Basic information Safety Supplier Related

treosulfan

Basic information Safety Supplier Related

treosulfan Basic information

Product Name:
treosulfan
Synonyms:
  • TREOSULPHAN
  • 1,2,3,4-butanetetrol 1,4-dimethanesulfonate
  • (2S,3S)-1-O,4-O-Di(methylsulfonyl)-L-threitol
  • CB-2562
  • L-Dihydroxy-Busulfan
  • Leo 40067
  • NSC 39069
  • THREOSULFAN
CAS:
299-75-2
MF:
C6H14O8S2
MW:
278.3
EINECS:
206-081-0
Product Categories:
  • API
Mol File:
299-75-2.mol
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treosulfan Chemical Properties

Melting point:
76-78 °C
Boiling point:
359.3°C (rough estimate)
Density 
1.305 (estimate)
refractive index 
1.5630 (estimate)
storage temp. 
Store at -20°C
solubility 
Acetone (Slightly), DMSO (Slightly), Methanol (Slightly), Water (Slightly)
form 
Solid
pka
12.36±0.20(Predicted)
color 
Off-White to Pale Beige
CAS DataBase Reference
299-75-2
IARC
1 (Vol. 26, Sup 7, 100A) 2012
EPA Substance Registry System
Treosulfan (299-75-2)
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Safety Information

RIDADR 
2811
HazardClass 
6.1(b)
PackingGroup 
III
Hazardous Substances Data
299-75-2(Hazardous Substances Data)
Toxicity
LDLo intravenous in dog: 222mg/kg
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treosulfan Usage And Synthesis

Uses

Treosulfan is used as myeloablative agent in conditioning regimen prior to allogeneic hematopoietic stem cell transplantation (HSCT)??. It can also be an effective agent for conditioning children with inborn errors of immunity (IEI).

Definition

ChEBI: Treosulfan is a methanesulfonate ester.

General Description

Odorless white crystalline powder.

Air & Water Reactions

Water soluble. Slowly hydrolyzes: decomposes within 3 hours at pH 7.5 and 77°F. .

Fire Hazard

Flash point data for treosulfan are not available; however, treosulfan is probably combustible.

Clinical Use

Alkylating agent for ovarian cancer

Safety Profile

Confirmed carcinogen. Poison by intravenous route. Human mutation data reported. When heated to decomposition it emits toxic fumes of SOx.

Metabolism

Treosulfan is a prodrug of a bifunctional alkylating agent, converted in vivo to epoxide compounds. Approximately 30
% of the substance is excreted unchanged in the urine within 24 hours, nearly 90
% of which is within the first 6 hours after administration.

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