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1366080

USP

Lidocaine Related Compound H

United States Pharmacopeia (USP) Reference Standard

Synonym(s):

N-(2,6-Dimethylphenyl)chloroacetamide, 1-Chloroacetylamino-2,6-dimethylbenzene, 2-Chloro-2′,6′-acetoxylidide, 2-Chloro-2′,6′-dimethylacetanilide, 2-Chloro-N-(2,6-dimethylphenyl)acetamide, N-(2,6-Dimethylphenyl)-2-chloroacetamide, N-(2,6-Xylyl)chloroacetamide, N-Chloroacetyl-2,6-dimethylaniline, Chloroacetamido-2,6-xylidine

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1 G
¥2,267.71

About This Item

Linear Formula:
ClCH2CONHC6H3(CH3)2
CAS Number:
Molecular Weight:
197.66
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24

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grade

pharmaceutical primary standard

API family

lidocaine

manufacturer/tradename

USP

mp

150-151 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

Cc1cccc(C)c1NC(=O)CCl

InChI

1S/C10H12ClNO/c1-7-4-3-5-8(2)10(7)12-9(13)6-11/h3-5H,6H2,1-2H3,(H,12,13)

InChI key

FPQQSNUTBWFFLB-UHFFFAOYSA-N

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1 of 4

This Item
S5393I4131I4506
biological source

human

biological source

human

biological source

-

biological source

-

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

form

lyophilized powder

form

lyophilized powder

form

essentially salt-free, lyophilized powder

form

essentially salt-free, lyophilized powder

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

packaging

vial of 0.5 mL

packaging

vial of 0.5 mL

packaging

-

packaging

-

contains

15 mM sodium azide

contains

15 mM sodium azide

contains

-

contains

-

General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Lidocaine Related Compound H USP reference standard for specifies quality tests and assay use.

Also used to prepare standard solutions for impurity analysis according to the given below monographs of United States Pharmacopeia (USP):
  • Lidocaine[1]
  • Lidocaine Hydrochloride Topical Solution[2]
  • Lidocaine Hydrochloride Oral Topical Solution[3]
  • Lidocaine Hydrochloride[4]

Analysis Note

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

Other Notes

Sales restrictions may apply.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Oligodeoxynucleotide analogues containing 3'-deoxy-3'-C- threo-hydroxymethylthymidine: Synthesis, hybridization properties and enzymatic stability.
Svendsen ML, et al.
Tetrahedron, 49(48), 11341-11352 (1993)
A Elmblad et al.
Nucleic acids research, 10(10), 3291-3301 (1982-05-25)
A method for the synthesis of mixed dimers, trimers and oligonucleotides on a solid support using monomeric protected nucleoside phosphochloridites (1a-d) has been developed and the different nucleoside reagents, and the results show that yields of different oligomers in a
K Miyoshi et al.
Nucleic acids research, 8(22), 5473-5489 (1980-11-25)
Synthesis of two oligothymidylic acids, tridecamer and nonadecamer, is described by a rapid and simple solid-phase method on two kinds of polyacrylamide supports derivatized from commercially available Enzacryl Gel K-2. The syntheses were performed by the phosphotriester method using di-
Tamara I Prykota et al.
Nucleosides, nucleotides & nucleic acids, 30(7-8), 544-551 (2011-09-06)
A new labeling technique attaching a fluorescent pteridine derivative (3, 5) via a linker onto the 3'-OH group of 5'-O-dimethoxytritylthymidine (7) was developed to lead to the conjugates 8 and 11. After detritylation to give 9 and 12, the final
A Guzaev et al.
Bioorganic & medicinal chemistry letters, 8(9), 1123-1126 (1999-01-01)
A novel solid-phase synthesis of 5'-radiolabeled oligonucleotides is described. The labeling reaction is carried out by the phosphoramidite method with the aid of [4,6-di-14C]-5'-dimethoxytritylthymidine building block 1. The feasibility of the method is demonstrated by preparation of 3'-phosphorylated dodecathymidylate phosphorothioate

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