Top
Georganics

Home All Chemicals Benzene-1,3-disulfonyl chloride
In stock

Benzene-1,3-disulfonyl chloride

CAS#[585-47-7]
G-codeGEO-03722
EC number209-556-0
Molecular formulaC6H4Cl2O4S2
Molecular weight275.12
Synonyms

1,3-Benzenedisulfonyl dichloride ; 3-Chlorosulfonylbenzenesulfonyl chloride ; m-Benzenedisulfonyl chloride ; m-Benzenedisulfonyl dichloride ; m-Phenylenedisulfonyl chloride ; 1,3-Benzenedisulfonyl chloride

Structure of Benzene-1,3-disulfonyl chloride
General description

For more information or to place an inquiry, please email us to
georganics@georganics.sk or use our contact form

Regulatory Information

Transport InformationCORROSIVE SOLID, ACIDIC, ORGANIC, N.O.S. UN3261 8/ PG II
GHS pictogram
GHS05_corrosiveGHS08_health_hazard
Signal WordDanger
Hazard Statements
H314 - H317 - H334

H314 – Causes severe skin burns and eye damage

H317 – May cause an allergic skin reaction

H334 – May cause allergy or asthma symptoms or breathing difficulties if inhaled

Precautionary Statements
P261 - P280 - P305+351+338 - P310

P261 – Avoid breathing dust/fume/gas/mist/vapours/spray:

P280 – Wear protective gloves/protective clothing/eye protection/face protection:

P305+351+338 – IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do – continue rinsing

P310 – Immediately call a POISON CENTER or doctor/physician:

Product categorization

Description

1,3-Benzenedisulfonyl chloride is useful reagent in organic chemistry for the preparation of pharmaceutical intermediates…

Show full description

General description:

Benzene-1,3-disulfonyl chloride (BDD) [585-47-7] or 1,3-benzenedisulfonyl chloride is dichloride of 1,3-benzenedisulfonic acid. It is a colorless (white) crystalline solid with the melting point of 59-62 °C.[1] It is soluble in common organic solvents. Compound is sensitive to moisture and reacts in water therefore should be stored in dry conditions. It has corrosive properties and can cause severe skin burns and eye damage. Convenient laboratory preparation is based on chlorination of appropriate disodium salt using phosphorus chloride[1] or thionyl chloride[2]. Alternative method starts with 1,3-benzenedithiol, which reacts with chlorine in acetic acid.[3]

Application of Benzene-1,3-disulfonyl chloride:

1,3-Benzenedisulfonyl chloride is useful reagent in organic chemistry for the preparation of pharmaceutical intermediates.[4] It was used in the synthesis of isonitriles as dehydration agent of formamides.[2] Benzene-1,3-disulfonyl chloride is commonly used in the synthesis of biological active sulfonamides[5] and in the preparation of composite polysulfonamide membranes.[6]

Product categorization (Chemical groups):

Main category: Second level: Third level: ______________________________________________________________________________________
[1] Ch. J. Smedley, A. S. Barrow, Ch. Spiteri, M. C. Giel, P. Sharma, J. E. Moses Chem. Eur. J. 2017, 23, 9990. [2] R. Ghorbani-Vaghei, M. Amiri, H. Veisi Lett. Org. Chem. 2013, 10, 37. [3] Th. Zincke, O. Kruger Chemische Berichte 1912, 45, 3468. [4] A. M. Almerico, A. Campofelice, G. Culletta, L. Lentini, R. Melfi, A. Pace, R. Perriera, I. Pibiri, M. Tutone ACS Med. Chem. Lett. 2020, 11, 747. [5] S. Alavinia, J. Babamoradi, R. Ghorbani-Vaghei RSC Advances 2021, 11, 19147. [6] B.E. Ali, P. Majid, J. Mohsen, H. Hamzeh Chem. Eng. Res. Des. 2020, 155, 172.

Similar products