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674435

Sigma-Aldrich

16-Mercaptohexadecanoic acid

98%

Sinonimo/i:

MHDA

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CHF 344.00

About This Item

Formula condensata:
HS(CH2)15CO2H
Numero CAS:
69839-68-5
Peso molecolare:
288.49
Numero MDL:
MFCD00674018
Codice UNSPSC:
12352103
ID PubChem:
329760594
NACRES:
NA.23

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Saggio

98%

Stato

solid

Punto di fusione

65-69 °C

Temperatura di conservazione

2-8°C

Stringa SMILE

OC(=O)CCCCCCCCCCCCCCCS

InChI

1S/C16H32O2S/c17-16(18)14-12-10-8-6-4-2-1-3-5-7-9-11-13-15-19/h19H,1-15H2,(H,17,18)
INOAASCWQMFJQA-UHFFFAOYSA-N

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Descrizione generale

16-Mercaptohexadecanoic acid (MHA) is an alkanethiol with long chained −CH2 groups, which form a self-assembled monolayer (SAM) on a wide range of substrates.[1]

Applicazioni

Formation of interchain carboxylic anhydrides on self-assembled monolayers with Fluoro N,N,N′,N′-tetramethylforamidinium hexafluorophosphate.[2] This compound is used in self-assembly to produce hydrophilic SAMs. The resulting monolayers which are terminated with carboxylic acids can be further functionalized[3] with various amines and alcohols to introduce more complex end groups or multiple layers.[4]
MHA forms a SAM on gold surfaces by pen lithography (PPL). It finds potential application in bio-engineering.[5][6] It can also be used to functionalize gold-dypiramids, which can fabricate nano-resonators for shell-isolated nanoparticle enhanced Raman-spectroscopy (SHINERS).[7]

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
MKCQ3713
MKCD7271
MKBX8214V
MKBR1198V
MKBK8137V

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Young Shik Chi et al.
Langmuir : the ACS journal of surfaces and colloids, 22(16), 6956-6960 (2006-07-26)
In this paper, we report the reactivity of fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate (TFFH), a reagent for transformation of carboxylic acids into acid fluorides in solution, toward self-assembled monolayers (SAMs) of 16-mercaptohexadecanoic acid on gold. Contrary to the solution-based reactions, we found that
Guusje Delen et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 24(1), 187-195 (2017-11-23)
Control over assembly, orientation, and defect-free growth of metal-organic framework (MOF) films is crucial for their future applications. A layer-by-layer approach is considered a suitable method to synthesize highly oriented films of numerous MOF topologies, but the initial stages of
Chuanzhen Zhou et al.
Langmuir : the ACS journal of surfaces and colloids, 26(11), 8441-8449 (2010-04-21)
Ultrathin complex multilayer structures have many potential applications in molecular and organic electronics, sensing, biotechnology and other areas. Reported here is a method by which to construct multifunctional, multilayer, patterned structures, using alkanethiolate SAMs adsorbed on Au, UV photopatterning, and
Modification of surfaces of silver nanoparticles for controlled deposition of silicon, manganese, and titanium dioxides.
Abdulrahman HB, et al.
Applied Surface Science, 427, 334-339 (2018)
Sensitive detection of clozapine using a gold electrode modified with 16-mercaptohexadecanoic acid self-assembled monolayer.
Huang Fei, et al.
Talanta, 72(2), 457-462 (2007)
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