ChemicalBook > CAS DataBase List > Anifostine trihydrate

Anifostine trihydrate

Product Name
Anifostine trihydrate
CAS No.
112901-68-5
Chemical Name
Anifostine trihydrate
Synonyms
Amifostine;AMIFOSTIN;S-(2-((3-Aminopropyl)amino)ethyl) O,O-dihydrogen phosphorothioate trihydrate;WR2721;ANIFOSTINE;Ethyol trihydrate;Amifostine (150 mg);Amifostine (1019406);Anifostine trihydrate;Amphotericin trihydrate
CBNumber
CB4316378
Molecular Formula
C5H17N2O4PS
Formula Weight
232.23
MOL File
112901-68-5.mol
More
Less

Anifostine trihydrate Property

storage temp. 
2-8°C
solubility 
PBS (pH 7.2): 5 mg/ml
form 
powder
pka
pKa1 <2.0; pKa2 4.2; pKa3 9.0; pKa4 11.7(at 25℃)
InChIKey
JKOQGQFVAUAYPM-UHFFFAOYSA-N
CAS DataBase Reference
112901-68-5(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
26-36
WGK Germany 
3
RTECS 
TE6491000
HS Code 
2930909165
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
PHR2940
Product name
Amifostine
Purity
pharmaceutical secondary standard, certified reference material
Packaging
300MG
Price
$287
Updated
2024/03/01
Sigma-Aldrich
Product number
A5922
Product name
Amifostine trihydrate
Purity
≥97% (TLC), powder
Packaging
100mg
Price
$660
Updated
2024/03/01
Sigma-Aldrich
Product number
1019406
Product name
Amifostine trihydrate
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
150mg
Price
$644
Updated
2024/03/01
Cayman Chemical
Product number
14398
Product name
Amifostine (hydrate)
Purity
≥95%
Packaging
50mg
Price
$62
Updated
2024/03/01
Cayman Chemical
Product number
14398
Product name
Amifostine (hydrate)
Purity
≥95%
Packaging
100mg
Price
$109
Updated
2024/03/01
More
Less

Anifostine trihydrate Chemical Properties,Usage,Production

Description

Amifostine is a broad-spectrum cytoprotective agent, once used as a military anti-radiation agent, and now used as a protective drug for radiotherapy and chemotherapy. It has significantly effective in reducing the side effects of anticancer drugs such as cyclophosphamide, ciplatin, doxorubicin, and anti-HIV drugs such as 3-azido-3-deoxythymidine, without affecting the efficacy of anticancer or anti-HIV drugs curative effect. At present, the commercially available amifostine products include freeze-dried powder injection(ETHYOL )produced by American Life Sciences Co., Ltd. It is only available as a lyophilized powder for injection, but is thermally unstable.

Uses

Protectant (topical); radioprotector.

Uses

Amifostine may provide renal protection during PRRT using somatostatin analogs by mitigating radiation damage and reducing the absorbed kidney radiation dose. Amifostine remediates the degenerative effects of radiation on the mineralization capacity of the murine mandible.

brand name

Ethyol (MedImmune) [USAN previously used: Ethiofos.].

Biochem/physiol Actions

Radioprotective agent. Selectively protects normal tissues from the damaging effects of anti-neoplastic radiation therapy. Selectivity is due to preferential uptake by normal tissues and subsequent metabolic activation to 2-(3-aminopropyl)aminoethanethiol.

Synthesis

1). In the 50L stainless steel reactor, add 13.6kg of pure water, 19.2mol (7.6kg) of sodium thiophosphate dodecahydrate, add N-(2-bromoethyl)-1,3-propanediamine bisulfite under stirring Hydrobromide salt 19.8mol (6.8kg, 3% excess), 11.0kg DMSO was added slowly while maintaining the reaction temperature not to exceed 25°C. After the dropwise addition of DMSO, the reaction solution was monitored with silver nitrate solution until no black precipitate was precipitated, and the reaction was completed. Centrifugal filtration to obtain 6.1 kg of crude amifostine trihydrate.2). In the 50L stainless steel crystallization kettle, add 22.0kg of pure water, add 6.1kg of the crude 3-aminopropylamine ethyl thiophosphoric acid prepared in the previous step, dissolve at room temperature, add 95.0g of activated carbon, and stir at room temperature for 15 minutes , filter, add methanol 8.7kg to the mother liquor, cool down to 0 ℃ through cooling water, maintain 18 hours, centrifugal filter, obtain 4.8kg of 3-aminopropylamine ethyl thiophosphoric acid without crystal water once recrystallization.3). Add 20.0kg of pure water to the 50L stainless steel crystallization kettle, add 4.8kg of 3-aminopropylamine ethyl thiophosphoric acid without crystal water obtained by the first recrystallization, stir and dissolve at room temperature, add 75.0g of activated carbon , stirred at room temperature for 15 minutes, filtered, added 3.2kg of ethanol to the mother liquor, cooled to 0°C through cooling water, maintained for 18 hours, centrifugally filtered, and vacuum dried at 30°C to obtain 3.6kg of amifostine trihydrate.

Anifostine trihydrate Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Anifostine trihydrate Suppliers

LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2127
Advantage
70
AdooQ BioScience, LLC
Tel
+1 (866) 930-6790
Fax
+1 (866) 333-9607
Email
info@adooq.com
Country
United States
ProdList
2784
Advantage
58
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10658
Advantage
60
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9926
Advantage
65
Target molecule Corp.
Tel
857-239-0968
Fax
857-239-8801
Email
service1@targetmol.com
Country
United States
ProdList
2559
Advantage
60
InvivoChem
Tel
+1-708-310-1919 +1-13798911105
Fax
708-557-7486
Email
sales@invivochem.cn
Country
United States
ProdList
6393
Advantage
58
BOC Sciences
Tel
+1-631-485-4226
Fax
1-631-614-7828
Email
inquiry@bocsci.com
Country
United States
ProdList
19553
Advantage
58
Aladdin Scientific
Tel
+1-833-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57511
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354
Email
support@targetmol.com
Country
United States
ProdList
19973
Advantage
58
More
Less

View Lastest Price from Anifostine trihydrate manufacturers

Hebei Duling International Trade Co. LTD
Product
Anifostine trihydrate 112901-68-5
Price
US $50.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
50 tons
Release date
2023-04-18
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Amifostine Trihydrate 112901-68-5
Price
US $0.00/Kg/Bag
Min. Order
1KG
Purity
98%min
Supply Ability
100kgs
Release date
2021-11-16
Hebei Mojin Biotechnology Co., Ltd
Product
Anifostine trihydrate 112901-68-5
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-10-13

112901-68-5, Anifostine trihydrateRelated Search:


  • Amifostine (150 mg)
  • Anifostine trihydrate
  • Ethanethiol,2-[(3-aMinopropyl)aMino]-, 1-(dihydrogen phosphate), hydrate (1:3)
  • Amifostine trihydrate, >=98%
  • Aminopropylamino)ethylsulfanylphosphonic acid trihydrate
  • S-2-(3-AMINOPROPYLAMINO)ETHYL O,O-DIHYDROGEN PHOSPHOROTHIOATE
  • WR2721
  • Amifostine
  • Amifostinetrihydrateormonohydrate
  • Ethanethiol, 2-((3-aminopropyl)amino)-, dihydrogen phosphate (ester), trihydrate
  • Amifostine Disulfide (25 mg)
  • 2-(3-aminopropylamino)ethylsulfanylphosphonic acid trihydrate
  • AMIFOSTIN
  • AMINOPROPYL AMINOETHYLTHIOPHOSPHATE
  • Ethyol trihydrate
  • ANIFOSTINE
  • Aminopropylamino)ethylsulfanylphosphonic acid trihydrate USP/EP/BP
  • 2-(3-Aminopropylamino)ethylsulfanylphosphonic acid trihydrate USP/EP/BP
  • Amifostine trihydrate (WR2721)
  • Amifostine (1019406)
  • Amifostine Disulfide (1019417)
  • S-(2-((3-Aminopropyl)amino)ethyl) O,O-dihydrogen phosphorothioate trihydrate
  • DNA-damage,thiol,HIF-PH,cytoprotective,Broad-spectrum,Hypoxia-inducible factors,HIF-α1,WR-2721,MDM-2/p53,Inhibitor,p53,Amifostine trihydrate,WR 2721,inhibit,antiangiogenic,radioprotector,HIF/HIF Prolyl-Hydroxylase,HIFs
  • 2-(3-Amino-propylamino)ethylthiophosphonic acid,trihydrate
  • Amphotericin trihydrate
  • 112901-68-5
  • 1129-68-5
  • C5H15N2O3PS3H2O
  • C5H21N2O6PS
  • Cancer Research
  • Antitumor Agents
  • BioChemical
  • Therapy Adjuncts
  • Inhibitors
  • 112901-68-5