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1847-58-1

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  • 100% Natural 10:1 Herba Houttuyniae extract;Heartleaf houttuynia herb p.e.;Houttuynia cordata extract CAS NO.1847-58-1

    Cas No: 1847-58-1

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1847-58-1 Usage

Antiviral?Activities

Sodium new houttuyfonate (SNH), is an addition product of active ingredient houttuynin which could inhibit a variety of bacteria. Sodium new houttuyfonate (SNH) contains a hydrophilic sulfinyl head and a hydrophobic alkyl tail with 12 carbon atoms, which is considered to be surfactant-like structure. Although antibacterial mechanism of SNH remains unknown, it was indicated that Sodium new houttuyfonate (SNH) exerted its antimicrobial effect mainly through binding of non-polar tail group to bacterial hydrophobic membrane proteins or cytoplasmic enzymes. The hydrophobic lipid bilayer of cell membrane might be another target of aliphatic chain of SNH.? SNH was reported to exhibit potent inhibitory activity against Staphylococcus aureus, Staphylococcus epidermidis, and Klebsiella pneumoniae, etc.

Description

Different sources of media describe the Description of 1847-58-1 differently. You can refer to the following data:
1. Sodium lauryl sulfoacetate is an anionic surfactant. It increases proliferation of isolated chicken peripheral blood mononuclear cells (PBMCs) when used at concentrations ranging from 62.5 to 500 μg/ml. Sodium lauryl sulfoacetate (1, 2, and 4 mg/kg) increases the blood CD4+ to CD8+ T cell ratio induced by a Newcastle disease virus vaccine in chickens. Formulations containing sodium lauryl sulfoacetate have been used as surfactants in the manufacture of cosmetics.
2. Sodium Lauryl Sulfoacetate is derived from coconut and palm oils; a safe, skin-friendly surfactant (foaming agent) for both skin and hair. This mild plant-derived surfactant creates a rich, luxurious lather that effectively removes surface oil, dirt, and bacteria without stripping or drying sensitive skin or hair.

Chemical Properties

Sodium lauryl sulfate may be derived from either petroleum based or vegetable based sources. The SLS Tom’s of Maine uses is entirely derived from the vegetable sources of coconut and/or palm kernel oil. The oils can be split into glycerin and the component fatty acids, one of which is lauric acid. The lauric acid is isolated and then hydrogenated to form the lauryl alcohol. Alternately, the whole oil can be esterified and then hydrogenated to form the fatty alcohols of which lauryl alcohol would be isolated by fractionation. The lauryl alcohol is then combined with sulfur which then forms the salt, sodium lauryl sulfate.

Uses

Sodium Lauryl Sulfoacetate,can be used in the preparation of new surfactants of sodium cocoyl threoninate and sodium cocoyl glutamate that offer outstanding mildness, moisturization properties, and good foaming ability.

Application

Sodium lauryl sulfate is frequently used as a surfactant, or foaming agent. It may also serve as an emulsifier, helping oil based and water based ingredients to stay mixed. In many of our toothpastes SLS is used as a surfactant and helps to properly disperse the ingredients during brushing, and ensures easy rinsing and removal of debris (i.e. food particles).

benefits

Personal Care ProductsSLS has been an ingredient in shampoos since the 1930s. It works as a surfactant, trapping oil and dirt in hair so it can rinse away with water. An effective foaming agent, SLS can help create a rich lather in products like body and hand wash, facial cleansers and bubble. Likewise, SLS helps create the foaming action in toothpaste and also helps remove food particles from teeth.Cleaning ProductsSLS is an effective surfactant used in household cleaning products to help remove oily stains and residues, such as food stains in carpets. Because of its ability to break down oil and grease, SLS also is an ingredient in many industrial cleaning products, such as engine degreasers and industrial strength detergents.Food AdditiveAs a food additive, SLS is used as an emulsifier or thickener. For example, SLS helps make marshmallows and dried egg products light and fluffy. SLS also helps acids mix better with liquids, for example in fruit juices and punches.

Hazard

Depending on manufacturing processes, sodium laureth sulfate may be contaminated with measurable amounts of ethylene oxide and 1,4-dioxane. The International Agency for Research on Cancer ethylene oxide as a known human carcinogen and 1,4-dioxane as a possible human carcinogen. Ethylene oxide can also harm the nervous system iiand the California Environmental Protection Agency has classified it as a possible developmental toxicant based on evidence that it may interfere with human development. 1,4-dioxane is also persistent. In other words, it doesn’t easily degrade and can remain in the environment long after it is rinsed down the shower drain. 1,4-dioxane can be removed from cosmetics during the manufacturing process by vacuum stripping, but there is no easy way for consumers to know whether products containing sodium laureth sulfate have undergone this process.

Check Digit Verification of cas no

The CAS Registry Mumber 1847-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1847-58:
(6*1)+(5*8)+(4*4)+(3*7)+(2*5)+(1*8)=101
101 % 10 = 1
So 1847-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H28O5S.Na/c1-2-3-4-5-6-7-8-9-10-11-12-19-14(15)13-20(16,17)18;/h2-13H2,1H3,(H,16,17,18);/q;+1

1847-58-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium new houttuyfonate

1.2 Other means of identification

Product number -
Other names Dodecyl sodium sulfoacetate

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:1847-58-1 SDS

1847-58-1Synthetic route

dodecyl bromoacetate
3674-07-5

dodecyl bromoacetate

sodium lauryl sulphoacetate
1847-58-1

sodium lauryl sulphoacetate

Conditions
ConditionsYield
With sodium sulfite In water for 1h; Heating;
1-dodecyl alcohol
112-53-8

1-dodecyl alcohol

sodium lauryl sulphoacetate
1847-58-1

sodium lauryl sulphoacetate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: conc. HCl / toluene / 4 h / Heating
2: Na2SO3 / H2O / 1 h / Heating
View Scheme
methanesulfonic acid
75-75-2

methanesulfonic acid

lauryl acetate
112-66-3

lauryl acetate

sodium lauryl sulphoacetate
1847-58-1

sodium lauryl sulphoacetate

Conditions
ConditionsYield
Stage #1: methanesulfonic acid With sodium carbonate at 55℃; for 0.666667h;
Stage #2: lauryl acetate at 30℃; for 0.5h;

1847-58-1Downstream Products

1847-58-1Relevant articles and documents

Surface and Thermodynamic Properties of Octyl, Dodecyl, and Cetyl Sulfoacetates

Gad,El-Sukkary,Azzam

, p. 1085 - 1092 (1997)

Three anionic surfactants (Na-octysulfoacetate (A8), Na-dodecylsulfoacetate (A12), and Na-cetylsulfoacetate (A16) were prepared from alkyl bromoacetate. Several studies were carried out with aqueous surfactant solutions including surface tension, and electrical conductivity measurements. Surface properties, in particular, critical micelle concentration (CMC), effectiveness (ΠCMC), efficiency (Pc20), maximum surface excess (Γmax), and minimum surface area (Amin) were investigated at different concentrations at 20, 35 and 50°C, respectively. Free energies, enthalpies, entropies of micellization, and adsorption of the surfactants in the aqueous solution were studied.

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