418099
Benzaldehyde
purified by redistillation, ≥99.5%
동의어(들):
Bitter almond
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C6H5CHO
CAS 번호:
Molecular Weight:
106.12
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39023701
UNSPSC Code:
12352100
EC Number:
202-860-4
MDL number:
Beilstein/REAXYS Number:
471223
Assay:
≥99.5%
Bp:
178-179 °C (lit.)
Vapor pressure:
4 mmHg ( 45 °C)
vapor density
3.7 (vs air)
Quality Level
vapor pressure
4 mmHg ( 45 °C)
assay
≥99.5%
form
liquid
autoignition temp.
374 °F
purified by
redistillation
expl. lim.
1.4 %, 20 °F
refractive index
n20/D 1.545 (lit.)
pH
5.9 (20 °C)
bp
178-179 °C (lit.)
mp
−26 °C (lit.)
density
1.044 g/cm3 at 20 °C (lit.)
functional group
aldehyde, phenyl
SMILES string
O=Cc1ccccc1
InChI
1S/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6H
InChI key
HUMNYLRZRPPJDN-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
General description
Benzaldehyde (bitter-almond oil) is an aromatic compound commonly used in the cosmetics and flavor industries. The natural source of benzaldehyde is amygdalin, a glycoside found in apricots, bitter almonds, apples, cherries etc. Benzaldehyde is commercially produced by liquid phase chlorination and oxidation of toluene. Other methods reported to produce benzaldehyde include oxidation of benzyl alcohol, hydrolysis of benzal chloride and carbonylation of benzene.
Application
Benzaldehyde can be used as a precursor to synthesize:
- Cinnamaldehyde, cinnamic acid, ethyl cinnamate, benzoic acid, benzyl alcohol, benzyl benzoate and hydrobenzamide etc.
- Triphenylmethane derivatives by condensation with phenols, aromatic amines, and benzene. This reaction is useful for the production of malachite green dyes.
- Benzoylborane by reacting with borylmagnesium bromides.
- Multi-benzaldehyde functionalized poly(ethylene glycol) analog which is used as a cross-linker to develop an injectable hydrogel system.
signalword
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
저장 등급
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
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Synthesis, structure of borylmagnesium, and its reaction with benzaldehyde to form benzoylborane
Yamashita M, et al.
Journal of the American Chemical Society, 129(31), 9570-9571 (2007)
Highly selective oxidation of benzyl alcohol to benzaldehyde catalyzed by bimetallic gold?copper catalyst
Della Pina C, et al.
J. Catal., 260(2), 384-386 (2008)
Benzaldehyde
Bruhne F and Wright E
Ullmann's Encyclopedia of Industrial Chemistry (2000)
An injectable hydrogel formed by in situ cross-linking of glycol chitosan and multi-benzaldehyde functionalized PEG analogues for cartilage tissue engineering
Cao L, et al.
Journal of materials chemistry. B, 3(7), 1268-1280 (2015)
Spacing and site isolation of amine groups in 3-aminopropyl-grafted silica materials: The role of protecting groups.
Hicks JC, et al.
Chemistry of Materials, 18(21), 5022-5032 (2006)
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