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2-Mercaptoethanesulfonic acid

Product Name
2-Mercaptoethanesulfonic acid
CAS No.
3375-50-6
Chemical Name
2-Mercaptoethanesulfonic acid
Synonyms
Com;Hs-com;C03576;Reduced CoM;Reduced coenzyme M;2-Mercaptoethanesulfonate;MERCAPTOETHANESULFONIC ACID;2-MERCAPTOETHANESULFONIC ACID;2-sulfanylethanesulfonic acid;Mesna2-Mercaptoethanesulfonate
CBNumber
CB8186041
Molecular Formula
C2H6O3S2
Formula Weight
142.2
MOL File
3375-50-6.mol
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2-Mercaptoethanesulfonic acid Property

Density 
1.25 g/mL at 20 °C
solubility 
DMSO
form 
Powder
pka
pK1:;pK2:9.5(-1) (20°C)
BRN 
1098878
CAS DataBase Reference
3375-50-6(CAS DataBase Reference)
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Safety

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-27-36/37/39-45
RIDADR 
UN 3265 8/PG 3
WGK Germany 
2
10-23
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H314Causes severe skin burns and eye damage

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P310Immediately call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
63707
Product name
2-Mercaptoethanesulfonic acid solution
Purity
for protein sequence analysis, ampule, 3.0?M±0.1?M in H2O (T)
Packaging
10x1mL
Price
$212.4
Updated
2024/03/01
American Custom Chemicals Corporation
Product number
CHM0308673
Product name
2-MERCAPTOETHANESULFONIC ACID
Purity
95.00%
Packaging
5MG
Price
$499.82
Updated
2021/12/16
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2-Mercaptoethanesulfonic acid Chemical Properties,Usage,Production

Originator

Mistabronco,UCB,W. Germany,1973

Definition

ChEBI: An organosulfonic acid consisting of sulfonic acid having a 2-mercaptoethyl group attached to sulfur.

Manufacturing Process

2,100 g of β-S-thiuronium ethanesulfonate were placed in a solution of 2,100 cc of concentrated aqueous ammonia and 400 cc of water. The mixture was carefully warmed on a steam bath and an exothermic reaction ensured, at which point the β-S-thiuronium ethanesulfonate passed into solution. After standing for two hours at room temperature, the solution was concentrated until all of the excess ammonia had been removed.
The resultant clear solution from the ammonolysis reaction was processed through "Amberlite IR-120" ion exchange resin and converted into β-Smercaptoethanesulfonic acid in 93.7% yield (based on β-S-thiuronium ethanesulfonate).
It is expedient not to heat the reaction mixture rapidly since this increases the loss of ammonia and effects an incomplete reaction. Heating the mixture too rapidly may retard the ammonolysis reaction entirely. The amount of ammonia used is considered to be a satisfactory minimum and larger quantities of ammonia are not found to have any beneficial effect on the reaction. It is also expedient to remove the excess ammonia before processing the guanidinium β-mercaptoethanesulfonate solution through the ion exchange resin since the resin will also remove the ammonia with the result that the capacity of the resin for the exchange of guanidinium ions will be reduced.
Although the preparation of β-mercaptoethanesulfonic acid through the ammonolysis reaction is the preferred method, it is also possible to prepare the sulfonic acid by the sodium hydroxide hydrolysis of β-S-thiuronium ethanesulfonate followed by the ion exchange treatment. The resulting acid, however, is generally not as satisfactory as that prepared by the ammonolysis reaction.

Therapeutic Function

Mucolytic

Synthesis Reference(s)

Journal of the American Chemical Society, 77, p. 6231, 1955 DOI: 10.1021/ja01628a052

2-Mercaptoethanesulfonic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Mercaptoethanesulfonic acid Suppliers

Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12984
Advantage
57
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51456
Advantage
80
Career Henan Chemica Co
Tel
+86-0371-86658258 +8613203830695
Fax
0371-86658258
Email
laboratory@coreychem.com
Country
China
ProdList
30240
Advantage
58
Shaanxi Dideu Medichem Co. Ltd
Tel
+86-029-81138252 +86-18789408387
Fax
029-88380327
Email
1057@dideu.com
Country
China
ProdList
3958
Advantage
58
Energy Chemical
Tel
021-58432009 400-005-6266
Fax
021-58436166
Email
marketing@energy-chemical.com
Country
China
ProdList
44918
Advantage
58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd
Tel
17691182729 18161915376
Email
1046@dideu.com
Country
China
ProdList
10007
Advantage
58
SHANGHAI KEAN TECHNOLOGY CO., LTD.
Tel
+8613817748580
Fax
021-50175322
Email
cooperation@kean-chem.com
Country
China
ProdList
40066
Advantage
58
Shanghai Acmec Biochemical Technology Co., Ltd.
Tel
+undefined18621343501
Email
product@acmec-e.com
Country
China
ProdList
33338
Advantage
58
Hebei Weibang Biotechnology Co., Ltd
Tel
+8617732866630
Email
bess@weibangbio.com
Country
China
ProdList
18154
Advantage
58
Taiwan Hopax Chemicals Mfg. Co., Ltd
Tel
--
Fax
--
Email
hopax@hopax.com.tw
Country
China
ProdList
62
Advantage
55
Guangzhou WeiBo Chemical Co., Ltd.
Tel
--
Fax
--
Email
weibochem@163.com
Country
China
ProdList
6187
Advantage
67
Shanghai PI Chemicals Ltd.
Tel
--
Fax
--
Email
sales@pipharm.com
Country
China
ProdList
6344
Advantage
56
SHANGHAI TOSCO CHEMICAL
Tel
--
Fax
--
Email
xdm@toscochem.com
Country
China
ProdList
116
Advantage
47
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View Lastest Price from 2-Mercaptoethanesulfonic acid manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
2-Mercaptoethanesulfonic acid 3375-50-6
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20T
Release date
2024-07-19

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