Sulfuryl chloride

Suppliers

Names

[ CAS No. ]:
7791-25-5

[ Name ]:
Sulfuryl chloride

[Synonym ]:
Sulfuryl chloride
Sulphuryl dichloride
Sulfuryl dichloride
Sulphuryl chloride
EINECS 232-245-6
MFCD00011451
sulfonyl chloride

Chemical & Physical Properties

[ Density]:
1.667

[ Boiling Point ]:
69 ºC

[ Melting Point ]:
-54.1 °C

[ Molecular Formula ]:
Cl2O2S

[ Molecular Weight ]:
134.970

[ Flash Point ]:
69.1°C

[ Exact Mass ]:
133.899612

[ PSA ]:
42.52000

[ LogP ]:
1.24

[ Vapour density ]:
4.7 (vs air)

[ Vapour Pressure ]:
147.7±0.1 mmHg at 25°C

[ Index of Refraction ]:
1.479

[ Stability ]:
Reacts violently with water. Incompatible with acids, alcohols, bases, metals, amines, moisture.

[ Water Solubility ]:
reacts

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
WT4870000
CHEMICAL NAME :
Sulfuryl chloride
CAS REGISTRY NUMBER :
7791-25-5
LAST UPDATED :
199710
DATA ITEMS CITED :
6
MOLECULAR FORMULA :
Cl2-O2-S
MOLECULAR WEIGHT :
134.96
WISWESSER LINE NOTATION :
S O2-G2

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LCLo - Lowest published lethal concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
159 ppm/4H
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
TOXID9 Toxicologist. (Soc. of Toxicology, Inc., 475 Wolf Ledge Parkway, Akron, OH 44311) V.1- 1981- Volume(issue)/page/year: 3,62,1983 ** OTHER MULTIPLE DOSE TOXICITY DATA **
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
10 ppm/6H/2W-I
TOXIC EFFECTS :
Lungs, Thorax, or Respiration - changes in lung weight Blood - pigmented or nucleated red blood cells Blood - changes in erythrocyte (RBC) count
REFERENCE :
TOXID9 Toxicologist. (Soc. of Toxicology, Inc., 475 Wolf Ledge Parkway, Akron, OH 44311) V.1- 1981- Volume(issue)/page/year: 3,62,1983 ** TUMORIGENIC DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2850 mg/kg/1Y-I
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Skin and Appendages - tumors
REFERENCE :
GISAAA Gigiena i Sanitariya. For English translation, see HYSAAV. (V/O Mezhdunarodnaya Kniga, 113095 Moscow, USSR) V.1- 1936- Volume(issue)/page/year: 47(7),9,1982 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X4088 No. of Facilities: 33 (estimated) No. of Industries: 2 No. of Occupations: 2 No. of Employees: 2256 (estimated) No. of Female Employees: 657 (estimated)

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314-H335

[ Supplemental HS ]:
Reacts violently with water.

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338-P310

[ Target Organs ]:
Blood, Central nervous system, Liver

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R14;R34;R40

[ Safety Phrases ]:
S26-S45-S36/37-S36/37/39

[ RIDADR ]:
UN 2927 6.1/PG 2

[ WGK Germany ]:
2

[ RTECS ]:
WT4870000

[ Packaging Group ]:
I

[ Hazard Class ]:
8

[ HS Code ]:
2812101000

Synthetic Route

Precursor & DownStream

Precursor

  • Chlorosulfonic acid
  • pyrosulfuryl chloride
  • SULFUR DIOXIDE
  • Chlorine
  • Disulfur dichloride
  • Thionyl chloride
  • Sulfur dichloride
  • Aluminium chloride
  • Sulfur trioxide
  • Boron trichloride

DownStream

  • Stannane, dichlorobis[(chlorosulfonyl)oxy]
  • 1,2,3,4-tetrachloro-5-methylbenzene
  • 1-Hexadecanesulfonylchloride
  • 1,2,2-trichloropropane
  • 1,1,2-TRICHLOROPROPANE
  • 1,2,3-Trichloropropane
  • Ethyl 4-chlorobutanoate
  • Ethyl-2-chloro-n-butanoate
  • Ethyl-3-chloro-n-butanoate
  • METHYL 2-CHLOROBUTYRATE

Customs

[ HS Code ]: 2812101000

Articles

Trichlorophenol (TCP) sulfonate esters: a selective alternative to pentafluorophenol (PFP) esters and sulfonyl chlorides for the preparation of sulfonamides.

Chem. Commun. (Camb.) (10) , 1074-6, (2007)

2,4,6-Trichlorophenol (TCP) sulfonate esters undergo effective aminolysis under conventional heating and microwave irradiation; the reactivity of these species is such that chemoselective transformati...

Detection of Infertility-related Neutralizing Antibodies with a Cell-free Microfluidic Method.

Sci. Rep. 5 , 16551, (2015)

The unwanted emergence of neutralizing antibodies (nAbs) against an endogenous or a therapeutic protein can result in deficiency diseases or therapy failure. Here, we developed a cell-free microfluidi...

pH-activated nanoparticles for controlled topical delivery of farnesol to disrupt oral biofilm virulence.

ACS Nano 9(3) , 2390-404, (2015)

Development of effective therapies to control oral biofilms is challenging, as topically introduced agents must avoid rapid clearance from biofilm-tooth interfaces while targeting biofilm microenviron...


More Articles


Related Compounds

  • sulfuryl chloride fluoride
  • imidobis(sulfuryl chloride)
  • Isocyanatosulfuryl chloride
  • sulfuryl azide chloride
  • sulfuryl dibromide
  • sulfuryl propionate
  • tert-butyl N-{5-[(1S)-1-amino-2-hydroxyethyl]-2-hydroxyphenyl}carbamate
  • 2-(1H-indazol-3-yl)-2-methylpropan-1-ol
  • methyl (3S)-3-hydroxy-3-(1-methyl-1H-indol-6-yl)propanoate
  • 4-Methyl-4-[2-(methylsulfanyl)phenoxy]piperidine
  • 4-[1-(2,3-Dimethylphenyl)ethyl]piperidine
  • 2-Hydroxy-2-[1-(pentan-3-yl)cyclopropyl]acetic acid
  • 4-Amino-4-(difluoromethyl)cyclohexan-1-ol
  • 1,1,1-trifluoro-3-(4-methyl-1H-imidazol-5-yl)propan-2-amine
  • 2-Hydroxy-2-methyl-5-(thiophen-3-yl)pentanoic acid
  • tert-butyl N-{4-fluoro-2-[(4-hydroxypiperidin-4-yl)methyl]phenyl}carbamate
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.