674974
6-Mercaptohexanoic acid
90%
Synonyme(s) :
MHA
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A propos de cet article
Formule empirique (notation de Hill) :
C6H12O2S
Numéro CAS:
Poids moléculaire :
148.22
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Service technique
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Laissez-nous vous aiderQuality Level
assay
90%
refractive index
n20/D 1.4846
density
1.0715 g/mL at 25 °C
storage temp.
−20°C
SMILES string
OC(=O)CCCCCS
InChI
1S/C6H12O2S/c7-6(8)4-2-1-3-5-9/h9H,1-5H2,(H,7,8)
InChI key
CMNQZZPAVNBESS-UHFFFAOYSA-N
Gene Information
rat ... Ace(24310)
General description
6-Mercaptohexanoic acid (MHA) forms a self-assembled monolayer (SAM) that is used to cap a variety of materials like gold nanoparticles (AuNPs) and indium phosphide quantum dots (InPQDs). It is majorly used in immobilizing the surface molecules, which enhance the physio-chemical and electrical properties.
Application
MHA can be used in the surface modification of InP quantum nanowires for their potential uage in fluorescent chemical sensors that monitor cyanide ions. MHA may also be covalently bonded with liposomes that can form a SAM on the surface of gold for use as an insect odorant receptor in biosensor based applications.
Used to prepare thiol-functionalized 1.5 nm gold nanoparticles via a ligand exchange process with triphenylphosphine-stabilized nanoparticles. This compound is used in self-assembly to produce hydrophilic SAMs. The resulting monolayers which are terminated with carboxylic acids can be further functionalized with various amines and alcohols to introduce more complex end groups. Can also be used to control the rate of aggregation of gold colloidal nanoparticles using pH.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Classe de stockage
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Contenu apparenté
Wenjuan Wei et al.
Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi, 50(6), 821-830 (2016-01-05)
Treatment of Acinetobacter baumannii infections is challenging owing to widespread multidrug-resistant A. baumannii (MDR-AB) and the lack of novel agents. Although recent data suggest that levofloxacin (LVX) may have unique activity against MDR-AB in combination with colistin (CST), further preclinical
An Ultrasensitive Electrochemical Impedance-Based Biosensor Using Insect Odorant Receptors to Detect Odorants
Khadka R, et al.
Biosensors And Bioelectronics, 183, 441-445 (2018)
Panagiotis Papadopoulos et al.
Food microbiology, 84, 103249-103249 (2019-08-20)
Recently, there has been an increased tendency towards raw-milk consumption, which may pose a consumer risk, due to the possible presence of human pathogenic microorganisms, such as Staphylococcus aureus and even methicillin-resistant S. aureus (MRSA). The prevalence of S. aureus