| HS Code | 771724 |
| Chemical Name | n-Propanol |
| Molecular Formula | C3H8O |
| Cas Number | 71-23-8 |
| Molecular Weight | 60.10 g/mol |
| Purity | 99.5% |
| Appearance | Clear colorless liquid |
| Odor | Mild alcohol-like odor |
| Density | 0.804 g/cm3 at 20°C |
| Boiling Point | 97.1 °C |
| Melting Point | -127 °C |
| Flash Point | 23 °C (closed cup) |
| Autoignition Temperature | 412 °C |
| Vapor Pressure | 21.4 mmHg at 25°C |
| Solubility In Water | Miscible |
| Refractive Index | 1.384 at 20°C |
As an accredited N-Propanol 99.5% factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | N-Propanol 99.5% supplied in 1 L amber glass bottle with tamper-evident cap, clear hazard labeling, and chemical-resistant packaging. |
| Container Loading (20′ FCL) | 20′ FCL loaded with 80 palletized 200L drums of N-Propanol 99.5%, securely lashing and bracing for safe transport. |
| Shipping | N-Propanol 99.5% ships as a flammable liquid under UN1277, Class 3, Packing Group II. Use approved drums, IBCs, or containers with proper grounding. Affix flammable hazard labels and keep away from heat, sparks, and oxidizers. Ensure declarations and documentation meet applicable transport regulations. |
| Storage | Store N-Propanol 99.5% in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Keep containers tightly closed and upright, clearly labeled. Segregate from strong oxidizers and acids. Use approved flammable-liquid storage cabinets, grounded containers, and secondary spill containment. Ensure eyewash and fire extinguishing equipment are readily accessible nearby. |
| Shelf Life | Store tightly sealed, away from heat and ignition. Shelf life is typically 3 years from manufacture if unopened and properly stored. |
In solvent-borne flexographic surface printing on corona-treated biaxially oriented polypropylene and high-density polyethylene films, n-propanol 99.5% functions as a medium-volatility oxygenated co-solvent that maintains solubility of polyamide and nitrocellulose resins during high-speed ink circulation. A typical central-impression press formulation allocates 5–20 wt% n-propanol within a multi-solvent blend that also contains ethyl acetate and n-propyl acetate; percentages are adjusted to maintain 18–25 s Zahn cup #2 at 25 °C and to match the evaporation load of ceramic anilox rolls specified at 3.5–8.0 BCM and line speeds of 180–300 m/min. The low water content of n-propanol 99.5%, typically below 0.1 wt%, prevents polyamide precipitation and ink bodying in enclosed doctor blade chambers. On production lines, batch-to-batch variation in printable film wetting requires in-line corona treatment at 38–44 dyn/cm before the first color station. When press speed exceeds 250 m/min and ambient humidity exceeds 60% RH, retained n-propanol in printed reels increases unless solvent extraction fans maintain dew point below 8 °C in the press enclosure. Narrow-web presses with water-cooled anilox rollers report viscosity drift below 5% over an 8-hour shift when n-propanol purity is maintained above 99.5%. Printability and adhesion are validated on a production central-impression press by measuring print density under ISO 2834-1 and surface ink rub resistance by a 1.8 kg weight Sutherland rub test at 100 cycles or ASTM D5264. For food-contact printed laminates, compliance is evaluated under EU Regulation 1935/2004 and EC 2023/2006, with ink migration testing following EN 1186-1; volatile organic content is determined by ASTM D2369 or ISO 11890-1. Terminal finished products include snack food wrappers, confectionery overwrap, and pressure-sensitive labels where residual solvent must remain below 5 mg/m² in printed film as measured by headspace gas chromatography.
For polyester/melamine primer formulations applied to hot-dip galvanized steel and coil aluminium, n-propanol 99.5% reduces application viscosity without replacing the entire aromatic hydrocarbon fraction with hazardous air pollutants. High-solids polyester resins with hydroxyl numbers of 20–40 mg KOH/g are crosslinked with hexamethoxymethylmelamine at a polyester-to-melamine mass ratio near 80:20, and n-propanol is introduced at 8–15 wt% of the wet formulation to maintain a roll-coating viscosity of 60–120 mPa·s at 25 °C. The primer is applied by reverse roll coater at 8–20 g/m² dry film weight and cured at peak metal temperature 216–249 °C for 25–40 s. Because n-propanol has a boiling point of 97.2 °C and a flash point of 22 °C, the solvent release profile must be staged through infrared preheating zones before the final convection curing zone. Failure modes observed on high-speed coil lines include solvent popping when dry film weight exceeds 15 g/m² and peak metal temperature reaches 249 °C within 20 s; in such cases n-propanol is reduced to 5–8 wt% and the low-boiling fraction is replaced with n-butanol to retard skin formation. The opposite failure, soft undercured film with MEK double rubs below 20 cycles, occurs when the exhaust zone temperature falls below 216 °C and retained n-propanol inhibits acid-catalyzed crosslinking. Blocked p-toluenesulfonic acid catalyst at 0.3–0.8 wt% on resin solids holds pot life above 8 h at 25 °C. Coated material qualification includes EN 1396 for coil coated metal, EN 13523-9 for water immersion adhesion, and ASTM D4145 for T-bend flexibility. The addition of n-propanol must be managed under EU Directive 2010/75/EU where regenerative thermal oxidizer control of volatile organic compounds is required. Terminal articles are exterior cladding panels and domestic appliance skins.
Catalytic esterification of n-propanol 99.5% with acetic acid to n-propyl acetate is carried out in reactive distillation systems where the alcohol feed is passed through molecular sieve 3A to reduce water below 0.05 wt% before injection into the first reaction zone. Sulfuric acid at 0.5–1.0 wt% of total feed or p-toluenesulfonic acid monohydrate is used as homogeneous catalyst, with acetic acid fed at a molar excess of 1.1–1.3 mol per mol n-propanol. The reaction section is held at 95–110 °C; n-propyl acetate is withdrawn overhead and the organic phase is refluxed after decanting aqueous by-product, driving equilibrium toward esterification. Crude n-propyl acetate is then neutralized with sodium carbonate solution, water-washed, and distilled to a final purity exceeding 99.5% with acidity below 0.02% as acetic acid by ASTM D1613; color is assessed as 10 Pt-Co units maximum by ASTM D1209 and density at 20 °C by ASTM D4052. The water content of the finished ester is controlled below 0.05 wt% by ASTM D1364. Equipment using Hastelloy C276 reboiler tubes and 316L column internals avoids chloride stress corrosion when sulfuric acid is used. Terminal product n-propyl acetate is blended into flexographic inks, coil coating thinners, and industrial cleaning formulations. Published data for exact plate counts in this specific configuration is limited, but industrial designs typically specify 20–30 theoretical stages for high conversion.
In emulsifiable concentrate production for azole and strobilurin fungicides used on cereals and oilseed rape, n-propanol 99.5% is incorporated at 5–12 wt% as a polar co-solvent between the active ingredient solution in aromatic hydrocarbon and the aqueous spray dilution. A representative 480 g/L fungicide EC contains n-propanol, aromatic solvent, and a surfactant pair of calcium dodecylbenzene sulfonate and castor oil ethoxylate at total emulsifier loading 8–12 wt%. The concentrate is mixed in a jacketed high-shear vessel at 1500–3000 rpm for 25–35 min while temperature is maintained at 25–35 °C; vapor extraction is interlocked with the agitator because n-propanol reduces the closed-cup flash point to 23–35 °C depending on aromatic solvent ratio. Emulsion stability after dilution in CIPAC standard hard water is tested by CIPAC MT 36.3; re-emulsification at 24 h and 30 °C is assessed by CIPAC MT 36, and low-temperature storage is evaluated after 7 days at 0 °C by CIPAC MT 39.3. Regulatory compliance follows Regulation EC 1107/2009 for placing plant protection products on the market and CLP 1272/2008 for classification and labelling. The finished EC is filled into 1 L and 5 L HDPE containers and applied at 0.5–1.0 L/ha through hydraulic nozzles. Incompatibility occurs when dilution water hardness exceeds 1000 ppm as CaCO₃, producing cream separation and spray-tank filter clogging.
Preparative reversed-phase high-performance liquid chromatography of synthetic therapeutic peptides and insulin derivatives uses n-propanol 99.5% as the organic modifier when acetonitrile is restricted by supply interruption or incineration cost. The mobile phase is prepared with n-propanol at 20–40 vol% in water for injection and trifluoroacetic acid at 0.1 vol%, then filtered through 0.22 μm regenerated cellulose. C18 bonded silica columns of 15–30 cm internal diameter are equilibrated at linear velocities of 80–140 cm/h; crude peptide is loaded at 50–100 g/L of packed bed and eluted with a gradient from 20% to 45% n-propanol over 60–120 min. Fractions are collected by UV absorption at 214 nm and 280 nm, then concentrated on a rotary evaporator at 40–50 °C and 20–30 mbar followed by lyophilization. Because n-propanol is classified as a Class 3 solvent under ICH Q3C with a permitted daily exposure of 50 mg/day, residual solvent in the active pharmaceutical ingredient is measured by headspace gas chromatography using USP 467. Chromatographic method qualification follows USP 621, and in-process control of fraction purity is maintained under 21 CFR 211.110. Terminal products are lyophilized injection-grade peptide APIs for type 2 diabetes and hormone therapy.
When medical device manufacturers replace isopropanol with n-propanol 99.5% in final degreasing of titanium and stainless steel load-bearing components, the higher boiling point of n-propanol 97.2 °C and flash point 22 °C require explosion-proof ultrasonic immersion equipment with vapor extraction interlocked to the transducer circuit. The cleaning sequence immerses components in n-propanol 99.5% at 45–55 °C for 15–25 min under 40 kHz ultrasonics at 0.4–0.6 W/cm². A fresh n-propanol vapor rinse follows, then vacuum drying at 80–120 mbar for 30 min removes residual solvent from blind holes and thread roots. Cleanliness of the finished surfaces is verified by extraction and gravimetric analysis in accordance with ISO 19227:2018, with non-volatile residue limits of 0.05 mg/component; cytotoxicity of cleaned device materials is evaluated under ISO 10993-5. Chlorinated cutting fluids must be removed in an aqueous alkaline pre-wash before n-propanol immersion to avoid chloride-induced corrosion and acid formation on hot titanium surfaces. Plasma treatment follows at 13.56 MHz RF and 0.1–0.3 mbar oxygen to activate surfaces for osseointegration. Terminal parts include bone screws, dental abutments, and intramedullary nails.
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N-Propanol 99.5% (CAS 71-23-8, EC 200-746-9) is the linear primary alcohol CH3CH2CH2OH with a molar mass of 60.10 g/mol. The commercial designation “99.5%” is a purity model rather than a molecular isomer distinction: it identifies a bulk industrial grade with a certificate-of-analysis minimum assay of 99.5 wt% on an anhydrous basis, alongside controlled water, acidity, color and residue limits. This distinguishes the product from lower-purity n-propanol streams, from isopropanol despite the identical molar mass, and from reagent-grade 1-propanol used for laboratory calibration. Industrial packaging for the 99.5% grade is typically stainless steel ISO tank containers, 200 L tight-head high-density polyethylene drums, or nitrogen-blanketed bulk storage. At 101.325 kPa, the normal boiling point is 97.2 °C, the closed-cup flash point is 23 °C, and the vapor pressure at 20 °C is 2.0 kPa.
The high-purity n-propanol stream is used where water or acidity would interfere with downstream performance. In solvent applications, the linear C3 chain gives a slower evaporation profile than isopropanol at equal temperature. In derivative synthesis, the low water content reduces side reactions in moisture-sensitive processes such as esterification, amination and isocyanate-based formulations. These differences are expressed through specification values rather than through a separate equipment model number.
The certificate of analysis for production-scale n-propanol 99.5% normally reports the parameters shown in the following table. The assay is determined by gas chromatography with flame ionization detection; the method is calibrated against a certified reference material rather than assigned by area normalization alone. The water value is the central control parameter for most downstream users because n-propanol is fully miscible with water, and water cannot be removed by simple atmospheric distillation beyond the azeotropic limit.
| Parameter | Test method | Typical specification |
|---|---|---|
| Assay, anhydrous basis | GC-FID calibrated against certified reference material | ≥ 99.5 wt% |
| Water | ASTM D1364 | ≤ 0.10 wt% |
| Color | ASTM D1209 | ≤ 10 APHA |
| Density at 20 °C | ASTM D4052 | 0.803–0.805 g/cm³ |
| Distillation range | ASTM D1078 | 96.0–98.0 °C |
| Acidity as acetic acid | ASTM D1613 | ≤ 0.002 wt% |
| Non-volatile residue | ASTM D1353 | ≤ 0.002 wt% |
| Refractive index at 20 °C | ASTM D1218 | 1.385–1.387 |
The low water limit of 0.10 wt% is not a cosmetic specification. Water above this level can promote corrosion in aluminum ink reservoirs, alter evaporation from open trays, and consume isocyanate groups in two-component polyurethane systems. The acidity limit is similarly functional: residual acetic acid or other acidic species can destabilize acid-sensitive resins and accelerate metal pick-up in storage.
Commercially, the 99.5% material is obtained from the hydrogenation of propionaldehyde, which is itself produced by low-pressure rhodium-catalyzed hydroformylation of ethylene with carbon monoxide and hydrogen. The crude hydrogenation product contains water, unreacted propionaldehyde and minor heavy ends. Direct atmospheric fractionation cannot reach dry high-purity n-propanol because of the water azeotrope; therefore the finishing route uses a first distillation column to approach azeotropic composition, followed by molecular-sieve dehydration over 3A zeolite. Typical plant-scale equipment includes structured packing columns with more than 50 theoretical stages for separation of close-boiling by-products and a polishing bed of 3A zeolite operated at ambient temperature. Regeneration of the zeolite bed is performed under hot nitrogen at 200–250 °C; moisture breakthrough is monitored by on-line Karl Fischer analysis.
In solvent-based flexographic printing on central-impression presses running at 250–400 m/min, the ink-vehicle solvent blend must balance resin solubility, viscosity and evaporation. Isopropanol is a common diluent because its lower boiling point gives fast drying, but open ink pans and shallow anilox cells can exhibit viscosity drift when the press is stopped or when ambient temperature exceeds 30 °C. N-Propanol 99.5% has the same molar mass as isopropanol but a normal boiling point 14.6 °C higher and a vapor pressure at 20 °C of 2.0 kPa compared with 4.4 kPa for isopropanol. The practical result is a slower evaporation rate from the ink tray and from the cells of an anilox roll with cell depths in the 8–30 µm range. If a formulator replaces 20–30 wt% of the isopropanol fraction with n-propanol, print trials may show reduced mid-run viscosity increase and fewer ink-drying defects on the doctor blade, but retained solvent in the printed film can increase if dryer temperature is not adjusted upward. Comparative trial data for specific ink bases is limited; therefore a press-side viscosity curve at 25 °C and a retained-solvent measurement under the intended press speed should be used before locking the solvent ratio.
The Hansen solubility parameters for n-propanol are commonly tabulated as δD 16.0, δP 6.8, δH 17.4 MPa1/2, while isopropanol is typically reported as δD 15.8, δP 6.1, δH 16.4 MPa1/2. The higher polar and hydrogen-bonding components for n-propanol indicate that it is not a drop-in replacement in every resin system. Polyamide and nitrocellulose inks may tolerate the change with small adjustments in true and latent solvent ratios, but acrylic systems can show altered release from low-energy films if the n-propanol fraction is too high. This is a property difference, not a purity difference: at equal 99.5% assay, the two structural isomers still occupy different positions in the solvent formulation space.
The following table summarizes the practical physical-property differences among high-purity n-propanol, isopropanol and ethanol. The data are bulk liquid values for the pure compounds and do not vary with the 99.5% designation except through the presence of residual water.
| Property | N-Propanol 99.5% | Isopropanol 99.5% | Ethanol 99.5% |
|---|---|---|---|
| Molar mass | 60.10 g/mol | 60.10 g/mol | 46.07 g/mol |
| Boiling point at 101.325 kPa | 97.2 °C | 82.6 °C | 78.3 °C |
| Vapor pressure at 20 °C | 2.0 kPa | 4.4 kPa | 5.8 kPa |
| Density at 20 °C | 0.804 g/cm³ | 0.786 g/cm³ | 0.789 g/cm³ |
| Viscosity at 20 °C | 2.26 mPa·s | 2.04 mPa·s | 1.20 mPa·s |
| Surface tension at 20 °C | 23.8 mN/m | 21.7 mN/m | 22.3 mN/m |
| Closed-cup flash point | 23 °C | 12 °C | 13 °C |
| Autoignition temperature | 371 °C | 399 °C | 363 °C |
Among these three common alcohol solvents, n-propanol has the highest flash point and the lowest vapor pressure at 20 °C. That property position makes it useful where evaporation must be retarded, but it also increases the risk of retained solvent in printed or coated substrates. The selection is therefore process-dependent; the 99.5% grade does not remove the need for drying-capacity verification on a specific coating line.
At atmospheric pressure, the n-propanol-water binary forms a minimum-boiling azeotrope at approximately 87.7 °C with a composition near 71.7 wt% n-propanol. This physical constraint defines the finishing technology for the 99.5% grade. Aqueous crude n-propanol can be rectified to the azeotrope, but the remaining water cannot be removed by ordinary atmospheric distillation; further drying requires pressure-swing distillation, anhydrous entrainer distillation, or adsorption over 3A molecular sieve. The 3A sieve has a pore aperture of approximately 0.3 nm, which adsorbs water while excluding the larger n-propanol molecule. In storage, the product must be kept under nitrogen blanketing to prevent moisture re-entry and maintain the ≤0.10 wt% water upper limit. Equipment suitable for handling includes 304 or 316 stainless steel transfer piping and pumps; carbon steel is generally acceptable for dry solvent, but water-containing product can accelerate corrosion at welds. Elastomer seals should be specified as EPDM or polytetrafluoroethylene, because natural rubber and certain nitrile grades can swell in n-propanol service.
As a chemical intermediate, N-Propanol 99.5% is used in the synthesis of n-propyl acetate by esterification with acetic acid, in the production of n-propylamines by amination, and in the manufacture of propylene glycol n-propyl ether by reaction with propylene oxide. In these applications, water above 0.10 wt% can reduce catalyst life or generate by-products, particularly in acid-catalyzed esterification. The 99.5% grade is therefore selected less for its solvent strength and more for its controlled water and acidity levels. Published data for all derivative synthesis configurations is limited, but the water limit is the parameter most frequently specified in technical bids for continuous n-propyl acetate plants.
The practical storage boundary is determined by the flash point and water limit. Bulk tanks should be fitted with pressure-vacuum vents set at 5–10 kPa(g), flame arrestors, and dry nitrogen pads. Drum transfer should use grounded and bonded positive-displacement or centrifugal pumps rated for flammable liquids. Open transfers that allow vapor release above the lower flammable limit must be avoided. Because n-propanol is fully miscible with water but less dense than water, water contamination from tank cleaning or humid air can propagate through the entire bulk volume rather than settling as a separate phase. This is different from water-immiscible solvents such as toluene or butyl acetate, where water can be drained from a bottom leg.
Under the United Nations transport scheme, n-propanol is assigned to UN 1274, hazard class 3, packing group III, on the basis of its flash point. Under the European CLP regulation, the product is classified as flammable liquid category 3 with H226. The lower flammable limit in air is typically cited as 2.1 vol% and the upper flammable limit as 13.5 vol%; the closed-cup flash point of 23 °C places the material close to the boundary between packing group II and III, which is why flash-point verification on each tank or drum batch is performed by ASTM D56 or ASTM D3828. For pharmaceutical manufacturing, n-propanol is listed in ICH Q3C as a Class 3 residual solvent with a permitted daily exposure of 50 mg/day, subject to the usual justification that residual levels are controlled in accordance with the relevant monograph or registration. The product is REACH registered as a full-tonnage industrial chemical; downstream users must apply their own exposure scenarios and ensure loading racks, drumming lines and production vessels comply with ATEX equipment requirements for zone 1 or zone 2 areas, depending on the process.