D-PANTOTHENYL ALCOHOL

CAS: 81-13-0 NUTRIENT SUPPLEMENT

D-PANTOTHENYL ALCOHOL, also known as Dexpanthenol or pantothenol, is the alcohol analogue of pantothenic acid (vitamin B5) and is used as a nutrient supplement form of provitamin B5 in food and supplement contexts.

What It Is

D-PANTOTHENYL ALCOHOL is a biologically relevant form of provitamin B5, known chemically as the alcohol analogue of pantothenic acid. It corresponds to a specific enantiomer of panthenol that is utilized in nutritional and supplement applications. Its CAS number 81-13-0 identifies the D form of the compound, which has been widely characterized in chemical and regulatory sources. Dexpanthenol functions as a precursor to pantothenic acid, which is essential for the biosynthesis of coenzyme A in biological systems. Within food science and nutrition, it is categorized as a nutrient supplement, meaning it provides a source of a vitamin precursor when added to food products or dietary supplements. This compound’s inclusion in food and supplement products is tied to its metabolic role and nutritional contribution rather than its effects on taste or texture. This substance often appears in ingredient lists for fortified foods and beverages, as well as in dietary supplement formulations that aim to supply vitamin B5 or its precursors. Its recognition in food and supplement contexts stems from its metabolic conversion to pantothenic acid, which participates in fundamental enzymatic reactions in the body. The D isomer specifically is considered the biologically active form, whereas other stereoisomers may have less defined metabolic activity. Chemically, D-PANTOTHENYL ALCOHOL is a viscous, colorless to slightly yellow liquid under standard conditions. It is hygroscopic and soluble in water and certain alcohols. Its role as a nutrient supplement distinguishes it from other food additives that are used for technological effects like preservation or coloring. The compound’s identity and function are established in scientific and regulatory databases, supporting its use in food and supplement applications.

How It Is Made

D-PANTOTHENYL ALCOHOL is typically produced through the reduction of pantothenic acid or related precursors that yield the corresponding alcohol form known as panthenol. In chemical manufacturing contexts, the conversion involves reducing the carboxylic acid group of pantothenic acid to an alcohol group, resulting in the panthenol molecule. Industrial synthetic methods use established organic chemistry techniques, ensuring the correct stereochemistry for the D isomer. Manufacturers producing this compound for food, supplement, or cosmetic use apply purification steps to achieve high assay purity, often specifying minimal levels of residual solvents and impurities. Purity specifications are generally guided by pharmacopeial or ingredient standards relevant to intended use categories. While food-grade and supplement-grade material typically demands rigorous quality control, the core chemical synthesis pathways mirror those used for laboratory preparation of this vitamin precursor. The manufacturing process is designed to yield a stable, consistent product that conforms to safety and quality expectations. Because this compound is integrated into foods and supplements as a nutritional ingredient rather than a technological processing aid, producers emphasize purity and identity verification. Analytical techniques like chromatography and spectroscopy are applied during quality assurance to confirm the compound’s structure, stereochemistry, and absence of contaminants. Key physical properties such as solubility and hygroscopicity influence how the compound is formulated into final product matrices. Overall, the production of D-PANTOTHENYL ALCOHOL aligns with standard organic synthesis practices for vitamin precursors, supported by quality oversight to meet regulatory and industry standards for nutrient supplements.

Why It Is Used In Food

D-PANTOTHENYL ALCOHOL is used in food and dietary supplement applications primarily because it serves as a precursor to pantothenic acid (vitamin B5), an essential nutrient that supports metabolic functions in humans. When included in food or supplements, it acts as a nutrient fortificant that contributes to the overall vitamin content of the product. This can be particularly useful in fortified foods and beverages where manufacturers seek to enhance the nutritional profile or address dietary gaps. As a provitamin form of B5, D-PANTOTHENYL ALCOHOL is metabolized to the active vitamin in the body after ingestion, thereby contributing to the pool of essential nutrients that support energy metabolism, synthesis of coenzyme A, and other biochemical pathways. Its inclusion in food products is framed around nutritional benefit rather than technological effects such as texture modification or preservation. Food scientists and formulators may select this ingredient for its compatibility with other micronutrients and its stability in typical processing and storage conditions. It can be incorporated into a range of product formats, including beverages, nutrition bars, meal replacements, and dietary supplements, where the goal is to provide additional vitamins in a bioavailable form. The functional logic for its use is anchored in established nutrient fortification practices that aim to support balanced diets and meet regulatory or voluntary labeling standards for vitamin content.

Adi Example Calculation

Because D-PANTOTHENYL ALCOHOL does not have a standalone ADI defined by regulatory bodies, an illustrative example focuses on the context of pantothenic acid nutrient intake. Suppose a fortified beverage contains an amount of D-PANTOTHENYL ALCOHOL designed to supply the equivalent of a standard vitamin B5 serving for an average adult. If the product delivers a milligram-level equivalent of B5 precursor, this aligns with typical recommendations for vitamin intake without representing excessive exposure. In this hypothetical scenario, the calculation would involve converting the amount of precursor to an equivalent pantothenic acid contribution, recognizing that metabolic conversion efficiency supports integration into normal metabolic pathways. The illustrative calculation underscores the difference between nutrient supply and hazard-based exposure limits used for other additives. It highlights how nutrient context frames safety considerations rather than numeric ADI limits.

Safety And Health Research

Safety assessments for compounds like D-PANTOTHENYL ALCOHOL emphasize general toxicity data, metabolic fate, and tolerability rather than specific adverse effects at typical intake levels from fortified foods or supplements. As a nutrient precursor, it is metabolized to pantothenic acid, an essential B vitamin with well-characterized biological functions. The metabolic pathways involved suggest that the compound’s inclusion in food and supplements supplies a physiologically relevant precursor without introducing novel mechanisms of toxicity. Regulatory frameworks that address nutrient ingredients consider factors such as purity of the supplied material, absence of harmful impurities, and evidence from existing usage patterns. Toxicological evaluations typically address endpoints such as acute toxicity and basic dose-response relationships. Because pantothenic acid and its analogues are naturally occurring and widely present in food matrices, the safety assessment foregrounds expected metabolic incorporation rather than unique toxicological concerns. The absence of extensive regulatory restrictions and the historical use of related compounds in nutritional applications contribute to the overall safety profile for this ingredient. Nevertheless, safety research supports careful formulation practices to avoid levels that would exceed common dietary intakes by large margins. Overall, scientific and regulatory perspectives frame the compound’s safety in terms of standard nutrient fortification practice rather than hazard-based constraints.

Regulatory Status Worldwide

Regulatory status for D-PANTOTHENYL ALCOHOL varies by country and jurisdiction, and it is important to distinguish between food additive approval and nutrient supplement use. In the United States, the compound may be included as a nutrient or vitamin precursor under the framework that governs substances added to food, which includes provisions for generally recognized as safe (GRAS) ingredients. However, there is no explicit CFR listing identified for this specific compound in standard food additive regulations, and direct FDA approval as a food additive is not confirmed in available regulatory inventories. This reflects the broader framework under which nutrient supplements and food ingredients are evaluated, where GRAS status may be established through notification or expert consensus rather than explicit regulation. In the context of dietary supplements, the FDA oversees the category under DSHEA, which places responsibility on manufacturers to ensure safety and accurate labeling for nutrient ingredients, including D-PANTOTHENYL ALCOHOL when used to supply vitamin B5. Globally, equivalent regulatory approaches may permit its inclusion in fortified foods or supplements subject to local rules for nutrient fortification. Because of the compound’s established use as a vitamin precursor and nutrient ingredient in food and supplement products, regulatory consideration focuses on ensuring appropriate purity and safety data. It is not classified under restricted additive categories, and where permitted, its use aligns with fortification practices consistent with public health objectives.

Taste And Functional Properties

D-PANTOTHENYL ALCOHOL itself has limited impact on the taste profile of foods because its primary purpose in formulations is nutritional rather than sensory. When used at levels typical for nutrient fortification, it contributes negligible flavor or aroma characteristics. In food matrices, the compound generally remains organoleptically neutral, allowing it to be included without altering the intended sensory properties of the product. From a functional standpoint, this compound exhibits solubility in aqueous and certain alcoholic systems, which facilitates its integration into beverages and liquid supplement formats. Its hygroscopic nature suggests that formulators must account for moisture interactions during processing and storage, especially in dry-mix applications. The stability of this molecule under typical conditions of food manufacturing supports its use across a range of pH levels and temperatures encountered during standard product preparation. Because the compound serves as a nutrient, its presence does not influence food texture or structure in the way that emulsifiers or stabilizers might. Instead, its role is confined to supplying a precursor to an essential vitamin without contributing to functional properties like gelation, aeration, or shelf-life extension. Its utility is defined by nutritional science rather than sensory modulation, making it appropriate for products where nutrient content claims or fortification are central to product positioning.

Acceptable Daily Intake Explained

The concept of acceptable daily intake (ADI) refers to the maximum amount of a substance that can be consumed daily over a lifetime without appreciable risk. For nutrient precursors like D-PANTOTHENYL ALCOHOL, formal ADI values specific to the compound itself are not established in the same way that they are for food additives with defined toxicological thresholds. This is because the compound’s metabolic role feeds into established vitamin pathways rather than presenting unique toxicological concerns at typical levels of use in fortified food products or supplements. In regulatory practice, nutrient ingredients are assessed in terms of their contribution to overall nutrient intake and alignment with dietary reference intakes for the corresponding vitamins. The safety rationale for using this compound in food and supplements focuses on ensuring that total intake of pantothenic acid and its precursors does not exceed levels compatible with normal metabolism. Because pantothenic acid is an essential nutrient, there is a broad safety margin for its precursors when used at levels typical for fortification. Therefore, while D-PANTOTHENYL ALCOHOL does not have a specific ADI numeric value set by authoritative agencies, its inclusion in fortified foods and supplements fits within frameworks that treat nutrient ingredients in relation to established nutritional requirements. This reflects a regulatory approach that distinguishes nutrient supply from hazard-based additive assessment.

Comparison With Similar Additives

When compared with other nutrient fortificants like niacin or folic acid, D-PANTOTHENYL ALCOHOL’s role is similar in supplying a form of an essential nutrient that integrates into metabolic pathways. While niacin and folic acid may have specific regulatory intake thresholds due to distinct metabolic effects, pantothenic acid precursors generally exhibit broad safety margins at typical levels used for fortification. In contrast to non-nutrient additives such as colorants or preservatives, which have defined functional thresholds and ADI values established by regulators, nutrient precursors like this compound are evaluated in the context of nutritional contribution. Their comparison with other nutrient additives reflects shared considerations around bioavailability, metabolic incorporation, and formulation synergy rather than hazard-driven limitations. This positions D-PANTOTHENYL ALCOHOL among additive categories focused on enhancing dietary nutrient profiles rather than modifying sensory or preservation characteristics.

Common Food Applications Narrative

D-PANTOTHENYL ALCOHOL is incorporated into a variety of fortified and nutritional food and supplement products where the goal is to enhance vitamin content for consumers. As a provitamin form of B5, it appears in beverages designed for energy support, nutrition bars that aim to supply micronutrients, and specialized meal replacements tailored for balanced diets. In these applications, it contributes as a source of pantothenic acid without substantially affecting the sensory experience of the product. Manufacturers that produce fortified foods leverage this ingredient to meet voluntary or regulatory nutrient labeling guidelines. For example, breakfast cereals, dairy alternatives, and health-focused beverages often include vitamin precursors like D-PANTOTHENYL ALCOHOL to deliver a broader spectrum of B vitamins. This aligns with broader trends in food fortification that seek to address common dietary gaps through added micronutrients. Beyond food matrices, dietary supplements like tablets, capsules, and liquid mixtures may use this compound to deliver targeted vitamin B5 support, particularly in formulations marketed for metabolic health or nutritional balance. Because its use extends to both conventional and specialty products, the ingredient serves a role in boosting overall nutrient density in modern food and supplement portfolios.

Safety & Regulations

FDA

  • Notes: Specific FDA food additive approval or GRAS listing for this ingredient is not confirmed from available evidence.

EFSA

  • Notes: No explicit EFSA additive authorization or ADI information was found.

JECFA

  • Notes: JECFA evaluation for a numeric ADI specific to this ingredient was not identified.

Sources

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