Mixed Alkanolamines
  • Chapter 3: Synthesis Approach
    • Analogues and Homologues
    • Specificity and Selectivity
  • Chapter 4: Nucleophilic Substitution
    • Theory
      • Sn1
      • Sn2
    • Practice
      • Esters
        • Direct Esterification
          • Esterification Reaction from Methy Ester
          • Esterification Reaction from Fatty Acid
        • Trans esterification
      • Amides
        • Amidification from Methyl Ester
        • Amidification from Fatty Acids
        • Amidification from Triglycerides
      • Carboxylates
        • Carboxylation with Anhydrides
        • Soap from Methyl Ester
        • Soap from Fatty Acid
        • Soap from Triglyceride
        • Carboxylates
      • Amphoterics
        • Amido Betaines
        • Alkyl Betaines
        • Amino Propionates
        • Sulfobetaines
        • Phosphobetaines
      • Quats
        • Alkyl Quat—Benzyl Chloride
        • Alkyl Quat—Dimethyl Sulfate
      • Monoalkyl Phosphate
        • Phosphation Reaction with Polyphosphoric Acid
      • Sarcosinates
      • Taurates
        • Schotten-Baumann Taurates
      • Isoethionates
  • Chapter 5: Sulfation/Sulfonation
    • Theory
      • Sulfonation
      • Sulfanation
    • Practice
      • Sulfonation—SO3
      • Chlorosulfonic Sulfation
      • Sulfamic Acid Sulfation
      • Sulfonation of Alpha Olefin Sulfonate
  • Chapter 6: Fatty Tertiary Amine Oxidation
    • Theory
      • Surfactant Activity
      • Antimicrobial Activity
    • Practice
      • Amine Oxides
      • Peroxide Oxidation of Tertiary Amine
  • Chapter 7: Reduction
    • Theory
      • Hydrogenation
      • Dehydrogenation
      • Reduction
      • Oxidation
      • Catalysts
    • Practice
      • Hydrogenation
      • Hydrogenolysis
      • Group Specific Hydrogenolysis
  • Chapter 8: Radical Polymers
    • Theory
      • Conventional Radical Polymerization
      • Kinetics
      • Controlled “Pseudo-living” Radical Polymerization
      • Atom Transfer Radical Polymerization (ATRP)
      • Reversible Addition-Fragmentation Transfer (RAFT)
      • Nitroxi-Mediated Radical Polymerization (NMRP)
    • Practice
      • Non-Living Polymerization
        • Nonionic
        • Cationic
        • Anionic
      • Living Radical Polymerization
        • Reversible-Addition Fragmentation Transfer Radical Polymerization (RAFT)
        • Nitroxide-Mediated Radical Polymerization (NMRP)
        • Atom Transfer Radical Polymerization (ATRP)
  • Chapter 9: Other Polymers
    • Theory
      • Polyesters
      • Polyamides
      • Polyurethanes
    • Practice
      • Polyesters
      • Polyamides
      • Polyurethanes
  • Chapter 10: Aldol Condensation
    • Theory
    • Practice
      • Guerbet Alcohol
  • Chapter 11: Diels-Alder Reactions
    • Theory
    • Practice
      • Dimer Acid
        • Tall Oil (Tallol)
  • Chapter 12: Ring Opening Reactions
    • Theory
    • Practice
      • Alkoxylation
      • Ethenification
      • Carboxylates
        • Reaction with Anhydrides
      • Butryolactone Ring Opening
        • Reaction to Make Carboxy
  • Chapter 13: Ring Closing Reactions
    • Theory
      • Ring-Containing Components
        • 3-Membered Rings
        • 4-Membered Rings
        • 5-Membered Rings
        • 6-Membered Rings
    • Practice
      • Imidazoline
      • Sorbitan Esters
      • Lactams
      • Alkylpolyglucoside
  • Chapter 14: Analytical
    • The mg KOH/gm System
      • Alkali Value
      • Acid Value
      • Hydroxyl Value
      • Saponification Value
      • Summary
  • Chapter 15: Analytical Methods
  • Index

Anthony J. O'Lenick, Jr., has more than 30 years of experience in innovative personal care ingredients. He is president of Siltech LLC, a company he founded in 1989, specializing in functional silicones and specialty surfactants. O'Lenick has five published books, more than 40 technical articles and is the inventor of more than 260 patents.

Other books published by this author/editor:

Thomas O'Lenick earned his BS in chemistry from Georgia Southern University in 2005, and is now a doctoral candidate in polymer and organic chemistry at the University of Tennessee in Knoxville. O'Lenick is the inventor of four patents and author of six publications.

"We find Organic Chemistry for Cosmetic Chemists and Understanding Fragrance Chemistry great reference books for anyone involved in the cosmetic and personal care industries. They provide a review, as well as insight into areas that many of us may have forgotten. We recommend the books as secondary books for chemistry, as well as for perfume courses and as library reference books."

—Larry Smith, Professor
—Virginia Bonofiglio, Chairperson
Fashion Institute of Technology (FIT)

"This is a useful organic chemistry book targeted at the cosmetic chemist. There are many organic chemistry books that cover this content—but none I am aware of that are targeted at the cosmetic chemist or condensed to the precise chemistries that the cosmetic chemist needs. This is an essential text for the cosmetic chemist and it should also be useful to those who wish to create intellectual property within this subject area."

—Robert Y. Lochhead, PhD
The School of Polymer & High Performance Materials
The University of Southern Mississippi

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