Sodium Laureth Sulfate CAS 9004-82-4 Mastering Sulfate Surfactants: An In-Depth Analysis from Chemical Structure to Formulation Application

Mastering Sulfate Surfactants: An In-Depth Analysis from Chemical Structure to Formulation Applications

Sulfate surfactants, such as Sodium Lauryl Sulfate (SLS) and Sodium Laureth Sulfate (SLES), had a global annual production exceeding 2 million tons in 2022, with projections reaching 3.4 million tons by 2032. While most formulators are familiar with or have encountered these ingredients, the depth of their knowledge regarding structural characteristics and formulation application details may be insufficient. This article systematically summarizes the chemical structure, physicochemical properties, and application techniques of sulfate surfactants, aiming to enhance the effectiveness and precision of formulation design, thereby facilitating the development of safer and more efficient personal care products.

1 Representative Sulfate Surfactants

In personal care formulations, the most commonly used sulfate surfactants are Alkyl Sulfates and Alkyl Ether Sulfates derived from fatty alcohols. Typical examples include Sodium Lauryl Sulfate (SLS), also known as Sodium Dodecyl Sulfate (SDS), and Sodium Laureth Sulfate (SLES).

The common feature of these surfactants is a hydrophilic head group containing a sulfate ester group (–OSO₃⁻)​ connected to a hydrophobic hydrocarbon chain. However, they differ in the number of polyoxyethylene (ethoxy) units​ and the associated cations​ (e.g., Na⁺ and NH₄⁺).

1.1 Chemical Structure and Properties

Table 1 summarizes the chemical names, structural formulas (simplified), and molecular weights of some representative sulfate surfactants used in personal care:

Surfactant (Common Name)	Structural Formula (Abbreviated)	Molecular Weight (g/mol)
Sodium Lauryl Sulfate (SLS)	CH₃–(CH₂)₁₁–O–SO₃⁻ Na⁺	288.4
Sodium Laureth Sulfate (SLES)	CH₃–(CH₂)₁₁–(OCH₂CH₂)ₙ–OSO₃⁻ Na⁺ (n ≈ 2–3)	~382–421*
Ammonium Lauryl Sulfate (ALS)	CH₃–(CH₂)₁₁–O–SO₃⁻ NH₄⁺	283.4

*Note: Sodium Laureth Sulfate (SLES) is typically a mixture of ethoxylated lauryl alcohol sulfate esters. Common commercial grades include “laureth-2 sulfate” (n=2 ethoxy groups) and “laureth-3 sulfate” (n=3 ethoxy groups). The molar mass of ~421 g/mol corresponds to an average of about 3 ethoxy units, while laureth-2 sulfate has a molecular weight of approximately 382 g/mol. The exact value varies slightly depending on the degree of ethoxylation (for SLES).

1.2 Key Physicochemical Properties

Hydrophile-Lipophile Balance (HLB Value)

Sulfate surfactants are extremely hydrophilic. For instance, SLS has an HLB value as high as approximately 40, far exceeding the conventional 0–20 HLB scale used for nonionic emulsifiers. This reflects its very high water solubility and high compatibility with oil-in-water (O/W) systems. SLES also exhibits a similarly high HLB value (≈40), stemming from its structure that combines an ionic sulfate group and polyether segments, granting it good stabilizing effects in aqueous formulations. In contrast, many milder nonionic surfactants typically have HLB values in the teens or lower. Such a high HLB indicates that these sulfates strongly favor the aqueous phase in formulations, contributing almost nothing to lipophilicity.

Critical Micelle Concentration (CMC)

CMC is the minimum concentration at which surfactant monomers begin to self-assemble into micelles. The CMC of SLS at 25°C is approximately 8.2 mM​ (equivalent to 0.2–0.3% w/w), which is relatively low for an anionic surfactant with a C₁₂ alkyl chain, indicating good surface activity even at low concentrations. Introducing ethoxylate (EO) units further lowers the CMC: the CMC of SLES is typically about 0.8–1 mM, roughly an order of magnitude lower than that of SLS. Research indicates that beyond the first EO unit, further ethoxylation has a limited effect on the CMC. This low CMC value means that only small amounts of SLS/SLES are needed in formulations to achieve effective micelle formation and surface tension reduction. In water, SLS micelles have an aggregation number of about 60​ and a relatively high charge density (degree of ionization ≈30%). SLES micelles, due to their bulkier ethoxylate structure, have a slightly smaller aggregation number (e.g., aggregation numbers for laureth-3 sulfate are reported around 40).

Water Solubility and Krafft Point

As sodium salts of sulfated alcohols, both SLS and SLES can form clear aqueous solutions. However, their solubility varies with temperature:

• The Krafft point of SLS is about 16°C. Below this temperature, its solubility drops sharply, potentially forming hydrated crystals. For example, a 0.1–0.5% SLS solution may not fully dissolve at around 21°C and requires heating above 25°C for complete dissolution.
• The ethoxylate structure of SLES significantly lowers its Krafft point, maintaining good solubility even at temperatures close to 0°C. This makes SLES more suitable for stable formulations in low-temperature environments.

Both exhibit good solubility in soft and hard water, but high electrolyte concentrations affect their dissolution behavior. They are almost insoluble in nonpolar solvents and have limited solubility in short-chain alcohols (e.g., ethanol).

Salt Effect and pH Stability

As ionic surfactants, alkyl sulfates exhibit a common “salting-out” effect at high salt concentrations:

• Adding electrolytes (especially multivalent cations) can lower their CMC and may induce phase separation or precipitation.
• For example, in neutral solution, SLS (SDS) will precipitate from aqueous solution when the Na⁺ concentration exceeds approximately 0.4 M. The solubility of its sodium salt is limited (about 0.5 M at room temperature). Beyond this range, precipitation of solid or liquid crystalline phases can occur due to cation “depletion.”
• Divalent cations​ (e.g., Ca²⁺ and Mg²⁺ in hard water) are more prone to form insoluble salts with sulfates. Although SLS is more water-hardness resistant than soaps (fatty acid salts) and less prone to forming “soap scum,” it can still precipitate as calcium or magnesium lauryl sulfate​ under high concentrations of Ca²⁺/Mg²⁺.
• The ethoxylate structure of SLES grants it higher electrolyte tolerance. With an ethoxylation degree ≥2, it can prevent precipitation in moderately hard water and reduce adsorption on salt or soil surfaces. Therefore, SLES is preferred in formulations like shampoos that require tolerance to ionic interference.

Regarding pH stability, sulfate surfactants are very stable in the neutral to alkaline range and can be safely used in alkaline cleansers without hydrolysis. However, in strongly acidic environments (pH < ~4), especially at elevated temperatures, their sulfate half-ester structure may slowly hydrolyze, releasing sulfuric acid and the corresponding alcohol. At room temperature, both SLS and SLES are reasonably stable even in slightly acidic formulations (e.g., personal care products with pH 5–7). In contrast, sulfonates (e.g., alkylbenzene sulfonates) are stable even under strongly acidic conditions. Therefore, sulfates are typically not used in strongly acidic formulations, or require cosurfactants (e.g., amphoteric types) to protect their stability and reduce irritation.

Physicochemical Properties Summary:

• Lauryl sulfates are highly hydrophilic surfactants with extremely high HLB values.
• They form micelles and effectively reduce surface tension at low concentrations.
• They are soluble in water, but SLS requires temperatures above its Krafft point, while SLES is also soluble at low temperatures.
• They perform well with moderate electrolytes but may precipitate in high salt or hard water.
• They are stable under neutral to slightly acidic conditions, but may hydrolyze under strongly acidic/high-temperature conditions.

2 Performance in Personal Care Formulations

2.1 Foaming Characteristics

Sulfate surfactants are favored for their excellent foaming ability:

• SLS​ rapidly produces a large volume of foam with large, air-rich bubbles.
• SLES​ produces a finer, creamier, and more stable foam, making it a primary foaming agent in shampoos and body washes.

During use, the substantial foam generated by SLS gives users an impression of “powerful cleansing,” contributing to its widespread use. In standard foam tests (e.g., Ross-Miles foam height), SLS and SLES outperform most other types of surfactants. While foam itself does not directly participate in the cleaning process, it aids in product distribution on skin and hair and enhances user experience. Additionally, sulfate surfactants exhibit foaming synergy with amphoteric surfactants (e.g., betaines), maintaining foam stability during use. For instance, a shampoo containing about 10% SLES​ can form dense foam even in the presence of oils or conditioning agents, thanks to its strong foaming power.

2.2 Cleansing Ability

Detergency and Cleaning Power

Lauryl sulfates are efficient cleansers, effective at removing oils, dirt, and particulate soil. Their excellent cleaning power stems from two points:

• Strong wetting action: They lower the surface tension of water, allowing it to penetrate oil layers.
• Micelle formation: They encapsulate and solubilize oily soils.

SLS is particularly notable for its degreasing ability and is commonly used experimentally to disrupt and solubilize proteins and lipids (e.g., protein denaturation in SDS-PAGE). In personal care, sulfate-containing cleansing products effectively remove sebum, makeup residue, etc.

Soil Emulsification Capacity

At concentrations above the CMC, micelles formed by SLS/SLES can effectively emulsify oily soils and carry them into the wash water. However, they have a relatively weak ability to suspend particulate or heavy soils themselves; therefore, high-molecular-weight polymers or auxiliary surfactants are often added to formulations to enhance anti-redeposition capability. For daily mild oil-based soils (e.g., sebum, cosmetics), sulfate surfactants are highly competent. Products containing them often leave a “squeaky clean” feeling, indicative of thorough oil removal, though this strong cleansing power can also lead to potential irritancy issues.

2.3 Skin and Eye Irritation

A known disadvantage of sulfate surfactants is their relatively strong irritating potential:

• SLS​ is considered a more irritating surfactant. It can penetrate and denature skin proteins, disrupt the skin barrier, and lead to discomfort like erythema and itching. It is even used as a positive control irritant in dermatological tests. Even at concentrations of a few percent, SLS can cause discomfort with prolonged exposure.
• In contrast, SLES is milder. Its ethoxylate structure increases molecular volume, reducing its ability to penetrate the skin, thus making it less irritating. Studies by the Cosmetic Ingredient Review (CIR) Expert Panel indicate that while SLES can be irritating at high concentrations, it does not cause sensitization. In actual consumer products, with optimized formulations, SLES has very low irritation potential. SLES is typically used at 10–15%​ in conventional shampoos and cleansers, which are rinse-off products with short contact time, making it relatively safe for the skin. Conditioners, plant oils, or polymers are often added to formulations to further alleviate dryness.
• ALS​ is slightly milder than SLS (possibly because NH₄⁺ is gentler on the skin than Na⁺) but still not as mild as SLES.

Summary:​ Due to its better mildness, SLES is generally preferred over SLS​ in wash-off products. Baby shampoos and products for sensitive skin often completely avoid SLS, and sometimes even SLES, opting for milder alternatives like sulfosuccinates, Alkyl Polyglucosides (APG), or amino acid-based surfactants.

2.4 Compatibility Techniques with Other Ingredients

Compatibility and Synergy with Other Surfactants

As anionic surfactants, SLS and SLES are compatible with most anionic and nonionic surfactants but are incompatible with cationic surfactants.

1. When coexisting with cationics like quaternary ammonium conditioning agents, they form insoluble complexes or neutralize each other, leading to inactivation. Therefore, they should not coexist in the same formulation (e.g., it’s acceptable to use shampoo followed by conditioner, but not to mix them together).
2. They have synergistic effects with amphoteric surfactants​ (e.g., betaines) and nonionic surfactants​ (e.g., alkyl polyglucosides). These synergies include:
   • Enhancing foam richness and stability.
   • Reducing irritation: Amphoteric surfactants can also inhibit protein denaturation, making formulations gentler on the skin.
   • Improving the response to salt thickening, making it easier to adjust the product to a desired gel-like consistency.
   • For example, mixing SLES with a betaine (e.g., CAPB) at a 3:1 weight ratio​ significantly improves foam quality and reduces irritation.
3. Sulfate surfactants can also be combined with alkanolamides (e.g., Cocamide DEA) to further enhance creamy foam sensation and viscosity.
4. Adding small amounts of amphoacetates​ or sulfosuccinates​ (e.g., sulfosuccinate esters) can further improve mildness and foam stability.
5. Additionally, they can be combined with nonionics (e.g., polysorbates, alkyl polyglucosides) to adjust foam or dissolve fragrances.

Viscosity and Foam Control

• Viscosity Control: The response of sulfate surfactants to added salt is characterized by an initial increase in viscosity (due to charge screening between micelles leading to rod-like micelle formation) followed by a decrease in viscosity with excess salt. SLES exhibits a pronounced viscosity peak upon salt addition, which is beneficial for formulating thick shampoos. Combining with CAPB can optimize this salt-thickening effect. SLS itself is typically supplied as a high-concentration paste (30% active) with inherent viscosity; adding salt can actually reduce viscosity due to a salting-out effect. Therefore, SLES is usually preferred for high-viscosity products.
• Foam Control: Sulfate surfactants produce foam quickly. Adding small amounts of foam stabilizers (e.g., betaines, amine oxides) can prolong foam life, suitable for applications requiring persistent foam like shaving foams or bubble baths.

Summary

Sulfate surfactants offer high-performance advantages in personal care:

• Rich foam.
• Excellent cleaning power.
• Synergy with cosurfactants to optimize foam, viscosity, and mildness.

Their main limitation lies in their inherent irritation potential, especially for SLS. However, by using milder derivatives (e.g., SLES, ALS) and optimizing formulations (cosurfactants, conditioning agents), a good balance between cleansing efficacy and skin friendliness can be achieved. Well-designed products based on SLES/ALS can maintain cleaning power while delivering the comfortable experience consumers expect.

3 Synthetic Routes

3.1 Production Overview

Sulfate surfactants like SLS and SLES are typically manufactured via a two-step industrial process:

1. Sulfation: Reaction of a fatty alcohol with a sulfating agent to generate a sulfuric acid ester intermediate.
2. Neutralization: Reaction of the acidic intermediate with a base to yield the final surfactant salt.

The fatty alcohols used are primarily from natural sources​ (e.g., lauryl alcohol derived from coconut or palm kernel oil) or synthetic sources​ (e.g., via Ziegler or Oxo processes). The carbon chain length is generally C₁₂–C₁₄ for optimal performance.

Step 1: Sulfation

Taking lauryl alcohol (CH₃–(CH₂)₁₁–CH₂OH) as an example, it can be sulfated by:

• Traditional Method: Using concentrated sulfuric acid (H₂SO₄). This is an equilibrium reaction requiring excess acid, producing many by-products and being corrosive to equipment. It is now less commonly used.
• Modern Methods:
  • Chlorosulfonic acid (ClSO₃H): Reacts with lauryl alcohol to yield lauryl sulfuric acid and hydrogen chloride gas (HCl), which needs recovery via water or alkaline scrubbing systems.
  • Sulfur trioxide (SO₃) gas: The industrial method of choice. SO₃, usually diluted in an inert gas (e.g., air or nitrogen), is used in continuous reactors (e.g., falling film reactors) to react with the alcohol.

Reaction Control Points:

• Use a near 1:1 molar ratio to control side reactions.
• The reaction is highly exothermic, requiring cooling to maintain temperatures <50°C.
• This prevents by-products like charring, discoloration, or sulfone formation.
• The product is the acidic form of the sulfate ester (e.g., lauryl sulfuric acid).

Step 2: Neutralization

The acidic sulfate ester intermediate is immediately neutralized with a base to produce the desired salt product:

• SLS: Neutralized with sodium hydroxide (NaOH) or sodium carbonate to form sodium lauryl sulfate.
• ALS (Ammonium Lauryl Sulfate): Neutralized with aqueous ammonia (NH₃ or NH₄OH).
• SLES: After sulfation, neutralized with NaOH to form sodium laureth sulfate.

This step is typically performed in a continuous reaction system, with water added to adjust to a standard concentration. By-products may include small amounts of sodium sulfate (Na₂SO₄), originating from residual sulfuric acid or excess alkali. Commercial-grade SLS/SLES often contains 1–3% Na₂SO₄ impurities. Final products are often lightly bleached with hydrogen peroxide​ to improve color by removing residual unsaturated impurities.

3.2 Pre-treatment Step for SLES: Ethoxylation

For producing SLES, lauryl alcohol is first ethoxylated​ by adding 2–3 moles of EO (ethylene oxide)​ under pressure to form lauryl ether alcohol. This mixture (called lauryl alcohol ethoxylate) is then sulfated and neutralized as described above. Therefore, the production process for SLES is:

Ethoxylation → Sulfation → Neutralization

Ethoxylation is performed using catalysts (e.g., KOH), yielding a mixture with a distribution of EO units. Common products are laureth-2 sulfate​ and laureth-3 sulfate. While higher ethoxylation increases mildness, it also raises costs with diminishing returns.

3.3 Feedstocks

Primary sources of fatty alcohol feedstocks for SLS/SLES production include:

• Natural Sources: Coconut oil, Palm kernel oil → Hydrolyzed to fatty acids → Hydrogenated to alcohols (e.g., lauryl alcohol C₁₂, myristyl alcohol C₁₄). The resulting “coconut alcohol” mixture (approximately 70% C₁₂, 30% C₁₄) can be sulfated to produce so-called Sodium Coco-Sulfate. This explains why SLS is often labeled as a “natural ingredient derived from coconut oil.”
• Synthetic Sources: Fatty alcohols produced via processes like Ziegler or Oxo, with a broader chain length distribution. Some commercial products (e.g., pareth sulfates) are sulfates of petroleum-derived alcohol ethoxylates.

Other raw materials include:

• Sulfur (to produce SO₃)
• Ethylene (to produce EO)

The source of these feedstocks determines the product’s economics and environmental impact.

3.4 Process Technology and Efficiency

Modern production uses continuous reaction units with precise process control:

• Film Reactors​ enable efficient contact between the alcohol and SO₃, completing the reaction within seconds.
• High Conversion Rate: Main product yield is typically >98%, with minimal by-products.
• High Atom Economy: Theoretically, all SO₃ ends up in the target product.
• Heat Recovery Systems​ are often used to absorb the exothermic heat. The process is typically conducted under vacuum or inert atmosphere to remove HCl or excess heat.

The Ethoxylation process​ is energy-intensive, requiring heating and pressurization, and can also generate trace by-products (e.g., 1,4-dioxane).

The Neutralization process​ is also continuously controlled, effectively utilizing the base and ensuring consistent product quality.

Therefore, SLS/SLES production is a mature, high-yield, and cost-effective industrial process, explaining its low cost and widespread application.

3.5 Safety and Environmental Considerations

The production of sulfate surfactants involves hazardous chemicals:

• SO₃, ClSO₃H​ are highly corrosive and toxic substances, requiring enclosed reactors and gas absorption systems (e.g., for HCl).
• Factories must adhere to strict operational safety protocols and engineering controls to ensure personnel health.
• Environmental Friendliness: The process generates minimal organic waste. By-products are mainly inorganic salts (e.g., NaCl, Na₂SO₄) that can be treated or recovered.
• Energy consumption is moderate, with many manufacturers implementing heat integration for optimization.

A notable concern is the formation of trace amounts of 1,4-dioxane (a potential carcinogen)​ during ethoxylation. Reputable manufacturers employ vacuum stripping or other purification steps to control its level in the final product to below a few ppm, subject to regulatory monitoring.

Overall, SLS/SLES production is a mature, safe, and efficient chemical process.

Summary: SLS/SLES Combined Performance Advantages

• Efficient foaming + Powerful cleaning + Low cost.
• Can produce the dense foam consumers expect.
• Compatible with common dyes, fragrances, and conditioning agents.
• Good water solubility, allowing formulation into clear or pearlescent products.
• Rinses cleanly with minimal residue (especially true for SLS).
• Quick-foaming, suitable for a variety of formulation systems.
  Based on the provided document, here is a complete English summary of the article titled “A Comprehensive Guide to Sulfate Surfactants: From Chemical Structure to Formulation Applications.”
• 1. Chemical Structure and Key Properties
• Main Types: The article focuses on the two most common sulfate surfactants in personal care formulations: alkyl sulfates​ (e.g., Sodium Lauryl Sulfate, SLS/SDS) and alkyl ether sulfates​ (e.g., Sodium Laureth Sulfate, SLES).
• Structural Features: Both share a sulfate ester group (–OSO₃⁻) as the hydrophilic head attached to a hydrophobic hydrocarbon tail. The key structural difference is that SLES incorporates polyoxyethylene (ethoxylate, EO) units.
• Key Physicochemical Properties:
  • High Hydrophilicity: Possess very high HLB values (~40), making them strongly water-phase oriented.
  • High Surface Activity: They have a low Critical Micelle Concentration (CMC), especially SLES, meaning they are effective at low concentrations for reducing surface tension and forming micelles.
  • Water Solubility: SLS solubility decreases at low temperatures (below its Krafft point​ of ~16°C), while SLES remains soluble in cold water due to its ethoxylate structure.
  • Stability: They are stable in neutral to alkaline conditions but can slowly hydrolyze​ under strongly acidic conditions (pH < ~4) and elevated temperatures. They are sensitive to electrolytes; high salt or hard water (divalent cations like Ca²⁺/Mg²⁺) can cause precipitation, though SLES has better electrolyte tolerance than SLS.
• 2. Performance in Personal Care Formulations
• Excellent Foaming: SLS rapidly produces large volumes of foam, while SLES generates a finer, creamier, and more stable lather, making it a preferred primary foaming agent.
• Strong Cleansing Power: They effectively lower surface tension and emulsify oils and dirt via micelle formation, offering strong degreasing action, which can sometimes be overly stripping.
• Irritation Potential: SLS is considered a relatively strong irritant that can compromise the skin barrier. SLES is milder due to its larger molecular size from ethoxylation, which reduces skin penetration. Ammonium Lauryl Sulfate (ALS) is moderately milder than SLS.
• Formulation Compatibility:
  • Incompatible​ with cationic​ surfactants (e.g., quats in conditioners), forming insoluble complexes.
  • Exhibit good synergy​ with amphoteric​ (e.g., betaines) and nonionic​ surfactants, enhancing foam, reducing irritation, and aiding in viscosity modulation (e.g., through salt-thickening response).
  • SLES shows a more pronounced salt-thickening effect, making it easier to formulate into high-viscosity products like shampoos.
• 3. Synthesis, Production, and Economics
• Primary Synthesis Route: Typically a two-step process: Sulfation​ (using reagents like SO₃) followed by Neutralization. SLES production requires an initial Ethoxylation​ step to add ethylene oxide (EO) units.
• Feedstock Sources: Primarily derived from natural oils (e.g., coconut oil, palm kernel oil) or synthetic processes.
• Mature and Efficient Process: Modern production uses continuous, automated processes like film reactors, ensuring high conversion rates and cost-effectiveness. A notable byproduct concern in SLES production is trace amounts of 1,4-dioxane, which is controlled to low ppm levels in the final product.
• 4. Summary of Advantages and Limitations
• Key Advantages: High-performance foaming, excellent cleansing, good water solubility, easy rinsability, and low cost.
• Main Limitation: Potential for skin/eye irritation, particularly with SLS.
• Conclusion: Through the use of milder derivatives like SLES and optimized formulations (e.g., combining with amphoteric or nonionic co-surfactants), sulfate surfactants can achieve a good balance between cleansing efficacy and skin-friendliness in personal care products.

ACF Chemical Co., Ltd.      Athena     phone/whatsapp：008613805212761  email：ceo@acfchemical.com website： https://acfchemical.com No. 45 Pengwan Road, Qianwan Bonded Port Area, Qingdao Area, China (Shandong)                                      welcome to vist our factory.                                      sample is free ACF Chemical Qingdao Co., Ltd. was established in 1987. the company has over decades of experience in the production of methacrylate and acrylate series products, as well as high-efficiency polymerization inhibitors and rubber and plastic antioxidant series products. The company’s leading products are high-efficiency polymerization inhibitor series products, with an annual production capacity of 1,000 tons of tert-butylhydroquinone (TBC), 800 tons of polymerization inhibitor TH-701, 500 tons of polymerization inhibitor TH-A294, 500 tons of polymerization inhibitor TH-100BE, 500 tons of phenothiazine, and 200 tons of hydroquinone.
2-Ethylhexyl nitrate	27247-96-7
Toluenesulfonamide(0/PTSA)	1333-07-9
LABSA (Linear-Alkylbenzenesulfonic Acid)	27176-87-0
MMT  Methylcyclopentadienyl manganese tricarbonyl	12108-13-3
C12/18 TERTIARY AMINE(MB)	68391-04-8
Alkyl (C12-C14) Glycidyl Ether (AGE)	68609-97-2
NMA(N-methylaniline)	100-61-8
N-ethylaniline	103-69-5
C12-14-alkyldimethylamines	84649-84-3
Aniline	62-53-3
TETA ( Triethylene Tetraamine )	112-24-3
2EH(2-Ethylhexylamine)	104-75-6
Sodium Lauryl Ether Sulfate (SLES)	68585-34-2
Titanium dioxide powder coating, paint grade.
1-Propene, 2-methyl-, homopolymer, hydroformylation products , reaction products with ammonia	337367-30-3
PEG-40 Castor Oil (Castor oil 40 EO, Castor oil ethoxylated 40 EO)	61791-12-6
Hydrogenated PEG-40 Castor Oil (Hydrogenated castor oil 40 EO, hydrogenated castor oil ethoxylate 40 EO) – CAS 61788-85-0	61788-85-0
Ethoxylated cocoamine EO 2 (PEG-2 cocoamine) – CAS 61791-14-8	61791-14-8
Hydrogenated Tallow Amine ethoxylate EO 8 (PEG-8 Hydrogenated Tallow Amine) – CAS: 61791-26-2	61791-26-2
Phenyl Glycidyl Ether	122-60-1
Neopentane Glycol Diglycidyl Ether	17557-23-2
Benzyl Glycidyl Ether	89616-40-0
Diethylene Glycol Diglycidyl Ether	39443-66-8
Butyl glycidyl ether	2426-08-6.
HydrogenatedTallowAmine	61788-45-2
Dodecyltrimethylammoniumbromide	1119-94-4
Didodecyldimethylammoniumbromide	3282-73-3
Dioctyldimethylammoniumbromide	3026-69-5
Sodium Dimethyl Dithiocarbamate (SDD)	128-04-1
Potassium Dimethyl Dithiocarbamate (KDD)	128-03-0
Boron Trifluoride Etherate	109-63-7
3-Glycidoxypropyltrimethoxysilane	2530-83-8
*MTHP  – Methyl Tetra Hydro Pyran	4717-96-8
2-(2-Methoxyethoxy)ethanol	111-77-3
HYDROQUINONE MONOMETHYL ETHER	150-76-5
MONO ISOPROPYLAMINE	75-31-0
Isopropyl Acetate (IPAC)	108-21-4
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PROPYLENE GLYCOL MONOMETHYL ETHER ACETATE （PMA)	108-65-6
PROPYLENE GLYCOL MONOMETHYL ETHER   (PM)	107-98-2
DIPROPYLENE GLYCOL DIMETHYL ETHER (DPDM)	111109-77-4
DIPROPYLENE GLYCOL MONOMETHYL ETHER ACETATE  （DPMA）	88917-22-0
POLY(VINYL CHLORIDE-CO-VINYL ACETATE)	9003‑22‑9
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2-3 Epoxypropyl Neodecanoate	26761-45-5
2-Ethylhexyl Acrylate (2-EHA)	103-11-7
12-Hydroxystearic Acid (12-HSA)	106-14-9
Hexahydrophthalic anhydride (HHPA)	85-42-7
Allyl alcohol	107-18-6
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N,N-Dimethyldecylamine	1120-24-7
N,N-Dimethyldodecylamine	112-18-5
N,N-Dimethyltetradecylamine	112-75-4
N,N-Dimethylhexadecylamine	112-69-6
N,N-Dimethyloctadecylamin	124-28-7
N,N-Dimethyl-C12-14-alkylamine	68439-70-3
DMA12/18	68391-04-8/61788-93-0
N-Coconut-1,3-propyl diamine	61791-63-7
N-Tallowalkyl 1,3-propanediamines   DAT	61791-55-7
Dodecyl trimethyl ammonium chloride	112-00-5
N-Hexadecyltrimethylammonium chloride	112-02-7
Octadecyl trimethyl ammonium chloride	112-03-8
Dioctyldimethylammonium chloride	5538-94-3
MT(M-Toluidine)	108-44-1
PT(P-Toluidine)	106-49-0
O-Toluidine  OT	95-53-4
C16-18-alkyldimethyl   Octadecyl/Hexadecyl dimethylamines	68390-97-6
Octadecyl/behenyl dimethylamines	124046-42-0
N-3-Laurylamidopropyl dimethylamine	3179-80-4
N-3-(Hydrogenated cocoamido)propyl dimethylamines	288095-05-6
1,8-DIAZABICYCLO[5.4.0]UNDEC-7	57671-19-9
DIETHYLPHENYL ACETAMIDE (DEPA)	84-66-2
3-(2-ETHYLHEXYLOXY) PROPYLAMIN	5397-31-9
LS 944	70624-18-9
LS 770	52829-07-9
LS 2020	192268-64-7
LS 123	129757-67-1
LS 3853	167078-06-0
LS 610	106990-43-6+70198-29-7
UV P	2440-22-4
UV 2	65816-20-8
UV 99-2	127519-17-9
UV 234	70321-86-7
UV 327	3864-99-1
UV 360	103597-45-1
UV 928	73936-91-1
UV 1164	2725-22-6
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Hydroxy propyl acrylate; HPA	25584-83-2
Benzyl Triethyl Ammonium Chloride	56-93-9
Benzyltriethylammonium bromide	56-37-1
Benzyltributylammonium bromide	23616-79-7
Tetrabutylammonium bromide	37451-68-6
Benzyltrimethylammonium bromide	5350-41-4
Benzyltributylammonium chloride	5197-95-5
Tetrabutylphosphonium bromide	3115-68-2
Methyltriphenylphosphonium bromide	1779-49-3
4-dimethylaminopyridine	1122-58-3
Tetrabutylammonium iodide	311-28-4
Tetraethyl ammonium bromide	71-91-0
Triphenylphosphine	603-35-0
Potassium Persulfate	7727-21-1
Triphenylethyl phosphorus bromide	1530-32-1
1, 2-Bis (diphenylphosphino) Ethane	1663-45-2
1,3-Bis(diphenylphosphino)propane	6737-42-4
1,5-Bis(diphenylphosphino)pentane	2 7721-02-4
(R)-(+)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl	76189-55-4
(R)-(+)-(1,1′-binaphthalene)-2,2′-diol	18531-94-7
[1,3-Bis(diphenylphosphino)propane]nickel(II) chloride	15629-92-2
Minodronic Acid	155648-60-5
Nitrilotriacetic acid	139-13-9
n-Propyl acrylate	925-60-0
N-(Hydroxymethyl)acrylamide; NMA	924-42-5
N,N’-Methylenebisacrylamide; MBA	110-26-9
N,N-Dimethylacrylamide; DMAA	2680-03-7。
N,N-dimethyldocosylamine	21542-96-1
N-Methyldioctylamine	4455-26-9
N-methyldidodecylamine	2915-90-4
N-3-Oleylamidopropyl dimethylamine	109-28-4
N-3-Erucylamidopropyl dimethylamine	60270-33-9
N-Oleyl 1,3-propanediamine	7173-62-8
N-tallow alkyltripropylenetetra	68911-79-5
N-[3-(isodecyloxy)propyl]propane-1,3-diamine	72162-46-0
N-Methyldiethanolamine	105-59-9
N,N-dimethylcyclohexylamine	98-94-2
N,N,N’-trimethylamino-N’-ethylethanolamine	2212-32-0
N,N-Dimethylethanolamine	108-01-1
N,N’-1,3-Phenylene bismaleimide	3006-93-7
N,N’-4,4′-Diphenylene-Bismalemide	13676-54-5
N-Cyclohexyl maleimide	1631-25-0
N-Phenyl maleimide	941-69-5
N-benzyl maleimide	1631-26-1
N,N-Diethylaniline	91-66-7
N,N-DIMETHYL -P-TOLUIDINE	99-97-8
DMA(N,N-dimethylaniline)	121-69-7
NDPT(N,N-dihydroxyethyl-p-toluidine)	3077-12-1
3-Diethylaminophenol	91-68-9
Diethanolamine	111-42-2
N,N-Dimethylbenzylamine	103-83-3
Trifluoromethanesulfonic acid	1493-13-6
p-Terphenyl	92-94-4
MethylEthylKetone	78-93-3
1-Butanol	71-36-3
2-Naphthol	135-19-3
N,N-Diethylhydroxylamine	3710-84-7
N,N-diethyl-m- toluamide DEET	134-62-3
Oleic acid	112-80-1
POLY(VINYL METHYL ETHER)	9003-09-2。
Triethanolamine	102-71-6
Bis(2-ethylhexyl)amine	106-20-7
Cocoamine	61788-46-3
Diethylaminoethanol	100-37-8
N,N-Dimethylcapramide	14433-76-2
N,N-Dimethylethylamine	598-56-1
Morpholine	110-91-8
Dichloroacetic acid	79-43-6
819；Phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide	162881-26-7
M-tolyl diethanolamine (MTDA)	91-99-6
P-Tolyl Diethanolamine (PTDA)	3077-12-1.
Dimethyl Thio Toluene diamine (DMTDA)	106264-79-3
Dimethyl P-Toluidine (DMPT)	99-97-8
Methyl-N-hydroxyethyl-p-toluidine (MHPT)	2842-44-6
Diisopropanol Para Toluidine (DIPT)	38668-48-3
Sodium Laureth Sulfate	9004-82-4