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CAS RN: 122292-85-7 | Product Number: T3633

(-)-Trichostatin A


Purity: >98.0%(HPLC)
Synonyms:
  • [S-(E,E)]-(-)-7-[4-(Dimethylamino)phenyl]-N-hydroxy-4,6-dimethyl-7-oxo-2,4-heptadienamide
Product Documents:
10MG
€393.00
1   ≥100 

*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).


Product Number T3633
Purity / Analysis Method >98.0%(HPLC)
Molecular Formula / Molecular Weight C__1__7H__2__2N__2O__3 = 302.37 
Physical State (20 deg.C) Solid
Storage Temperature Frozen (<0°C)
Condition to Avoid Heat Sensitive
CAS RN 122292-85-7
Reaxys Registry Number 5291762
PubChem Substance ID 354334997
Specifications
Appearance White to Orange to Green powder to crystal
Purity(HPLC) min. 98.0 area%
Optical purity(LC) min. 95.0 ee%
Properties (reference)
Specific Rotation -133° (C=0.3,MeOH)
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H302 + H312 + H332 : Harmful if swallowed, in contact with skin or if inhaled.
H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P261 : Avoid breathing dust.
P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P302 + P352 + P312 : IF ON SKIN: Wash with plenty of water. Call a POISON CENTER/doctor if you feel unwell.
P304 + P340 + P312 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. Call a POISON CENTER/doctor if you feel unwell.
Related Laws:
Transport Information:
HS Number 2928009090
Application
(-)-Trichostatin A: The Less Active Enantiomer of Trichostatin A

(-)-Trichostatin A (S-enantiomer) is the less active enantiomer (distomer) of trichostatin A (R-enantiomer) [T2477] as a HDAC inhibitor. However, it has been reported that HDAC inhibition assays with R- and S-trichostatin A in 2016 showed that the R-enantiomer was a broad-range HDAC inhibitor, whereas the S-enantiomer had moderate selectivity for HDAC6.

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