| HS Code | 426198 |
| Appearance | Colorless to slightly yellow transparent liquid |
| Ionicity | Nonionic to weak cationic |
| Ph | 5.0-7.0 (1% aqueous solution) |
| Solidcontent | 30% ± 1% |
| Viscosity | 1000-3000 mPa·s (25°C) |
| Density | 1.00-1.05 g/cm³ (25°C) |
| Watersolubility | Easily soluble or dispersible in water |
| Stability | Super stable to acid, alkali, electrolyte, and shear |
| Hydrophilicity | Excellent hydrophilic performance |
| Handfeeling | Soft and smooth |
| Yellowing | Low yellowing tendency |
| Storagestability | Stable under normal storage conditions |
As an accredited Super Stable Hydrophilic Silicone Oil RH-NB-8973 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in 200 kg sealed plastic drums with inner liners, labeled RH-NB-8973, for safe industrial handling and storage. |
| Container Loading (20′ FCL) | Super Stable Hydrophilic Silicone Oil RH-NB-8973 is securely loaded into a 20′ FCL container for export shipment. |
| Shipping | RH-NB-8973 is typically shipped in sealed HDPE drums or IBC totes, labeled and packed to prevent leakage. Store cool, dry, and ventilated, away from moisture and contamination. Transport per local regulations and the supplier’s SDS; confirm hazard classification before shipment. |
| Storage | Store Super Stable Hydrophilic Silicone Oil RH-NB-8973 in its original, tightly closed container in a cool, dry, well-ventilated area, away from direct sunlight, heat, and ignition sources. Keep upright to prevent leakage or contamination; avoid freezing and contact with strong oxidizers or acids. Do not store near foodstuffs or incompatible materials. Follow the manufacturer’s SDS and local regulations. |
| Shelf Life | RH-NB-8973 typically has a shelf life of about 12 months when stored in original, unopened containers under cool, dry conditions away from sunlight. |
On a production-scale continuous padding range processing polyester/nylon knitted mesh, RH-NB-8973 is metered into a 50 L to 80 L bath at 10 g/L to 30 g/L active concentration. The pad mangle is set to a two-roll vertical configuration with roll hardness 70 Shore A and nip pressure 2.0 bar to 2.8 bar, giving wet pickup of 68% to 82%. Bath pH is maintained between 5.0 and 6.0 with dilute acetic acid because prolonged exposure above pH 8.0 at 40°C reduces silicone polyether emulsion stability and produces visible scum on trough walls. When relative humidity in the finishing plant exceeds 60%, fabric pre-drying at 100°C for 30 s is required before the final cure step to prevent uneven finish migration. Drying at 120°C for 45 s and curing at 160°C for 90 s with a set-point tolerance of ±5°C avoids yellowing on cellulose-containing blends. Treated fabric is tested for wicking behaviour according to AATCC 79; a drop absorption time below 3 s on polyester microfibre is retained after 5 home-laundering cycles under AATCC 135. Compliance is documented against OEKO-TEX Standard 100 Annex 4 and ZDHC MRSL v3.1. The terminal textile structures include nylon tricot liner fabric and polyester mesh for sportswear, where moisture transport and controlled fibre-to-fibre friction are combined without hydrophobic build-up.
| Test method | Parameter | Control limit |
|---|---|---|
| OEKO-TEX Standard 100 Annex 4 | Extractable silicone fraction | No exceedance of applicable annex limit |
| ZDHC MRSL v3.1 | Residual solvent screening | Below 10 ppm reporting limit |
| AATCC 79 | Drop absorption time | ≤ 3 s on polyester microfibre |
| AATCC 135 | Dimensional change after 5 cycles | ± 3% |
Flexible polyether slabstock lines operating with low-pressure multi-component mixing heads show cell coarsening when the surfactant package loses interfacial activity under water-blown conditions; RH-NB-8973 is introduced at 0.6 pphp to 1.2 pphp of polyol, replacing a portion of the conventional non-hydrolytic silicone surfactant. The processing conflict is controlling bubble wall drainage before the gelation point without allowing over-stabilization that traps excessive open-cell windows. Mixing head speed of 4,500 rpm to 5,500 rpm and polyol stream temperature of 22°C to 26°C are held within ±1°C because viscosity drift from premature water reaction modifies surfactant domain size. Foam density is measured at 28 kg/m³ to 32 kg/m³ under ASTM D3574-17, and indentation force deflection is reported at 25% and 65% compression according to ISO 3386-1:2014. The hydrophilic component of RH-NB-8973 reduces the equilibrium surface tension of the aqueous phase to the 21 mN/m to 23 mN/m range, which maintains fine cell nucleation without the hydrophobic cell-wall drainage that leads to pinholes at higher tin catalyst loadings. Hydrolytic stability is critical because water is the chemical blowing agent at 2.5 pphp to 4.0 pphp, and the exothermic reaction temperature reaches 130°C to 150°C in the block core. Avoid combination with tertiary amine catalyst packages exceeding 0.2 pphp, because excessive amine-driven cell opening and silicone-induced surface tension reduction can combine to produce partial collapse near the slab centre. Terminal slabstock is fabricated into mattress cores and automotive seating cushion blanks.
Post-addition of RH-NB-8973 at 0.05 wt% to 0.30 wt% on total binder solids is made after the letdown stage in a high-speed disperser operating at 900 rpm to 1,200 rpm. The addition sequence avoids high-temperature grind phase exposure because the hydrophilic silicone oil can coat pigment dispersant micelles and reduce colour development. Air-dry alkyd topcoats formulated with cobalt-free drier packages require a pH of 8.0 to 8.8; RH-NB-8973 remains soluble without forming an oily border at the container wall under 50°C accelerated storage for 14 days, evaluated according to ASTM D1849-95. Coefficient of friction reduction is measured by ASTM D4518-91 static friction on coated glass panels; slip resistance values of 0.15 to 0.25 static coefficient are typical after 7 days of cure. Blocking resistance is assessed by ASTM D4946-89; face-to-face panels under 0.5 psi at 43°C for 24 h should separate without film delamination. Gloss retention is measured with ISO 2813:2014 at 60°; gloss loss above 3% indicates oversupply or accumulation at the air-coating interface. Avoid simultaneous addition with high levels of organo-modified clay thickeners above 0.8 wt% because competitive binding to clay platelet edges can produce viscosity loss and visible seeding. The terminal articles are interior alkyd trim enamels and water-reducible wood topcoats, where silicone migration during film formation is controlled by polymer polar groups.
In leave-on skin lotions thickened with carbomer, RH-NB-8973 is incorporated at 0.5% to 2.0% w/w after the emulsion has cooled below 40°C and after neutralization to pH 5.0 to 6.5. The addition sequence is dictated by the nonionic silicone polyether structure: direct addition to an acidic carbomer solution below pH 4.0 causes temporary viscosity collapse, and hot addition above 70°C increases the risk of entrapping air in lamellar gel networks. Stirring is maintained at 300 rpm to 500 rpm in a side-scraped vacuum kettle; sweep agitation is preferred over high-shear homogenization to avoid excessive shear thinning. The finished emulsion is evaluated for microbial robustness under ISO 11930:2019 and preservative efficacy with USP 51 challenge organisms. Skin compatibility documentation follows Regulation (EC) No 1223/2009 Annex I safety assessment. Silicone oil migration to the liquid-air interface is measured by surface tension reduction to 28 mN/m to 30 mN/m at 0.5% dilution. Formulation compatibility is limited in high-electrolyte systems above 3% sodium chloride, where phase separation may occur. The terminal cosmetic formats include face serums and non-greasy moisturizers, where RH-NB-8973 functions as a wetting agent for hydrophobic emollients without forming a continuous occlusive film.
Tank-mix compatibility of RH-NB-8973 is established at 0.05% to 0.15% v/v, either as a built-in wetting agent in suspension concentrate formulations or as a tank-mix adjuvant. Spray solution dynamic surface tension is measured by CIPAC MT 148; values below 35 mN/m at 100 ms bubble lifetime are needed for droplets to spread on waxy leaf surfaces. Equipment on production-scale boom sprayers uses flat-fan nozzles at 2.0 bar to 3.5 bar and a droplet volume median diameter of 200 µm to 350 µm; excessive reduction of surface tension below 25 mN/m increases driftable fines and reduces rainfastness of contact fungicide deposits. The hydrophilic silicone oil is therefore used mainly with systemic active ingredients such as glyphosate and tebuconazole, where leaf penetration is more important than residuality. Compatibility with hard water is tested at 342 ppm calcium carbonate equivalents according to CIPAC MT 18, and phase separation is recorded above 500 ppm divalent cation. Regulatory classification follows inert ingredient rules under 40 CFR 180.910 and storage stability under FAO/WHO JMPR guidelines. Terminal spray programs include soybean glyphosate pass and orchard tebuconazole applications.
Synthetic staple fibre spin finish used in nonwoven hygiene materials is prepared by diluting RH-NB-8973 to 0.3% to 1.0% solids in demineralized water and applied by kiss-roll applicator at 0.15% to 0.40% oil-on-fibre. Web thermal bonding at 135°C to 145°C with calender roll pressure of 60 N/mm to 100 N/mm triggers the key conflict: silicone oil must survive the thermal cycle without hydrophobic degradation and then re-wet the polypropylene fibre surface. Hydrolytically stable structure prevents the release of trimethylsilanol fragments that would otherwise deposit on calender rolls and create dark edge deposits within 8 h of continuous operation. Re-wettability is tested under ISO 9073-6:2003 liquid strike-through time; the target is below 3 s for a 22 g/m² polypropylene spunbond nonwoven. Peel strength of the thermal bond is measured by ASTM D1876; a reduction greater than 10% compared to control indicates fibre surface over-lubrication. The terminal articles are topsheet layers in sanitary pads and diaper acquisition layers, where rapid liquid penetration is required after package compression.
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Super Stable Hydrophilic Silicone Oil RH-NB-8973 is a 100% active nonionic polyether-modified polydimethylsiloxane supplied as a clear to faint-yellow liquid. The product carries pendant polyoxyethylene-polyoxypropylene grafts attached through hydrolysis-resistant Si-C linkages rather than conventional Si-O-C bridges, which differentiates it from standard water-dispersible silicone oils in acidic and alkaline process baths. Dynamic viscosity at 25 °C is specified as 800–1,500 mPa·s by ISO 3219, density at 25 °C is 1.04–1.06 g/cm³ by ASTM D4052, and the pH of a 1% aqueous dispersion is 6.0–7.5 by ISO 4316. RH-NB-8973 disperses in water without added co-surfactant at 0.025–8.0 wt%, although high-shear predispersion is required when bath temperature falls below 15 °C. The material is used in textile wet finishing, nonwoven surfactant top-ups, personal care rinse-off systems, agricultural spray adjuvants, and waterborne coating post-add applications. It does not function as a volatile silicone carrier; under ambient storage it remains a non-volatile liquid and does not evolve hydrogen during aqueous dilution.
| Property | Specification range or limit | Test method |
|---|---|---|
| Appearance at 25 °C | Clear to faint-yellow liquid | Visual |
| Dynamic viscosity at 25 °C | 800–1,500 mPa·s | ISO 3219 |
| Density at 25 °C | 1.04–1.06 g/cm³ | ASTM D4052 |
| Non-volatile content | 100% | ISO 3251 |
| pH of 1% aqueous dispersion | 6.0–7.5 | ISO 4316 |
| Cloud point of 1% aqueous solution | 62–68 °C | DIN EN 1890 method A |
| Surface tension of 0.1% aqueous solution | 22–24 mN/m | ASTM D1331 |
| Pour point | -10 °C maximum | ASTM D97 |
High-shear predispersion is preferred for stock emulsions above 10% concentration. In a Silverson L5M-A rotor-stator mixer operating at 3,000 rpm for 10 min, RH-NB-8973 forms a translucent nanoemulsion with median droplet size 120–180 nm by dynamic light scattering at 25 °C. Paddle mixing alone produces droplet sizes of 500–800 nm, with visible creaming after 48 h at rest. For high-concentration premixes, reverse addition is recommended: water is fed slowly into the oil phase under high shear to suppress transient gel bodies and reduce entrained air. Progressive cavity or gear pumps with line velocity 0.5–1.5 m/s are suitable for transfer; centrifugal pumps with excessive impeller shear should be avoided where repeated recirculation may raise emulsion temperature above 40 °C.
Hydrolytic drift is the principal failure mode for nonionic polyether silicones in cellulosic finishing. Conventional Si-O-C-bridged polyether silicones undergo acid-catalysed cleavage at the siloxane-polyether bond, releasing silanol fragments that recondense, raise bath viscosity, and deposit on pad rolls. RH-NB-8973 replaces the hydrolyzable bridge with a Si-C-grafted polyether architecture, which reduces chain scission under the weakly acidic conditions created by crease-resistant resin systems. Ageing of a 5.0 g/L aqueous finish at pH 4.0 and 40 °C for 72 h produced a viscosity change of ≤5% measured by ISO 3219 and no visible creaming after centrifugation at 3,000 g for 30 min. Under identical conditions, a conventional Si-O-C polyether analogue showed a 12–18% viscosity increase and visible roller deposit. This is operationally relevant on continuous pad lines where bath dwell times exceed 8 h and resin baths stabilise between pH 4.0 and 5.5.
On a Werner Mathis HVF padder operating at 2.0 bar nip pressure and 12 m/min line speed, 5.0 g/L RH-NB-8973 on 180 g/m² bleached cotton interlock delivered a vertical wicking height of 4.2–4.8 cm after 30 min by AATCC 79, after drying at 120 °C for 90 s and curing at 150 °C for 90 s. A conventional Si-O-C polyether silicone in the same bath gave 2.7–3.2 cm. Wash durability by AATCC 61-2A retained 80–85% of the initial wicking height after five cycles. Whiteness retention by AATCC 110 showed a Δb of 0.3–0.6, lower than the 1.5–2.0 Δb typical of amino-functional silicone softeners. At relative humidity above 60%, pre-drying at 100 °C for 60 s before curing prevents water spot defects on finished fabric.
Rinse-off and leave-on personal care systems can use RH-NB-8973 at 0.5–2.0 wt% as a non-yellowing wetting and conditioning aid. In a stability chassis containing 12.0 wt% sodium laureth sulfate and 3.0 wt% cocamidopropyl betaine at pH 5.5, storage at 45 °C for 12 weeks produced no phase separation and no change in optical transmittance measured at 600 nm. Wetting of hair fibres after a single rinse reduced water contact angle from 85–90° to 55–60° using a Krüss DSA25 drop shape analyzer. Published comparative data for this specific surfactant chassis is limited; the observed values are single-batch manufacturer stability data and should be re-verified with final fragrance, thickener, and preservative systems. Alcoholic systems above 20% ethanol require a premix with a nonionic co-surfactant because direct addition may produce localised gel aggregates.
Post-addition of 0.05–0.2 wt% RH-NB-8973 in waterborne acrylic coil coating topcoats under a Cowles blade at 300–500 rpm for 15 min reduces crater defects without depressing block resistance. In a 100 μm drawdown over phosphated steel, surface defect count was reduced from 10–12 craters per m² to ≤2 craters per m², with no loss of recoat adhesion by ISO 2409 cross-cut. The product is not a defoamer; excessive addition above 0.5 wt% can stabilise microfoam and should be avoided in high-speed airless spray application.
The practical selection among hydrophilic silicone oils can be reduced to three variables: linkage stability, yellowing tendency, and handle. Conventional Si-O-C polyether silicone oils are inexpensive and fast-wetting but have a narrow pH operating window. Amino-functional silicones deliver a dense, durable handle but yellow under forced storage and can impair hydrophilicity. RH-NB-8973 occupies a middle position with Si-C architecture and polyether chain length sufficient to maintain water absorption after curing. The table below summarises the comparative profile at equal 0.5% active content in distilled water.
| Property | RH-NB-8973 | Conventional Si-O-C polyether silicone | Amino-functional hydrophilic silicone |
|---|---|---|---|
| Linkage type | Si-C grafted polyether | Si-O-C bridged polyether | Aminoalkyl-modified siloxane |
| pH stability window at 25 °C | 3.0–10.0 | 5.0–7.5 | 4.0–8.0 |
| Equilibrium surface tension at 0.1 wt% | 22–24 mN/m | 24–26 mN/m | 28–32 mN/m |
| Wicking height after 30 min | 4.2–4.8 cm | 2.7–3.2 cm | 1.5–2.5 cm |
| Whiteness retention Δb | 0.3–0.6 | 0.4–0.8 | 1.5–2.0 |
| Wash durability by AATCC 61-2A | 80–85% | 50–60% | 85–90% |
Agricultural spray adjuvants based on polyether silicones are sensitive to electrolyte composition of the carrier. At 0.03–0.08 wt% RH-NB-8973 in deionised water, equilibrium surface tension declines from 72 mN/m to 22–24 mN/m by ASTM D1331; spread diameter on a PTFE film at 25 °C reaches 6–8 mm after 30 s. When the same concentration is introduced into a carrier containing 2.0 wt% ammonium sulfate and 540 g/L glyphosate potassium salt, the cloud point shifts from 62–68 °C to 38–44 °C, and phase separation appears if RH-NB-8973 exceeds 0.05 wt%. Jar tests should use 500 mL of actual tank water at 200 rpm agitation for 30 min before adding the silicone; if water hardness exceeds 300 mg/L as CaCO₃, a polycarboxylate chelating agent at 0.1–0.2 wt% restores clarity. Published crop efficacy data for RH-NB-8973 is limited, and the material should not be substituted for a registered pesticide adjuvant without local regulatory review.
Storage of RH-NB-8973 should be in closed HDPE or 316L stainless steel containers at 5–40 °C. Below 5 °C, viscosity rises and water dispersibility slows; warm to 25 °C with low-shear mixing before sampling. In unopened containers, the product has a shelf life of 24 months from production date. Avoid contact with strong oxidizers, concentrated mineral acids below pH 1.0, and aromatic solvents that can strip the polyether graft from the siloxane backbone during long-term storage. Compounding with strong amine-based alkoxy silanes in the same premix should be avoided because silanol condensation may raise molecular weight and reduce hydrophilicity. Spill control should follow local industrial wastewater rules and prevent undiluted liquid from entering drains in large volume.