o-Anisaldehyde
Synonym(s):o-Anisaldehyde;2-Methoxybenzaldehyde;o-Anisaldehyde;Salicylaldehyde methyl ether
- CAS NO.:135-02-4
- Empirical Formula: C8H8O2
- Molecular Weight: 136.15
- MDL number: MFCD00003308
- EINECS: 205-171-7
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-12-18 14:15:32
What is o-Anisaldehyde?
Description
o-Methoxybenzaldehyde has a faint, sweet, floral odor. It blends well with cassia. It has a spice-like flavor, quite bitter above 30 - 40 ppm. May be prepared from salicylaldehyde and dimethyl sulfate in weak alkaline solution.
Chemical properties
light yellow to pale brown
Chemical properties
Colorless to cream amber crystalline powder; sweet powdery hawthorn guaiacol vanilla acetophenone almond aroma.
Occurrence
Reported found in Cassia oil, cinnamon bark, and Cinnamon bark oil (Cinnamomum zeylanicum Blume), Sri Lanka (0.09–0.15%)
The Uses of o-Anisaldehyde
Intermediate.
The Uses of o-Anisaldehyde
2-Methoxybenzaldehyde has been used to examine the acaricidal activity of Periploca sepium oil and its active component against Tyrophagus. It has also been used to obtain good enantioselectivities using Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding in asymmetric Henry reaction.
The Uses of o-Anisaldehyde
2-Methoxybenzaldehyde has been used to obtain good enantioselectivities using Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding in asymmetric Henry reaction.
Definition
ChEBI: 2-Methoxybenzaldehyde is a carbonyl compound.
Aroma threshold values
Medium strength odor; anisic type; recommend smelling in a 10.00% solution or less.
Taste threshold values
Sweet powdery guaiacol musty vanilla floral almond taste at 50 ppm in water.
Synthesis Reference(s)
Journal of Heterocyclic Chemistry, 11, p. 943, 1974 DOI: 10.1002/jhet.5570110616
Tetrahedron Letters, 25, p. 1843, 1984 DOI: 10.1016/S0040-4039(01)90056-5
Biochem/physiol Actions
Naturally-occurring aromatic aldehyde with acaricidal activity. May condense with L-tryptophan in foods to form the corresponding phenolic tetrahydro-β-carboline-3-carboxylic acid which is a potent antioxidant.
Safety Profile
Moderately toxic by ingestion. A skin irritant. Mutation data reported. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes.
Properties of o-Anisaldehyde
Melting point: | 34-40 °C(lit.) |
Boiling point: | 238 °C(lit.) |
Density | 1.127 g/mL at 25 °C(lit.) |
refractive index | 1.5608 |
FEMA | 4077 | O-ANISALDEHYDE |
Flash point: | 244 °F |
storage temp. | 2-8°C |
solubility | Solubility Slightly soluble in water; soluble in ethanol |
form | Low Melting Crystalline Mass |
color | Light yellow to pale brown |
Specific Gravity | 1.127 |
Odor | at 10.00 % in propylene glycol. sweet powdery hawthorn guaiacol vanilla acetophenone almond |
PH Range | Non1 uorescence (3.1) to green 1 uorescence (4.4) |
Water Solubility | insoluble |
Sensitive | Air Sensitive |
JECFA Number | 2062 |
BRN | 606301 |
Major Application | Battery, hair dyes, bird repellents, cosmetics, antibacterial, antipyretic |
CAS DataBase Reference | 135-02-4(CAS DataBase Reference) |
NIST Chemistry Reference | Benzaldehyde, 2-methoxy-(135-02-4) |
EPA Substance Registry System | Benzaldehyde, 2-methoxy- (135-02-4) |
Safety information for o-Anisaldehyde
Signal word | Warning |
Pictogram(s) |
Exclamation Mark Irritant GHS07 |
GHS Hazard Statements |
H315:Skin corrosion/irritation H319:Serious eye damage/eye irritation H335:Specific target organ toxicity, single exposure;Respiratory tract irritation |
Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P264:Wash hands thoroughly after handling. P264:Wash skin thouroughly after handling. P271:Use only outdoors or in a well-ventilated area. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of soap and water. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. |
Computed Descriptors for o-Anisaldehyde
o-Anisaldehyde manufacturer
SOLFYN INTERNATIONAL LLP
Dr. ASCRO Bio Sciences Private Limited
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