| HS Code | 548387 |
| Chemical Name | Sodium Hydroxide |
| Chemical Formula | NaOH |
| Molecular Weight | 40.00 g/mol |
| Cas Number | 1310-73-2 |
| Appearance | White odorless pellets |
| Purity | ≥99.0% (cosmetic grade) |
| Ph 1 Aqueous Solution | ~13.5 |
| Solubility In Water | 1090 g/L at 20°C |
| Melting Point | 318 °C |
| Boiling Point | 1388 °C |
| Density | 2.13 g/cm³ at 25 °C |
| Odor | Odorless |
| Grade | Cosmetic grade |
| Storage | Keep in tightly closed container, dry, cool area |
| Safety | Corrosive; causes severe skin burns and eye damage |
As an accredited Cosmetic Grade Sodium Hydroxide (NaOH) Pellets factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in 25 kg net double polyethylene-lined woven polypropylene bags, sealed to protect cosmetic-grade NaOH pellets from moisture and contamination. |
| Container Loading (20′ FCL) | 20′ FCL: 20-foot container loaded with 25kg sealed bags of cosmetic-grade NaOH pellets, palletized, secured, and ventilated. |
| Shipping | Cosmetic Grade Sodium Hydroxide Pellets ship in sealed, corrosion-resistant containers with hazard labeling. Due to their caustic nature, ground transport only, avoiding moisture and extreme heat. Quantities require UN-approved packaging and documented safety data. Signature upon delivery ensures compliance with hazardous material regulations for safe handling. |
| Storage | Store in a tightly sealed, corrosion-resistant container in a cool, dry, well-ventilated area. Protect from moisture and humidity, as NaOH pellets are hygroscopic. Keep away from acids, metals, and incompatible chemicals. Ensure the area is clearly labeled and inaccessible to children or pets. Use appropriate PPE when handling. |
| Shelf Life | Shelf life: 2 years when stored tightly sealed in a cool, dry place; prolonged exposure to air degrades purity. |
Across cold-process saponification lines converting coconut, olive, palm, and shea oil blends into solid cleansing bars, sodium hydroxide pellets are dissolved in reverse-osmosis water to a lye concentration of 28%–38% w/w. The raw material addition ratio is not a fixed percentage of total batch mass but is calculated from the ISO 3657:2020 saponification value of each lipid and the specified superfat percentage. In a 100 kg fat phase composed of 40 kg Cocos nucifera oil, 35 kg Elaeis guineensis oil, and 25 kg Olea europaea oil at 5% superfat, the required NaOH pellet mass is 40×0.181×0.95 + 35×0.142×0.95 + 25×0.135×0.95 = 14.8 kg, equivalent to 14.8% of the fat phase. The downstream production process begins with NaOH pellet dissolution in a jacketed 316L stainless steel vessel; the exotherm raises solution temperature to 80–90°C, and the lye is cooled to 38–49°C before dosing into the oil phase under scraped-wall agitation at 60–80 rpm. False trace occurs when lye temperature exceeds 49°C or when shea butter-rich phases are mixed below 30°C, generating air-entrained emulsion that cannot degas during molding. After reaching trace, the batch is poured into slab or cavity molds and held under insulation at 30–45°C for 18–48 h to complete gel phase; insufficient gel temperature causes soda ash efflorescence at the bar surface through atmospheric CO₂ reaction with residual free alkali. Compliance for this operation is anchored to ISO 22716:2007 cosmetic GMP, EU Regulation (EC) No 1223/2009 for finished cosmetic goods, and 21 CFR 701.20 for ingredient labeling when the soap carries cosmetic claims. The table below provides saponification inputs for four common cosmetic soap feedstocks.
| Lipid feedstock | ISO 3657:2020 saponification value (mg KOH/g) | NaOH equivalent (g NaOH/g oil) | NaOH mass per 10 kg oil at 5% superfat (kg) |
|---|---|---|---|
| Cocos nucifera oil | 254 | 0.181 | 1.72 |
| Elaeis guineensis oil | 200 | 0.142 | 1.35 |
| Olea europaea oil | 190 | 0.135 | 1.28 |
| Butyrospermum parkii butter | 180 | 0.128 | 1.22 |
Inside continuous saponification reactors or jacketed crutchers, industrial soap noodle production using cosmetic grade NaOH pellets operates with NaOH introduced as a 40–50% w/w aqueous solution into pre-heated fats and oils at 80–100°C. The formulation addition ratio is calculated from the ISO 3657:2020 saponification value of the fat phase plus a deliberate excess of 0.5–1.5% over stoichiometric, leaving free alkali in the finished soap at 0.02–0.10% Na₂O to prevent fatty acid specks. In crutcher batches of 10,000–30,000 kg, open steam injection brings the soap mass toward 95°C; lye addition is slowed when the batch temperature passes 90°C to prevent foam-over caused by rapid steam liberation in the headspace. The downstream process includes drying the saponified mass to moisture 11–14%, passing the dried soap through simplex mills, and extruding it through vacuum plodders with cone length-to-diameter ratio 1.8:1–2.2:1. Barrel temperature is maintained at 35–45°C and die head temperature at 40–48°C; residual moisture above 14% causes wall slip in the plodder barrel and die-temperature instability below 30°C, leading to rough extrusion and surface lamination defects. Compliance standards for this manufacturing route include ISO 22716:2007, the USP Sodium Hydroxide monograph for chloride and carbonate limits, and Ph. Eur. monograph 0677 for cosmetic raw material acceptance. Terminal finished product types include soap noodles supplied to downstream bar finishing lines, extruded and stamped toilet bars, and glycerin-retained translucent soap bars where alkaline content is adjusted to target clarity.
In lye-based hair relaxer manufacture, NaOH pellets function as the primary alkali active in oil-in-water cream systems; the formulation addition ratio for ready-to-use straightener creams is controlled at 1.8–2.0% w/w active NaOH, staying below the EU Regulation (EC) No 1223/2009 Annex III entry 15a limit of 2.0% w/w for hair straightener preparations. This finished product category also triggers 21 CFR 740.10(b) alkali warning labeling, which requires the statement “Contains alkali. Avoid contact with eyes. Can cause blindness. Keep out of reach of children” on the primary container. In production, the pellets are dissolved in deionized water to a 25–35% NaOH solution and cooled to 25–30°C before introduction into the water phase. A 316L vacuum homogenizer receives the oil phase—petrolatum, mineral oil, cetearyl alcohol, and emulsifying wax—heated to 70–75°C; the water phase containing NaOH is combined with the oil phase at 45–50°C, followed by high-shear dispersion at 1,500–3,000 rpm for 10–15 minutes. NaOH addition while the emulsion is above 50°C saponifies ester-linked fatty emulsifiers and produces visible oil separation during cooling. The final cream is adjusted with cetyl alcohol or PEG-75 lanolin to a Brookfield RVT T-D spindle viscosity of 80,000–160,000 cP at 2.5 rpm and 25°C. Finished pH is typically 12.8–13.0. Terminal finished product types include jarred lye hair relaxer creams, tube-pack consumer and professional hair relaxer formulations, and salon backbar straightening creams.
NaOH pellets are incorporated into cuticle remover gels and liquids at a formulation addition ratio of 2.0–5.0% w/w ready-to-use preparation, constrained by EU Regulation (EC) No 1223/2009 Annex III entry 15a for nail cuticle solvents. A 316L stainless steel vessel is charged with deionized water at 20–25°C; NaOH pellets are added in 5–10 kg increments under propeller agitation at 60–90 rpm, and the exotherm is controlled to remain below 40°C before hydroxyethylcellulose is dispersed. The production sequence is critical: NaOH added after the thickener causes localized alkaline hydrolysis of the cellulose backbone, producing irreversible viscosity loss and stringy rheology. A representative cuticle remover formula contains 3.0% NaOH, 5% glycerin, 1.5% hydroxyethylcellulose, and 0.1% tetrasodium EDTA; final pH is 12.5–13.5 measured according to ISO 4316:1977. The batch is mixed under a cold water jacket to offset hydration exotherm, and viscosity is checked with a Brookfield RVT Helipath using a T-bar spindle at 2.5 rpm, with a typical target of 12,000–35,000 cP. Industry compliance standards include ISO 22716:2007 cosmetic GMP and 21 CFR 701.20 ingredient labeling requirements for nail care cosmetics. Terminal finished product types include roll-on cuticle remover gel, brush-applied cuticle softener liquid, and professional salon callus softening preparations.
When stearate-based emulsifier synthesis uses NaOH pellets as the neutralizer for stearic acid, palmitic acid, and C16–C18 fatty acid blends, the reaction is performed in glass-lined or 316L stainless steel jacketed reactors heated to 75–85°C under nitrogen sparging. The formulation addition ratio is stoichiometric at 1.00 mol NaOH per 0.98–1.00 mol fatty acid to form in-situ sodium stearate/palmitate emulsifier; in final oil-in-water cream batches containing 5–8% stearic acid, this corresponds to a NaOH pellet mass fraction of 2.0–3.5% of total formula when pre-neutralization is used. The pellets are dissolved to a 10–20% w/w aqueous solution and dosed over 30–60 minutes to prevent localized over-neutralization that creates insoluble sodium carbonate or over-saponified gel domains. Reactor agitation is maintained at 50–80 rpm; endpoint is confirmed when the acid value drops below 2 mg KOH/g and a 10% dilution reaches pH 8.0–9.5. The neutralized soap phase is then transferred to a separate oil-in-water emulsion vessel and combined with deionized water, humectants, and nonionic emulsifiers at 70–75°C, followed by high-shear dispersion at 1,500–3,000 rpm for 10–20 minutes. Compliance standards for this reactive intermediate production include ISO 22716:2007, the USP Sodium Hydroxide monograph for chloride and sulfate limits, and EU Regulation (EC) No 1223/2009 for finished cosmetic goods. Terminal finished product types include vanishing cream bases, o/w lotion concentrates, and cold cream substitutes based on sodium stearate emulsifier systems.
Depilatory cream bases formulated with potassium thioglycolate or calcium thioglycolate hydrate use NaOH pellets only as a secondary pH adjuster, with a formulation addition ratio of 0.2–1.2% w/w NaOH in the finished cream, delivered as a 5–10% aqueous solution after the thioglycolate active has been dispersed at 35–40°C in the emulsion. The target ready-to-use pH is 12.5–12.7, positioned within the EU Regulation (EC) No 1223/2009 Annex III entry 2a allowance for thioglycolic acid and its salts, where consumer preparations must not exceed pH 12.7. Production vessels are 316L steel vacuum mixers; sodium hydroxide pellets are dissolved in the water phase prior to emulsion formation but only after the thickener and chelating agents are fully hydrated. If NaOH is introduced before the thioglycolate salt, the local pH spike accelerates air oxidation of thioglycolate to dithiodiglycolic acid and reduces depilatory efficacy; if the final pH falls below 12.5, hair-keratin reduction slows and contact time becomes insufficient. Homogenization is performed at 35–40°C with anchor stirrer at 20–30 rpm and vacuum at 0.6–0.8 bar to minimize oxygen ingress. Viscosity after NaOH addition is adjusted to 15,000–30,000 cP at 25°C. Compliance standards include ISO 22716:2007 and FDA cosmetic labeling requirements for hair removal products under 21 CFR 701.20. Terminal finished product types include leg and body depilatory creams, sensitive-skin depilatory lotions, and professional backstage hair removal creams.
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Cosmetic Grade Sodium Hydroxide (NaOH) Pellets, product designation CG-NaOH-P990, are white anhydrous spheroidal pellets with a molecular weight of 40.00 g/mol, CAS 1310-73-2, and EC 215-185-5. The material is specified for saponification, pH adjustment, and neutralization in rinse-off and leave-on cosmetic manufacturing where residual carbonate, chloride, iron, mercury, and nickel must be controlled below general industrial limits. Release specifications are aligned with the USP-NF Sodium Hydroxide monograph for total alkali and sodium carbonate, but the procurement profile adds lower trace-metal ceilings relevant to dermal exposure. The manufacturing site is certified to ISO 9001:2015 and operates according to ISO 22716:2007 cosmetic GMP guidance. The product is supplied in 25 kg HDPE-lined fibre drums, and each drum carries a lot number and certificate of analysis. Table 1 lists the representative certificate-of-analysis profile.
| Parameter | Limit | Determination basis |
|---|---|---|
| Total alkali, as NaOH | 99.0–100.5% w/w | Acid-base titration per USP-NF Sodium Hydroxide monograph |
| Sodium carbonate | ≤0.5% w/w | Double-indicator alkalinity titration or barium chloride precipitation |
| Chloride, as NaCl | ≤50 ppm | Turbidimetric chloride determination or ion chromatography |
| Iron | ≤10 ppm | ICP-OES after acid digestion |
| Mercury | ≤0.1 ppm | Cold-vapour AAS |
| Nickel | ≤5 ppm | ICP-MS after acid digestion |
| Water-insoluble matter | ≤0.005% w/w | Gravimetric after aqueous dissolution and filtration |
| Bulk density | 0.90–1.10 kg/L | Untapped bulk density, graduated cylinder |
The total alkali minimum of 99.0% w/w is intentionally above the USP-NF lower acceptance threshold of 95.0% w/w. Residual sodium carbonate does not contribute to saponification and generates carbon dioxide during acid neutralization. In high-shear mixers operating at 3,000–6,000 rpm, carbon dioxide release can produce micro-foam in emulsion phases. Sodium carbonate also consumes two equivalents of mineral acid per mole and can create an apparent pH plateau between 10.3 and 6.4 because the carbonate/bicarbonate buffer system spans these pKa values.
Cold-process saponification demand is fixed by the saponification value of the oil phase. For a vegetable oil blend with SV 190 mg KOH/g, the stoichiometric NaOH requirement is 135.5 g/kg oil; this is derived from 190 × 40.00 / 56.11. If a technical-grade pellet containing 1.5% w/w sodium carbonate is used, the active NaOH fraction falls to 98.5%, and a 5.0% superfat formula effectively rises to 6.4% when the same nominal mass is dispensed. The carbonate limit of ≤0.5% w/w in CG-NaOH-P990 therefore preserves stoichiometric control in small cold-process batches where the lye phase is prepared as a 30–50% w/w solution.
Dissolution of pellets must be performed by adding NaOH to well-mixed purified water, not water to pellets; the integral heat of solution at infinite dilution is -44.5 kJ/mol, and localized boiling can occur when the solution strength exceeds 50% w/w. During lye preparation, atmospheric carbon dioxide is absorbed at the air-liquid interface above pH 10, forming sodium carbonate. Production-scale lye tanks with nitrogen blanketing or closed transfer piping show less carbonate drift than open tanks; published data for this specific configuration are limited. Residual carbonate above 0.8% w/w has been associated with haze in translucent cold-process bars after 72 h cure at 25°C and 50–60% RH. The haze mechanism is consistent with sodium carbonate crystallization, but quantitative failure rates on manufacturing lines are not uniformly reported. In a jacketed 25 kg pilot mixer, the oil phase is held at 40–50°C and the lye phase at 20–25°C; the two phases are combined under 1,500 rpm high-shear dispersion until trace is reached.
In soap noodle and syndet bar production, sodium hydroxide is often metered as a 32–50% w/w solution into a scraped-surface heat exchanger or continuous saponification reactor. The reactor temperature is maintained at 80–95°C; in plug-flow configurations, complete saponification is typically reached within 10–20 min. The lower carbonate specification matters because neutralization of free fatty acids in syndet bars with carbonate-containing NaOH generates CO₂ that can produce pinholes in extruded billets. Vacuum plodders operating at -0.08 to -0.09 MPa remove air but cannot remove dissolved carbonate gas if it forms after the vacuum port.
Technical diaphragm-grade and mercury-cell-grade sodium hydroxide differ from cosmetic-grade material primarily in chloride, iron, mercury, and nickel. Technical grades can contain chloride up to 500 ppm and iron up to 50 ppm, and mercury-cell grades may retain mercury at levels above the cosmetic procurement ceiling. CG-NaOH-P990 is sourced from membrane-cell feedstocks or equivalent low-mercury technology; mercury is capped at ≤0.1 ppm, nickel at ≤5 ppm, and iron at ≤10 ppm. The chloride ceiling is ≤50 ppm because chloride contributes to pitting corrosion of unlined 316L stainless steel at pH above 10 and temperatures above 60°C. Iron and nickel are limited because transition metals can catalyze oxidative degradation of unsaturated lipids and fragrance compounds in emulsion bases. Table 2 compares representative procurement limits for CG-NaOH-P990 with technical-grade ranges where published specifications exist.
| Parameter | Cosmetic Grade CG-NaOH-P990 | Technical Diaphragm/Mercury Grade |
|---|---|---|
| Total alkali, as NaOH | 99.0–100.5% w/w | 98.0–99.0% w/w |
| Sodium carbonate | ≤0.5% w/w | 0.5–2.0% w/w |
| Chloride, as NaCl | ≤50 ppm | 100–500 ppm |
| Iron | ≤10 ppm | 10–50 ppm |
| Mercury | ≤0.1 ppm | 0.1–1.0 ppm for mercury-cell material; membrane-cell material is lower |
| Nickel | ≤5 ppm | Not routinely controlled |
Ranges for technical grade are representative; plant configuration and cell technology cause variation. The term “cosmetic grade” is not harmonized under a single global monograph; it is a procurement specification, not a pharmacopoeial compendial grade. Buyers should specify total alkali, carbonate, mercury, nickel, and chloride in the purchase order because otherwise no uniform standard applies. These impurity differences are most visible in acid-neutralization and emulsion-stability testing. Carbonate content influences the volume of acid required to reach a target pH and the amount of gas liberated; chloride and iron can alter corrosion and oxidation behavior. A procurement specification alone does not guarantee performance in a specific formulation, so the incoming lot should be evaluated by acid-base titration and, where necessary, elemental impurity analysis.
Addition of sodium hydroxide for final pH adjustment in oil-in-water emulsions is performed as a 10% w/w aqueous solution at a dosing rate of 0.05–0.10 pH unit/min in 500 kg production vessels. The rate limit exists because the hydroxide feed must be diluted and injected below the liquid surface; localized pH above 7.5 can deprotonate carbomer acid groups and reduce viscosity. A carbomer dispersion thickened to 12,000–18,000 mPa·s at pH 6.0 (Brookfield RV, spindle 6, 20 rpm, 25°C) can lose structure at the point of addition when concentrated NaOH is applied without sufficient mixing. Quantitative viscosity-loss data at production scale is limited, but the rheological mechanism is consistent with microgel deswelling and charge neutralization.
The target final pH for most leave-on emulsions is 5.5–6.5; at pH 6.0, the free hydroxide ion concentration is 10⁻⁸ mol/L, so the material does not persist as free caustic in the finished formula. Sodium hydroxide is not unrestricted for all cosmetic product categories under Regulation (EC) No 1223/2009; the formulator must verify the current Annex III entry for sodium hydroxide and document the final pH and residual alkali content in the Cosmetic Product Safety Report. For high-pH depilatory or hair-relaxing products, the use concentration is product-specific and must be evaluated by a qualified safety assessor.
Sodium hydroxide pellets are deliquescent. At 25°C and 60% RH, surface moisture uptake begins; above 70% RH, open-container mass gain exceeding 1.0% within 24 h is typical because the pellets form a NaOH·H₂O surface film. Packaging therefore consists of heat-sealed polyethylene liners inside 25 kg HDPE fibre drums. Storage areas should maintain low humidity and should avoid floor-level moisture. For bulk storage in carbon steel or lined steel silos, dry air purge with a dew point below -40°C is required to prevent surface wetting. Stainless steel 316L is preferred for continuous solution tanks at concentrations above 25% w/w and temperatures above 50°C; carbon steel is acceptable below 50°C with stress-relief post-weld treatment because caustic stress corrosion cracking can occur in carbon steel at elevated temperatures.
A 50% w/w NaOH stock solution has a crystallization point near 12°C; transfer lines and storage tanks for this solution require heat tracing or dilution to 25–30% w/w in unheated warehouses. The material is incompatible with aluminum, zinc, tin, and their alloys; contact with aluminum generates hydrogen according to 2Al + 2NaOH + 6H₂O → 2Na[Al(OH)₄] + 3H₂. In confined hoppers or transfer chutes, hydrogen accumulation is a safety hazard. Acidic materials must be stored separately. Occupational exposure is controlled to the ACGIH TLV-C of 2 mg/m³ for sodium hydroxide aerosol. The material is classified as Skin Corr. 1A, H314 and Eye Dam. 1, H318 under CLP. When preparing stock solutions, purified water with low carbonate hardness should be used; hard water with 250 mg/L CaCO₃ total hardness can precipitate calcium carbonate upon alkalization. The recommended re-test interval for unopened drums is 12 months; drums stored above 30°C or in humid environments should be sampled at 6-month intervals for total alkali and carbonate drift. Safety data sheets must be consulted before first use.