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Basic Information
CAS No.: 7446-09-5
Name: Sulfur dioxide
Article Data: 2732
Molecular Structure:
Molecular Structure of 7446-09-5 (Sulfur dioxide)
Formula: SO2
Molecular Weight: 64.0648
Synonyms: Sulfursuperoxide (6CI);E 220;Fermenticide liquid;Sulfur dioxide (SO2);Sulfuroxide;Sulfur oxide (SO2);Sulfurous acid anhydride;Sulfurous anhydride;Sulfurous oxide;Sulphur dioxide;
EINECS: 231-195-2
Density: 1.59 g/cm3
Melting Point: -73 °C
Boiling Point: -10 °C
Solubility: Water: 9.4 g/100ml (20℃)
Appearance: Colourless gas
Hazard Symbols: ToxicT
Risk Codes: 23-34
Safety: 9-26-36/37/39-45
Transport Information: UN 2037 2.3
PSA: 66.23000
LogP: 0.41060
Related products
Synthetic route
10545-99-0

sulfur dichloride

7446-11-9

sulfur trioxide

A

7719-09-7

thionyl chloride

B

7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In neat (no solvent) below -10°C or under pressure;;A 100%
B n/a
...Expand

barium sulfide

A

barium sulfate

B

7446-09-5

sulfur dioxide

Conditions
ConditionsYield
With oxygen 1000°C;A 100%
B 0%
With O2 1000°C;A 100%
B 0%
921-01-7, 3374-22-9, 4371-52-2, 40143-64-4, 40143-66-6, 40143-69-9, 52-90-4

rac-cysteine

1606142-70-4

N-benzyl-2,4-dinitro-N-(prop-2-yn-1-yl)benzenesulfonamide

A

N-propargylbenzylamine

N-propargylbenzylamine

B

3165-76-2

S-(2,4-Dinitrophenyl)-cystein

C

7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In aq. phosphate buffer for 0.5h; pH=7.4;A n/a
B n/a
C 100%
...Expand
921-01-7, 3374-22-9, 4371-52-2, 40143-64-4, 40143-66-6, 40143-69-9, 52-90-4

rac-cysteine

C16H17N3O7S

A

3165-76-2

S-(2,4-Dinitrophenyl)-cystein

B

139944-56-2

2-methoxy-N-propylaniline

C

7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In aq. phosphate buffer for 0.5h; pH=7.4;A n/a
B n/a
C 100%
...Expand
921-01-7, 3374-22-9, 4371-52-2, 40143-64-4, 40143-66-6, 40143-69-9, 52-90-4

rac-cysteine

N-butyl-N-(2-methoxyphenyl)-2,4-dinitrobenzenesulfonamide

A

3165-76-2

S-(2,4-Dinitrophenyl)-cystein

B

65570-20-9

butyl-(2-methoxy-phenyl)amine

C

7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In aq. phosphate buffer for 0.5h; pH=7.4;A n/a
B n/a
C 100%
...Expand
921-01-7, 3374-22-9, 4371-52-2, 40143-64-4, 40143-66-6, 40143-69-9, 52-90-4

rac-cysteine

N-methyl-2,4-dinitro-N-(prop-2-yn-1-yl)benzenesulfonamide

A

35161-71-8

N-methylpropargylamine

B

3165-76-2

S-(2,4-Dinitrophenyl)-cystein

C

7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In aq. phosphate buffer for 0.5h; pH=7.4;A n/a
B n/a
C 100%
...Expand
921-01-7, 3374-22-9, 4371-52-2, 40143-64-4, 40143-66-6, 40143-69-9, 52-90-4

rac-cysteine

N-benzyl-N-(3-(N-(2-methoxybenzyl)-2,4-dinitrophenylsulfonamido)propyl)-2,4-dinitrobezenesulfonamide

A

3165-76-2

S-(2,4-Dinitrophenyl)-cystein

B

C18H24N2O

C

7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In aq. phosphate buffer for 0.5h; pH=7.4;A n/a
B n/a
C 100%
...Expand
921-01-7, 3374-22-9, 4371-52-2, 40143-64-4, 40143-66-6, 40143-69-9, 52-90-4

rac-cysteine

N-benzyl-N-(3-(N-(4-methoxybenzyl)-2,4-dinitrophenylsulfonamido)propyl)-2,4-dinitrobezenesulfonamide

A

3165-76-2

S-(2,4-Dinitrophenyl)-cystein

B

C18H24N2O

C

7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In aq. phosphate buffer for 0.5h; pH=7.4;A n/a
B n/a
C 100%
...Expand
921-01-7, 3374-22-9, 4371-52-2, 40143-64-4, 40143-66-6, 40143-69-9, 52-90-4

rac-cysteine

1606142-72-6

N-benzyl-N-(3-(N-(2-methoxyphenyl)-2,4-dinitrophenylsulfonamido)propyl)-2,4-dinitrobenzenesulfonamide

A

3165-76-2

S-(2,4-Dinitrophenyl)-cystein

B

C17H22N2O

C

7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In aq. phosphate buffer for 0.5h; pH=7.4;A n/a
B n/a
C 100%
...Expand
921-01-7, 3374-22-9, 4371-52-2, 40143-64-4, 40143-66-6, 40143-69-9, 52-90-4

rac-cysteine

1606142-73-7

N-benzyl-N-(3-(N-(3-methoxyphenyl)-2,4-dinitrophenylsulfonamido)propyl)-2,4-dinitrobenzenesulfonamide

A

3165-76-2

S-(2,4-Dinitrophenyl)-cystein

B

C17H22N2O

C

7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In aq. phosphate buffer for 0.5h; pH=7.4;A n/a
B n/a
C 100%
...Expand
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Consensus Reports

For Sulfur dioxide's consensus: EPA Extremely Hazardous Substances List. Reported in EPA TSCA Inventory. EPA Genetic Toxicology Program.

Standards and Recommendations

OSHA PEL: TWA 2 ppm; STEL 5 ppm
ACGIH TLV: TWA 2 ppm; STEL 5 ppm; Not Classifiable as a Human Carcinogen
DFG MAK: 0.5 pm (1.3 mg/m3)
NIOSH REL: (Sulfur Dioxide) TWA 0.5 ppm
DOT Classification:  2.3; Label: Poison Gas

Analytical Methods

For occupational chemical analysis use OSHA: #ID-107 or NIOSH: Sulfur Dioxide, 6004.

Specification

The Sulfur dioxide with CAS registry number of 7446-09-5 is also known as Sulphur dioxide. It belongs to product categories of Refrigerants; Inorganics; Chemical Synthesis; Compressed and Liquefied Gases; Synthetic Reagents; Compressed and Liquefied GasesMaterials Science; Alternative Energy; Electrolytes. This chemical is a colourless gas and should be stored in ventilated and dry place. Sulfur dioxide is the chemical compound with the formula SO2. It is a toxic gas with a pungent, irritating smell, that is released by volcanoes and in various industrial processes.

Physical properties about Sulfur dioxide are: (1)#H bond acceptors: 2; (2)Index of Refraction: 1.51; (3)Molar Refractivity: 12.053 cm3; (4)Molar Volume: 40.269 cm3; (5)Polarizability: 4.778 10-24cm3; (6)Surface Tension: 66.8939971923828 dyne/cm; (7)Density: 1.591 g/cm3; (8)Enthalpy of Vaporization: 24.94 kJ/mol; (9)Boiling Point: -10 °C at 760 mmHg; (10)Vapour Pressure: 2533.46899414063 mmHg at 25°C

Preparation of Sulfur dioxide: It is prepared by the combustion of hydrogen sulfide and organosulfur compounds.

2H2S+3O2→2H2O+2SO2

Uses of Sulfur dioxide: It is an intermediate in the production of sulfuric acid, being converted to sulfur trioxide and sometimes used as a preservative for dried apricots and other dried fruits. It is an important compound in winemaking, and is designated as parts per million in wine and also a good reductant. What's more, It or its conjugate base bisulfite is produced biologically as an intermediate in both sulfate-reducing organisms and in sulfur oxidizing bacteria as well. It is a candidate material for refrigerants and a versatile inert solvent that has been widely used for dissolving highly oxidizing salts. Treatment of aryl diazonium salts with sulfur dioxide and cuprous chloride affords the corresponding aryl sulfonyl chloride.

When you are using this chemical, please be cautious about it. As a chemical, it is toxic by inhalation and may cause burns. During using it, wear suitable protective clothing, gloves and eye/face protection. Keep container in a well-ventilated place. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. If accident happens or you feel unwell seek medical advice immediately.

You can still convert the following datas into molecular structure:
1. Canonical SMILES: O=S=O
2. InChI: InChI=1S/O2S/c1-3-2
3. InChIKey: RAHZWNYVWXNFOC-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
frog LCLo inhalation 1pph/15M (10000ppm)   "Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1396, 1935.
guinea pig LCLo inhalation 1039ppm/24H (1039ppm)   Contributions from Boyce Thompson Institute. Vol. 10, Pg. 281, 1939.
human LCLo inhalation 1000ppm/10M (1000ppm) LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION Clinical Toxicology. Vol. 5, Pg. 198, 1972.
human LCLo inhalation 3000ppm/5M (3000ppm)   Tabulae Biologicae. Vol. 3, Pg. 231, 1933.
human TCLo inhalation 3ppm/5D (3ppm) LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES Toxicology and Applied Pharmacology. Vol. 22, Pg. 319, 1972.
human TCLo inhalation 12ppm/1H (12ppm) LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES Sangyo Igaku. Japanese Journal of Industrial Health. Vol. 14, Pg. 449, 1972.
mammal (species unspecified) LCLo inhalation 3000ppm/5M (3000ppm)   Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 138, Pg. 65, 1928.
mouse LC50 inhalation 3000ppm/30M (3000ppm) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)		 Journal of Combustion Toxicology. Vol. 4, Pg. 236, 1977.
rat LC50 inhalation 2520ppm/1H (2520ppm)   National Technical Information Service. Vol. AD-A148-952,