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Modified starch
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Modified starch, also called starch derivatives, is prepared by physically, enzymatically, or chemically treating native starch to change its properties.[1] Modified starches are used in practically all starch applications, such as in food products as a thickening agent, stabilizer or emulsifier; in pharmaceuticals as a disintegrant; or as binder in coated paper. They are also used in many other applications.[2]
Starches are modified to enhance their performance in different applications and are one of the components of UPFs (Ultra Processed Foods). Starches may be modified to increase their stability against excessive heat, acid, shear, time, cooling, or freezing, to change their texture, to decrease or increase their viscosity, to lengthen or shorten gelatinization time or to increase their visco-stability.
Modification methods
[edit]



An ancient way of modifying starch is malting grain, which humans have done for thousands of years. The plant's own enzymes modify the grain's starches. The effects can be modulated by varying the duration and the ambient conditions of the process. However, malting alone is not a limitless or optimized tool for every desirable end product. In recent centuries, humans have expanded their repertoire of starch-modifying methods by learning how to use simple substances such as acids, alkalis, and enzymes from nature to modify starches in tailored ways.
Acid-treated starch (INS 1401),[3] also called thin boiling starch, is prepared by treating starch or starch granules with inorganic acids, e.g. hydrochloric acid (equivalent to stomach acid), breaking down the starch molecule and thus reducing the viscosity.
Other treatments producing modified starch (with different INS and E-numbers) are:
- dextrin (INS 1400),[3] roasted starch with hydrochloric acid
- alkaline-modified starch (INS 1402)[3] with sodium hydroxide or potassium hydroxide
- bleached starch (INS 1403)[3] with hydrogen peroxide
- oxidized starch (INS 1404, E1404)[3] with sodium hypochlorite, breaking down viscosity
- enzyme-treated starch (INS 1405),[3] maltodextrin, cyclodextrin
- monostarch phosphate (INS 1410, E1410) with phosphorous acid or the salts sodium phosphate, potassium phosphate, or sodium triphosphate to reduce retrogradation
- distarch phosphate (INS 1412, E1412) by esterification with for example sodium trimetaphosphate, crosslinked starch modifying the rheology, the texture
- acetylated starch (INS 1420, E1420)[3] esterification with acetic anhydride
- hydroxypropylated starch (INS 1440, E1440), starch ether, with propylene oxide, increasing viscosity stability
- hydroxyethyl starch, with ethylene oxide
- starch sodium octenyl succinate (OSA) starch (INS 1450, E1450) used as emulsifier adding hydrophobicity
- starch aluminium octenyl Succinate (INS 1452, E1452)
- cationic starch, adding positive electrical charge to starch
- carboxymethylated starch with monochloroacetic acid adding negative charge
and combined modifications such as
- phosphated distarch phosphate (INS 1413, E1413)
- acetylated distarch phosphate (INS 1414, E1414)
- acetylated distarch adipate (INS 1422, E1422),
- hydroxypropyl distarch phosphate (INS 1442, E1442),
- acetylated oxidized starch (INS 1451, E1451).[3]
Modified starch may also be a cold-water-soluble, pregelatinized or instant starch which thickens and gels without heat, or a cook-up starch which must be cooked like regular starch. Drying methods to make starches cold-water-soluble are extrusion, drum drying, spray drying or dextrinization.
Other starch derivatives, the starch sugars, like glucose, high fructose syrup, glucose syrups, maltodextrins, starch degraded with amylase enzyme are mainly sold as liquid syrup to make a sweetener.
Examples of use and functionality of modified starch
[edit]Pre-gelatinized starch is used to thicken instant desserts, allowing the food to thicken with the addition of cold water or milk.[citation needed] Similarly, cheese sauce granules such as in Macaroni and Cheese, lasagna, or gravy granules may be thickened with boiling water without the product going lumpy. Commercial pizza toppings containing modified starch will thicken when heated in the oven, keeping them on top of the pizza, and then become runny when cooled.[4]
A suitably modified starch is used as a fat substitute for low-fat versions of traditionally fatty foods,[5] e.g. industrial milk-based desserts like yogurt[6] or reduced-fat hard salami[7] having about 1/3 the usual fat content. For the latter type of uses, it is an alternative to the product Olestra.
Modified starch is added to frozen products to prevent them from dripping when defrosted. Modified starch, bonded with phosphate, allows the starch to absorb more water and keeps the ingredients together.[8] Modified starch acts as an emulsifier for French dressing by enveloping oil droplets and suspending them in the water. Acid-treated starch forms the shell of jelly beans. Oxidized starch increases the stickiness of batter.
Carboxymethylated starches are used as a wallpaper adhesive, as textile printing thickener, as tablet disintegrants and excipients in the pharmaceutical industry.
Cationic starch is used as wet end sizing agent in paper manufacturing.
Genetically modified starch
[edit]Modified starch should not be confused with genetically modified starch, which refers to starch from genetically engineered plants, such as those that have been genetically modified to produce novel fatty acids or carbohydrates which might not occur in the plant species being harvested. In Europe the term "Genetically Modified Organism" is used solely where "the genetic material has been altered in a way that does not occur naturally through fertilisation and/or natural recombination".[9] The modification in "genetically modified" refers to the genetic engineering of the plant DNA, whereas in the term "Modified Starch" seen on mandatory ingredient labels it refers to the later processing or treatment of the starch or starch granules.
Genetically modified starch is of interest in the manufacture of biodegradable polymers and noncellulose feedstock in the paper industry, as well as the creation of new food additives. For example, researchers aim to alter the enzymes within living plants to create starches with desirable modified properties, and thus eliminate the need for enzymatic processing after starch is extracted from the plant.[10]
See also
[edit]- Acceptable daily intake – Measure of a substance in food or water
- Retrogradation (starch) – Gelatinization of starch
- Starch gelatinization – Process of breaking down the intermolecular bonds of starch by water
- Resistant starch – Dietary fiber
References
[edit]- ^ Vickie Vaclavik; Vickie A. Vaclavik; Elizabeth W. Christian (2007). Essentials of food science (3rd ed.). Springer. p. 61. ISBN 978-0-387-69939-4.
- ^ Starch derivatization: fascinating and unique industrial opportunities, K. F. Gotlieb, A. Capelle, Wageningen Academic Publishers, 2005, ISBN 978-90-76998-60-2
- ^ a b c d e f g h "Codex General Standard for Food Additives (GSFA) Online Database" (PDF).
- ^ Zhang, Honghong; Fan, Haoran; Xu, Xueming; Xu, Dan (January 2024). "Deterioration mechanisms and quality improvement methods in frozen dough: An updated review". Trends in Food Science and Technology. 143 – via Science Direct.
- ^ Lin, Qianzhu; Jiang, Ling; Li, Xiaojing; Sang, Shangyuan; Ji, Hangyan; Jin, Zhengyu; Qiu, Chao (June 2024). "Starch based fat replacers in food system: Modification, structured design, and application". Food Bioscience. 59 – via Science Direct.
- ^ He, Jun; Han, Yumei; Liu, Min; Wang, Yanan; Yang, Yang; Yang, Xujin (2019). "Effect of 2 types of resistant starches on the quality of yogurt". Inner Mongolia Agricultural University. 102:3956 (3964): 8 – via American Dairy Science Association.
- ^ Skrede, G (1989). "Comparison of various types of starch when used in meat sausages". Meat Science. 25 (1): 21–36 – via PubMed.
- ^ Ačkar, Đurđica; Grec, Marijana; Grgić, Ivanka; Gryszkin, Artur; Styczyńska, Marzena; Jozinović, Antun; Miličević, Borislav; Šubarić, Drago; Babić, Jurislav (August 17, 2022). "Physical Properties of Starches Modified by Phosphorylation and High-Voltage Electrical Discharge (HVED)". Polymers. 14 (16): 3359 – via PubMed.
- ^ "GMO". European food Standards Agency. 24 April 2013.
- ^ Zeeman, Samuel C.; Kossmann, Jens; Smith, Alison M. (2 June 2010). "Starch: Its Metabolism, Evolution, and Biotechnological Modification in Plants". Annual Review of Plant Biology. 61 (1): 209–234. doi:10.1146/annurev-arplant-042809-112301. PMID 20192737. Retrieved 16 July 2021.
Suggested reading
[edit]- Ridgwell, Jenny (2001). GCSE food technology for OCR (2nd ed.). Oxford: Heinemann. ISBN 978-0-435-41951-6.
- Revise for OCR GCSE Food Technology, Alison Winson. 2003.
- Degradable Polymers, Recycling, and Plastics Waste Management. S Huang, Ann-Christine Albertsson. 1995.
- Modified Starch, Jenny Ridgwell, Ridgwell Press, 2001, ISBN 978-1-901151-07-7
Modified starch
View on GrokipediaFundamentals
Structure of Native Starch
Starch is a naturally occurring polysaccharide primarily composed of two glucose polymers: amylose and amylopectin. Amylose constitutes 15-30% of most native starches and consists of linear chains of α-D-glucose units linked by α-1,4 glycosidic bonds, typically ranging from 250 to several thousand glucose residues in length.[6] Amylopectin, making up the remaining 70-85%, is highly branched with α-1,4 linked glucose chains connected by α-1,6 glycosidic bonds at branch points approximately every 24-30 glucose units, forming a highly organized, tree-like structure.[6] These components are synthesized and stored in plant amyloplasts as discrete granules, providing an energy reserve.[7] Native starch granules exhibit a semi-crystalline organization, characterized by alternating amorphous and crystalline regions that form concentric layers or growth rings around a central hilum. The crystalline regions, comprising about 15-45% of the granule, arise from the radial alignment of amylopectin double helices packed into lamellae approximately 9 nm thick, while amorphous regions contain branch points and amylose molecules.[8] Granule sizes vary widely from less than 1 μm to over 100 μm, influencing functional properties such as swelling and enzymatic susceptibility.[9] For example, corn starch granules are typically polygonal and range from 5-25 μm, potato starch granules are often oval or spherical with sizes of 10-100 μm, and wheat starch shows a bimodal distribution with large lenticular granules (15-45 μm) and small spherical ones (2-10 μm).[10] Botanical sources lead to distinct variations in amylose-to-amylopectin ratios, which affect granule architecture and overall starch behavior. Normal corn starch has an amylose content of about 25%, while waxy maize varieties contain nearly 0% amylose and nearly 100% amylopectin, resulting in smoother, more uniform granules. High-amylose corn or barley starches can reach up to 70% amylose, leading to elongated or irregular granule shapes and increased crystallinity. Potato starch typically features 20-25% amylose, contributing to its large granule size and high swelling capacity.[6] Native starch possesses inherent properties stemming from its molecular and granular structure, including strong hydrophilicity due to abundant hydroxyl groups on glucose units that form hydrogen bonds with water. This results in insolubility in cold water but significant swelling upon heating. The tendency for retrogradation, where gelatinized starch molecules realign into ordered crystalline structures during cooling or storage, is prominent in high-amylose starches and leads to texture firming in food applications. Gelatinization, the process of granule disruption and leaching of amylose upon heating in water, occurs over a temperature range of 50-80°C, varying by botanical source and influenced by factors like amylose content and granule size.[11][12][1]Reasons for Modification
Native starch, composed primarily of amylose and amylopectin, exhibits several inherent limitations that restrict its direct use in industrial applications. These include poor solubility in cold water, tendency to undergo retrogradation—which leads to firming and staling in processed foods—and syneresis, where water separates from the gelled structure during storage or freeze-thaw cycles.[6] Additionally, native starch is highly sensitive to environmental factors such as pH extremes, elevated temperatures, and mechanical shear, often resulting in granule rupture, viscosity breakdown, and loss of thickening power during processing.[13] Shear thinning behavior further complicates its handling, as the paste viscosity decreases rapidly under agitation, making it unsuitable for high-shear operations common in food manufacturing.[14] To address these shortcomings, starch modification aims to enhance functional properties tailored to industrial demands. Key objectives include improving thermal, acid, and shear stability to withstand rigorous processing conditions without structural breakdown.[1] Modifications also seek to provide better viscosity control, maintaining consistent thickening over time and reducing unwanted changes like retrogradation or syneresis.[1] Furthermore, alterations can reduce digestibility by creating resistant starch fractions that resist enzymatic breakdown in the gut, supporting nutritional goals such as lower glycemic responses.[15] Tailoring textural attributes, such as gelation strength and emulsification capacity, enables starch to mimic or improve upon the functionalities of more expensive ingredients in formulations.[16] Economic and functional drivers further underscore the necessity of modification. Starch serves as a cost-effective alternative to synthetic hydrocolloids and gums due to its abundance from renewable sources like corn and potatoes, offering similar thickening and stabilizing effects at lower prices.[17] In response to consumer demand for clean-label products, modifications—particularly physical and enzymatic methods—provide natural alternatives to chemical additives, aligning with regulatory and market preferences for minimally processed ingredients.[18] The recognition of native starch's limitations dates to the early 20th century, as industrial food processing expanded. By the 1920s and 1930s, challenges in baking and canning highlighted issues like rapid staling from retrogradation and instability in heated mixtures, prompting initial derivatization efforts to improve paste properties for commercial viability.[19]Modification Techniques
Chemical Modifications
Chemical modifications of starch involve covalent alterations to its molecular structure, primarily targeting the hydroxyl groups on the anhydroglucose units of amylose and amylopectin, to enhance functional properties such as solubility, stability, and viscosity. These modifications are achieved through reactions like esterification, etherification, oxidation, and cross-linking, which introduce functional groups or form intermolecular bridges, typically with a degree of substitution (DS) ranging from 0.01 to 0.2. This low DS ensures minimal disruption to the native granule while imparting targeted improvements, such as increased hydrophobicity or resistance to shear.[20][11][1] Esterification substitutes hydroxyl groups with ester linkages, commonly via acetylation using acetic anhydride under alkaline conditions to produce acetylated starch (E1420), where acetyl groups constitute less than 2.5% dry weight basis. Another variant is octenyl succinylation with octenyl succinic anhydride, yielding octenyl succinate starch (E1450) with octenyl succinyl groups below 3% dry weight basis, which introduces amphiphilic properties due to the hydrophobic octenyl chain. These reactions occur preferentially at the C6 primary hydroxyl, followed by C3 and C2 positions, reducing inter- and intramolecular hydrogen bonding, thereby lowering gelatinization temperature and enhancing solubility.[20][11][21] Etherification introduces ether linkages, exemplified by hydroxypropylation with propylene oxide in the presence of an alkaline catalyst, resulting in hydroxypropyl starch (E1440) with hydroxypropyl groups up to 7% dry weight basis. This substitution, also targeting hydroxyl groups (primarily C6), sterically hinders chain alignment, improving paste clarity, freeze-thaw stability, and solubility while maintaining granule integrity at DS levels of 0.01-0.2. The process disrupts retrogradation by interrupting hydrogen bond formation in the crystalline regions.[20][11][1] Oxidation converts hydroxyl groups into carbonyl or carboxyl functionalities using oxidizing agents like sodium hypochlorite or hydrogen peroxide, producing oxidized starch (E1404) with carboxyl content limited to 1.1% dry weight basis. This depolymerizes the starch chains partially, increasing hydrophilicity, solubility, and paste clarity while reducing viscosity and granule integrity through chain scission and crystallinity loss. For instance, hypochlorite oxidation at pH 9-10 introduces aldehyde and carboxyl groups mainly at C6 and C3, facilitating applications like paper sizing where enhanced film-forming properties are needed.[20][11][1] Cross-linking forms covalent bridges between starch chains to reinforce granule structure, using agents such as phosphorus oxychloride or adipic anhydride, yielding phosphate cross-linked products like distarch phosphate (E1412). These reactions create intra- or intermolecular phosphate or ester bonds under controlled conditions, preserving granule integrity against heat, acid, and shear while reducing swelling and solubility compared to native starch. The low DS (0.01-0.2) ensures stability without excessive rigidity; for example, cross-linked starch resists breakdown in high-temperature processing like canned foods.[20][11][21] These modifications are typically performed via the wet process, starting with starch slurried in water (30-40% solids) through wet milling, followed by pH adjustment to 4-10 (often alkaline with NaOH for esterification and etherification), reaction at 30-50°C for 0.5-24 hours with catalysts if needed, neutralization, filtration, washing to remove byproducts, and drying to 10-15% moisture. Reaction conditions are optimized to control DS and avoid over-substitution, which could lead to excessive solubility loss or granule disruption.[20][11][14][1]Physical Modifications
Physical modifications of starch involve non-chemical treatments that alter the granular structure and physicochemical properties through mechanical, thermal, or radiative means, without introducing new molecular bonds or functional groups. These methods reorganize the crystalline domains within starch granules, leading to changes such as modified pasting viscosity and amylose leaching behavior, while maintaining the "clean-label" status desirable in food applications. Unlike chemical or enzymatic approaches, physical modifications rely solely on physical forces, offering advantages like the absence of reagents and broad applicability for enhancing starch functionality in various industries.[1] Heat-moisture treatment (HMT) is a hydrothermal process conducted at temperatures of 90–120°C with limited moisture levels of 10–30% for durations ranging from 1 to 16 hours. This treatment induces reorganization of the crystalline and amorphous regions in starch granules, resulting in reduced amylose leaching during gelatinization and lowered pasting viscosity, without forming new functional groups. HMT improves the freeze-thaw stability of starch-based products by restricting water mobility and syneresis, making it particularly useful for frozen foods. As a reagent-free method, HMT aligns with clean-label preferences and is often applied to cereal and tuber starches to enhance thermal stability.[22][23] Annealing involves controlled hydration of starch at temperatures below its gelatinization point, typically 40–60°C with excess water (over 40% moisture) for extended periods of 24–72 hours. The process promotes molecular rearrangement within the granule, increasing crystallinity and perfection of existing crystalline domains while avoiding granule disruption. This leads to reduced retrogradation upon cooling, as the more ordered structure resists amylose recrystallization, and alters pasting properties by elevating the gelatinization temperature. Annealing provides a simple, non-chemical way to improve starch stability in hydrated systems, such as gels and puddings, without introducing additives.[1][23] Pregelatinization disrupts starch granules through thermal-mechanical processes like drum drying or extrusion, where starch is exposed to heat and shear, often at 120–180°C in high-moisture conditions followed by rapid drying. Drum drying gelatinizes starch on heated rollers before dehydration, while extrusion uses high-temperature short-time (HTST) processing under pressure to shear and expand the material. These methods fragment hydrogen bonds and partially degrade granules, increasing cold-water solubility and viscosity without creating new chemical groups, thus producing instant or cold-swell starches suitable for quick-cooking products. The clean-label appeal and efficiency of extrusion make it a preferred technique for manufacturing ready-to-eat foods like instant cereals.[22][24] Irradiation employs ionizing radiation, such as gamma rays from cobalt-60 sources or electron beams, at doses typically ranging from 5 to 50 kGy to modify starch structure. This treatment causes depolymerization by breaking glycosidic bonds in amylose and amylopectin chains, reducing molecular weight and crystallinity while avoiding the formation of new functional groups. The resulting changes include decreased pasting viscosity and increased water solubility, which enhance digestibility and reduce retrogradation in processed starches. Irradiation offers a reagent-free, scalable method for improving starch functionality in non-food applications like adhesives, though it requires controlled dosing to prevent excessive degradation.[25][26]Enzymatic Modifications
Enzymatic modifications of starch involve the use of specific biocatalysts to hydrolyze glycosidic bonds or rearrange glucan chains, enabling precise control over molecular structure and functionality without harsh chemical treatments.[27] These modifications enhance starch properties such as solubility, viscosity, and digestibility, making it suitable for diverse industrial applications while maintaining biodegradability.[28] Key enzymes include α-amylase, which performs endohydrolysis of α-1,4 glycosidic bonds to shorten amylose and amylopectin chains randomly; β-amylase, an exo-enzyme that cleaves α-1,4 bonds from non-reducing ends to produce maltose units; and glucoamylase, which hydrolyzes both α-1,4 and α-1,6 bonds sequentially to yield glucose monomers.[27][28] Branching enzymes, such as starch branching enzyme II (SBE2), introduce α-1,6 branches by transferring glucan segments, remodeling amylopectin structure to increase short-chain content.[27] Transglucosidases, including cyclodextrin glycosyltransferase (CGTase), facilitate the transfer of glucosyl units to form new bonds or cyclic structures.[28] Hydrolysis processes primarily utilize α-amylase to produce maltodextrins, which are low-molecular-weight carbohydrates with dextrose equivalent (DE) values of 3-20, achieved through controlled partial breakdown of starch granules.[27] Cyclodextrin production employs CGTase to cyclize α-1,4-glucan chains from liquefied starch, forming cyclic oligosaccharides like α-, β-, and γ-cyclodextrins that serve as inclusion complexes in pharmaceuticals and food. β-Cyclodextrin, designated as E459 in the European Union, is manufactured via initial α-amylase liquefaction followed by CGTase action, yielding ring structures with six to eight glucose units for enhanced stability and flavor masking. Dual enzyme systems, such as α-amylase combined with pullulanase or amylopullulanase and amyloglucosidase, promote resistant starch formation by hydrolyzing specific bonds to favor retrogradation into indigestible structures, increasing resistant starch content up to 80% in treated flours. These modifications typically occur under mild conditions to preserve enzyme activity, with optimal pH ranging from 4 to 7 and temperatures of 40-60°C, allowing time-controlled reactions for partial versus complete hydrolysis.[27] For instance, immobilized α-amylase systems operate effectively at pH 4.5-6.5 and 40-50°C, enhancing reusability and process efficiency in continuous industrial setups. Enzymatic alternatives to acid thinning reduce granule size and viscosity similarly but with greater specificity, avoiding non-specific degradation.[27] Overall, these biocatalytic approaches offer eco-friendly, targeted enhancements to native starch's linear amylose and branched amylopectin components.[28]Applications and Properties
Functional Enhancements
Modified starches are engineered to overcome limitations of native starch, such as retrogradation, which leads to undesirable texture changes upon cooling.[1] One primary enhancement is increased shear stability, achieved through cross-linking that introduces covalent bonds between starch molecules, preventing viscosity breakdown during mechanical processing.[29] This modification maintains consistent paste viscosity under high shear conditions, unlike native starch which experiences significant thinning.[29] For instance, cross-linked starches exhibit higher storage modulus (G') and loss modulus (G'') in rheological tests, indicating improved gel strength.[29] Acid and heat tolerance is another key improvement from esterification, where hydroxyl groups on starch are substituted with ester linkages, enhancing resistance to degradation in low pH or elevated temperature environments.[30] Esterified starches show thermal degradation onset around 370°C, compared to 320°C for native forms, allowing better performance in acidic or hot processing.[30] This substitution disrupts hydrogen bonding and reduces crystallinity, contributing to overall stability.[30] Emulsifying capacity is notably boosted by modifications such as octenyl succinic anhydride (OSA) esterification, which introduces hydrophobic octenyl groups to the starch surface, enabling effective stabilization of oil-in-water emulsions.[31] OSA-modified starch adsorbs at interfaces to form Pickering emulsions with steric stabilization, resulting in smaller droplet sizes (e.g., 76–110 μm) and higher emulsification indices (0.77–0.78) than native starch (0.60).[31] Digestibility control is enhanced through strategies that promote resistant starch formation, such as retrogradation, which creates crystalline amylose structures resistant to enzymatic breakdown, or enzymatic branching to increase amylose content and linear glucans.[32] These modifications reduce rapidly digestible starch while elevating slowly digestible and resistant fractions, supporting applications requiring controlled glycemic response.[32] Modified starches are classified by their functional profiles, including thin-boiling types that exhibit low viscosity for easy dispersion, thick-boiling variants with high gel strength for firm textures, and stabilized forms that resist retrogradation and syneresis.[1] Thin-boiling starches, often from acid hydrolysis, provide clarity and reduced paste thickness, while thick-boiling ones maintain integrity under stress, and stabilized types ensure consistent performance over time.[1] These enhancements are quantified using techniques like rheology to assess viscosity curves under shear, differential scanning calorimetry (DSC) to measure gelatinization enthalpy and thermal transitions, and solubility/swelling indices to evaluate water interaction.[1] Rheological analysis reveals stable viscosity profiles in modified starches, DSC shows shifts in peak temperatures, and swelling power indicates controlled granule expansion.[1]| Property | Native Starch Example | Modified Starch Example |
|---|---|---|
| Gelatinization Temperature | 60–70°C (e.g., corn starch) | Instant solubility (pregelatinized) or elevated to 69–80°C (cross-linked/annealed) |
| Viscosity under Shear | Significant drop during processing | Stable, minimal breakdown (cross-linked) |
| Solubility | Low at room temperature | High (thin-boiling or pregelatinized) |
| Emulsification Index | ~0.60 (poor stabilization) | 0.77–0.78 (OSA-modified) |
| Thermal Stability | Degradation ~320°C | ~370°C (esterified) |