ChemicalBook > CAS DataBase List > Tiopronin

Tiopronin

Product Name
Tiopronin
CAS No.
1953-02-2
Chemical Name
Tiopronin
Synonyms
Thiola;Thiopronin;N-(2-MERCAPTOPROPIONYL)GLYCINE;2-(2-Mercaptopropanamido)acetic acid;Capen;2-MPG;Vincol;SF-572;Thiora;Epatiol
CBNumber
CB2106227
Molecular Formula
C5H9NO3S
Formula Weight
163.19
MOL File
1953-02-2.mol
More
Less

Tiopronin Property

Melting point:
93-98 °C
Boiling point:
418.3±30.0 °C(Predicted)
Density 
1.249 (estimate)
refractive index 
1.5216 (estimate)
storage temp. 
Inert atmosphere,2-8°C
solubility 
DMSO (Slightly), Methanol (Slightly)
pka
3.36±0.10(Predicted)
form 
solid
color 
White
Merck 
14,9453
BRN 
1859822
CAS DataBase Reference
1953-02-2(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
36/37
WGK Germany 
3
RTECS 
MC0596500
HS Code 
2930.90.4950
Toxicity
LD50 i.v. in mice: 2.1 g/kg (Fujimura)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

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

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
M6635
Product name
N-(2-Mercaptopropionyl)glycine
Packaging
5G
Price
$103
Updated
2023/06/20
Sigma-Aldrich
Product number
M6635
Product name
N-(2-Mercaptopropionyl)glycine
Packaging
10G
Price
$192
Updated
2023/06/20
TCI Chemical
Product number
T2614
Product name
Tiopronin
Purity
>97.0%(GC)(T)
Packaging
5g
Price
$108
Updated
2024/03/01
TCI Chemical
Product number
T2614
Product name
Tiopronin
Purity
>97.0%(GC)(T)
Packaging
25g
Price
$280
Updated
2024/03/01
Cayman Chemical
Product number
23720
Product name
Tiopronin
Purity
≥98%
Packaging
1g
Price
$32
Updated
2024/03/01
More
Less

Tiopronin Chemical Properties,Usage,Production

Description

Tiopronin is a sulfiydryl derivative of N-propylglycine useful in the treatment of cystine urolithiasis in children. It is also reportedly effective in the management of rheumatoid polyarthritis, possibly due to its inhibitory effect on the free oxygen radicals produced by inflammatory macrophages and granulocytes.

Description

Tiopronin is an antioxidant that has diverse biological activities. It reduces free radical production by murine macrophages and granulocytes in vitro in a dose-dependent manner. Tiopronin induces expression of hypoxia-inducible factor 1α (HIF-1α) and increases VEGF secretion in human colon carcinoma cells. Rectal administration (500 μL of a 10 mM solution) reduces myeloperoxidase activity and reduces pro-inflammatory cytokine production in the colon in a rat model of colitis. Tiopronin (80-320 mg/kg per day) reduces the incidence of cleft palate in fetuses born to female mice orally exposed to teratogenic methylmercury chloride. Tiopronin (100 mg/kg) reduces heme oxygenase 1 mRNA expression, lipid peroxidation, and transverse aortic constriction in a mouse model of cardiac hypertrophy. Tiopronin (20 mg/kg) is hepatoprotective, increasing activity of the antioxidant enzymes superoxide dismutase and glutathione peroxidase and reversing hepatocyte degeneration in a rat model of high-fat diet-induced non-alcoholic steatohepatitis.

Chemical Properties

White Solid

Originator

Roussel-Uclaf (Japan)

Uses

N-(2-Mercaptopropionyl)glycine or Tiopronin has been used:

  • in the preparation of polyethylenimine (PEI)-coated gold microparticles (PEI-gold) for biolistic delivery of nucleic acids
  • to study the role of reactive oxygen species (ROS) at the reperfusion stage in in vivo isoflurane preconditioning-induced neuroprotection
  • as a ROS inhibitor to study its effect on lysophosphatidylcholine (LPC)-induced inflammasome activation

Uses

It is used as antidote against heavy metal poisoning; hepatoprotectant; mucolytic.

Definition

ChEBI: Tiopronin is a N-acyl-amino acid.

Manufacturing Process

α-Benzylmercaptopropionic acid (melting point 76°C to 78°C; 100 g) prepared by condensation of α-mercaptopropionic acid with benzyl chloride is allowed to stand overnight with 80 g of thionyl chloride. After removal of excess thionyl chloride distillation in vacuo gives 70 g of α-benzylmercaptopropionic acid chloride of boiling point 138°C to 139°C/7 to 8 mm Hg.
Then, 25 g of glycine is dissolved in 165 ml of 2 N sodium hydroxide solution and 70 g of α-benzylmercaptopropionic acid chloride and 100 ml of 2 N sodium hydroxide solution are dropped thereinto simultaneously at 3°C to 5°C. The solution is then stirred at room temperature for 3 to 4 hours to complete the reaction, the reaction solution is washed with ether, the aqueous layer is acidified with hydrochloric acid, and the resulting crystals are collected by filtration. These are recrystallized from a mixture of methanol and ethyl acetate to give 60 g of α-benzylmercaptopropionylglycine of melting point 133°C to 134°C.
This α-benzylmercaptopropionylglycine (60 g) is dissolved in 400 ml of liquid ammonia, kept at about -50°C, and 12 g of sodium metal is gradually added thereto. After the reaction, excess ammonia is removed therefrom, the residue is dissolved in water, washed with ether and the residual aqueous layer is adjusted to pH 1 with hydrochloric acid and concentrated in vacuo in a stream of hydrogen sulfide. The crystalline residue is dried and recrystallized from ethyl acetate to give 25 g of α-mercaptopropionylglycine of melting point 95°C to 97°C.

brand name

Thiola

Therapeutic Function

Antidote (heavy metal)

Biochem/physiol Actions

N-(2-Mercaptopropionyl)glycine (NMPG) is a thiol compound associated with autoimmune hypoglycemia. It is a diffusible antioxidant and reduces the severity of colonic injury. NMPG also relieves myeloperoxidase activity and stimulates hypoxia-inducible factor-1 (HIF-1) - vascular endothelial growth factor (VEGF) pathway for ulcer healing.

Veterinary Drugs and Treatments

Tiopronin is indicated for the prevention of cystine urolithiasis in patients where dietary therapy combined with urinary alkalinization is not completely effective. It may also be useful in combination with urine alkalinization to dissolve stones.

Tiopronin Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Tiopronin Suppliers

Jiangxi ravel Biotechnology Co.,Ltd
Tel
400-880-2824 18107960669
Fax
18140514863
Email
79046690@qq.com
Country
China
ProdList
1267
Advantage
58
Suzhou Laihui Biotechnology Co., Ltd.
Tel
180-13160973 18013160973
Fax
0512-68236973
Email
rywaybio@gmail.com
Country
China
ProdList
298
Advantage
55
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15839
Advantage
69
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Fax
0086-571-85864795
Email
sales@capotchem.com
Country
China
ProdList
18207
Advantage
66
Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9809
Advantage
59
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
XiaoGan ShenYuan ChemPharm co,ltd
Tel
15527768850
Email
1791901229@qq.com
Country
China
ProdList
8843
Advantage
52
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11707
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14435
Advantage
57
Hunan Hui Bai Shi Biotechnology Co., Ltd.
Tel
0731-85526065 13308475853
Email
ivy@hnhbsj.com
Country
China
ProdList
4552
Advantage
62
Wuhan Fortuna Chemical Co., Ltd
Tel
027-59207852 13308628970
Fax
QQ3130921841
Email
buy@fortunachem.com
Country
China
ProdList
2871
Advantage
58
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
meilunui@163.com
Country
China
ProdList
4727
Advantage
58
BioBioPha Co., Ltd.
Tel
0871-65217109 13211707573;
Fax
0871-65215563
Email
y.liu@mail.biobiopha.com
Country
China
ProdList
5653
Advantage
65
ShangHai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847 13636370518
Fax
021-55068248
Email
shyysw007@163.com
Country
China
ProdList
4940
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9718
Advantage
55
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9865
Advantage
52
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12335
Advantage
58
Shanghai Topbiochem Technology Co., Ltd
Tel
021-58170097
Email
info@topbiochem.com
Country
China
ProdList
9459
Advantage
58
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Fax
+86 21 50676805
Country
China
ProdList
9891
Advantage
58
Haoyuan Chemexpress Co., Ltd.
Tel
021-58950125
Fax
(86) 21-58955996
Email
info@chemexpress.com
Country
China
ProdList
7552
Advantage
61
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22514
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-400-6206333 18521732826
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
The future of Shanghai Industrial Co., Ltd.
Tel
021-61552785
Fax
021-55660885
Email
sales@shshiji.com
Country
China
ProdList
9545
Advantage
55
China Nobel Chem Co., Limited
Tel
+86(0)21 60484900
Fax
+86(0)21 60484900
Country
China
ProdList
764
Advantage
50
Chengdu AstaTech Trading Co., Ltd./AstaTech (Chengdu) Pharma. Co., Ltd.
Tel
+86-28-85122536 85324413
Fax
+86-28-85326443
Email
market@astatech.cn
Country
China
ProdList
8026
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
3239
Advantage
55
TargetMol Chemicals Inc.
Tel
021-021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7783
Advantage
58
Wuhan DKY Technology Co.,Ltd.
Tel
27-81302488 18007166089
Fax
027-81302088
Email
info@dkybpc.com
Country
China
ProdList
2024
Advantage
58
Shanghai JONLN Reagent Co., Ltd.
Tel
400-0066400 13621662912
Fax
021-55660885
Email
422131432@qq.com
Country
China
ProdList
9978
Advantage
55
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41462
Advantage
60
Shanghai DiBai Chemicals Co., Ltd.
Tel
021-54359730 400-008-9730
Fax
021-54353864
Email
info@chemxyz.com
Country
China
ProdList
3991
Advantage
60
ChongQing Purel Bio-Pharmaceutical Technology Co., Ltd.
Tel
023-89130144 18523560356
Fax
023-67534737
Email
zhyong1011@163.com
Country
China
ProdList
299
Advantage
58
ChemStrong Scientific Co.,Ltd
Tel
0755-0755-66853366 13670046396
Fax
0755-28363542
Email
sales@chem-strong.com
Country
China
ProdList
18042
Advantage
56
Wuxi Zhongkun Biochemical Technology Co., Ltd.
Tel
0510-85629785 18013409632
Fax
051085625359
Email
sales@reading-chemicals.com
Country
China
ProdList
15178
Advantage
58
Wuhan Dahua Pharmaceutical Co., Ltd.
Tel
027-59262863 13277907145 3091977954
Fax
027-59420980
Country
China
ProdList
4943
Advantage
58
Shanghai HuanChuan Industry Co.,Ltd.
Tel
021-61478794
Fax
021-61478794
Email
sales@hcshhai.com
Country
China
ProdList
9793
Advantage
50
Lihe Wuhan New Chemical Materials Co., Ltd.
Tel
027-88395709
Fax
027-88391805
Country
China
ProdList
429
Advantage
50
Shanghai Song Yuan Chemical Technology Co., Ltd.
Tel
010-1234567 18521000990
Fax
86-021-33275113
Email
sonyuanchemical@163.com
Country
China
ProdList
6479
Advantage
50
Hubei Jusheng Technology Co.,Ltd
Tel
027-59599241 18871490274
Fax
027-59599241
Email
1400878000@qq.com
Country
China
ProdList
9958
Advantage
58
Dalian Wondersun Biochemical Technology Co., Ltd.
Tel
0411-88165855
Fax
0411-88165855
Email
sales@wdspharma.com
Country
China
ProdList
56
Advantage
50
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51456
Advantage
80
Watson Biotechnology Co.,Ltd
Tel
027-59207879 1972026995 18140587686
Fax
QQ:1972026995
Email
sales@3600chem.com
Country
China
ProdList
4668
Advantage
55
Wuhan Senwayer Century Chemical Co.,Ltd
Tel
027-86652399 13627115097;
Fax
86-27-59707018
Email
sales@senwayer.com
Country
China
ProdList
267
Advantage
55
SanoChem (Chengdu) Tech. Co., Ltd.
Tel
28-87999436 02887999436
Fax
QQ:2746983436
Email
sales@sano-chem.com
Country
China
ProdList
3795
Advantage
55
Hubei Kangbaotai Finechem Co., Ltd.
Tel
+86 (27) 8778653
Fax
+86 (27) 8773-8652
Email
13720228325@163.com
Country
China
ProdList
337
Advantage
58
Chengdu RunZeBenTu Chemical Co., Ltd
Tel
028-88469284 18000562381
Email
rzbtsj@163.com
Country
China
ProdList
9951
Advantage
56
More
Less

View Lastest Price from Tiopronin manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Tiopronin 1953-02-2
Price
US $0.00/Kg/Bag
Min. Order
1KG
Purity
98.5%min; CP/JP
Supply Ability
3500kg/month
Release date
2021-06-03
Hangzhou Hyper Chemicals Limited
Product
Tiopronin 1953-02-2
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
USP, BP
Supply Ability
5,000KG
Release date
2024-06-13
Hebei Yanxi Chemical Co., Ltd.
Product
Tiopronin 1953-02-2
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
100tons
Release date
2023-08-16

1953-02-2, TioproninRelated Search:


  • A-MERCAPTOPROPIONYL GLYCINE
  • ALPHA-MERCAPTO PROPIONYL GLYCINE
  • LABOTEST-BB LT00451995
  • TIOPRONIN
  • N-(2-MERCAPTOPROPIONYL)GLYCINE
  • TOPRONIN
  • (2-Mercaptopropionamido)acetic acid
  • (2-Mercaptopropionyl)glycine
  • Acadione
  • a-Mercaptopropionyglycine
  • BRN 1859822
  • Capen
  • Captimer
  • CCRIS 1935
  • DL-(a-Mercaptopropionyl)glycine
  • Epatiol
  • Glycine, N-(2-mercapto-1-oxopropyl)- (9CI)
  • Glycine, N-(2-mercaptopropionyl)- (7CI, 8CI)
  • Hepadigest
  • Meprin (detoxicant)
  • MPG (hepatoprotective)
  • Mucolysin
  • N-(2-Meraptopropionyl)glycine
  • Sutilan
  • Sutilan Cusi
  • Thiola
  • Thiolpropionamidoacetic acid
  • Thiopronin
  • Thiopronine
  • Thiosol
  • Tiopronin, Vetranal
  • N-(2-MERCAPTOPROPIONYL)GLYCINE 99%
  • Tioglis
  • Tiopronino
  • Tioproninum
  • Vincol
  • n-(2-mercapto-1-oxopropyl)-glycin
  • [(2-mercaptopropanoyl)amino]acetic acid
  • N-(α-Mercaptopropionyl)glycine
  • SF-572
  • 2-(2-Sulfanylpropanoylamino)acetic acid
  • 2-MPG
  • Thiora
  • N-(.alpha.-Mercaptopropionyl) glycine
  • N-(2-Mercaptopropionyl)glycine, Tiopronin
  • (±)-N-(2-Mercapto-1-oxopropyl)glycine
  • 2-(2-mercaptopropanoylamino)acetic acid
  • 2-(2-sulfanylpropanoylamino)ethanoic acid
  • Tiopronin/N-(2-mercaptopropionyl)glycine
  • Tiopronin (Thiola)
  • Tiopronin (base and/or unspecified salts)
  • 2-[(2-mercapto-1-oxopropyl)amino]acetic acid
  • 2-(2-sulfanylpropanamido)acetic acid
  • Tiopronin (APIs)
  • N-(2-MercaptopropionyL
  • Glycine, N-(2-mercapto-1-oxopropyl)-
  • 2-(2-Mercaptopropanamido)acetic acid
  • Tiopronin USP/EP/BP