Ceramide NP

Product Specifications

Chemical NameN-[(2S,3S,4R)-1,3,4-trihydroxyoctadecan-2-yl]octadecanamide / N-Stearoyl Phytosphingosine / Ceramide NP (Ceramide 3 / 神经酰胺 NP / 神经酰胺 3)
SourceNon-GMO precision bio-fermentation (Wickerhamomyces ciferrii / Pichia ciferrii yeast) generating human-identical phytosphingosine, followed by green chemical acylation with vegetable stearic acid
SpecificationHigh-Purity Cosmetic Grade: Ceramide NP ≥ 95.00% (HPLC on anhydrous basis); Ultra-Pure Clinical & Pharma Grade: Ceramide NP ≥ 98.00% and ≥ 99.00% (HPLC; high-melting crystalline white powder); Pre-Dispersed Nano-Liposomal Liquid Grade: Ceramide NP 1.00%, 2.50%, and ≥ 5.00% (Encapsulated with hydrogenated lecithin and cholesterol for direct cold-process aqueous addition); Physiological Barrier Triad Complexes: Formulated complexes combining Ceramide NP + Ceramide AP + Ceramide EOP + Phytosphingosine + Cholesterol in a 3:1:1:1 biomimetic ratio.
AppearancePure Crystalline Grades (≥95%–99%): Fine white to off-white microcrystalline powder or flakes; Nano-Liposomal Grades (1%–5%): Translucent to milky opalescent fluid / nano-dispersion.

Master Physiological Intercellular Lipid & Benchmark Stratum Corneum Barrier Molecule produced via sustainable, non-GMO bio-fermentation using Wickerhamomyces ciferrii (Pichia ciferrii) and precision acylation with stearic acid. Standardized to high-purity crystalline powder (Ceramide NP ≥ 95.0%–99.0% by HPLC) displaying the exact human-identical (2S,3S,4R) stereochemical configuration, alongside specialized water-dispersible nano-liposomal and pre-solubilized liquid dispersions (1.0%–5.0%). It integrates into the intercellular lamellar bilayer sheets of the stratum corneum, bridging the physiological 3:1:1:1 lipid matrix alongside cholesterol and free fatty acids. Formulated to seal skin barrier micro-fissures, suppress transepidermal water loss (TEWL), buffer retinoid and acid-induced dermatitis, and restore structural hydration in atopic, eczema-prone, and post-procedure compromised skin. Serves as the premier raw material for clinical skin-barrier repair creams, post-procedure restorative recovery serums, neuro-cosmetic anti-redness emulsions, and oral nutricosmetic beauty-from-within capsules.

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Ceramide NP (Purity ≥95.0%-99.0% HPLC / Bio-Identical Yeast Fermentation / Nano-Liposomal Liquid) | Gold Standard Intercellular Lipid for Stratum Corneum Barrier Repair, TEWL Reduction & Deep Hydration

1. Product Overview & Value Proposition

Ceramide NP (N-stearoyl phytosphingosine, formerly designated as Ceramide 3 under the Motta classification system, 神经酰胺 NP / 神经酰胺 3), produced via biotechnology-driven yeast fermentation of Wickerhamomyces ciferrii (Pichia ciferrii), is globally recognized as the cornerstone physiological lipid active in clinical barrier restoration, medical dermatology, and advanced neuro-cosmetics. In healthy human epidermal physiology, ceramides constitute approximately 50% of the total lipid mass of the intercellular stratum corneum matrix (alongside 25% cholesterol and 15% free fatty acids). Within this protective architecture, Ceramide NP is quantitatively one of the most abundant and functionally vital short-chain ceramides, composed of an 18-carbon saturated stearic acid chain aminated to an endogenous phytosphingosine base exhibiting the pure, human-identical (2S,3S,4R) stereochemical conformation.

In cutaneous biophysics, the primary barrier preventing environmental xenobiotic penetration and desiccation is the intercellular lamellar lipid bilayer (organized into alternating Long Periodicity Phase [~13 nm] and Short Periodicity Phase [~6 nm] crystalline sheets). Ceramide NP intercalates between saturated fatty acid chains and cholesterol molecules, acting as a molecular rivet that transitions disordered liquid-phase lipids into dense, highly ordered orthorhombic crystalline gel phases. When epidermal ceramides are depleted—whether through chemical over-cleansing, atopic dermatitis, aging, or aggressive clinical exfoliation—the lamellar lattice collapses, triggering acute transepidermal water loss (TEWL), severe micro-fissuring, pruritus, and uninhibited allergen penetration. Topically applied bulk Ceramide NP restores this structural integrity: it reduces TEWL by up to 50% within 24 to 48 hours, accelerates epidermal junction recovery following fractional laser or chemical peel procedures, and actively buffers against the erythema, flaking, and “retinoid dermatitis” associated with synthetic Vitamin A therapy. We provide distinct commercial grades tailored to various cosmetic manufacturing processes:

  • Ultra-Pure Crystalline Powder (≥ 95.0%, 98.0% & 99.0% HPLC): High-melting, solvent-free bio-identical crystalline powder engineered for traditional high-temperature emulsion compounding, medical-grade barrier repair ointments, and intensive anhydrous barrier balms.
  • Cold-Water-Dispersible (CWD) Nano-Liposomal & Liquid Dispersions (1.0%–5.0%): Pre-solubilized, high-pressure homogenized nano-emulsions utilizing hydrogenated lecithin and vegetable phytosterols. Bypasses the challenging 90°C melting point of raw crystals, dissolving seamlessly into cold-process formulations, clear facial essences, watery toners, and soothing hydrogel sheet masks without recrystallization or clouding.
  • Physiological Multi-Ceramide Systems: Custom co-processed lipid matrices combining Ceramide NP with Ceramide AP, Ceramide EOP, Phytosphingosine, and Free Plant Sterols in the exact 3:1:1:1 ratio necessary to replicate the human stratum corneum.
  • Clean Oral Nutricosmetic Grades: High-purity phytoceramide grades engineered for dietary supplement capsules and functional beverage drink mixes to fortify whole-body skin moisture retention from within.

As an established bulk Ceramide NP manufacturer and direct active ingredient supplier, our facilities operate precision non-GMO microbial fermentation vessels, automated chromatographic purification lines, and clean solvent crystallization systems. To empower agile skincare brands, cosmetic formulators, and contract manufacturing organizations (CMOs), we pair uncompromising analytical quality with flexible commercial terms: accessible low MOQ procurement for benchtop pilot trials, multi-ingredient shipment consolidation across our cosmetic bioactives (Bakuchiol, Ectoine, L-Ergothioneine, PDRN, Glabridin), and dedicated on-the-ground China-wide raw material sourcing assistance tailored to your exact manufacturing requirements.

2. Product Specifications (Analytical Quality)

Test Item Standard Cosmetic Grade (≥95.0%) Ultra-Pure Pharma Grade (≥98%-99%) Nano-Liposomal Liquid (2.5%-5.0%) Test Method
Chemical Identification Conforms to authentic N-stearoyl phytosphingosine reference standard retention time & FTIR spectrum FTIR / HPLC-ELSD / 1H-NMR
Ceramide NP Assay (Dry Basis) ≥ 95.00% (HPLC-ELSD) ≥ 98.00% / ≥ 99.00% (Clinical Target) 2.50% – 5.00% (Active Ceramide NP) HPLC-ELSD / HPLC-CAD
Stereochemical Configuration 100% human-identical (2S,3S,4R) configuration (Synthesized via yeast fermentation) Chiral HPLC / Specific Optical Rotation
Free Phytosphingosine Content ≤ 1.00% ≤ 0.50% ≤ 0.20% HPLC-ELSD
Free Stearic Acid Content ≤ 2.00% ≤ 1.00% Part of liposomal carrier GC-FID
Melting Point Range 100.0°C – 106.0°C 103.0°C – 108.0°C N/A (Liquid nano-emulsion) Capillary Melting Apparatus
Appearance & Color White to off-white microcrystalline powder Pure snow-white crystalline powder / flakes Translucent to milky opalescent fluid Visual / Organoleptic
Odor & Sensory Fingerprint Practically odorless; neutral, clean sensory profile; zero rancidity or amine odor Organoleptic
Aqueous Dispersion Behavior Insoluble in cold water; soluble in hot cosmetic oils/esters (>85°C-90°C) 100% dispersible in cold water (Translucent nano-emulsion; d50 ≤ 100 nm) Visual / Dynamic Light Scattering (DLS)
Particle Size 100% passing 80 mesh (Ultra-fine micronized powder) Average droplet size < 100 nm Sieve Analysis / Laser Diffraction
Loss on Drying / Moisture ≤ 2.00% ≤ 1.00% Water-based fluid carrier USP <731> (105°C) / Karl Fischer
Residue on Ignition (Ash) ≤ 0.50% ≤ 0.10% ≤ 0.50% USP <281> (600°C)
Heavy Metals (Pb) < 1.0 ppm (As < 1.0 ppm, Cd < 0.5 ppm, Hg < 0.1 ppm; Prop 65 compliant) ICP-MS
Residual Solvents (Ethanol, Heptane) ≤ 3,000 ppm Ethanol; ≤ 1,000 ppm Heptane (Complies with USP <467>) GC-HS
Microbiological Limits Total Aerobic Microbial Count ≤ 100 CFU/g; Yeast & Mold ≤ 10 CFU/g; Pathogens Absent USP/EP Standard

3. Functional Applications (Mechanism of Action)

Deploying pharmaceutical-grade Ceramide NP across clinical barrier repair creams, post-procedure recovery formulations, and sensitive-skin cosmetics provides scientifically verified cellular and biophysical actions:

  • Intercellular Lamellar Lipid Bilayer Assembly: The stratum corneum matrix is governed by alternating lamellar lipid bilayers composed of ceramides, cholesterol, and free fatty acids. Ceramide NP’s linear 18-carbon saturated stearic acyl tail tightly packs alongside adjacent lipid chains, while its multi-hydroxyl phytosphingosine polar headgroup engages in extensive hydrogen bonding with adjacent lipid headgroups. This drives the transition of disordered liquid lipids into a highly impermeable orthorhombic crystalline lattice, sealing epidermal micro-fissures and fortifying structural barrier integrity.
  • Suppression of Transepidermal Water Loss (TEWL): Clinical evaporimeter assessments prove that topical application of Ceramide NP rapidly reduces TEWL by 30% to 50% in compromised or chemically stripped skin within 24 to 48 hours. By restoring the hydrophobic moisture-retention barrier, it traps water molecules within the deep stratum corneum, preventing dehydration, flaking, and winter xerosis.
  • Buffering Against Retinoid & Exfoliating Acid Dermatitis: High-potency active ingredients (such as all-trans-retinol, retinaldehyde, and glycolic/salicylic acids) notoriously dissolve intercellular lipids, triggering barrier breakdown, stinging, and redness. Co-formulating with Ceramide NP replenishes depleted lipid reserves in real time, neutralizing retinization irritation and enabling higher consumer tolerance to clinical resurfacing regimens.
  • Downregulation of Keratinocyte Inflammatory Cytokines: Disruptions in the skin barrier provoke keratinocytes to release pro-inflammatory cytokines, specifically Interleukin-1 alpha (IL-1α), Tumor Necrosis Factor-alpha (TNF-α), and Interleukin-8 (IL-8). By rapidly resealing the physical barrier, Ceramide NP dampens the mechanical trigger for cytokine synthesis, calming chronic skin erythema, rosacea-prone flushing, and neuro-sensitive skin reactivity.
  • Restoration of Eczema & Atopic Dermatitis Phenotypes: In atopic skin, endogenous sphingomyelinase and β-glucocerebrosidase enzyme activity is deficient, resulting in severe ceramide depletion (especially Ceramide NP and EOS). Exogenous supplementation of bio-identical Ceramide NP normalizes stratum corneum lipid ratios, restores antimicrobial barrier defenses against Staphylococcus aureus colonization, and reduces reliance on topical corticosteroids.
  • Moisture Sealing in Clean Nutricosmetic Beverage Formulations: When formatted as an oral nutricosmetic powder (or paired with dietary glucosylceramides), ceramides are absorbed in the small intestine, repackaged into circulating chylomicrons, and transported to the basal layer of the epidermis, reinforcing systemic skin barrier hydration from the inside out.

4. Formulation Combinations & Trending Market Applications

Capitalize on the expanding clinical skin-barrier repair, dermatological recovery, and clean-beauty markets by formulating with our versatile Ceramide NP portfolio:

  • The Master Clinical “3:1:1:1 Biomimetic Barrier Triad” Cream: Our Ceramide NP (≥98%, 0.2%–0.5% or 5% Nano-Liquid, 4.0%–6.0%) + Ceramide AP (0.1%) + Ceramide EOP (0.05%) + Plant-Derived Cholesterol (≥95%, 0.2%) + Free Fatty Acids (Palmitic/Stearic Acid, 0.2%) + Phytosphingosine (≥95%, 0.05%). The globally recognized gold-standard physiological matrix: precisely replicates the human stratum corneum’s natural 3:1:1:1 molar ratio, providing rapid lamellar reconstruction in eczema, atopic dermatitis, and barrier-stripped skin.
  • The “Retinoid-Buffer & Barrier Rescue” Night Emulsion: Our Ceramide NP (≥95%, 0.2%) + Bakuchiol (≥99.0%, 1.0%) + Ectoine (≥99.0%, 1.5%) + Plant-Derived Squalane (5.0%–8.0%) + Niacinamide (≥99.5%, 3.0%). A high-performance rejuvenating formula: Bakuchiol stimulates collagen turnover, while Ceramide NP and Ectoine form a protective lipid-hydration shield that prevents erythema, flaking, and retinoid irritation.
  • The “Post-Laser & Aesthetic Procedure” Soothing Fluid: Our Pre-Dispersed Nano-Liposomal Ceramide NP (5% Active, 4.0%) + PDRN (Sodium DNA ≥98%, 0.2%) + Madecassoside 95% (0.2%) + D-Panthenol (Vitamin B5, 2.0%) + Sodium Hyaluronate (Multi-Molecular Weight, 0.5%). A high-tolerance, cold-process barrier elixir designed for fragile, sensitized, post-laser, or post-microneedling recovery to seal moisture, clear post-inflammatory erythema, and accelerate tissue re-epithelialization.
  • The Oral Nutricosmetic “Internal Ceramide Glow” Sachet: Our Dietary Ceramide Powder (0.5%–1.0% active ceramides, 100 mg) + Hydrolyzed Marine Collagen Peptides (3,000–5,000 mg) + Sodium Hyaluronate (Food Grade, 100 mg) + Natural Astaxanthin Powder 2% (200 mg delivering 4 mg active astaxanthin) + Vitamin C (100 mg). A targeted beauty-from-within drink packet designed to fortify systemic epidermal lipid bilayers, increase whole-body skin hydration, and shield against UV-induced collagen degradation.

5. Why Choose Us As Your Long-Term Active Ingredient Partner?

  • Flexible Low MOQ Policy: Mitigate product launch risk. As an agile low MOQ Ceramide NP bulk supplier, our orders start as low as 100 g for ultra-pure pharma crystalline grades (≥98%–99%), 500 g for standard cosmetic powder (≥95%), and 1 kg for cold-water-dispersible nano-liposomal liquids (1%–5%), scaling smoothly up to recurring multi-ton commercial manufacturing contracts.
  • 100% Bio-Identical Yeast Fermentation: Sourced strictly from non-GMO *Wickerhamomyces ciferrii* microbial fermentation, guaranteeing the precise human-identical (2S,3S,4R) stereochemical configuration. We certify complete absence of animal-derived tissues (BSE/TSE-free) and eliminate synthetic racemic isomers that lack physiological lamellar packing efficiency.
  • Multi-Product Portfolio Consolidation: Streamline your supply chain by sourcing your complete barrier repair and anti-aging active suite (Ceramide NP, Bakuchiol, Ectoine, L-Ergothioneine, PDRN, Glabridin, Ferulic Acid, Sodium Hyaluronate), longevity vitamins (L-5-MTHF-Ca, β-NMN), and botanical extracts under a single, cost-effective freight shipment to reduce customs overhead and landed freight costs.
  • Value-Added China Sourcing Service: In addition to our dedicated fermentation suites, liposomal nano-homogenization facilities, and vacuum crystallization lines, our on-the-ground technical team audits upstream raw material feedstocks, validates HPLC-ELSD purity testing paperwork, and procures specialized functional ingredients across China tailored to your exact manufacturing roadmap.

6. Quality & Supply Chain Assurance

  • Precision Microbial Fermentation & Synthetic Stereospecificity: Raw phytosphingosine is biosynthesized via closed-loop, automated fermentation of non-GMO *W. ciferrii*, followed by clean chemical acylation with vegetable stearic acid. This guarantees a chemically defined, single-substance Ceramide NP molecule displaying exact stereospecificity, free from petroleum-derived contaminants or animal pathogens.
  • Advanced Nano-Liposome Emulsification Technology: Raw crystalline Ceramide NP possesses a high melting point (~105°C), making it prone to recrystallization into gritty particles if cooled improperly in conventional emulsions. Our pre-solubilized nano-liposomal grades disperse crystalline ceramide into sub-100-nanometer droplets stabilized by hydrogenated lecithin and cholesterol, enabling room-temperature addition and crystal-free shelf stability.
  • Validated HPLC-ELSD Analytical Monograph: Because ceramides lack strong UV chromophores, standard UV detection can produce erratic readings. We test every commercial batch via High-Performance Liquid Chromatography coupled with Evaporative Light Scattering Detection (HPLC-ELSD) or Charged Aerosol Detection (HPLC-CAD), ensuring exact active quantification and strict limitation of free fatty acids and residual sphingoids.
  • Formulation Compatibility & Physical Stability: Our crystalline and nano-liposomal grades maintain chemical stability across broad cosmetic pH ranges (pH 4.0 to 7.5). They withstand standard cosmetic shear and homogenization pressures, resisting oxidative cleavage and discoloration over extended accelerated shelf-life cycles.
  • Comprehensive ICP-MS & Heavy Metal Screening: Batch-tested via high-resolution ICP-MS to ensure heavy metals (Lead, Arsenic, Cadmium, Mercury) strictly comply with California Prop 65, European Cosmetic Regulation (EC) No 1223/2009, and China Safety and Technical Standards for Cosmetics. Sealed in food/pharma-grade double-polyethylene liners within light-proof, nitrogen-flushed aluminum bottles (100 g, 1 kg) and heavy-duty 25 kg fiber export drums.

7. FAQ

Q1: What is the functional and chemical difference between Ceramide NP (Ceramide 3) and other ceramides like Ceramide AP, EOP, and NS?
A1: Ceramides are categorized by their specific combination of sphingoid base and fatty acid chain:

  • Ceramide NP (Ceramide 3): Composed of a Phytosphingosine (P) base bonded to a Normal saturated fatty acid (N) (stearic acid). It constitutes the foundational structural backbone of stratum corneum lamellae, specifically responsible for packing lipids into crystalline gel phases and preventing moisture evaporation.
  • Ceramide AP (Ceramide 6 II): Composed of Phytosphingosine (P) and an α-hydroxy fatty acid (A). It supports natural cellular desquamation and epidermal smooth-cell turnover.
  • Ceramide EOP (Ceramide 1): An ultra-long-chain esterified ω-hydroxy fatty acid linked to Phytosphingosine. It acts as the molecular “tie-chain” that rivets adjacent lamellar bilayers together.
  • Ceramide NS (Ceramide 2): Composed of a Sphingosine (S) base and Normal fatty acid (N). It delivers rapid surface emollience. While single ceramides provide benefits, pairing Ceramide NP with AP and EOP provides complete biomimetic barrier repair.

Q2: Why is bio-identical yeast-fermented Ceramide NP superior to synthetic racemic or bovine ceramides?
A2: Human skin naturally produces ceramides exclusively in the (2S,3S,4R) stereochemical configuration. Non-GMO yeast fermentation (*Wickerhamomyces ciferrii*) synthesizes phytosphingosine with this exact optical stereospecificity, allowing it to seamlessly fit into the human stratum corneum’s lamellar lipid lattice. Synthetic chemical synthesis often produces racemic mixtures (mixtures of D- and L-enantiomers) that cannot pack efficiently into lamellar bilayers, reducing barrier repair potency. Animal-derived ceramides carry substantial risks of viral contamination, BSE/TSE, and consumer regulatory rejection.

Q3: How do cosmetic formulators overcome the high melting point and recrystallization challenges of raw Ceramide NP?
A3: Pure Ceramide NP crystals melt between 102°C and 108°C and are insoluble in water, making them notoriously prone to “crashing out” or forming gritty sand-like crystals in creams if cooled improperly. Formulators successfully incorporate Ceramide NP using three proven techniques:

  • High-Temperature Oil Phase Solubilization: Heat the oil phase to 85°C–90°C in the presence of polar cosmetic emollients (such as isostearyl alcohol, octyldodecanol, or C12-15 alkyl benzoate) and high-HLB emulsifiers (like polyglyceryl esters or hydrogenated lecithin) to melt and solubilize crystals before emulsification.
  • The 3:1:1:1 Co-Melting Technique: Pre-blend Ceramide NP with cholesterol and stearic acid; this physiological mixture depresses the individual melting points, facilitating smooth lamellar liquid crystal formation at lower temperatures (~75°C–80°C).
  • Utilizing Pre-Dispersed Nano-Liposomal Liquids: Utilize our 1.0%–5.0% nano-liposomal liquid dispersions, which can be added directly into the water phase or during the cool-down phase (<45°C) without heating, high shear, or recrystallization risks.

Q4: What is the clinically supported usage percentage of Ceramide NP in skincare products?
A4: Formulating percentages vary by delivery format and target clinical claim:

  • Daily Barrier Hydration Creams & Lotions: 0.05% to 0.2% of pure Ceramide NP crystalline powder (delivers measurable reductions in TEWL and restores hydration).
  • Intensive Clinical Repair Balms & Eczema Treatments: 0.2% to 0.5% of pure crystalline powder (or 4.0%–10.0% of our pre-dispersed nano-liposomal liquid).
  • Aqueous Toners, Clear Essences & Sheet Masks: 1.0% to 3.0% of our pre-solubilized nano-liposomal liquid (yielding a stable, non-cloudy, transparent essence).
  • Retinoid & Acid Buffering Serums: 0.1% to 0.3% of pure powder co-formulated with 1.0% Bakuchiol or Ectoine.

Q5: What is the MOQ for bulk Ceramide NP orders?
A5: We support agile product commercialization with flexible minimum order quantities starting from just 100 g for ultra-pure pharma crystals (≥98%–99%), 500 g for standard cosmetic grade (≥95%), and 1 kg for cold-water-dispersible nano-liposomal liquids (1%–5%), scaling smoothly up to recurring multi-ton commercial manufacturing contracts.

8. References

  1. PubChem: N-Stearoylphytosphingosine (Ceramide NP) Compound Summary (CID 5702602) – National Center for Biotechnology Information.
  2. PubMed Central: The Role of Ceramides in Skin Barrier Function, Atopic Dermatitis, and Transepidermal Water Loss: A Review of Biochemical Mechanisms and Clinical Replacement Therapies – National Institutes of Health research database.

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