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About This Item
Linear Formula:
SOCl2
CAS Number:
Molecular Weight:
118.97
UNSPSC Code:
12352300
NACRES:
NA.21
PubChem Substance ID:
EC Number:
231-748-8
Beilstein/REAXYS Number:
1209273
MDL number:
Assay:
≥99%
Form:
liquid
vapor pressure
97 mmHg ( 20 °C)
Quality Level
product line
ReagentPlus®
assay
≥99%
form
liquid
refractive index
n20/D 1.518 (lit.)
bp
79 °C (lit.)
mp
−105 °C (lit.)
density
1.631 g/mL at 25 °C (lit.)
anion traces
chloride (Cl-): 59.0-60.2%
SMILES string
ClS(Cl)=O
InChI
1S/Cl2OS/c1-4(2)3
InChI key
FYSNRJHAOHDILO-UHFFFAOYSA-N
General description
Thionyl chloride is an inorganic acid chloride mainly used to prepare carboxylic acid chlorides from carboxylic acids.
Application
Thionyl chloride may be used in the following processes:
- To facilitate the synthesis of indenones from 3-hydroxyindanones via dehydroxylation.
- Surface modification of amorphous carbon nanotubes (α-CNTs) in stearic acid-dichloromethane solution.
- To functionalize silica gel for thioacetalization of aldehydes.
- Conversion of tert-butyl esters to acid chlorides.
- Conversion of aliphatic and aromatic sulfoxides to sulfides in the presence of triphenylphosphine.
- As an activator to generate ketenes in-situ for preparing 2-azetidinones.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3
target_organs
Respiratory system
supp_hazards
Storage Class
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Thionyl chloride assisted functionalization of amorphous carbon nanotubes: A better field emitter and stable nanofluid with better thermal conductivity.
Sarkar SK, et al.
Mat. Res. Bul., 1-8 (2015)
Fox MA and Whitesell JK
Organic Chemistry, 607-607 null
Thionyl chloride (or oxalyl chloride) as an efficient acid activator for one-pot synthesis of [Beta]-lactams.
Ebrahimi E & Jarrahpour A.
Iranian Journal of Science and Technology, 38(A1), 49-49 (2014)

