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SWEP, also known as Sodium Lauryl Ether Sulfonate, is a surfactant derived from the sulfonation of lauryl alcohol ethoxylates. It is an anionic surfactant with excellent wetting, foaming, and emulsifying properties. Its hydrophilic and hydrophobic groups allow it to interact with various substances, making it a versatile ingredient in various applications.

1918-18-9

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1918-18-9 Usage

Uses

Used in the Herbicide Industry:
SWEP is used as an active ingredient for enhancing the effectiveness of herbicides. Its surfactant properties help in the better dispersion and absorption of the herbicide on plant surfaces, leading to improved weed control and reduced chemical usage.
Used in the Cosmetics Industry:
SWEP is used as a foam booster and stabilizer in personal care products such as shampoos, shower gels, and bubble baths. Its excellent foaming and wetting properties contribute to a rich lather and improved cleaning performance.
Used in the Detergent Industry:
SWEP is used as a wetting agent and emulsifier in various cleaning products, including laundry detergents and dishwashing liquids. Its ability to reduce surface tension helps in the better penetration of cleaning agents into fabrics and dishes, resulting in more effective stain removal.
Used in the Textile Industry:
SWEP is used as a wetting agent and detergent in the textile industry, particularly during the scouring and bleaching processes. Its surfactant properties facilitate the removal of impurities, oils, and greases from fibers, leading to improved fabric quality and appearance.
Used in the Oil and Gas Industry:
SWEP is used as an emulsifier in the oil and gas industry to stabilize water-in-oil emulsions. Its ability to reduce interfacial tension between water and oil helps in the separation of water from crude oil, improving the efficiency of oil extraction and processing.
Used in the Agricultural Industry:
SWEP is used as a wetting agent and emulsifier in agrochemical formulations, such as pesticides and fertilizers. Its surfactant properties enhance the dispersion and absorption of these chemicals on plant surfaces, leading to improved nutrient uptake and pest control.
Chemical Properties:
SWEP is a crystalline solid that is insoluble in water and kerosene but soluble in acetone and dimethylformamide. These solubility properties make it suitable for use in various formulations and applications across different industries.

Hazard

Toxic by ingestion.

Check Digit Verification of cas no

The CAS Registry Mumber 1918-18-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1918-18:
(6*1)+(5*9)+(4*1)+(3*8)+(2*1)+(1*8)=89
89 % 10 = 9
So 1918-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H7Cl2NO2/c1-13-8(12)11-5-2-3-6(9)7(10)4-5/h2-4H,1H3,(H,11,12)

1918-18-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name swep

1.2 Other means of identification

Product number -
Other names Methyl 3,4-dichlorocarbanilate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1918-18-9 SDS

1918-18-9Relevant articles and documents

Anti-methicillin resistant staphylococcus aureus compound and its medical use

-

Paragraph 0075-0078, (2021/02/02)

The present invention relates to a compound represented by chemical formula 1 having an antibacterial effect against Staphylococcus aureus, particularly Staphylococcus aureus resistant to existing antibacterial agents such as methicillin or the like, and to a medicinal use of the compound.

Indole synthesis based on a modified koser reagent

Fra, Laura,Millán, Alba,Souto, José A.,Mu?iz, Kilian

supporting information, p. 7349 - 7353 (2014/07/21)

A new metal-free method for the rapid and productive preparation of indoles has been developed. This process is based on sterically congested hypervalent iodine compounds of the family of Koser reagents, and iodosobenzene in combination with 2,4,5-tris-isopropylbenzene sulfonic acid provides the highest yields and fastest reaction times. This reagent alone promotes the chemoselective oxidative cyclization of 2-amino styrenes to indoles in high yields under mild conditions. Convenient route to indole: A fast, productive, and operationally simple indole synthesis was developed.

Triazolecarboxamide herbicides

-

, (2008/06/13)

Compounds of the formula: STR1 wherein X is O or S; R and R1 are substituted or unsubstituted alkyl, alkenyl, alkynyl or cycloalkyl or R and R1 may be joined to form a heterocyclic ring; R2 is substituted or unsubstituted cycloalkyl; and n is 0, 1 or 2 are disclosed as well as their postemergence and preemergence selective herbicide use against both monocot and dicot weeds in crops such as sugarbeets, cotton, soybeans and rice.

Process for the preparation of N,O-disubstituted urethanes suitable as a starting material for the preparation of isocyanates

-

, (2008/06/13)

A process for the preparation of N,O-disubstituted urethanes. Primary amines and alcohols are reacted with organic compounds having carbonyl groups at 120° to 350° C. Suitable carbonyl-containing compounds include N-unsubstituted urethanes. N-mono-substituted, N,N'-disubstituted ureas, or polyureas may be used in combination with the N-unsubstituted urethane. The product urethanes are particularly suitable for the preparation of isocyanates.

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides

-

, (2008/06/13)

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides of the formula STR1 where R1 is hydrogen, a metal atom or an unsubstituted or substituted ammonium radical, R2 is a saturated or unsaturated straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical or 3 to 7 carbon atoms, a branched saturated or unsaturated aliphatic radical of 3 to 10 carbon atoms, a halogen-, alkoxy- or alkylmercapto-substituted aliphatic radical of 2 to 10 carbon atoms tetrahydrofuryl substituted methyl, a cycloalkoxy-substituted aliphatic radical of 4 to 10 carbon atoms, unsubstituted or halogen-substituted benzyl or phenyl, halophenyl, or alkylphenyl of a total of up to 10 carbon atoms, R3 is hydrogen, a straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical of 3 to 7 carbon atoms, a branched aliphatic radical of 3 to 10 carbon atoms, haloalkyl, or alkoxyalkyl of 2 to 10 carbon atoms and X is oxygen and may also be sulfur if R2 is unsubstituted or halogen-substituted benzyl, processes for their preparation, and herbicides containing the above compounds.

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