MedKoo Cat#: 574108 | Name: Norlidocaine HCl
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Norlidocaine is an active metabolite of lidocaine formed via N-deethylation of lidocaine by the hepatic cytochrome P450 (CYP) isoform CYP3A4. Topical administration reduces thrombus formation in microvascular injury. Plasma levels of Norlidocaine following lidocaine administration have been used to monitor declining liver function in patients with cirrhosis.

Chemical Structure

Norlidocaine HCl
Norlidocaine HCl
CAS#7729-94-4 (HCl)

Theoretical Analysis

MedKoo Cat#: 574108

Name: Norlidocaine HCl

CAS#: 7729-94-4 (HCl)

Chemical Formula: C12H19ClN2O

Exact Mass: 242.1186

Molecular Weight: 242.75

Elemental Analysis: C, 59.38; H, 7.89; Cl, 14.60; N, 11.54; O, 6.59

Price and Availability

Size Price Availability Quantity
1mg USD 210.00
5mg USD 390.00
10mg USD 635.00
25mg USD 975.00
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Synonym
MEGX HCl, Monoethylglycinexylidide HCl, Norlidocaine
IUPAC/Chemical Name
N-(2,6-dimethylphenyl)-2-(ethylamino)-acetamide, monohydrochloride
InChi Key
KPXFVVHMUVBVGI-UHFFFAOYSA-N
InChi Code
InChI=1S/C12H18N2O.ClH/c1-4-13-8-11(15)14-12-9(2)6-5-7-10(12)3;/h5-7,13H,4,8H2,1-3H3,(H,14,15);1H
SMILES Code
CC1=CC=CC(C)=C1NC(CNCC)=O.Cl
Appearance
Solid powder
Purity
>95% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Product Data
Biological target:
Norlidocaine is an active metabolite of lidocaine formed via N-deethylation of lidocaine by the hepatic cytochrome P450 (CYP) isoform CYP3A4.
In vitro activity:
TBD
In vivo activity:
TBD
Solvent mg/mL mM comments
Solubility
DMF 1.0 4.12
DMSO 5.0 20.60
Ethanol 2.0 8.24
PBS (pH 7.2) 5.0 20.60
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 242.75 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
TBD
In vitro protocol:
TBD
In vivo protocol:
TBD
1. Reichel, C., Skodra, T., Nacke, A., et al. The lignocaine metabolite (MEGX) liver function test and P-450 induction in humans. Br. J. Clin. Pharmacol. 46(6), 535-539 (1998). 2. Luostarinen, V., Evers, H., Lyytikäinen, M.T., et al. Antithrombotic effects of lidocaine and related compounds on laser-induced microvascular injury. Acta Anaesthesiol. Scand. 25(1), 9-11 (1981).