ChemicalBook > CAS DataBase List > Sulfalen

Sulfalen

Product Name
Sulfalen
CAS No.
152-47-6
Chemical Name
Sulfalen
Synonyms
smp2;Vetkel;longum;as18908;dalysep;sulfalen;f.i.5978;kelfizin;Policydal;SULFALENE
CBNumber
CB3725126
Molecular Formula
C11H12N4O3S
Formula Weight
280.3
MOL File
152-47-6.mol
More
Less

Sulfalen Property

Melting point:
176°
Boiling point:
488.6±55.0 °C(Predicted)
Density 
1.3936 (rough estimate)
refractive index 
1.6200 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO (Slightly), Methanol (Slightly, heated)
form 
Solid
pka
pKa 6.20(H2O t = 25.0±0.5 I = 0.2) (Uncertain)
color 
White to Yellow
λmax
250nm(NaOH aq.)(lit.)
Merck 
14,8910
CAS DataBase Reference
152-47-6(CAS DataBase Reference)
More
Less

Safety

RTECS 
WP0175000
HS Code 
2935.90.9500
HazardClass 
IRRITANT
Toxicity
LD50 in mice (g/kg): 2.164 orally; 1.41 i.v. (US 3098069)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H361Suspected of damaging fertility or the unborn child

H362May cause harm to breast-fed children

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P263Avoid contact during pregnancy/while nursing.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

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

P308+P313IF exposed or concerned: Get medical advice/attention.

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

TCI Chemical
Product number
S0917
Product name
Sulfalene
Purity
>98.0%(HPLC)(T)
Packaging
5g
Price
$114
Updated
2024/03/01
TCI Chemical
Product number
S0917
Product name
Sulfalene
Purity
>98.0%(HPLC)(T)
Packaging
25g
Price
$286
Updated
2024/03/01
TRC
Product number
S699230
Product name
Sulfamethoxypyrazine
Packaging
250mg
Price
$1455
Updated
2021/12/16
ChemScene
Product number
CS-8165
Product name
Sulfalene
Purity
99.90%
Packaging
50mg
Price
$108
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0004273
Product name
SULFAMETHOXYPYRAZINE
Purity
95.00%
Packaging
25MG
Price
$401.16
Updated
2021/12/16
More
Less

Sulfalen Chemical Properties,Usage,Production

Chemical Properties

White to Yellow Solid

Originator

Longum,Farmitalia,W. Germany,1962

Uses

A possible antimalarial drug.

Definition

ChEBI: Sulfamethopyrazine is a member of pyrazines, a sulfonamide and a sulfonamide antibiotic.

Manufacturing Process

2-Amino-3,5-Dibromo-Pyrazine: 112.7 ml of bromine in 375 ml of acetic acid are slowly added at 0° to +2°C, while stirring, to a solution of 95.11 grams of 2-amino-pyrazine and 326.5 grams of acetic acid trihydrate (CH3COONa·3H2O) in 1,480 ml of acetic acid. This addition requires about 2 to 3 hours and it is carried out in the dark. The mixture is then allowed to stand at room temperature (25° to 30°C) for 15 to 16 hours. About 1.5 liters of acetic acid are distilled off under vacuum (12 to 14 mm Hg) at 35°C and the brown and viscous residue is poured into 500 grams of ice-water under stirring.
Aqueous 20% sodium hydroxide is added in order to obtain a pH = 8 and then the product is filtered and air-dried. The air-dried product is extracted 6 times with 150 ml of ether; the filtered ethereal solutions are evaporated to dryness and the residue (50 to 52 grams) is crystallized from hot water. The yield is 34.36 grams, melting at 114°C.
2-Amino-3-Methoxy-5-Bromo-Pyrazine: 7 grams of 2-amino-3,5-dibromopyrazine are boiled for 9 hours in a methanolic solution of sodium methylate (obtained from 0.65 gram of Na and 18.5 ml of methanol). By cooling a crystalline product is obtained, filtered and washed once with methanol and 2 to 3 times with water. The yield is 5.4 grams, melting at 138°C.
2-Amino-3-Methoxy-Pyrazine: 3 grams of 2-amino-3-methoxy-5-bromopyrazine are hydrogenated, in methanolic solution at room temperature and at atmospheric pressure, in the presence of 1 gram of palladium over charcoal (10%) and 0.9 gram of potassium hydroxide. When the stoichiometric amount of hydrogen is absorbed, the suspension is filtered and the filtrate is evaporated to dryness. The residue is extracted with acetone, the acetonic solution is evaporated and the residue (1.8 grams, melting at 75° to 82°C) is crystallized from cyclohexane. The yield is 1.5 grams, melting at 85°C.
2-(p-Acetylaminobenzene-sulfonamido)-3-Methoxy-Pyrazine: 1.5 grams of 2- amino-3-methoxy-pyrazine dissolved in 15 ml of anhydrous pyridine are treated, under cooling and stirring, with 2.81 grams of pacetylaminobenzenesulfonyl chloride, at small portions in about 30 minutes. The mixture is allowed to stand for 20 hours at room temperature and then is heated to 50°C for 4 hours.
The solution is concentrated to one-third of its volume, under vacuum, and poured into ice-water under stirring. The precipitate is filtered and washed with water. 2.21 grams melting at 218° to 220°C are obtained. The MP (crystallized from alcohol) is 224°C.
2-Sulfanilamido-3-Methoxy-Pyrazine: 1.5 grams of the product from the preceding step and 7 to 8 ml of aqueous 10% sodium hydroxide are boiled for 1 hour. The cooled solution is slightly acidified to pH 6 with aqueous 2 N hydrochloric acid and the product is filtered. The yield is 1.25 grams, melting at 175°C.

brand name

Kelfizina (Abbott).

Therapeutic Function

Antibacterial

Pharmaceutical Applications

2-Sulfanilamido-3-methoxypyrazine. A very long-acting compound (plasma half-life 60 h). Adequate blood levels can be maintained by giving a dose of 2 g once weekly. The protein binding is c. 70%. It has been successfully used in the single-dose treatment of urinary tract infection. As with other long-acting compounds, sulfametopyrazine has been associated with an increased incidence of erythema multiforme.

Synthesis

Sulfalene, 3-methoxy-2-sulfanilamidopyrazine (33.1.41), like other sulfanilamides, is synthesized by the standard scheme from 4-acetylaminobenzenesulfonyl chloride, which is reacted with 3-amino-2-methoxypyrazine, which is synthesized by two technologically available methods. The first of these methods consists of direct bromination of 2-aminopyrazine using acetic acid as a solvent, which gives 3,5-dibromo-2-aminopyrazine (33.1.34). Reacting this with sodium methoxide gives 3-methoxy-5-bromo-2-aminopyrazine (33.1.35). Hydrogen reduction using a palladium on carbon catalyst replaces the bromine atom at C5 of the product with a hydrogen atom, giving 3-methoxy-2-aminopyrazine (33.1.36).
This same 3-methoxy-2-aminopyrazine (33.1.36) is synthesized from 3-hydroxypyrazin- 2-carboxamide. Reacting this with phosphorous oxychloride replaces the hydroxyl group with a chlorine atom while the carboxamide group simultaneously undergoes dehydration to form 3-chloro-2-cyanopyrazine (33.1.37). Next, reacting this with sodium methoxide gives 3-methoxy-2-cyanopyrazine (33.1.38). The cyano group in this compound is hydrolyzed by a base in the presence of hydrogen peroxide to a carboxamide group, giving 3-methoxy-2-carboxamideopyrazine (33.1.39). The resulting product undergoes a Hofmann rearrangement when reacted with sodium hypochlorite, giving the desired 3-methoxy-2 aminopyrazine (33.1.36). Reacting this with 4-acetylaminobenzenesulfonyl chloride and subsequent hydrolysis of the acetyl group with a base to (33.1.40) gives sulfalene.

Sulfalen Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Sulfalen Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
TAIYUAN RHF CO.,LTD.
Tel
+86 351 7031519
Fax
+86 351 7031519
Email
sales@RHFChem.com
Country
China
ProdList
2341
Advantage
56
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32344
Advantage
50
XiaoGan ShenYuan ChemPharm co,ltd
Tel
0712-0712-2580635 15527768850
Email
1791901229@qq.com
Country
China
ProdList
8849
Advantage
52
Wuhan Fortuna Chemical Co., Ltd
Tel
027-027-59207852 13308628970
Fax
QQ3130921841
Email
buy@fortunachem.com
Country
China
ProdList
2893
Advantage
58
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12338
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22519
Advantage
55
Guangzhou Isun Pharmaceutical Co., Ltd
Tel
020-39119399 18927568969
Fax
020-39119999
Email
isunpharm@qq.com
Country
China
ProdList
4428
Advantage
55
Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-57798810
Fax
025-57019371
Email
sales@sunlidabio.com
Country
China
ProdList
3750
Advantage
55
TargetMol Chemicals Inc.
Tel
021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7934
Advantage
58
Wuhan DKY Technology Co.,Ltd.
Tel
27-81302488 18007166089
Fax
027-81302088
Email
info@dkybpc.com
Country
China
ProdList
2024
Advantage
58
Hubei XinyuanShun Chemical Co., Ltd.
Tel
13971561712, 13995564702, 027-50664929
Fax
027-50664927
Email
hbeixys2001@163.com
Country
China
ProdList
3123
Advantage
55
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41438
Advantage
60
Wuhan Dahua Pharmaceutical Co., Ltd.
Tel
027-59262863 13277907145 3091977954
Fax
027-59420980
Country
China
ProdList
4951
Advantage
58
Hubei Jusheng Technology Co.,Ltd
Tel
027-59599241 18871490274
Fax
027-59599241
Email
1400878000@qq.com
Country
China
ProdList
9972
Advantage
58
Henan CoreyChem Co., Ltd
Tel
0371-86658258
Fax
0371-60996044
Email
info@coreychem.com
Country
China
ProdList
10457
Advantage
58
Changzhou Hopschain Chemical Co.,Ltd.
Tel
0519-85528066 13775048983
Fax
0519-85528066
Email
sales@hopschem.com
Country
China
ProdList
31557
Advantage
55
Shandong Xiya Chemical Co., Ltd.
Tel
4009903999 13395398332
Fax
0539-6365991
Email
sales@xiyashiji.com
Country
China
ProdList
20810
Advantage
60
Raw material medicin reagent co.,Ltd
Tel
025-57798860
Email
sales@njromanme.com
Country
China
ProdList
4534
Advantage
58
ShangHai Biochempartner Co.,Ltd
Tel
17754423994 17754423994
Fax
QQ:2853530913
Email
2853530910@QQ.com
Country
China
ProdList
8011
Advantage
62
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131981
Advantage
58
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Fax
010-60605840
Email
psaitong@jm-bio.com
Country
China
ProdList
12308
Advantage
58
Anhui kuer Bioengineering Co., Ltd
Tel
0551-65171243 13810511747
Email
kuer@kuerhuaxue.com
Country
China
ProdList
2997
Advantage
55
Shanghai Orgchem Co.,Ltd.
Tel
+86-21-5877 1921
Fax
+86-21-5877 1925
Email
info@chemofchina.com
Country
China
ProdList
9661
Advantage
55
JinJin Le Chemical Co., Ltd
Tel
10106090
Email
jjlchem2@163.com
Country
China
ProdList
9986
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
021-021-52271985 17721149837
Fax
+86 (21) 52271987
Email
sales@9dingchem.com
Country
China
ProdList
19806
Advantage
60
Shenzhen Regent Biochemical Technology Co., Ltd.
Tel
0755-0755-85201366 18938635012
Fax
0755-85201366
Email
sales@regentsciences.com
Country
China
ProdList
9293
Advantage
58
Aikon International Limited
Tel
025-66028182 18112977050
Fax
(3)02557626880
Email
cfzhang@aikonchem.com
Country
China
ProdList
15820
Advantage
58
Wuhan FengyaoTonghui Chemical Products Co., Ltd.
Tel
027-87466105 15377573527
Email
2678564200@qq.com
Country
China
ProdList
17997
Advantage
58
Shanghai Jizhi Biochemical Technology Co. Ltd.
Tel
400-400-400-9004166 18616739031
Email
3007523370@qq.com
Country
China
ProdList
52712
Advantage
58
Shaanxi Jiandu Pharmaceutical Chemical Co. Ltd.
Tel
029-87576359 17691182729
Fax
029-88380327
Email
1018@dideu.com
Country
China
ProdList
1982
Advantage
58
Fan De(Beijing) Biotechnology Co., Ltd.
Tel
15911056312
Email
liming@bio-fount.com
Country
China
ProdList
9730
Advantage
58
Guangzhou Tomums Life Science Co., Ltd.
Tel
020-31155029 18902330969
Fax
020-31155029
Email
sales@tomums.cn
Country
China
ProdList
4698
Advantage
58
SHANDONG ZHI SHANG CHEMICAL CO.LTD
Tel
+86 18953170293
Fax
+86 0531-67809011
Email
sales@sdzschem.com
Country
China
ProdList
2931
Advantage
58
Tianjin Kaifu Pharmaceutical Technology Co., Ltd.
Tel
18081075745
Email
chemflowtech@sina.com
Country
China
ProdList
1886
Advantage
58
Hebei Mojin Biotechnology Co., Ltd
Tel
+8613288715578
Email
sales@hbmojin.com
Country
China
ProdList
12456
Advantage
58
ANHUI WITOP BIOTECH CO., LTD
Tel
+8615255079626
Email
eric@witopchemical.com
Country
China
ProdList
23556
Advantage
58
Xi'an MC Biotech, Co., Ltd.
Tel
029-89275612 +8618991951683
Fax
8618991951683
Email
mcbio_sales@163.com
Country
China
ProdList
2255
Advantage
58
Hefei TNJ Chemical Industry Co.,Ltd.
Tel
0551-65418671
Fax
0551-65418697
Email
sales@tnjchem.com
Country
China
ProdList
34572
Advantage
58
Wuhan Fortuna Chemical Co., Ltd
Tel
+86-27-59207850 +86-13986145403
Fax
86-27-59524646
Email
info@fortunachem.com
Country
China
ProdList
5989
Advantage
58
Dideu Industries Group Limited
Tel
+86-29-89586680 +86-15129568250
Email
1026@dideu.com
Country
China
ProdList
29016
Advantage
58
Baoji Guokang Healthchem co.,ltd
Tel
+8615604608665 15604608665
Email
dominicguo@gk-bio.com
Country
CHINA
ProdList
9427
Advantage
58
Hebei Qige Biological Technology Co. Ltd
Tel
+86 +8618733132031
Country
CHINA
ProdList
1313
Advantage
58
AFINE CHEMICALS LIMITED
Tel
0571-85134551
Fax
008657185134895
Email
info@afinechem.com
Country
CHINA
ProdList
15377
Advantage
58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
Tel
86-571-88216897,88216896 13588875226
Fax
86-571-88216895
Email
sales@hzclap.com
Country
CHINA
ProdList
6313
Advantage
58
Chemwill Asia Co.,Ltd.
Tel
86-21-51086038
Fax
86-21-51861608
Email
chemwill_asia@126.com
Country
CHINA
ProdList
23931
Advantage
58
Hubei Jusheng Technology Co.,Ltd.
Tel
18871490254
Fax
027-59599243
Email
linda@hubeijusheng.com
Country
CHINA
ProdList
28180
Advantage
58
Hebei Guanlang Biotechnology Co., Ltd.
Tel
+86-19930503282
Fax
whatapp+8619930503282
Email
alice@crovellbio.com
Country
China
ProdList
8823
Advantage
58
Hubei Jinsuo Biological Technology Co., Ltd.
Tel
00123456789
Email
hubeijinsuo@163.com
Country
China
ProdList
1547
Advantage
58
More
Less

View Lastest Price from Sulfalen manufacturers

Hebei Duling International Trade Co. LTD
Product
Sulfalen 152-47-6
Price
US $1.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10000
Release date
2023-01-06
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Sulfamethoxypyrazine 152-47-6
Price
US $0.00-0.00/Kg/Drum
Min. Order
1KG
Purity
99%min CP
Supply Ability
1000KGS
Release date
2021-07-21
Hebei Mojin Biotechnology Co., Ltd
Product
Sulfalene 152-47-6
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-09-08

152-47-6, SulfalenRelated Search:


  • 2-(p-aminobenzenesulfanamide)-3-methoxypyrazine
  • 2-(p-aminobenzenesulfonamido)-3-methoxypyrazine
  • sulfamethopyrazine
  • sulfametopyrazine
  • sulfapyrazinemethoxine
  • sulfapyrazinemethoxyine
  • sulfapyrazinemethoxyne
  • SULFAMETHOXYPYRAZINE(SULFALENE)
  • SULPHAMETHOXYPYRAZINE(SMPZ)
  • SULFAMETHOXYPYRAZINE(2-SULFANILAMIDO-3-METHOXYPYRAZINE)
  • Sulphanyl acid N-(3-methoxypyrazin-2-yl) amide
  • 4-Amino-N-(3-methoxy-2-pyrazinyl)-benzenesulfonamide
  • 2-Methoxy-3-sulfanilaMidopyrazine
  • Kelfizine W
  • N1-(3-Methoxypyrazinyl)-sulfanilaMide
  • Policydal
  • Vetkel
  • n1-(3-methoxy-2-pyrazinyl)sulfanilamide
  • sulfalen
  • SULFALENE
  • SULFAMETHOXYPYRAZINE
  • 4-amino-N-(3-methoxypyrazin-2-yl)benzene-1-sulfonamide
  • 2-sulfanilamido-3-methoxypyrazine
  • 3-methoxy-2-sulfanilamidopyrazine
  • 3-methoxy-2-sulfapyrazine
  • 3-methoxypyrazinesulfanilamide
  • 4-amino-n-(3-methoxypyrazinyl)-benzenesulfonamid
  • 4-amino-n-(3-methoxypyrazinyl)benzenesulfonamide
  • as18908
  • dalysep
  • f.i.5978
  • farmitalia204/122
  • kelfizin
  • kelfizina
  • kelfizine
  • longum
  • n(sup1)-(3-methoxy-2-pyrazinyl)-sulfanilamid
  • n(sup1)-(3-methoxy-2-pyrazinyl)sulfanilamide
  • n(sup1)-(3-methoxypyrazinyl)-sulfanilamid
  • n(sup1)-(3-methoxypyrazinyl)sulfanilamide
  • nsc-110433
  • polycidal
  • smp2
  • 4-aMino-N-(3-Methoxypyrazin-2-yl)benzenesulfonaMide
  • 4-Amino-N-(3-methoxypyrazin-2-yl)
  • Sulfalene&gt
  • Benzenesulfonamide, 4-amino-N-(3-methoxy-2-pyrazinyl)-
  • N-(3-Methoxypyrazin-2-yl)sulfanilamide
  • Sulfalen USP/EP/BP
  • Sulfalen(SMPZ)
  • Sulfamethoxizine
  • SULFAMETHOXY
  • Sulfalene(Sulfametopyrazine)
  • 152-47-6
  • Pharmaceuticals
  • Sulfur & Selenium Compounds
  • API
  • Amines