Chemodex

Tetracaine

Product Code:
 
CDX-T0454
Product Group:
 
Inhibitors and Activators
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
+4°C
1 / 1
Chemical Structure
❮❯

Chemical Structure

No additional charges, what you see is what you pay! *

CodeSizePrice
CDX-T0454-G0055 g£65.00
Quantity:
CDX-T0454-G02525 g£114.00
Quantity:
CDX-T0454-G05050 g£188.00
Quantity:
Prices exclude any Taxes / VAT
How to order with us   Contact us
Stay in control of your spending. These prices have no additional charges, not even shipping!
* Rare exceptions are clearly labelled (only 0.14% of items!).
Multibuy discounts available! Contact us to find what you can save.
This product comes from: Switzerland.
Typical lead time: 7-10 working days.
Contact us for more accurate information.
  • Further Information
  • Documents
  • References
  • Show All

Further Information

Alternate Names/Synonyms:
4-(Butylamino)benzoic acid 2-(dimethylamino)ethyl ester
Appearance:
White to off-white powder.
CAS:
94-24-6
Class:
6.1
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS06,GHS08
Handling Advice:
Protect from light and moisture.
Hazards:
H301, H317, H351
InChi:
InChI=1S/C15H24N2O2/c1-4-5-10-16-14-8-6-13(7-9-14)15(18)19-12-11-17(2)3/h6-9,16H,4-5,10-12H2,1-3H3
InChiKey:
GKCBAIGFKIBETG-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 94-24-6. Formula: C15H24N2O. MW: 264.36. Synthetic. Tetracaine is a potent local anaesthetic and a channel function allosteric inhibitor that blocks voltage-sensitive release of Ca2+ from sarcoplasmic reticulum. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely. inhibitor of voltage-gated sodium channels such as NaV1.4 and NaV1.8. Shown also to reversibly block nicotinic acetylcholine (ACh) receptors (nAChRs).
MDL:
MFCD00053787
Molecular Formula:
C15H24N2O
Molecular Weight:
264.36
Package Type:
Vial
PG:
III
Precautions:
P280, P301+P310
Product Description:
Tetracaine is a potent local anaesthetic and a channel function allosteric inhibitor that blocks voltage-sensitive release of Ca2+ from sarcoplasmic reticulum. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely. inhibitor of voltage-gated sodium channels such as NaV1.4 and NaV1.8. Shown also to reversibly block nicotinic acetylcholine (ACh) receptors (nAChRs).
Purity:
>98% (TLC)
Signal word:
Danger
SMILES:
CCCCNC1=CC=C(C(OCCN(C)C)=O)C=C1
Solubility Chemicals:
Soluble in DMSO or methanol. Almost insoluble in water.
Source / Host:
Synthetic
Transportation:
Excepted Quantity
UN Nummer:
2811
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) S. Hishinuma & M.K. Uchida; Br. J. Pharmacol. 103, 1393 (1991) | (2) L. Desmedt, et al.; J. Gen. Physiol. 101, 103 (1993) | (3) E. Jaimovich & E. Rojas; Cell Calcium. 15, 356 (1994) | (4) S. Gyoerke, et al.; J. Physiol. 500, 297 (1997) | (5) C.L. Overend, et al.; J. Physiol. 502, 471 (1997) | (6) D. Mears, et al.; Cell Calcium 25, 59 (1999) | (7) R. Cobo, et al.; Front. Mol. Neurosci. 11, 193 (2018)