Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

135828

Sigma-Aldrich

Benzamide

99%

Synonym(s):

Benzoic acid amide

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H5CONH2
CAS Number:
55-21-0
Molecular Weight:
121.14
Beilstein:
385876
EC Number:
200-227-7
MDL number:
MFCD00007968
UNSPSC Code:
12352100
PubChem Substance ID:
24848219
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

Assay

99%

mp

125-128 °C (lit.)

solubility

ethanol: soluble 50 mg/mL, clear to very slightly hazy, colorless to light yellow

functional group

amide
phenyl

SMILES string

NC(=O)c1ccccc1

InChI

1S/C7H7NO/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)

InChI key

KXDAEFPNCMNJSK-UHFFFAOYSA-N

Gene Information

human ... PARP1(142)

Looking for similar products? Visit Product Comparison Guide

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
39933712072694304
Benzamide 99%

135828

Benzamide

Benzamide purified by sublimation, ≥99.5%

399337

Benzamide

Benzamidine ≥95.0%

12072

Benzamidine

Benzamide (phenyl-1-13C) 99 atom % 13C

694304

Benzamide (phenyl-1-13C)

solubility

ethanol: soluble 50 mg/mL, clear to very slightly hazy, colorless to light yellow

solubility

ethanol: soluble 50 mg/mL, clear to slightly hazy, colorless to light yellow

solubility

-

solubility

-

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

-

mp

125-128 °C (lit.)

mp

125-128 °C (lit.)

mp

-

mp

125-128 °C (lit.)

functional group

amide

functional group

amide, phenyl

functional group

amine, phenyl

functional group

-

Gene Information

human ... PARP1(142)

Gene Information

human ... PARP1(142)

Gene Information

human ... F10(2159), F2(2147), PLAT(5327), PLAU(5328), PLG(5340), PRSS1(5644)

Gene Information

-

General description

Benzamide on radioiodination by different labeling procedures results in large-scale production of radioiodinated benzamides having potential therapeutic application for patients with metastatic malignant melanoma[1].

Benzamide is used as a building block in organic synthesis for the preparation of various biologically active compounds. [2]

Application

Benzamide was used to study the mechanism of photocatalytic decomposition of aqueous solution of acetic acid, acetamide and acetonitrile in the presence of semiconductors[3]. It was used to develop a robust screening method to study biotransformations using (+)-γ-lactamase enzyme[4].

Biochem/physiol Actions

Inhibits poly(ADP-ribose) polymerase (PARP).

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Statements

H302,H341

Hazard Classifications

Acute Tox. 4 Oral - Muta. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

356.0 °F - closed cup

Flash Point(C)

180 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
  • Specification Sheet

    • Choose from one of the most recent versions:

    Certificates of Analysis (COA)

    Lot/Batch Number
    STBK5339
    STBK3229
    STBK1028
    STBJ8084
    STBJ8054

    Don't see the Right Version?

    If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

    Search for a COA

    Already Own This Product?

    Find documentation for the products that you have recently purchased in the Document Library.

    Visit the Document Library

    Walter Mier et al.
    Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 55(1), 9-14 (2013-11-28)
    The performance of cytotoxic drugs is defined by their selectivity of uptake and action in tumor tissue. Recent clinical responses achieved by treating metastatic malignant melanoma with therapeutic modalities based on gene expression profiling showed that malignant melanoma is amenable
    Photocatalytic Decompositions of Carboxylic Acid Derivatives by Semiconductors.
    Park KH and Kim JH.
    Bull. Korean Chem. Soc., 12(4), 439-439 (1991)
    Willian G Birolli et al.
    Pesticide biochemistry and physiology, 156, 129-137 (2019-04-28)
    Chiral pesticides have been used in agriculture, including (±)-lambda-cyhalothrin ((±)-LC), which is a pyrethroid insecticide widely employed on crops for protection against different types of insects. However, enantioselectivity is poorly studied in biodegradation processes. Therefore, the (±)-LC enantioselective biodegradation by
    Jamin D Steffen et al.
    Journal of medicinal chemistry, 54(15), 5403-5413 (2011-06-23)
    The metabolism of poly(ADP-ribose) (PAR) in response to DNA strand breaks, which involves the concerted activities of poly(ADP-ribose) polymerases (PARPs) and poly(ADP-ribose) glycohydrolase (PARG), modulates cell recovery or cell death depending upon the level of DNA damage. While PARP inhibitors
    Anne Marie Hickey et al.
    Biotechnology journal, 4(4), 510-516 (2009-03-18)
    A (+)-gamma-lactamase was precipitated, cross-linked and the resulting solid crushed prior to immobilisation within a capillary column microreactor. The microreactor was subsequently used to study enzyme stability, activity, kinetics and substrate specificity. The thermophilic (+)-gamma-lactamase retained 100% of its initial
    View All Related Papers

    Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

    Contact Technical Service