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A7808812

Thalidomide , ≥98% , 50-35-1

Synonym(s):
(±)-2-(2,6-Dioxo-3-piperidinyl)-1H-isoindole-1,3(2H)-dione;(±)-Thalidomide - CAS 50-35-1 - Calbiochem;(±)-2-(2,6-Dioxo-3-piperidinyl)-1H-isoindole-1,3(2H)-dione;(±)-Thalidomide

CAS NO.:50-35-1

Empirical Formula: C13H10N2O4

Molecular Weight: 258.23

MDL number: MFCD00153873

EINECS: 200-031-1

Pack Size Price Stock Quantity
250mg RMB84.80 In Stock
1G RMB188.80 In Stock
5G RMB414.40 In Stock
25g RMB812.00 In Stock
100g RMB2079.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 269-271°C
Boiling point: 401.48°C (rough estimate)
Density  1.2944 (rough estimate)
refractive index  1.5300 (estimate)
storage temp.  Keep in dark place,Sealed in dry,Room Temperature
solubility  45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 0.6 mg/mL
form  White solid
pka 10.70±0.40(Predicted)
color  white
Water Solubility  <0.1 g/100 mL at 22 ºC
λmax 300nm(lit.)
Merck  14,9255
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey UEJJHQNACJXSKW-UHFFFAOYSA-N

Description and Uses

(±)-Thalidomide is an immunomodulatory compound with diverse biological activities, including anticancer, anti-inflammatory, and teratogenic properties. It prevents polymorphonuclear leukocyte (PMN) chemotaxis when used at concentrations of 1, 10, and 100 μg/ml. (±)-Thalidomide increases IL-2-induced proliferation and IFN-γ production in primary human T cells in vitro. It enhances natural killer (NK) cell-mediated cytotoxicity in MM.1S multiple myeloma cells. Thalidomide (4 mg/animal) reduces lung IL-6, TGF-β, VEGF, angiopoietin-1, angiopoietin-2, and collagen type Iα1 expression, inhibits pulmonary angiogenesis, and attenuates fibrosis in a mouse model of bleomycin-induced pulmonary fibrosis. It induces apoptosis in primary human embryonic fibroblasts (EC50 = 8.9 μM) and induces limb and eye defects in chicken embryos (EC50 = 50 μg/kg egg weight). Formulations containing thalidomide have been used in the treatment of multiple myeloma and erythema nodosum leprosum (ENL) in non-pregnant individuals.

antiinfective (topical)

Safety

Symbol(GHS) 
GHS06,GHS08
Signal word  Danger
Hazard statements  H301-H312-H360D
Precautionary statements  P201-P202-P264-P280-P301+P310-P302+P352+P312
Hazard Codes  T
Risk Statements  46-61-21-25-62-22
Safety Statements  53-22-26-36/37/39-45
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  TI4375000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29337900
Toxicity LD50 oral in mouse: 2gm/kg

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