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8.01756

Sigma-Aldrich

Benzaldehyde

for synthesis

Synonym(s):

Benzaldehyde, Bitter almond oil

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About This Item

Empirical Formula (Hill Notation):
C7H6O
CAS Number:
Molecular Weight:
106.12
MDL number:
UNSPSC Code:
12352114
EC Index Number:
202-860-4
NACRES:
NA.22

vapor pressure

1.3 hPa ( 20 °C)

Quality Level

Assay

≥99.0% (GC)

form

liquid

autoignition temp.

190 °C

potency

1300 mg/kg LD50, oral (Rat)
>1250 mg/kg LD50, skin (Rabbit)

expl. lim.

1.4-8.5 % (v/v)

pH

5.9 (1 g/L in H2O)

bp

179 °C/1013 hPa

mp

-26 °C

transition temp

flash point 64 °C

solubility

3.3 g/L

density

1.05 g/cm3 at 20 °C

storage temp.

2-30°C

InChI

1S/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6H

InChI key

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Application

Benzaldehyde can be used as a reactant to synthesize:
  • β-amino ketone derivatives by Cu nanoparticles catalyzed one-pot, three-component Mannich reaction with various aromatic ketones and amines.
  • Enantioselective 1-phenyl-1-propanol by asymmetric addition of diethylzinc in the presence of fenchone-based derivatives as catalysts.
  • Benzoylborane by reacting with a boryl Grignard reagent (borylmagnesium).
  • Diethyl benzylidenemalonate by piperidine catalyzed reaction with diethyl malonate.

Analysis Note

Assay (GC, area%): ≥ 99.0 % (a/a)
Density (d 20 °C/ 4 °C): 1.044 - 1.046
Identity (IR): passes test

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

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

WGK

WGK 1

Flash Point(F)

145.4 °F - closed cup

Flash Point(C)

63 °C - closed cup


Certificates of Analysis (COA)

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Synthesis, structure of borylmagnesium, and its reaction with benzaldehyde to form benzoylborane.
Makoto Yamashita et al.
Journal of the American Chemical Society, 129(31), 9570-9571 (2007-07-17)
Novel one-pot Cu-nanoparticles-catalyzed Mannich reaction
Kidwai M, et al.
Tetrahedron Letters, 50(12), 1355-1358 (2009)
Reactions under microwave conditions
Tetrahedron Organic Chemistry Series (2005)
B Goldfuss et al.
The Journal of organic chemistry, 65(1), 77-82 (2000-05-18)
Three (-)-fenchyl alcohol derivatives, ¿(1R,2R,4S)-exo-(2-Ar)-1,3, 3-trimethylbicyclo[2.2.1] heptan-2-ol, Ar = o-anisyl (2), 2-N-methylimidazolyl (3), 2-N,N-dimethylbenzylamine (4)¿ were synthesized, characterized by X-ray analyses, and employed as precatalysts in diethyl zinc additions to benzaldehyde. Directions and relative degrees of enantioselectivities are rationalized by

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