760714

S-(4-Bromobutyl) thioacetate

96% (GC)

• Sinónimos: 1-Butanethiol, 4-bromo-, acetate, Acetic acid, thio-,S-(4-bromobutyl) ester, Ethanethioic acid, S-(4-bromobutyl) ester
• Fórmula empírica (notación de Hill): C₆H₁₁BrOS
• Número de CAS: 14475-59-3
• Peso molecular: 211.12
• MDL number: MFCD22666439
• UNSPSC Code: 12352103
• PubChem Substance ID: 329766891
• NACRES: NA.23

Propiedades

• assay: 96% (GC)
• form: liquid
• contains: copper as stabilizer
• composition: (copper wire added to bulk material for stabilization)
• storage condition: under inert gas
• refractive index: n20/D 1.518
• density: 1.388 g/mL at 25 °C
• storage temp.: −20°C
• SMILES string: CC(=O)SCCCCBr
• InChI: 1S/C6H11BrOS/c1-6(8)9-5-3-2-4-7/h2-5H2,1H3
• InChI key: ABARMQVSPZAYRI-UHFFFAOYSA-N

Descripción

General description

S-(4-Bromobutyl) thioacetate is used as a precursor in the formation of organic self-assembled monolayers (SAMs) on metals. Deprotection reactions can then converts the thioacetate group to thiol. These are chemisorbed onto metal surfaces to form self-assembled monolayers with a high degree of structural order. They are often used as a molecular template to form functional nanostructures.

Application

Used in the formation of Self-Assembled Monolayers on gold electrodes to modify its work function.

Features and Benefits

High chemical stability in air or solution. Thioacetate prevents undesirable oxidation of thiol groups in oxygen containing atmosphere. Forms homogeneous interface structure in SAMs.

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H302,H315,H319,H335
• pcodes: P261 - P264 - P270 - P301 + P312 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• target_organs: Respiratory system
• Storage Class: 10 - Combustible liquids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable