1,8-Octanedithiol
1,8-Octanedithiol Basic information
- Product Name:
- 1,8-Octanedithiol
- Synonyms:
-
- 1,8-OCTANEDITHIOL
- 1,8-DIMERCAPTOOCTANE
- FEMA 3514
- NANOTHINKS(R) THIO8
- OCTAMETHYLENE DIMERCAPTAN
- OCTANE-1,8-DITHIOL
- 1 8-OCTANEDITHIOL 97+%
- NANOTHINKS THIO8
- CAS:
- 1191-62-4
- MF:
- C8H18S2
- MW:
- 178.36
- EINECS:
- 214-738-8
- Mol File:
- 1191-62-4.mol
1,8-Octanedithiol Chemical Properties
- Melting point:
- 1°C(lit.)
- Boiling point:
- 269-270 °C (lit.)
- Density
- 0.97 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.505(lit.)
- FEMA
- 3514 | 1,8-OCTANEDITHIOL
- Flash point:
- >230 °F
- form
- Liquid
- pka
- 10.19±0.10(Predicted)
- color
- Colorless to pale yellow
- Odor
- at 0.10 % in propylene glycol. sulfurous meaty mushroom earthy
- Odor Type
- sulfurous
- Sensitive
- Air Sensitive
- JECFA Number
- 541
- BRN
- 1735431
- Stability:
- Stable. Combustible. Incompatible with strong oxidizing agents, strong bases.
- LogP
- 4.21
- CAS DataBase Reference
- 1191-62-4(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 22-36/37/38-20/21/22
- Safety Statements
- 36-36/37/39-26
- RIDADR
- UN 1170
- WGK Germany
- 3
- RTECS
- RG9610000
- HS Code
- 29309090
MSDS
- Language:English Provider:1,8-Octanedithiol
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
1,8-Octanedithiol Usage And Synthesis
Chemical Properties
liquid
Chemical Properties
1,8-Octanedithiol has a sulfurous, meaty odor. FEMA indicates that total dithiol added to any food should not exceed 1.0 ppm
Uses
OCT may be used as a processing additive that can functionalize the electrode layer to enhance the power efficiency of P3HT:PCBM solar cells. It may also be used to form a SAM on gold electrodes to enhance the electrochemical properties.
Definition
ChEBI: 1,8-Octanedithiol is an alkanethiol.
General Description
1,8-Octanedithiol (OCT) is an alkanedithiol, which forms a self-assembled monolayer (SAM) on a variety of metal surfaces. OCT contains linearly arranged carbon-carbon bonds (C?C) and two sulfur atoms at the end facilitating the attachment with the surface atoms of the substrates. It mainly forms an organo-metallic system, which can be used to improve the electron transport medium for a wide range of electronic applications.
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