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trofosfamide

Product Name
trofosfamide
CAS No.
22089-22-1
Chemical Name
trofosfamide
Synonyms
A-4828;Ccris 4442;Brn 0532530;Asta Z 4828;trofosfamide;TROPHOSPHAMIDE;Trofosfamide,Bacterial,Inhibitor,inhibit;2H-1,3,2-Oxazaphosphorin-2-amine, N,N,3-tris(2-chloroethyl)tetrahydro-, 2-oxide (9ci);3-(2-Chloroethyl)-2-(bis(2-chloroethyl)amino)perhydro-2H-1,3,2-oxazaphosphorine 2-oxide;3-(2-Chloroethyl)-2-(bis(2-chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorin 2-oxide
CBNumber
CB3877124
Molecular Formula
C9H18Cl3N2O2P
Formula Weight
323.58
MOL File
22089-22-1.mol
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trofosfamide Property

Melting point:
47-49°C
alpha 
D25 -28.6° (c = 2 in CH3OH)
Boiling point:
104°C
Density 
1.35±0.1 g/cm3(Predicted)
storage temp. 
-20°C Freezer
solubility 
DMF: 50mg/mL; DMSO: 30mg/mL; Ethanol: 50mg/mL; PBS (pH 7.2): 10mg/mL
form 
A crystalline solid
pka
-0.46±0.20(Predicted)
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Safety

Toxicity
LD50 i.p. in mice: 212 mg/kg (Brock, Potel)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H340May cause genetic defects

H350May cause cancer

H360May damage fertility or the unborn child

H372Causes damage to organs through prolonged or repeated exposure

H413May cause long lasting harmful effects to aquatic life

Precautionary statements

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

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

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

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P314Get medical advice/attention if you feel unwell.

P321Specific treatment (see … on this label).

P330Rinse mouth.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Cayman Chemical
Product number
21874
Product name
Trofosfamide
Packaging
5mg
Price
$32
Updated
2024/03/01
Cayman Chemical
Product number
21874
Product name
Trofosfamide
Packaging
10mg
Price
$50
Updated
2024/03/01
Cayman Chemical
Product number
21874
Product name
Trofosfamide
Packaging
25mg
Price
$109
Updated
2024/03/01
Cayman Chemical
Product number
21874
Product name
Trofosfamide
Packaging
50mg
Price
$169
Updated
2024/03/01
ChemScene
Product number
CS-0078076
Product name
Trofosfamide
Purity
>98.0%
Packaging
50mg
Price
$200
Updated
2021/12/16
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trofosfamide Chemical Properties,Usage,Production

Chemical Properties

Off-White Low Melting Solid

Originator

Ixoten,Asta,W. Germany,1973

Uses

Antineoplastic; one derivative

Definition

ChEBI: Trofosfamide is a member of ifosfamides.

Manufacturing Process

259 g (1 mol) of N,N-bis-(2-chloroethyl)-phosphoric acid amide dichloride, 209 g (1.2 mols) of N-(2-chloroethyl)-N-(3-hydroxypropyl)-amine hydrochloride (crude), 1,000 cc of ethylene dichloride and 344 g (3.4 mols) of triethylamine are the reactants. N,N-bis-(2-chloroethyl)-phosphoric acid amide dichloride is dissolved in the methylene dichloride. N-(2-chloroethyl)-N-(3- hydroxypropyl)-amine hydrochloride is suspended in this solution and triethylamine is added thereto dropwise with stirring. The temperature of the solution rises to boiling, After the termination of the addition, the mixture is heated to boiling for another 6 hours. Thereafter, the reaction mixture is cooled down and allowed to stand overnight at about 0°C. The precipitated triethylamine hydrochloride is filtered off with suction. The resulting solution is evaporated, the residue (about 370 g) is triturated with about 3.2 liters of ether and is heated to boiling for a short period of time.
The ethereal solution is decanted from the insolubles (about 90 g). The solution is rendered to pH 6.5 to 7 by the addition of ethereal hydrochloric acid and then is filtered over charcoal and thereafter is evaporated. During evaporation, the temperature should not rise above 40°C. The residue is dissolved in ether and in an amount corresponding to half of its weight (240 g of residue, dissolved in 120 cc of ether), the ethereal solution is cooled to - 5°C and is inoculated. After standing for 25 hours, 140 g have been separated by crystallization. After separation by filtration with suction, the mother liquor is diluted with ether to 5 times its volume, the solution is filtered over charcoal, is again evaporated and the residue is again dissolved in a volume corresponding to half of the weight of the residue. Another cooling to -5°C and inoculation produces further 18 g of the desired compound. MP: 50° to 51°C. Total yield: 161 g (50% of the theoretical)

Therapeutic Function

Cancer chemotherapy

Safety Profile

Poison by intraperitoneal, subcutaneous, and intravenous routes. Moderately toxic by ingestion. Human mutation data reported. Human systemic effects by unspecified routes: hematuria, leukopenia, and thrombocytopenia. When heated to decomposition it emits very toxic fumes of Cl-, NOx, and POx.

trofosfamide Preparation Products And Raw materials

Raw materials

Preparation Products

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trofosfamide 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
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9806
Advantage
58
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Fax
010-60605840
Email
psaitong@jm-bio.com
Country
China
ProdList
12306
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 +86-13028896684;
Email
sales@rrkchem.com
Country
China
ProdList
57412
Advantage
58
Fan De(Beijing) Biotechnology Co., Ltd.
Tel
15911056312
Email
liming@bio-fount.com
Country
China
ProdList
9729
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11217
Advantage
58
Shanghai hongqu biomedical technology co. LTD
Tel
88888888888
Email
hongquchem@qq.com
Country
China
ProdList
5132
Advantage
58

22089-22-1, trofosfamide Related Search:


  • trofosfamide
  • TROPHOSPHAMIDE
  • 2-(Bis(2-chloroethyl)amino)-3-(2-chloroethyl)tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide
  • 2H-1,3,2-Oxazaphosphorin-2-amine, N,N,3-tris(2-chloroethyl)tetrahydro-, 2-oxide (9ci)
  • 2H-1,3,2-Oxazaphosphorine, 2-(bis(2-chloroethyl)amino)-3-(2-chloroethyl)tetrahydro-, 2-oxide
  • 3-(2-Chloroethyl)-2-(bis(2-chloroethyl)amino)perhydro-2H-1,3,2-oxazaphosphorine 2-oxide
  • 3-(2-Chloroethyl)-2-(bis(2-chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorin 2-oxide
  • A-4828
  • Asta Z 4828
  • Brn 0532530
  • Ccris 4442
  • Trofosfamide,Bacterial,Inhibitor,inhibit
  • 22089-22-1
  • C9H18Cl3N2O2P
  • C9H14D4Cl3N2O2P
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Isotope Labelled Compounds
  • Pharmaceuticals