Wood Chemistry PSE 406 Lecture 131 Wood Chemistry PSE 406/Chem E 470 Lecture 13 Diterpenes and Triterpenes.

Slides:



Advertisements
Similar presentations
Phytochemical analysis for plant’s crude extract
Advertisements

Wood Chemistry PSE 406 Lecture 121 Wood Chemistry PSE 406/Chem E 470 Lecture 12 Wood Extractives Introduction Terpenes and Sesquiterpenes.
Wood Chemistry PSE 406/Chem E 470
Pulping and Bleaching PSE 476/Chem E 471
Extractive Components of Wood Barbara Cole University of Maine.
Pulping and Bleaching PSE 476
Wood Chemistry PSE 406: Lecture 151 Wood Chemistry PSE 406/Chem E 470 Lecture 15 Stilbenes, Flavonoids, and Condensed Tannins.
Wood Chemistry PSE 406/Chem E 470
1 Agenda Chemical Description of Wood »Carbohydrates »Extractives »Lignin Loss of Components During Kraft Pulping Reactions in the Early Portion of the.
Pulping and Bleaching PSE 476/Chem E 471 Lecture #15 Kraft Pulping Review of Reactions/Kinetics Lecture #15 Kraft Pulping Review of Reactions/Kinetics.
Resins and resins combination
Lipids.
Lipids
Mevalonic Acid Pathway Many constituents are unsaturated hydrocarbons Ketons, alcohols, simple hydrocarbons are formed Through acetate-mevalonate pathway.
Lecture on the topic: Lipids, their structure and properties. For the 1st year students of specialty “General medicine". Discipline: Chemistry. Lecturer:
Lipids Qualitative. Lipids are the body’s principal energy reserve. About 85% of the deaths caused by cardiovascular disease are due to arteriosclerosis.
CHEM 1152 Dr. Sheppard Spring 2015
Karaganda State Medical University. Chemistry department.
The Lipid By: Kirsten Anderson Ajla Basic Hammad Ahmed Miguel Cabrera Kamila Barnak Joshua Edoimioya.
Organic and biochemistry Assistance Lecturer Amjad Ahmed Jumaa Elimination reactions. Bimolecular elimination (E2). Unimolecular elimination.
Wood Chemistry PSE Lecture 171 Wood Chemistry PSE 406/Chem E 470 Lecture 17 Chemical Isolation and Analysis I.
PSE 406: Lecture 151 Wood Chemistry PSE 406 Lecture 15 Stilbenes, Flavonoids, Condensed and Hydrolysable Tannins, other Miscellaneous Extractives and Inorganic.
An Introduction to Organic Chemistry. Orgins Originally defined as the chemistry of living materials or originating from living sources Wohler synthesized.
Lipids General Characteristics Classification Biological function
Wood Chemistry PSE 406/Chem E 470
Lipids. LIPIDS Lipids are a large and diverse group of naturally occurring organic compounds that are related by their solubility in nonpolar organic.
Wood Chemistry PSE 406: Lecture 161 Wood Chemistry PSE 406/Chem E 470 Lecture 16 Wood Extractives, Components and Analysis.
What you should remember from last lecture 1.Organic compounds are based on carbon, and form the basis of biology and of many of the materials that you.
Macromolecules 2: Lipids Grade 10 Biology. Your Assignment.
Chapter 13 Lipids Tiara Bartol and Brant Houghton.
Lipids The term Lipid applies to a class of compounds that are soluble in organic solvent and nearly in soluble in water. Chemically:
Cleansing Action of Soap The carboxylate end of the long-chain molecule is ionic and therefore is preferentially dissolved in water The hydrocarbon.
LIPIDS.
Volatile oil. Volatile oils different from fixed – secreted in oil cells in specialised structures ducts, gland, cell or glandular hairs – frequently.
PSE 406 Lecture 121 Wood Chemistry PSE 406 Lecture 12 Wood Extractives.
Lipids 1. Storage Lipids 2. Structural Lipids in Membranes 3. Working with Lipids.
What is Lipid Lipids: Lipids: insoluble in water, but soluble in organic solvents including diethyl ether, chloroform, methylene chloride, and acetone.
Volatile oils Shahana Sharmin Pharmacognosy-II PHR 205.
Hydrocarbons Systematic naming Alcohols. P,S,T.
Carboxylic acids and Esters
Biomolecules: carbohydrates and lipids
LIPIDS Varied in structure
Lipids: Fats & Oils.
Lecture 11 Lignin Structure
long term energy storage
Lipids: Fats & Oils.
Lipids: Fats & Oils.
Lipids: Fats & Oils.
Lipids: Fats & Oils.
Lipids: Fats & Oils.
Lipids: Fats & Oils.
LIPIDS Diverse group of organics Insoluble in water
Lipids: Fats & Oils.
Lipids: Fats & Oils.
Lipids: Fats & Oils.
Wood Chemistry PSE 406/Chem E 470
Lecture 9 Lignin Biosynthesis
Lipids: Fats & Oils.
dehydration synthesis Fats Structure: fatty acid = long HC “tail” with carboxyl (COOH) group “head” enzyme Look at structure… What makes them hydrophobic?
Lipids: Fats & Oils.
Lipids.
Lipids: Fats & Oils.
What do you use fats for? All around your body?
Lipids: Fats & Oils.
Lipids: Fats & Oils.
Lipids: Fats & Oils.
Wood Chemistry PSE 406/Chem E 470
Lipids: Fats & Oils.
Catalyst Take out your homework so that we may go over it.
Lecture 11 Lignin Structure
Presentation transcript:

Wood Chemistry PSE 406 Lecture 131 Wood Chemistry PSE 406/Chem E 470 Lecture 13 Diterpenes and Triterpenes

Wood Chemistry PSE 406 Lecture 132 Pitch Chemicals l When you grab a softwood tree and your hand sticks to the tree, you have discovered pitch. l Pitch consists of about 50/50 terpenes and resin acids. Resin acids are glassy like chemicals also made of isoprene units. l The Christmas tree I’m holding didn’t have any pitch left.

Wood Chemistry PSE 406 Lecture 133 Pitch as a Bandage l When a softwood tree is wounded, it releases pitch to “seal” the wound. »Terpenes serve as the antiseptic and then evaporate. »Resin acids serve as the bandage (and also as an antiseptic).

Wood Chemistry PSE 406 Lecture 134 Rosin l The term rosin refers to a mixture of resin acids produced through the distillation of pitch. l Gum rosin: distillation of gum resins (wound resin) »US 197 metric tons (1998) l Tall oil rosin: from the Swedish word talloja which means pine oil. Produced during the kraft pulping process. »US 247,000 metric tons (1998) l Wood rosin: Distillation of old stumps. »US 30,000 metric tons (1998)

Wood Chemistry PSE 406 Lecture 135 Diterpenes: Structure l 4 isoprene units linked head to tail l Neutrals: »Hydrocarbons, phenolics, alcohols, ketones and aldehydes l Acids: Typically referred to as resin acids l Acid content much higher in heartwood than sapwood

Wood Chemistry PSE 406 Lecture 136 Diterpenes: Structure l Ring structures »Acyclic, mono, di, tri and tetracyclic »Macrocylcic (10-15 carbons)

Wood Chemistry PSE 406 Lecture 137 Diterpenes: Location in Tree l Composition is very species dependent l Mainly found in conifers ( %) »Oleoresin: ~70% resin acids (tricyclic/COOH) »Heartwood: Large amount of neutral diterpenoids that have been modified through various reactions: –Aromatization, hydroxylation, oxidation, & rearrangements (often losing C atom) l Tropical Hardwoods: »Sandalwood: 12-14% resin

Wood Chemistry PSE 406 Lecture 138 Diterpenes Physical Properties l Rosin (mixture of diterpenoids) is glass like: it slowly softens when heated – does not have a melting point l Pure resin acids are crystalline »Pimaric acid mp = °C l Tricylcic structure quite stable: Amber l Volatilization »Some diterpenoids can be volatilized with steam »Problem in TMP plants (health reasons) l Solubility: Abietic acid –Insoluble in water –Some solubility in base

Wood Chemistry PSE 406 Lecture 139 Diterpenes Pulp and Paper Problems l Toxicity »Diterpenoids are primary pollutants in pulp mill effluents »Very toxic to fish »Difficult to remove in treatment systems »LD 50 not particularly high (abietic 180mg/kg) »Inhalation problems in saw mills l Stickies

Wood Chemistry PSE 406 Lecture 1310 Uses of Diterpenes l Rosin: Mixture of resin acids »Gum Rosin »Tall Oil Rosin l Uses of Rosin »Printing Inks, Paper Size, Rubber, Adhesives, Miscellaneous

Wood Chemistry PSE 406 Lecture 1311 Triterpenes & Sterols Chemical Composition l 6 isoprene units linked head to tail l Many are classified as steroids (sterane structure) »Triterpenoids and sterols have same synthetic pathway so they should not be separated »Both start from squalene and then branch off

Wood Chemistry PSE 406 Lecture 1312 Triterpenes & Sterols Chemical Composition

Wood Chemistry PSE 406 Lecture 1313 Triterpenes & Sterols Chemical Composition l Triterpenoids exist in three forms »Free form »Esters of fatty acids »Glycosides l Can contain a large variety of functional groups »Carboxyl »Ethers »Acetyl »Alcohols »Ketones

Wood Chemistry PSE 406 Lecture 1314 Triterpenes& Sterols Physical Properties  -sitosterol l Crystalline »mp 140°C l Solubility »Organic solvents: ether, alcohols, etc l Boiling Point »Merck index: no boiling point listed. Found in tall oil pitch - does not distill

Wood Chemistry PSE 406 Lecture 1315 Triterpenes & Sterols Role in Nature l Sterols are found in plants as both free sterols, as sterol esters (of fatty acids) and as sterol glycosides l Serve as components of membranes »Work with phospolipids to create membranes which are only permeable to certain chemicals l Sterol esters »Believed to serve as transport agent to get sterols from site of biosynthesis to membrane l Sterol glycosides ?????????

Wood Chemistry PSE 406 Lecture 1316 Sterol levels in plants l Levels of sterols variable depending on plant. »Broccoli: 3.4g/kg »Banana: 0.5g/kg »Alfalfa 2.1 g/kg »Aspen (wood): 5 g/kg l Free sterols are found in vegetable oils. »Peanut oil: 1-2 mg/kg oil »Corn oil: 2-4 mg/kg 1. J Food Comp Anal , TAPPI, (5)

Wood Chemistry PSE 406 Lecture 1317 Triterpenes & Sterols Tree Information l Found in both hardwoods and softwoods »Not a very large component in softwoods »  -sitosterol major component »Larger amounts in tropical hardwoods l Not found to any extent in oleoresin l Found throughout the tree »Concentration actually higher as go from bark to pith –Not involved in heartwood formation –Higher concentration of sterols in younger trees

Wood Chemistry PSE 406 Lecture 1318 Triterpenes & Sterols Pulp and Paper Problems l Sterol esters are difficult to saponify: known as nonsaponifiables »Some chemical conversions during pulping but mostly stable. »Large number of reactions during bleaching – saponification l Hydrophobic nature of sterol esters cause them to be a major pitch problem in papermaking »Major components of pitch deposits

Wood Chemistry PSE 406 Lecture 1319 Sterols from Trees Benecol (1) l Benecol: cholesterol reducing product. »Known since 1950s that vegetable sterols can reduce blood cholesterol. –High levels of sterols can cause other problems »1970s shown that plant stanols were effective at lowering cholesterol without negative effects. –Stanols not fat soluble so difficult to use. –Finnish company (Rasio) developed a procedure in late 1980s early 1990s to produce stable fat soluble stanol esters from plant derived sterols.

Wood Chemistry PSE 406 Lecture 1320 Sterols from Trees : Benecol (2) l Sitostanol »Similar structure to sitosterol »Saturated sterol »Found in Nordic Pine l In Benecol the sitostanol is in the form of a fatty acid ester.