Tetradecyl sulfate sodium salt - ≥95% , CAS No.1191-50-0

CAS: 1191-50-0 Cat. No.: T166336 Peso molecular: 316.43 Número EC: 214-737-2 PubChem CID: 23665770

GRADE & PURITY ≥95%

Synonyms

sodium n-tetradecyl sulphate | sodiumtetradecylsulfate | Texapon K 14 | DTXSID4042416 | Natri tetradecylsulfas | Q27255739 | Silica (SiO2) Photoelectric Crystal | J-004075 | Tetradecyl sulfate sodium salt | AKOS015912587 | Sulfuric acid, monotetradecyl es

Storage

Room temperature

Shipped In

Normal

Descripción general

Tetradecyl sulfate sodium salt is a detergent-like sclerosant.
Tetradecyl sulfate sodium salt (Sodium tetradecyl sulphate) has been used: to investigate the effects of sclerosant foam preparation and composition on foam structure, the time course of liquid drainage and foam coarsenin. in sclerotherapy of telangiectases and reticular veins. in situ studies of self-assembled monolayers of adsorbed cationic or anionic surfactant molecules on atomically flat H-terminated Si(111) surfaces in aqueous solutions.

Specifications

Sinónimos

sodium n-tetradecyl sulphate | sodiumtetradecylsulfate | Texapon K 14 | DTXSID4042416 | Natri tetradecylsulfas | Q27255739 | Silica (SiO2) Photoelectric Crystal | J-004075 | Tetradecyl sulfate sodium salt | AKOS015912587 | Sulfuric acid, monotetradecyl es

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 504769516
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504769516
• Sonrisas canónicas: CCCCCCCCCCCCCCOS(=O)(=O)[O-].[Na+]
• IUPAC Name: sodium;tetradecyl sulfate
• InChIKey: UPUIQOIQVMNQAP-UHFFFAOYSA-M
• INCHI: 1S/C14H30O4S.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18-19(15,16)17;/h2-14H2,1H3,(H,15,16,17);/q;+1/p-1
• Isómeros SMILES: CCCCCCCCCCCCCCOS(=O)(=O)[O-].[Na+]
• PubChem CID: 23665770
• Peso molecular: 316.43

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Organic sulfuric acids and derivatives
      • Subclass Sulfuric acid esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Organic sulfuric acids and derivatives
• Subclass: Sulfuric acid esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Sulfuric acid monoesters
• Alternative Parents: Alkyl sulfates Organooxygen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkyl sulfate - Sulfate-ester - Sulfuric acid monoester - Organic alkali metal salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organooxygen compound - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as sulfuric acid monoesters. These are organic compounds containing the sulfuric acid monoester functional group, with the generic structure ROS(O)(=O)=O, (R=organyl group).
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

POLK Tbio DNA polymerase kappa (8653 Activities)

Discover Target: POLK

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)

Discover Target: RECQL

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

BLM Tchem Bloom syndrome protein (4248 Activities)

Discover Target: BLM

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

GCN5 Histone acetyltransferase GCN5 (89 Activities)

Discover Target: GCN5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rorc Nuclear receptor ROR-gamma (89407 Activities)

Discover Target: Rorc

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)

Discover Target: fba

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive.
• Punto de fusión (°C): 182-192°C
• Peso molecular: 316.430 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 14
• Exact Mass: 316.168 Da
• Monoisotopic Mass: 316.168 Da
• Topological Polar Surface Area: 74.800 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 275.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

Referencias

1. Du Guang-Jun, Xing Si-Yan, Wu Ning, Wang Tong, Jiang Yue-Hui, Song Tao, Yang Bai-Bing, Dai Yu-Tian.  (2024)  Injectable agents for the induction of Peyronie’s disease in model rats: a comparative study.  ASIAN JOURNAL OF ANDROLOGY,      [PMID:39177415] [10.4103/aja202430]

2. Haichao Yu, Yan Xu, Jinfeng Zhao, Jiayue Huang.  (2026)  Detection of pesticides using an optical biosensor based on liquid crystal microdroplets.  JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART B-PESTICIDES FOOD CONTAMINANTS AND AGRICULTURAL WASTES,      [PMID:41660853] [10.1080/03601234.2026.2626194]