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674249

Sigma-Aldrich

11-Mercapto-1-undecanol

99%

Sinonimo/i:

11-Hydroxy-1-undecanthiol, 11-Hydroxyundecane-1-thiol

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About This Item

Formula condensata:
HS(CH2)11OH
Numero CAS:
73768-94-2
Peso molecolare:
204.37
Numero MDL:
MFCD00239433
Codice UNSPSC:
12352103
ID PubChem:
329760584
NACRES:
NA.23

Saggio

99%

Stato

solid

Punto di fusione

33-37 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

OCCCCCCCCCCCS

InChI

1S/C11H24OS/c12-10-8-6-4-2-1-3-5-7-9-11-13/h12-13H,1-11H2
ULGGZAVAARQJCS-UHFFFAOYSA-N

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Applicazioni

Oxidation to the corresponding disulfide by N-phenyltriazolinedione (Aldrich Catalog No. 280992) without the need for hydroxyl protection. This compound is used to produce hydrophilic SAMs. The resulting monolayers which are terminated with alcohols can be further functionalized with various groups even when attached to gold nanoparticles.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

>235.4 °F - closed cup

Punto d’infiammabilità (°C)

> 113 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
MKBG9572V
MKBG9915V
MKBF8564V
07631EH

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Jinda Fan, J.; Chen, S.; Gao, Y.
Colloids and Surfaces, B: Biointerfaces, 28, 199-207 (2003)
N-Phenyltriazolinedione as an efficient, selective, and reusable reagent for the oxidation of thiols to disulfides
Angelos C, et al.
Tetrahedron Letters, 47, 9211-9211 (2006)
Rui R Costa et al.
Biomacromolecules, 19(8), 3401-3411 (2018-07-04)
We introduce elastin-like recombinamers (ELRs) as polypeptides with precise amino acid positioning to generate polypeptide coatings with tunable rigidity. Two ELRs are used: V84-ELR, a hydrophobic monoblock, and EI-ELR, an amphiphilic diblock. Both were modified with the amine-reactive tetrakis (hydroxymethyl)
Chapman, R. G.; et al.
Journal of the American Chemical Society, 122, 8303-8303 (2000)
M Alles et al.
Biofouling, 31(5), 469-480 (2015-07-15)
Fouling release (FR) coatings are increasingly applied as an environmentally benign alternative for controlling marine biofouling. As the technology relies on removing fouling by water currents created by the motion of ships, weakening of adhesion of adherent organisms is the
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