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Commentary on 1,3-Dioleoyl-2-Palmitoyl Triglyceride: A Ground-Level Take

Historical Development

Interest in structured triglycerides like 1,3-Dioleoyl-2-Palmitoyl Triglyceride (DOPP) grew as food scientists and chemists started pushing beyond basic oils and fats to get specific properties. A few decades ago, the concept of designer lipids moved from academic curiosity to industrial reality. Researchers wanted to improve the nutritional value and texture of processed food and infant formula. By the late 20th century, improvements in lipid chemistry—notably enzymatic interesterification—made it practical to create molecules like DOPP on purpose, instead of just finding them in nature by accident. Today, labs and factories treat these structured triglycerides as essential building blocks for special nutrition products, thanks to progress in catalysis, analytical methods, and globalized fat sourcing.

Product Overview

In the world of lipids, DOPP brings a lot to the table. It looks simple: a triglyceride with two oleic acid groups and a palmitic acid chain. What sets it apart comes down to placement. Structuring oleoyl and palmitoyl residues at specific positions tunes melting point, digestibility, and suitability for sensitive populations—like infants or hospitalized patients. Unlike common fats, DOPP’s design avoids the randomness of most dietary triglycerides, which giants like Cargill, DSM, and Nestlé recognized early as a big deal for nutritional purity and product consistency.

Physical & Chemical Properties

DOPP shows up as a pale to light yellow oil at room temperature. The palmitic acid at the 2-position brings firmness, whereas the oleic groups at 1 and 3 keep things fluid. This balance drops the melting point well below animal fats, making it much smoother on the tongue and easier to work with in industrial settings. It’s got a saponification value similar to olive oil—around 190–195 mg KOH/g—and an iodine value that reflects the double bonds of the oleic chains. It dissolves well in most nonpolar solvents and stays stable during moderate heating, which matters in food production, cosmetics, and even pharma.

Technical Specifications & Labeling

Most commercial DOPP supplies get tagged with technical specs: purity above 98%, moisture content below 0.1%, peroxide value under 1.0 meq/kg, and fatty acid composition backed up by GC analysis. Producers document the triglyceride form through HPLC and NMR data. In regulated markets, the material carries a CAS number (often 104372-58-1) and detailed batch records. In food applications, allergen statements, origin of feedstock (palm, olive, or GMO-free), and clear ingredient labeling bring trust and traceability, which satisfies regulatory and consumer worries.

Preparation Method

DOPP production leans heavily on enzymatic interesterification. One common route starts with palm stearin and high-oleic oils. A lipase with sn-1,3 specificity swaps out the fatty acids, nesting palmitic acid in the middle. Unlike chemical interesterification, which requires high temperature and catalysts, enzymes keep costs lower and preserve subtle flavors. Skilled operators avoid unwanted byproducts, which show up fast in finished formulas. Once the reaction’s done, the triglyceride gets purified by distillation and crystallization, followed by vacuum drying to pull away any traces of reactant or water.

Chemical Reactions & Modifications

DOPP serves as a flexible starting point for further chemistry. Hydrogenation can fully harden it for use in chocolate, though most applications want it unmodified to maintain nutritional benefits. Acyl migration sometimes creeps in during processing, so keeping temperature and time under control matters if the exact structure is needed. You can react DOPP with limited alcoholysis to release mono- or diglycerides, handy for emulsifiers. For advanced drug delivery, chemicalists have tried linking DOPP to polyethylene glycol or peptides, creating lipid-based carriers for slow-release medications or vitamins.

Synonyms & Product Names

Over the years, DOPP has gone by several names—chemists often call it 1,3-dioleoyl-2-palmitoylglycerol or OPO. Industry labels include “sn-2 Palmitate Oil” or “Structured Triglyceride Type OPO”. In product catalogs you might spot systematic names, trade names, or batch numbers flavored by the parent company, but the structure—oleoyl at 1 and 3, palmitoyl at 2—remains consistent.

Safety & Operational Standards

Plants making DOPP follow the same strict codes as other food- and pharma-grade fats. GMP guides every step—ingredient selection, allergen risk mitigation, batch segregation, and environmental control. Workers suit up against both contamination and fires. Labs watch for heavy metals, solvents, and microbial load. Finished batches run through rigorous shelf-life and oxidation tests, since structured lipids can break down under light and oxygen. Global regulators, including the US FDA and EFSA, keep companies honest by reviewing both ingredient status and safe use levels.

Application Area

DOPP’s biggest spotlight comes in infant formula. When breast milk can’t be used, nutritionists look for fats that closely match its molecular layout. DOPP steps up by mimicking human milk’s palmitic acid positioning, improving calcium absorption and gut tolerance in babies. Hospitals and dietary supplement makers also use it to up the calories in enteral nutrition for patients who struggle to digest regular fats. In the food industry, DOPP add smoothness to spreads and dairy analogs. Fewer folks know it shows up in cosmetics, where it gives moisturizers a non-greasy, quick-absorbing character.

Research & Development

The academic world keeps digging into better ways to make DOPP with higher purity and sustainability. Teams at universities tweak enzymes and raw materials to raise yields and lower palm oil use, which ties into broader palm sustainability worries. Analytical chemists explore LC-MS and NMR to spot even trace impurities, since those affect both safety and performance in nutrition applications. Clinics watch how DOPP in infant formula impacts bone health, growth, and microbiome formation—big social topics in global health policy.

Toxicity Research

As with any synthetic lipid, safety gets serious attention. Chronic and acute toxicity studies in animals and humans haven’t found harmful effects at intended use levels. In vitro digestion models show DOPP breaks down the same way as milk fat, releasing similar monoglycerides and fatty acids. No long-term buildup in tissues, no carcinogenicity, and fewer signs of pro-inflammatory action—these facts put minds at ease in regulatory agencies and with pediatricians. Vigilance remains: new studies continue tracking tiny metabolites and allergy potential as structured fats move into mainstream diets.

Future Prospects

Looking forward, DOPP’s role keeps expanding as new processing tech lowers costs and improves environmental impact. Demand for sustainable, well-characterized triglycerides grows fast, especially in Asia and emerging economies. As plant-based diets spread, DOPP and related molecules promise to bridge sensory gaps between dairy and non-dairy, or improve complete nutrition for vulnerable groups. More precise enzyme engineering, green chemistry, and zero-waste lipid processing will give this molecule a future beyond food, extending its reach into medical, cosmetic, and nutraceutical products worldwide.




What is 1,3-Dioleoyl-2-Palmitoyl Triglyceride used for?

Why This Ingredient Stands Out in Products

Most labels on skin creams or nutritional supplements read like a stream of puzzle pieces. One ingredient, 1,3-Dioleoyl-2-Palmitoyl Triglyceride, sounds like a chemistry quiz, but its story traces back to living, everyday benefits. I’ve watched how cosmetic chemists or nutritionists react when this triglyceride turns up—they recognize it because it’s more than filler. It mimics some key lipids our skin and bodies know well. That “natural fit” brings practical advantages, especially for anyone struggling with dryness or ingredient sensitivities.

Lipids and Skin: More Than Moisture

My first memory of working with this triglyceride came during a project in a small skincare lab. We mixed test batches for a winter cream, aiming for real help against the relentless dry air. Among a crowd of oils, this one kept the formula rich, yet smooth to the touch. It blends easily and sticks to a natural fatty acid balance close to what healthy skin produces. As a result, creams made with it often help restore the barriers that fight flakiness or rough patches.

1,3-Dioleoyl-2-Palmitoyl Triglyceride acts as an emollient. That means it leaves the skin feeling soft and strengthened without that greasy after-feel so many people dislike. Brands pick it for formulas meant for sensitive skin since it rarely causes irritation. Studies have backed up its value in soothing and repairing the topmost layers—good news for folks with eczema, psoriasis, or just stubborn winter skin.

Beyond Skincare: The Food Angle

People often overlook its role in food science. It’s not a household name like coconut oil, but it finds its way into specialist nutrition formulas, especially in infant formula and clinical diets. Why? The molecular structure lets it act almost like the fat in human breast milk. It supports fat absorption, which is vital for infants or anyone who has trouble digesting regular fats. I learned about this from a friend whose child depended on formula—suddenly, the choice of fat blend turned from theoretical chemistry to a very real impact on her baby’s stomach.

Looking for Alternatives and What That Really Means

Some pressure comes from people asking for more plant-based or “clean label” ingredients. There’s a push to find options that don’t strip away natural resources or trigger allergies. 1,3-Dioleoyl-2-Palmitoyl Triglyceride scores well in these debates because many suppliers source it from vegetable oils. It supports sustainability without skipping performance. For a formulator, that’s gold: you get stability, skin comfort, and a backstory you can stand behind in a product pitch or at the kitchen table.

Toward Safer, Smarter Use

Safety always looms large. So far, research shows low risk for the average consumer. As with any ingredient, overuse or mixing with harsh chemicals changes results, but it holds up well under real-world conditions. Companies should routinely share full testing results and keep an eye on ingredient traceability—not only to meet regulations but to maintain trust.

Consumers need honest labels and manufacturers must stay transparent about sourcing. This approach lines up with today’s demand for evidence, trust, and care—values that rarely fail anyone, whether applied to skin, a supplement, or a baby’s formula.

Is 1,3-Dioleoyl-2-Palmitoyl Triglyceride safe for skin application?

The Science Behind the Ingredient

1,3-Dioleoyl-2-Palmitoyl Triglyceride goes by a less intimidating name in a cosmetic context: a specialized plant-based fat. Manufacturers blend it into lotions, serums, and balms as an emollient, meaning it locks moisture in the skin. The structure of this ingredient mimics some of the fats found naturally in human skin, so it can deliver a smooth, nourishing feel without causing irritation. Most sources for this triglyceride come from common edible oils like olive or palm, giving it a long track record in both food and personal care settings.

Safety Data and Real-World Use

Most skin scientists and dermatologists view 1,3-Dioleoyl-2-Palmitoyl Triglyceride as safe if the product is used responsibly. The Cosmetic Ingredient Review panel, an authoritative voice in the U.S., keeps a watchful eye on new and old cosmetic ingredients. They report few issues with this compound when it’s processed and handled with proper quality controls. In daily life, people with sensitive skin sometimes worry about breakouts or rashes from new products, but data shows this triglyceride rarely triggers those issues. Its makeup is similar to ingredients in nut and seed oils, which helps skin keep its barrier healthy.

Some of my earliest memories using skin creams included formulas with these sorts of triglycerides. My own experience matches what’s in the literature: gentle, quick-absorbing, and no sticky residue. I remember slathering a moisturizer on my cracked hands one winter, and the relief from itch and dryness made me a convert. You notice right away if an ingredient creates tingling or breakouts, and those moments never showed up here.

Who Should Keep an Eye Out?

Allergic reactions always grab headlines but happen more often with botanical extracts or strong scents, not with standard triglycerides. For anyone with extreme nut or palm allergies, a quick review of the source material makes sense. People with complicated skin conditions, like eczema or chronic dermatitis, might want to patch test a new formula anyway. Most over-the-counter products that feature this triglyceride follow global safety guidelines, including levels set by the FDA and EU cosmetic authorities.

What the Evidence Shows

Peer-reviewed articles support the safety profile. Research published by the Journal of the Society of Cosmetic Chemists evaluates ingredients like this for both acute and long-term toxicity. They found no evidence of hormone disruption, carcinogenicity, or severe irritation—even when the ingredient is used often. Sometimes brands market this triglyceride as “bio-mimetic,” since the molecule behaves like natural skin lipids. This gives formulators a way to make creams that calm irritation and help restore dry or damaged skin.

Steps Toward Responsible Skincare

Transparency on ingredient sourcing still matters. More companies now disclose how they harvest and process fats and oils to produce cosmetic triglycerides. This helps build trust and gives people a better shot at finding sustainable and ethical brands. For those worried about palm oil's environmental impact, some lines now use triglycerides from olive, sunflower, or coconut instead.

Reading ingredient labels and researching sources keeps consumers informed. If a reaction does show up—redness or bumps—stopping use is the smart move, and seeking professional help makes sense in stubborn cases. But broadly, this unique triglyceride earns its spot in skin care, balancing safety, performance, and affordability.

What are the benefits of 1,3-Dioleoyl-2-Palmitoyl Triglyceride in cosmetics?

What Sets This Ingredient Apart

Most people walk through a cosmetics store and glance over ingredient lists without thinking twice. Every once in a while, a molecule shows up that really punches above its weight. 1,3-Dioleoyl-2-Palmitoyl Triglyceride fits this bill. Unlike many lab-made fillers, this ingredient shares a closer bond with the skin’s real structure. Our skin contains its own natural lipids, and this triglyceride has a similar vibe. That’s why it feels so smooth and doesn’t leave a heavy film behind.

Moisture: Lock It In, Don’t Fake It

I remember trying creams that made my skin feel great for five minutes, then left it more parched. With 1,3-Dioleoyl-2-Palmitoyl Triglyceride, things play out differently. Studies show this lipid can bolster the skin’s own protective layer, trapping moisture where it belongs. Dermatologists regularly point to strong barrier support as the front line against everything from itching to flaking. Real stories from consumers, and my own experience, back up the data: products with this triglyceride bring lasting comfort and a softer feel.

Putting Up a Shield Against Pollution

City living means dodging a constant drizzle of pollutants. Part of staying healthy involves giving the skin a fighting chance. 1,3-Dioleoyl-2-Palmitoyl Triglyceride doesn’t just moisturize—it strengthens the skin’s shield. With a tougher barrier, unwanted particles and irritants struggle to get under the surface. There’s truth in those studies from European labs showing reduced inflammation thanks to this very molecule. That means fewer days battling redness, and less need for heavy makeup to cover up.

Feeling Good, Not Greasy

Texture matters just as much as chemistry. Classic oils often sit on top of the skin or clog pores. I’ve tried enough greasy serums to know the tradeoff isn’t worth it. 1,3-Dioleoyl-2-Palmitoyl Triglyceride gives creams a silky texture. Think soft, velvety touch that vanishes after a gentle rub, leaving no shiny afterglow. Product developers love that quality too, since consumers actually stick with a cream that feels invisible.

Safer Ingredients for All Skin Types

For anyone prone to breakouts, picking a face cream turns into a nerve-wracking guessing game. This triglyceride clears that fog. It doesn’t block pores and rarely causes allergic reactions, which stands out in a world full of harsh actives. Multiple studies back up its safety profile, making it a solid option for kids, adults, and even sensitive skin. Leading dermatology groups across the United States and Asia recognize it as a “skin-friendly” ingredient on their recommended lists.

What Cosmetic Brands Should Do

Brands see strong results wherever they include 1,3-Dioleoyl-2-Palmitoyl Triglyceride in moisturizers or lotions. More than boosting skin texture, companies earn customer trust by using ingredients rooted in solid research. I’ve noticed top brands highlighting this molecule in their marketing, signaling a shift toward thoughtful formulations instead of hype. This approach can help reduce confusion among shoppers searching for safe, science-backed choices. Investing in better, skin-identical lipids creates a ripple effect, raising industry standards and delivering lasting results right to the consumer’s mirror.

Is 1,3-Dioleoyl-2-Palmitoyl Triglyceride derived from natural sources?

The Origins Behind the Ingredient

The world loves a label. “Natural” is slapped on everything from granola bars to cosmetics, and people reach for these products in hopes of something better. In food science and beauty products, ingredient lists often turn cryptic. 1,3-Dioleoyl-2-Palmitoyl Triglyceride, a mouthful even for chemists, shows up now and then. I’ve looked at ingredient decks for years, and this one stands out because many want to know if it comes straight from nature – or if it’s just wearing the name.

The chemical name doesn’t love plain speech. It breaks down to a triglyceride built from two oleic acid chains and one palmitic acid chain. Both these fatty acids naturally appear in plant oils and animal fats. For example, olive oil overflows with oleic acid. Palm oil and animal fats carry palmitic acid. About a decade ago, I started seeing more triglycerides tailored for specific applications, but the truth is: the backbone often begins with ordinary vegetable oil.

The Creation Process

Manufacturers source these fatty acids mainly from natural oils. In practice, producers sometimes use clever chemistry to isolate exactly the chains they want, sticking them together in controlled ways, rather than relying on the natural assortment that comes straight from pressing olives or coconuts. This process can involve enzymes or heat, separating and recombining the fatty acids in a precise way. It brings a certain predictability for food texture or cosmetics, which consumers like.

While the triglyceride’s raw materials can draw straight from naturally grown plants or animal fats, the final step veers into what many would call processing, even if the inspiration is nature. Despite this, you’ll see ingredient lists stretching the term “natural” much further than my grandmother would. Products with this ingredient often pass the “derived from natural sources” claim. The tricky part comes from how we think about that phrase. It’s one step removed from the olive or palm, but it didn’t start in a lab from nothing.

Importance for Consumers

A lot rides on clarity here. Folks buy “natural” hoping for something closer to its original source and less exposed to weird chemicals. Many care about sustainability, minimal processing, and allergen risk. For people with dietary restrictions or values built around whole foods, understanding the journey from raw oil to engineered triglyceride changes purchasing choices. The FDA and European authorities let producers call an ingredient “naturally derived” if its starting materials come from nature, even if clever chemistry makes the final product.

I’ve seen this confusion create real mistrust in product brands. Once, a friend allergic to peanuts asked me to help her read a snack bar label with an equally long ingredient. The phrase “vegetable oil-derived” put her at ease, but few packages tell you exactly which plants supplied the oil. Consumers read “derived from natural sources” and rarely get the next piece: which plant, and what methods got used from crop to package.

Where to Go from Here?

Brands could do much better with transparency. Simple breakdowns – olive, palm, or canola – help. So does spelling out if synthetic steps transformed the oils. Regulators should give better definitions for “natural” and “naturally derived” so shoppers don’t end up making decisions based on fuzzy language.

If you want to make truly informed choices, get comfortable asking questions and pushing brands for specifics when “natural” appears. All the science in the world doesn’t help unless you can actually understand what winds up in your body or on your skin.

Can 1,3-Dioleoyl-2-Palmitoyl Triglyceride cause allergic reactions?

What Is This Ingredient?

1,3-Dioleoyl-2-Palmitoyl Triglyceride sounds like something cooked up in a high school chemistry lab, but, at its core, it’s just a type of fat. Made from combining oleic and palmitic acids, this compound finds a home in a range of cosmetics, skincare products, sometimes in foods as a processed fat or emollient. I've stood in the grocery aisle, squinting at labels stuffed with complicated names—this one pops up on lotions and lip balms fairly often.

Should People Worry About Allergies?

From my experience, most folks won’t need to worry about this ingredient in the same way they would for common triggers like peanuts, shellfish, or pollen. Triglycerides like this usually don’t have the bits that set off most allergies, those pesky protein structures. Research backs this up. Scientific reviews and published case reports rarely list allergic reactions to this fat. Most dermatologists consider it low risk, and the Cosmetic Ingredient Review Expert Panel marks it as generally safe for use, especially since most reactions tie back to fragrance or preservatives, not the fat itself.

Not Everyone’s Skin Reacts the Same

Still, nobody’s skin responds exactly the same. The world isn’t short on stories about someone who used a “safe” ingredient and walked away with a rash. That’s especially true if you have eczema or have dealt with contact allergies before. Even with ingredients that seem harmless, outliers exist. When I work with folks who often break out, I usually suggest patch testing new products—including those with long, technical names.

How Would You Know If This Triglyceride Caused an Issue?

If you use a cream or food with this ingredient and get an itchy patch, redness, or even swelling, don’t brush it off as “just sensitive skin.” Itching and rash after using a new product raise the idea of a possible contact allergy. Most experts agree, real allergies to triglycerides like 1,3-dioleoyl-2-palmitoyl remain rare, but it can happen, especially if the fat is mixed with contaminants or oxidized oils. If you spot a reaction, put the product aside for a bit and see a doctor or dermatologist. They can figure out if this fat or something else in the mix raised trouble. In rare cases, seeing an allergist could help pin down the real cause.

Reducing the Risk

Pick skincare and foods from companies that post clear ingredient lists and avoid unnecessary perfume, color, or fillers. If you know you react to coconut, palm, or related oils, ask your doctor whether these specialty triglycerides could be an issue. I always keep a close eye on expiration dates. Oxidized fats don’t just smell off; they might feel rougher on sensitive skin. Buying smaller containers when trying something new keeps leftovers and old products from piling up, too.

Forward Steps for Everyone

One thing stands out: Trust your body’s signals. Don’t sweep a reaction aside. Specialists in clinical allergy recommend open lines of communication with your healthcare provider if your skin keeps surprising you. Ingredient transparency isn’t just good marketing; it helps people make safer, smarter choices. The science shows most people stay in the clear, but careful habits and open eyes offer better odds for everyone.

1,3-Dioleoyl-2-Palmitoyl Triglyceride
Names
Preferred IUPAC name 2-palmitoyl-1,3-dioleoyl glycerol
Other names Triolein, 2-palmitoyl-
2-palmito-1,3-dioleylglycerol
Glyceryl 1,3-dioleate 2-palmitate
Pronunciation /ˈwʌn θri daɪˈɔɪlɔɪl tuː pælˈmɪtɔɪl traɪˈɡlɪsəˌraɪd/
Preferred IUPAC name 2-palmitoyl-1,3-dioleoyl-glycerol
Other names Glyceryl 1,3-dioleate 2-palmitate
2-palmitoyl-1,3-dioleoyl-glycerol
Triolein, palmitic acid mixed triester
Olea-palmitin
1,3-dioleoyl-2-palmitoyl-sn-glycerol
Glycerol trioleate, palmitic acid monoester
Pronunciation /ˌwʌn θriː daɪˌoʊliːl tuː pælˈmɪtoʊɪl traɪˈɡlɪsəraɪd/
Identifiers
CAS Number 110944-63-5
Beilstein Reference 4761042
ChEBI CHEBI:86456
ChEMBL CHEMBL3291046
ChemSpider 58204906
DrugBank DB12121
ECHA InfoCard 03af425d-e774-47cf-b28d-4cb572a54a09
EC Number NA
Gmelin Reference 84809
KEGG C20496
MeSH D008057
PubChem CID 12351345
UNII 51U1M9SV58
UN number Not regulated
CAS Number 120158-87-0
Beilstein Reference 3874826
ChEBI CHEBI:85710
ChEMBL CHEMBL3291047
ChemSpider 53244110
DrugBank DB11234
ECHA InfoCard 03dbf3a8-df95-40ba-ae3a-3c85bc2671dd
EC Number NA
Gmelin Reference 66901
KEGG C19662
MeSH D009058
PubChem CID 9930889
UNII 4C9C59U3VI
UN number Not regulated
Properties
Chemical formula C55H104O6
Molar mass 885.4486 g/mol
Appearance White to off-white solid
Odor Odorless
Density 0.925 g/cm3
Solubility in water Insoluble in water
log P 13.7
Vapor pressure Vapor pressure: negligible
Refractive index (nD) 1.456
Viscosity Viscosity: 77.1 cP (at 40 °C)
Dipole moment 2.3784 D
Chemical formula C55H104O6
Molar mass 881.46 g/mol
Appearance White solid
Odor Odorless
Density 0.911 g/cm³
Solubility in water Insoluble in water
log P 18.2
Refractive index (nD) 1.454
Viscosity Viscosity: 82.6 mPa·s (at 40 °C)
Dipole moment 3.1 D
Thermochemistry
Std molar entropy (S⦵298) 384.9 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -1722.6 kJ/mol
Std enthalpy of combustion (ΔcH⦵298) -39180.3 kJ/mol
Std molar entropy (S⦵298) 923.9 J·mol⁻¹·K⁻¹
Std enthalpy of combustion (ΔcH⦵298) -38630 kJ/mol
Hazards
Main hazards No hazardous substance.
GHS labelling No GHS labelling.
Pictograms GHS07
Signal word Not Classified
Hazard statements Not a hazardous substance or mixture according to the Globally Harmonized System (GHS)
Precautionary statements P280-P305+P351+P338
Flash point > 230 °C
PEL (Permissible) PEL (Permissible Exposure Limit) for 1,3-Dioleoyl-2-Palmitoyl Triglyceride: **Not established**
REL (Recommended) 0.93 mg/m³
IDLH (Immediate danger) No IDLH established
Main hazards Not a hazardous substance or mixture.
GHS labelling No GHS labelling.
Pictograms GHS07
Precautionary statements Precautionary statements: Not a hazardous substance or mixture according to Regulation (EC) No. 1272/2008.
NFPA 704 (fire diamond) NFPA 704: "0-1-0
Flash point > 271.6 °C
PEL (Permissible) PEL (Permissible Exposure Limit) for 1,3-Dioleoyl-2-Palmitoyl Triglyceride: "Not established
IDLH (Immediate danger) Unknown
Related compounds
Related compounds 1,2-Dioleoyl-3-Palmitoyl Triglyceride
1,3-Dipalmitoyl-2-Oleoyl Triglyceride
1,2,3-Triolen
1,2,3-Tripalmitin
1-Oleoyl-2,3-dipalmitoyl-glycerol
Related compounds Triolein
Tripalmitin
1,2-Dioleoyl-3-palmitoyl-rac-glycerol
1,3-Dipalmitoyl-2-oleoyl-glycerol
1,2-Dipalmitoyl-3-oleoyl-glycerol