Skip to Content
Merck
All Photos(1)

Documents

76170

Supelco

Melting point standard 121-123°C

analytical standard

Synonym(s):

Benzoic acid

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

About This Item

Linear Formula:
C6H5COOH
CAS Number:
65-85-0
Molecular Weight:
122.12
Beilstein:
636131
EC Number:
200-618-2
MDL number:
MFCD00002398
UNSPSC Code:
20121904
PubChem Substance ID:
329766569
NACRES:
NA.24

grade

analytical standard

Quality Level

100

vapor density

4.21 (vs air)

vapor pressure

10 mmHg ( 132 °C)

autoignition temp.

1061 °F

shelf life

limited shelf life, expiry date on the label

bp

249 °C (lit.)

mp

121-123 °C (±0.3°C)
121-125 °C (lit.)

application(s)

food and beverages
pharmaceutical

format

neat

SMILES string

OC(=O)c1ccccc1

InChI

1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)

InChI key

WPYMKLBDIGXBTP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Benzoic acid melting point standard, 121-123 °C is useful as a melting point calibration standard while defining the purity of pharmaceutical chemicals. Its melting point value is determined with an average of 6 to 12 measurements using a Büchi B-545 instrument that is calibrated against primary standards.

Application

Melting point standard 121-123 °C, benzoic acid is an analytical standard used to calibrate melting point instruments, in the thermodynamic mode of operation. It is also used in R & D labs for chemical quality control (QC) and quality assurance (QA) to identify solid crystalline substances and to check their purity.

Features and Benefits

  • Melting point calibration standard traceable to primary standards (LGC, London)
  • Grade: Analytical Standard
  • Uncertainty of measurement up to ± 0.3 °C
  • Provided with certificates of analysis and safety data sheet
  • A product of analytical standard grade that meets the QC/QA requirements of melting point analysis

Pictograms

Health hazardCorrosion
GHS08,GHS05

Signal Word

Danger

Hazard Statements

H315,H318,H372

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT RE 1 Inhalation

Target Organs

Lungs

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCM0006
BCCK6317
BCCL0922
BCCH3582
BCCG8177

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

Kasture.V.A
Pharmaceutical Analysis, 1 (2008)
Renbo Wei et al.
Macromolecular rapid communications, 34(4), 330-334 (2013-01-03)
A new approach is developed to fabricate highly oriented mono-domain LCE nano/microstructures through micro-molding in capillaries. Gratings and microwires as two typical examples are fabricated and characterized by polarizing optical microscopy, optical microscopy, and scanning electron microscopy. The gratings with
G C Tremblay et al.
Pharmacology & therapeutics, 60(1), 63-90 (1993-10-01)
Detoxification of sodium benzoate by elimination as a conjugate with glycine, a nonessential amino acid, provides a pathway for the disposal of waste nitrogen. Since 1979, sodium benzoate has been widely used in the therapeutic regimen to combat ammonia toxicity
S Nacht et al.
Journal of the American Academy of Dermatology, 4(1), 31-37 (1981-01-01)
The transepidermal penetration and metabolic disposition of 14C-benzoyl peroxide were assessed in vitro (excised human skin) and in vivo (rhesus monkey). In vitro, the benzoyl peroxide penetrated into the skin, through the stratum corneum or the follicular openings, or both
Ly Dieu Tran et al.
Journal of the American Chemical Society, 134(44), 18237-18240 (2012-10-30)
An auxiliary-assisted, copper catalyzed or promoted sulfenylation of benzoic acid derivative β-C-H bonds and benzylamine derivative γ-C-H bonds has been developed. The method employs disulfide reagents, copper(II) acetate, and DMSO solvent at 90-130 °C. Application of this methodology to the
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