Products
| HS Code | 424858 |
| Chemical Name | Propan-2-ol |
| Chemical Formula | C3H8O |
| Cas Number | 67-63-0 |
| Molecular Weight | 60.10 g/mol |
| Purity | 99% minimum |
| Appearance | Clear colorless liquid |
| Odor | Characteristic alcohol odor |
| Boiling Point | 82.5 °C |
| Melting Point | -89.5 °C |
| Flash Point | 11.7 °C (closed cup) |
| Density | 0.785 g/cm³ at 20 °C |
| Refractive Index | 1.377 at 20 °C |
| Vapor Pressure | 4.4 kPa at 20 °C |
| Water Content | <0.1% (anhydrous) |
| Solubility | Miscible with water, ethanol, ether, chloroform |
| Vapor Density | 2.1 (air = 1) |
As an accredited Isopropyl Alcohol Grade 99% Anhydrous (IPA) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in 1-liter HDPE container with secure, child-resistant cap; labeled with hazard warnings and IPA purity specifications. |
| Container Loading (20′ FCL) | 20′ FCL: Isopropyl Alcohol 99% Anhydrous packed in UN-approved drums on pallets, secured, ventilated, away from heat/sunlight. |
| Shipping | Isopropyl Alcohol Grade 99% Anhydrous (IPA) is classified as a flammable liquid (Class 3). Ship via ground or air freight following hazmat regulations. Pack in UN-approved containers, away from ignition sources, and ensure proper labeling, documentation, and segregation from oxidizers during transit. |
| Storage | Store in tightly sealed, approved containers away from heat, sparks, and open flames. Keep in a cool, dry, well-ventilated area, ideally in a flammable-liquid safety cabinet. Protect from sunlight and moisture to preserve anhydrous grade. Segregate from oxidizers, acids, and peroxides. Use grounded containers and bonding during transfer to prevent static discharge. |
| Shelf Life | Shelf life is typically 2–3 years if stored sealed, away from heat, moisture, and light. |
In semiconductor and electronic assembly lines, anhydrous isopropanol at 99% assay is deployed as a final rinse and drying agent after aqueous processing because its low surface tension displaces retained water from narrow gaps, wire channels, and under low-standoff components. The working fluid is charged to an ultrasonic immersion bath at 100% neat strength for moisture-sensitive substrates, while a blend of 90% IPA and 10% deionized water at 10 MΩ·cm is selected in batch spray-under-immersion machines where no-clean flux pastes contain water-soluble organic acid activators. Process equipment includes 316L stainless steel tanks, 40 kHz ultrasonic transducers, and closed-loop filtration rated at 1 μm absolute; bath temperature is controlled between 25 °C and 35 °C because evaporation above this band creates vapour concentrations approaching the lower flammability limit. After immersion or spray rinsing, assemblies are dried with filtered nitrogen at 0.5–1.0 bar to prevent water spotting and to lower oxygen exposure during solvent evaporation. Terminal components include SMT stencil apertures after solder paste printing, BGA and CSP package footprints after reflow, wafer cassettes and FOUP surfaces, and optoelectronic lens elements before adhesive bonding. Compliance anchors are derived from IPC J-STD-001H contact cleanliness requirements, IPC TM-650 2.3.25 resistivity of solvent extract testing, ISO 14644-1 Class 5 particle limits, and ASTM D770-20 solvent specification. For high-reliability PCBAs, production lines commonly apply a ROSE ionic contamination threshold of 1.56 μg/cm² NaCl equivalence per IPC TM-650 2.3.25, though exact limits are job-specific. The principal operational boundary is water ingress in open tanks: anhydrous IPA absorbs atmospheric moisture in humid packaging areas during an eight-hour shift, and Karl Fischer measurements can drift from the as-supplied water content toward 0.5% or higher. Once water exceeds this range, dissolution of rosin-based flux residues shifts toward swelling and can redeposit residues on high-impedance areas. Polycarbonate and acrylic fixturing are incompatible due to stress crazing; nylon and PTFE carriers are preferred. Do not use IPA rinse cycles on energized assemblies or those with unsealed relays, solvent-sensitive conformal coatings, or open acoustic ports.
In pharmaceutical topical antiseptic processing, anhydrous IPA is metered into purified water at 20–25 °C in 316L stainless steel mixing vessels to a final concentration of 75% v/v for hand sanitizer or 70% v/v for surface and wipe saturant production. The blend sequence introduces IPA into the water phase under low-shear agitation to avoid localized solvent concentration, followed by 0.2 μm cartridge filtration and filling into HDPE bottles, laminated non-woven wipes, or unit-dose antiseptic pads. Compliance follows the USP Isopropyl Alcohol monograph for assay, water content, and acidity, ICH Q3C Class 3 residual solvent limits with a permitted daily exposure of 50 mg/day, and FDA 21 CFR 211.67 for equipment cleaning after batch campaigns. Terminal product classes include pump-bottle hand sanitizers, pre-saturated infection-control wipes, and skin antisepsis pads used before venipuncture. The formulation must be separated from terminal sterilization claims: isopropanol is not sporicidal, and a contact surface or product requiring absence of bacterial spores must be processed through an oxidizer-based disinfectant or steam cycle. Receiving tanks must be checked by Karl Fischer titration because the anhydrous grade should not fall below 99% before dilution. Avoid use on acrylic equipment windows and unpainted carbon steel penstocks, where repeated exposure produces stress crazing or flash rust in wet processing environments.
Solvent-based flexographic ink systems use anhydrous IPA as a letdown and press-side viscosity adjuster in alcohol-soluble polyamide and nitrocellulose inks. Finished ink formulations carry 5–20 wt% IPA in the solvent blend, while press wash-up trays may be charged with 100% IPA for in-place removal of dried ink from anilox rolls and doctor blade chambers. During production, pigment is first dispersed in a high-shear dissolver with resin and a slower ester or ketone tail, then IPA is added during letdown under low shear to reach a printing viscosity of 20–28 s on a #2 Zahn cup at 25 °C. This sequence prevents pigment agglomeration and avoids solvent shock that can precipitate polyamide resin. Terminal outputs include surface-printed flexible packaging films, pressure-sensitive labels, paper shopping sacks, and non-woven polypropylene tote bags. Compliance references ASTM D2369-20 for VOC content, ISO 11890-2:2020 for VOC determination in coatings, REACH Annex XVII restrictions on solvent handling, and IED 2010/75/EU for solvent consumption in flexographic units. Anhydrous water content is a critical batch parameter because water levels above 0.5–1.0% in alcohol-soluble polyamide inks cause resin precipitation and plate plugging. The operational boundary is flash-point control; press-side IPA containers require grounded dispensing, and vapour extraction is mandatory when the printing unit exceeds 60 m/min in enclosed spaces. Published data for a specific print deck configuration is limited; flammability controls are governed by site-specific risk assessment rather than a single ISO clause.
Where water contamination in gasoline produces cold-start phase separation, isopropanol is added as a co-solvent at 0.5–1.0 vol% of tank capacity; a typical aftermarket cartridge delivers 355 mL into 40–80 L fuel. The addition procedure is pour-in before refuelling so that the fuel flow rinses the filler neck and homogenizes the alcohol. IPA partitions into both petrol and water droplets, depresses the aqueous phase freezing point, and allows dispersed water to pass through injectors without ice plugging. Terminal products include fuel-system de-icing additives, water remover maintenance fluids, and intake system moisture control products. Registration for fuel additives in the United States is handled under 40 CFR Part 79, and vapour pressure behaviour is screened by ASTM D323. Excess IPA above 2 vol% is not recommended in spark-ignition engines without recalibration because oxygen content and latent heat shift open-loop cold-start enrichment and may increase lean misfire risk in older fuel injection maps.
Anhydrous IPA functions as the principal volatile solvent in alcohol-based pump and aerosol hair styling formulations, where use levels from 30 wt% to 70 wt% of the liquid concentrate precede propellant addition. The manufacturing sequence dissolves PVP/VA copolymer in ethanol at 20–25 °C under high-shear mixing, then adds anhydrous IPA after the polymer phase is clear to avoid resin shock and micro-gel formation. The concentrate is filtered through 10 μm bag filters, transferred to pressure-rated aerosol fillers, and gassed with dimethyl ether, propane, or butane blends to a final can pressure of 2.5–4.0 bar at 20 °C. Terminal product classes include pump hair sprays, aerosol styling mists, nail polish removers where IPA is blended at 30–50 wt% with methyl acetate or acetone, and cooling skin astringents. Compliance is anchored to ISO 22716 cosmetic GMP, EC 1223/2009 Annex III restricted substances, and CIR review of isopropanol safety for cosmetic exposure. Anhydrous water content reduces ester hydrolysis in methyl acetate-based nail remover blends and prevents polymer haze in spray films. The process boundary is VOC control; high IPA levels in aerosols require compliance with local volatile organic compound limits for personal care products, and filling lines are designed for flammable vapour extraction with 10–15 air changes/min in gassing rooms. Avoid compounding with concentrated mineral acids or oxidizers due to heat generation and fire risk.
Botanical extraction batches using anhydrous IPA as the primary non-halogenated solvent are run at a solvent-to-dried-biomass ratio of 5:1 to 10:1 v/w for oleoresin-rich raw materials. The process begins with percolation or high-shear homogenisation at 25–40 °C, followed by vacuum filtration through 5 μm depth media and evaporation in a rotary or falling-film unit at jacket temperature not exceeding 40 °C under reduced pressure to protect heat-sensitive marker compounds. Residual IPA in the concentrated extract is controlled to 50 mg/day permitted daily exposure under ICH Q3C and measured by headspace gas chromatography per USP <467>. Terminal products include dietary supplement botanical extracts, cosmetic plant extracts, and flavour precursor intermediates. Anhydrous grade is specified because water in aqueous IPA reduces partitioning of non-polar oleoresins and increases emulsification of pectins that complicate filtration. Operational boundary: IPA is not accepted as a direct food solvent in all jurisdictions; residual solvent declarations and food-contact registration must be confirmed against the destination market. Published data for a specific high-shear geometry is limited; scaling from pilot percolation to production falling-film evaporation requires verification of condenser efficiency and residual solvent recovery.
| Application scenario | Core standard or regulation | Test method or clause | Primary control parameter |
|---|---|---|---|
| Electronics and semiconductor rinse | IPC J-STD-001H, IPC TM-650 2.3.25, ISO 14644-1, ASTM D770-20 | ROSE ionic contamination, particle count, water content | 1.56 μg/cm² NaCl equivalence; Class 5 particle limits |
| Pharmaceutical topical antiseptic and equipment cleaning | USP Isopropyl Alcohol monograph, ICH Q3C, 21 CFR 211.67 | Assay, water content, residual solvent, bioburden | 75% v/v final IPA; 50 mg/day PDE |
| Flexographic ink and wash-up | ASTM D2369-20, ISO 11890-2:2020, REACH Annex XVII | VOC content, flash point, viscosity | 5–20 wt% letdown IPA; 20–28 s #2 Zahn |
| Fuel-system moisture control | 40 CFR Part 79, ASTM D323 | Fuel additive registration, vapour pressure | 0.5–1.0 vol% IPA in tank fuel |
| Cosmetic aerosol and nail remover | ISO 22716, EC 1223/2009 | VOC content, microbial limits, restricted substances | 30–70 wt% liquid concentrate IPA |
| Botanical extraction | USP <467>, ICH Q3C | Headspace GC residual solvent, residual IPA | 5:1–10:1 solvent-to-biomass; 50 mg/day PDE |
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Under ambient laboratory conditions, the product designation IPA-ANH-99 (CAS 67-63-0; EINECS 200-661-7; UN 1219, hazard class 3, packing group II) refers to an anhydrous isopropyl alcohol with a nominal assay of 99 wt% and a free water mass fraction not exceeding 0.10 wt%. The commercial designation indicates an anhydrous isopropyl alcohol intended for downstream processes where residual water interferes with condensation reactions, moisture-sensitive organometallic chemistry, rosin flux removal, or ionic cleanliness verification. Packaging for production-scale use includes 20 L and 200 L fluorinated HDPE drums and 316L stainless steel totes; laboratory quantities are supplied in 1 L and 4 L borosilicate glass containers. The material is classified as flammable liquid category 2 under CLP Regulation (EC) No 1272/2008, with a closed-cup flash point of 12 °C and an auto-ignition temperature of 399 °C. Because the dynamic viscosity is 2.3 mPa·s at 20 °C, high-shear transfer and fine-nozzle dispense in printing and cleaning equipment do not present viscosity-related pressure drops. The vapour pressure at 20 °C is 4.4 kPa, producing an evaporative drying time shorter than n-propanol but longer than acetone; this parameter is relevant for stencil cleaning cycles and for wipe-down procedures in controlled environments.
The primary distinction is not the nominal isopropanol assay but the free water content and the carbonyl specification. Technical 99% isopropanol may contain water in the range 0.20–0.50 wt% depending on supply chain and storage conditions, whereas anhydrous material is controlled to ≤0.10 wt% by Karl Fischer titration. The difference becomes significant in polyurethane prepolymer dilution, Grignard reagent preparation, and esterification reactions, where water consumes stoichiometric equivalents of the reactive species. A 0.10 wt% water content corresponds to approximately 55.5 mmol of water per kilogram of solvent; a technical solvent at 0.40 wt% water carries 222 mmol/kg. The production route for anhydrous isopropanol typically extends beyond simple distillation because isopropanol and water form an azeotrope at approximately 87.7 wt% alcohol at atmospheric pressure. Dehydration therefore requires azeotropic distillation with a volatile entrainer, pressure-swing distillation, or membrane pervaporation; the resulting specification is verified by grade classification under ASTM D770-21, with water measured by ASTM E203-16(2021) and distillation range measured by ASTM D1078-11(2019). Reagent-grade isopropanol may satisfy the same assay threshold but may not carry the same water limit or may have different trace cation profiles depending on whether it is prepared for trace-metal digestions. The anhydrous grade further differs from USP/NF isopropyl alcohol in that USP/NF monographs may allow water content above 0.10% and may not require the same non-volatile residue performance unless the supplier imposes additional specifications.
| Parameter | IPA-ANH-99 | Technical 99% | 70% aqueous IPA |
|---|---|---|---|
| Water content | ≤0.10 wt% | 0.20–0.50 wt% | 30.0 wt% |
| Assay, GC | ≥99.0 wt% | ≥99.0 wt% | 70.0 ± 0.5 wt% |
| Non-volatile residue | ≤1.0 mg/100 mL | supplier-dependent | not specified |
| Flash point, closed cup | 12 °C | 12 °C | 18 °C |
| Moisture-sensitive reaction use | suitable | limited | unsuitable |
A representative certificate of analysis for IPA-ANH-99 is structured around the following acceptance limits. The values are typical lot-release parameters and should be confirmed against the supplier’s current certificate of analysis.
| Property | Specification | Test method |
|---|---|---|
| Assay, GC, anhydrous basis | ≥99.0 wt% | ASTM D770-21 |
| Water, Karl Fischer | ≤0.10 wt% | ASTM E203-16(2021) |
| Acidity, as acetic acid | ≤0.002 wt% | ASTM D1613-17 |
| Non-volatile residue | ≤1.0 mg/100 mL | ASTM D1353-13(2021) |
| Color, Pt-Co/APHA | ≤10 | ASTM D1209-05(2019) |
| Distillation range at 760 mm Hg | 81.3–83.0 °C | ASTM D1078-11(2019) |
| Density at 20 °C | 0.785–0.787 g/cm³ | ASTM D4052-22 |
| Refractive index nD20 | 1.3770–1.3780 | ASTM D1218-21 |
The limit for non-volatile residue is operationally important for microelectronics cleaning because a residue of 1.0 mg/100 mL leaves a calculated maximum film of 1.0 mg per 100 mL of solvent evaporated on a flat substrate without subsequent rinsing; this is a solvent purity boundary, not a surface insulation resistance specification.
In printed circuit board assembly, IPA-ANH-99 is used in benchtop cleaning, stencil apertures, and post-rework flux removal. The relevant acceptance boundary is not the alcohol content but the contamination contribution of the solvent after evaporation. IPC J-STD-001 and IPC-TM-650 method 2.3.25 define the ROSE test for ionic cleanliness; an anhydrous solvent with non-volatile residue ≤1.0 mg/100 mL and low chloride/sulfate content reduces the solvent-related background signal in ion chromatography. For automated stencil cleaning systems, the solvent is sprayed through air-atomizing nozzles at 0.3–0.5 MPa and then vacuum-recovered; the low water content reduces the formation of white residue from rosin soap hydrolysis after evaporation. Rosin flux contains abietic acid and activators; water in the solvent can promote acid dissociation and leave hygroscopic salts that later absorb moisture and decrease surface insulation resistance. In high-density assemblies with component pitch below 0.5 mm, a wash process using anhydrous isopropanol is often followed by a final rinse with a virgin solvent batch because cross-contamination rises as the solvent bath approaches the cleaning-equipment maker’s recommended soil-loading limit. The closed-cup flash point of 12 °C requires automated cleaning equipment to be rated for flammable solvents under ATEX or NFPA 30; local ventilation must keep vapour concentration below 25% of the lower flammability limit, which is 2.0% by volume for isopropanol. Published data for specific surface insulation resistance improvements attributable solely to water content in IPA is limited; equipment evaluations should compare solvent residues using IPC-TM-650 2.6.3.7 before process qualification.
Precipitation of serum proteins in bioanalytical sample preparation uses IPA-ANH-99 at volumetric ratios between 1:1 and 4:1 solvent-to-plasma. The anhydrous condition avoids altering the aqueous/water ratio of the precipitation medium unpredictably, which is critical for reproducible analyte recovery in LC-MS/MS workflows. Because water content in the precipitating solvent changes the dielectric constant of the mixture, a shift from 0.10% to 0.50% water can alter the solubility threshold for hydrophilic metabolites and phospholipids. In tissue processing, anhydrous isopropanol is used in dehydration sequences before paraffin infiltration; the absence of appreciable water reduces carryover of formalin and improves the final clearing step. Laboratory use also includes preparation of HPLC mobile phases where the water content is weighed in the gradient calculation. The product is not a substitute for water-free solvents in Karl Fischer titrations without a blank determination because the solvent itself contains ≤0.10% water and contributes to the total drift. For cell culture hood disinfection, the product is diluted with USP purified water to the target 70% isopropanol concentration; the anhydrous form allows exact dilution to the recommended biocidal concentration rather than relying on a pre-diluted product with less reproducible final water content.
In pharmaceutical granulation and film coating, IPA-ANH-99 functions as a low-viscosity carrier in high-shear mixer process trains. The solvent is sprayed onto a moving powder bed through a peristaltic pump and two-fluid nozzle at atomizing air pressures between 0.15 MPa and 0.40 MPa. Because the solvent evaporates before binder migration can cause hardness gradients in the tablet core, the anhydrous specification reduces the risk of localized overwetting; defoaming agents are not required for typical hydroxypropyl methylcellulose solutions below 10 wt% solids. Process validation should include loss-on-drying and residual solvent testing under USP <467>. The ICH Q3C Class 3 listing for isopropanol permits residual levels up to 50 mg/day in pharmaceutical products; this is a regulatory boundary, not a solvent quality limit.
In solvent recovery loops where precipitation or extraction currently uses methanol or ethanol, IPA-ANH-99 presents a higher boiling point (82.3 °C at 760 mm Hg) and a lower vapour pressure than methanol, which reduces evaporative losses through open vents but increases the energy required for distillation recovery. The heat of vaporization of isopropanol is approximately 665 kJ/kg at the normal boiling point, compared with approximately 1100 kJ/kg for methanol and 841 kJ/kg for ethanol. The product is miscible with water, ethanol, acetone, and most common organic solvents, but is not as effective as methanol for dissolving highly polar ionic salts and not as effective as acetone for dissolving low-polarity oils. This selectivity is useful when the target analyte is a moderately polar small molecule and the impurity to be rejected is a polar salt or a nonpolar wax. In gas chromatography headspace methods, IPA-ANH-99 has a retention time between ethanol and n-propanol on a nonpolar stationary phase. Because the anhydrous form has a narrow distillation range, a recovered solvent stream can be monitored by density and refractive index to detect water accumulation before returning it to the process. A rise in water content above 0.50% shifts the density toward 0.800 g/cm³ and changes the refractive index by approximately 0.0005 units; these are not precise analytical methods but process-control indicators.
Moisture-cured polyurethane coatings and adhesives use anhydrous isopropanol as a diluent only when the resin system contains sufficient NCO capacity to tolerate the solvent water. A solvent containing 0.10 wt% water introduces 55.5 mmol water per kilogram; this water consumes 111 mmol of isocyanate groups per kilogram of solvent because one mole of water reacts with two equivalents of NCO. For a formulation containing 25 wt% solvent, the isocyanate consumption attributable to solvent water is approximately 2.78 mmol NCO per 100 g formulation. The resulting carbon dioxide can cause microfoam in thick films and should be accounted for when setting the NCO/OH index. Anhydrous IPA is therefore selected for laboratory crosslinking studies where the exact NCO/OH ratio must be fixed; technical 99% isopropanol with 0.30% water shifts the index by roughly 8.32 mmol NCO per 100 g formulation under the same solvent loading. The product is not suitable as a solvent for waterborne polyurethane dispersions because the addition of isopropanol changes particle stability and may induce gelation in certain polyester-based dispersions; formulation stability should be screened at 5% and 10% solvent addition levels before scale-up.
Moisture recontamination is an operational boundary, not a formulation flaw. Bulk storage of IPA-ANH-99 should be under a dry nitrogen pad or in closed systems, because open-top containers increase water content over time through atmospheric moisture uptake; the rate depends on exposed surface area, air velocity, and relative humidity. The product is strongly hygroscopic when the available air has high relative humidity. It should not be stored in unlined carbon steel vessels because dissolved oxygen and water can form acetic acid and promote iron contamination. Incompatibilities include strong oxidizers, strong acids, and mixtures with hydrogen peroxide; prolonged exposure to air and ultraviolet light can generate peroxides. Before use in a moisture-sensitive reaction, the solvent should be titrated or analyzed by Karl Fischer if the container has been opened more than once.