Welcome to LookChem.com Sign In|Join Free
  • or
Home > Products >  > 

2,2'-Thiodiethanol

Related Products

Hot Products

Name

2,2'-Thiodiethanol

EINECS 203-874-3
CAS No. 111-48-8 Density 1.18 g/cm3
PSA 65.76000 LogP -0.29580
Solubility N/A Melting Point -16 ºC(lit.)
Formula C4H10O2S Boiling Point 282 ºC at 760 mmHg
Molecular Weight 122.188 Flash Point 139.5 ºC
Transport Information N/A Appearance colourless liquid with characteristic odour
Safety 23-26-36/37/39-45 Risk Codes 36/37/38
Molecular Structure Molecular Structure of 111-48-8 (2,2'-Thiodiethanol) Hazard Symbols IrritantXi
Synonyms

Ethanol,2,2'-thiodi- (6CI,8CI);1,5-Dihydroxy-3-thiapentane;2,2'-Dihydroxydiethylsulfide;2,2'-Thiobisethanol;2,2'-Thiodiglycol;3-Thiapentane-1,5-diol;Bis(2-hydroxyethyl) sulfide;Bis(2-hydroxyethyl)thioether;Bis(b-hydroxyethyl)sulfide;Di(2-hydroxyethyl) sulfide;Diethanol sulfide;Kromfax Solvent;NSC6289;Tedegyl;Thiodiethylene glycol;Thiodiglycol;b,b'-Dihydroxydiethyl sulfide;b,b'-Dihydroxyethyl sulfide;b-Thiodiglycol;

Article Data 56

2,2'-Thiodiethanol Synthetic route

75-21-8

oxirane

111-48-8

2,2'-thiobis-ethanol

Conditions
ConditionsYield
With hydrogen sulfide at 20℃; Temperature;99.5%
With hydrogen sulfide
60-24-2

2-hydroxyethanethiol

111-48-8

2,2'-thiobis-ethanol

Conditions
ConditionsYield
With dihydrogen peroxide In ethanol; water at 20℃; for 0.0833333h; Green chemistry;98%
With dihydrogen peroxide In ethanol at 20℃; for 0.5h; Green chemistry;97%
With dihydrogen peroxide In ethanol at 20℃; for 1h; Catalytic behavior; Reagent/catalyst; Green chemistry; chemoselective reaction;90%
With dihydrogen peroxide In neat (no solvent, solid phase) at 20℃; for 0.583333h; Catalytic behavior; Green chemistry;76%
With dihydrogen peroxide In water at 20℃; for 0.1h; Rate constant; Mechanism; Thermodynamic data; ΔH(excit.), ΔS(excit.), stoichiometry, various pH, various concentrations;
96-49-1

[1,3]-dioxolan-2-one

60-24-2

2-hydroxyethanethiol

111-48-8

2,2'-thiobis-ethanol

Conditions
ConditionsYield
at 120 - 125℃;
With potassium carbonate In neat (no solvent) at 120℃; for 0.29h; Catalytic behavior; Temperature;
505-60-2

bis (2-chloroethyl) sulphide

111-48-8

2,2'-thiobis-ethanol

Conditions
ConditionsYield
With water; zinc(II) oxide
With water In ethanol Kinetics;
60-24-2

2-hydroxyethanethiol

107-07-3

2-chloro-ethanol

111-48-8

2,2'-thiobis-ethanol

Conditions
ConditionsYield
With sodium carbonate
107-07-3

2-chloro-ethanol

111-48-8

2,2'-thiobis-ethanol

Conditions
ConditionsYield
With potassium hydrosulfide at 0℃;
With sodium hydrogensulfide at 25℃;
With sodium sulfide; water Darstellung;
With potassium sulfide; water
With sodium sulfide; water
75-21-8

oxirane

60-24-2

2-hydroxyethanethiol

111-48-8

2,2'-thiobis-ethanol

Conditions
ConditionsYield
With triethylamine at 15℃; Rate constant; Mechanism; Thermodynamic data; other temperature, E(a);
693-30-1

mustard chlorohydrin

111-48-8

2,2'-thiobis-ethanol

Conditions
ConditionsYield
With water In ethanol at 25℃; Rate constant; further solvents, var. water concentration; charge separation in the transition state;
With water
505-60-2

bis (2-chloroethyl) sulphide

A

111-48-8

2,2'-thiobis-ethanol

B

64036-92-6

bis-(2-hydroxy-ethyl)-[2-(2-hydroxy-ethylsulfanyl)-ethyl]-sulfonium

C

C12H28O4S3(2+)

Conditions
ConditionsYield
In water Title compound not separated from byproducts;
64036-92-6

bis-(2-hydroxy-ethyl)-[2-(2-hydroxy-ethylsulfanyl)-ethyl]-sulfonium

A

111-48-8

2,2'-thiobis-ethanol

B

693-30-1

mustard chlorohydrin

C

505-60-2

bis (2-chloroethyl) sulphide

Conditions
ConditionsYield
With hydrogenchloride In water Product distribution; Mechanism;A 25.3 % Chromat.
B 64.8 % Chromat.
C 3.8 % Chromat.

2,2'-Thiodiethanol Consensus Reports

Reported in EPA TSCA Inventory.

2,2'-Thiodiethanol Specification

The β-Thiodiglycol, with the CAS registry number 111-48-8, is also known as 2,2'-Sulfanediyldiethanol. It belongs to the product category of Organics. Its EINECS registry number is 203-874-3. This chemical's molecular formula is C4H10O2S and molecular weight is 122.19. What's more, its IUPAC name is called 2-(2-Hydroxyethylsulfanyl)ethanol. β-Thiodiglycol is a viscous, clear to pale-yellow liquid. It is used as a solvent in a variety of applications ranging from dyeing textiles to inks in some ballpoint pens. In chemical synthesis, the production is used as a building block for protection products, dispersants, fibers, plasticizers, rubber accelerators, pesticides, dyes, and various other organic chemicals. In the manufacture of polymers, this chemical is used as a chain transfer agent. As an antioxidant, it is used as an additive in lubricants.

Physical properties about β-Thiodiglycol are: (1)# of Rule of 5 Violations: 0; (2)ACD/BCF (pH 5.5): 1; (3)ACD/BCF (pH 7.4): 1; (4)ACD/KOC (pH 5.5): 9.75; (5)ACD/KOC (pH 7.4): 9.75; (6)#H bond acceptors: 2; (7)#H bond donors: 2; (8)#Freely Rotating Bonds: 6; (9)Polar Surface Area: 65.76 Å2; (10)Index of Refraction: 1.523; (11)Molar Refractivity: 31.64 cm3; (12)Molar Volume: 103.5 cm3; (13)Surface Tension: 50 dyne/cm; (14)Density: 1.18 g/cm3; (15)Flash Point: 139.5 °C; (16)Enthalpy of Vaporization: 60.45 kJ/mol; (17)Boiling Point: 282 °C at 760 mmHg; (18)Vapour Pressure: 0.000407 mmHg at 25 °C.

Preparation of β-Thiodiglycol: this chemical can be prepared by Chlorohydrin with Sodium sulfide. This reaction needs reagent sulfuric acid at temperature of 90-95 °C.

2CH2Cl-CH2OH + Na2S → (CH2CH2OH)2S + 2NaCl

Uses of β-Thiodiglycol: it is used to produce other chemicals. For example, it can react with Methanol to get Bis-(2-methoxy-ethyl)-sulfane. The reaction occurs with reagent p-Toluenesulfonic acid monohydrate at temperature of 150 °C. The reaction time is 10 hours. The yield is 66 %.

β-Thiodiglycol can react with Methanol to get Bis-(2-methoxy-ethyl)-sulfane.

When you are dealing with this chemical, you should be very careful. This chemical is inflammation to the skin, eyes and respiratory system or other mucous membranes. Therefore, you should wear suitable protective clothing, gloves and eye/face protection. And in case of contacting with eyes, you should rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1) SMILES: OCCSCCO
(2) InChI: InChI=1S/C4H10O2S/c5-1-3-7-4-2-6/h5-6H,1-4H2
(3) InChIKey: YODZTKMDCQEPHD-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
guinea pig LD50 oral 3960mg/kg (3960mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

GASTROINTESTINAL: OTHER CHANGES

KIDNEY, URETER, AND BLADDER: OTHER CHANGES
Journal of Industrial Hygiene and Toxicology. Vol. 23, Pg. 259, 1941.
mouse LD50 subcutaneous 4gm/kg (4000mg/kg) GASTROINTESTINAL: OTHER CHANGES

LIVER: "HEPATITIS (HEPATOCELLULAR NECROSIS), DIFFUSE"

ENDOCRINE: OTHER CHANGES
Journal of Pharmacology and Experimental Therapeutics. Vol. 93, Pg. 1, 1948.
rabbit LD50 intravenous 3gm/kg (3000mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 93, Pg. 1, 1948.
rabbit LD50 skin 20mL/kg (20mL/kg)   Union Carbide Data Sheet. Vol. 11/3/1971,
rat LD50 oral 6610mg/kg (6610mg/kg)   Journal of Industrial Hygiene and Toxicology. Vol. 23, Pg. 259, 1941.
rat LD50 subcutaneous 4gm/kg (4000mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 93, Pg. 1, 1948.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 111-48-8