Caroverine hydrochloride

Chemodex
Product Code: CDX-C0258
Product Group: Other Biochemicals
Supplier: Chemodex
CodeSizePrice
CDX-C0258-M02525 mg£181.00
Quantity:
CDX-C0258-M100100 mg£596.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4 °C

Images

1 / 1
Chemical Structure

Chemical Structure

Further Information

Alternate Names/Synonyms:
1-[2-(Diethylamino)ethyl]-3-[(4-methoxyphenyl)methyl]-2(1H)-quinoxalinone monohydrochloride; P 201-1
Appearance:
White or slightly yellow fine powder.
CAS:
55750-05-5
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H302
InChi:
InChI=1S/C22H27N3O2.ClH/c1-4-24(5-2)14-15-25-21-9-7-6-8-19(21)23-20(22(25)26)16-17-10-12-18(27-3)13-11-17;/h6-13H,4-5,14-16H2,1-3H3;1H
InChiKey:
JRNWTJUIMRLKBV-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 55750-05-5. Formula: C22H27N3O2 . HCl . H2O. MW: 401.93 . 18.0. Synthetic. Nonselective NMDA and AMPA glutamate receptor antagonist. A class B calcium-channel-blocker, antiglutamatergic agent and shown to act as an antioxidant.
MDL:
MFCD01684929
Molecular Formula:
C22H27N3O2 . HCl . H2O
Molecular Weight:
401.93 . 18.0
Package Type:
Vial
Precautions:
P264, P270, P301, P312, P330, P501
Product Description:
Nonselective NMDA and AMPA glutamate receptor antagonist. A class B calcium-channel-blocker, antiglutamatergic agent and shown to act as an antioxidant.
Purity:
>99% (HPLC)
Signal word:
Warning
SMILES:
O=C1C(CC2=CC=C(OC)C=C2)=NC3=CC=CC=C3N1CC[NH+](CC)CC.[Cl-]
Solubility Chemicals:
Soluble in DMSO (10mg/ml). Insoluble in water.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at +4°C.

References

(1) K. Ehrenberger & D. Felix; Acta Otolaryngol. 115, 236 (1995) | (2) C. Geretsegger & R. Fartacek; Eur. Neuropsychopharmacol. 8, 191 (1998) | (3) N. Udilova, et al.; Biochem. Pharmacol. 65, 59 (2003) | (4) G.B. Feld, et al.; Neuropsychopharmacol. 38, 2688 (2013)

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