25155-30-0 Usage
Chemical Properties
white or light yellow flakes
Uses
Different sources of media describe the Uses of 25155-30-0 differently. You can refer to the following data:
1. A surfactant used in proteomics research.
2. Anionic detergent.
3. Sodium dodecylbenzenesulfonate has been used to stabilize dispersions of graphene nanoflakes (GNFs) during the preparation of the liquid phase of GNFs. It can also suspend single-walled carbon nanotubes as individuals in aqueous media and also give well-resolved spectral features.
General Description
Sodium dodecylbenzenesulfonate is a white to light yellow flakes, granules or powder. Sodium dodecylbenzenesulphonate is soluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Sodium dodecylbenzenesulphonate is used as a synthetic detergent.
Air & Water Reactions
Sodium dodecylbenzenesulphonate is soluble in water.
Reactivity Profile
SODIUM DODECYLBENZENESULFONATE is incompatible with strong oxidizers.
Health Hazard
Minor skin and eye irritant. INGESTION: May cause vomiting, diarrhea, and intestinal distension.
Flammability and Explosibility
Nonflammable
Industrial uses
These frothers are mixtures of alcohols containing 6–8 carbon atoms. They were at one
time marketed by DuPont and they are tailored frothers for specific ore types. The bestknown
frother from this group is methyl isobutyl carbinol (MIBC) and 2-ethyl hexanol.
Aliphatic alcohol frothers are used as mixtures of different carbon lengths and as a
mixture of hydrocarbon oils.
Safety Profile
Poison by intravenous
route. Moderately toxic by ingestion. A skin and
severe eye irritant. When heated to decomposiuon
it emits tomc fumes of NazO. See also
SULFONATES
Purification Methods
It crystallises from propan-2-ol or H2O. [Gray et al. J Org Chem 20 515 1955, Beilstein 11 IV 514.]
Alkyl benzene sulfonates
Most sodium dodecyl benzene sulfonates are a member of the linear alkyl benzene sulfonates, meaning that the dodecyl group (C12H25) is un branched. This dodecyl chain is attached at the 4- position of the benzene sulfonate group. Linear dodecyl-4-benzene sulfonate anions can exist in six isomers (ignoring optical isomers), depending on the carbon of the dodecyl group that is attached to the benzene ring. The isomer shown below left is 4-(5-dodecyl ) benzene sulfonate (4 indicating the position of the benzene ring, 5 indicating the position on the dodecane chain). Branched isomers, e.g. those derived from tetramerized propylene, are also known (below right) but are not as widely used because they biodegrade too slowly. Production Trillions of kilograms are produced annually. Given the large scale of the application, the alkyl benzene sulfonates have been prepared by many methods. In the most common route, benzene is alkylated by long chain mono alkenes (e.g. dodecene) using hydrogen fluoride as a catalyst. The purified dodecyl benzenes (and related derivatives) are then sulfonated with sulfur trioxide to give the sulfonic acid. The sulfonic acid is subsequently neutralized with sodium hydroxide.
Environmental considerations
Biodegradability has been well studied , and is affected by the isomerization (branching). The salt has an LD50 of 2.3 mg / liter for fish , about 4x more toxic than the branched tetra propylene benzene sulfonate. It is however biodegraded more rapidly. Oxidative degradation initiates at the alkyl chain.
Check Digit Verification of cas no
The CAS Registry Mumber 25155-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,5 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25155-30:
(7*2)+(6*5)+(5*1)+(4*5)+(3*5)+(2*3)+(1*0)=90
90 % 10 = 0
So 25155-30-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H30O3S.Na/c1-3-5-6-7-8-9-10-11-16(4-2)17-12-14-18(15-13-17)22(19,20)21;/h12-16H,3-11H2,1-2H3,(H,19,20,21);/q;+1/p-1
25155-30-0Relevant articles and documents
PREPARATION OF SURFACTANTS VIA CROSS-METATHESIS
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Paragraph 000454, (2015/09/28)
The present invention relates to compositions comprising 2-phenyl linear alkene benzenes or 2-phenyl linear alkene benzene sulfonates or 2-phenyl linear alkylbenzenes or 2-phenyl linear alkylbenzene sulfonates; where the benzene ring is optionally substituted with one or more groups designated R *, where R * is defined herein and to methods for making the same. This invention also relates to compositions, methods of making, use of, and articles of manufacuture comprising 2-ethoxylated hydroxymethylphenyl linear alkyl benzenes or 2-propoxylated hydroxymethylphenyl linear alkyl benzenes.
