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Merck
모든 사진(1)

주요 문서

418099

Sigma-Aldrich

Benzaldehyde

purified by redistillation, ≥99.5%

동의어(들):

Bitter almond

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크기 선택

100 ML
₩129,108
500 ML
₩339,416

₩129,108


재고 있음세부사항


벌크 견적 요청

크기 선택

보기 변경
100 ML
₩129,108
500 ML
₩339,416

About This Item

Linear Formula:
C6H5CHO
CAS Number:
Molecular Weight:
106.12
Beilstein:
471223
EC Number:
MDL number:
UNSPSC 코드:
12352100
eCl@ss:
39023701
PubChem Substance ID:
NACRES:
NA.22
분석:
≥99.5%
bp:
178-179 °C (lit.)
vapor pressure:
4 mmHg ( 45 °C)

₩129,108


재고 있음세부사항


벌크 견적 요청

vapor density

3.7 (vs air)

Quality Level

vapor pressure

4 mmHg ( 45 °C)

분석

≥99.5%

양식

liquid

autoignition temp.

374 °F

정제법

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.)

작용기

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

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일반 설명

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.[1][2]

애플리케이션

Benzaldehyde can be used as a precursor to synthesize:
  • Cinnamaldehyde, cinnamic acid, ethyl cinnamate, benzoic acid, benzyl alcohol, benzyl benzoate and hydrobenzamide etc.[2]
  • Triphenylmethane derivatives by condensation with phenols, aromatic amines, and benzene. This reaction is useful for the production of malachite green dyes.[2]
  • Benzoylborane by reacting with borylmagnesium bromides.[3]
  • Multi-benzaldehyde functionalized poly(ethylene glycol) analog which is used as a cross-linker to develop an injectable hydrogel system.[4]

픽토그램

Health hazardExclamation markEnvironment

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

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

개인 보호 장비

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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이미 열람한 고객

Benzaldehyde
Bruhne F and Wright E
Ullmann's Encyclopedia of Industrial Chemistry (2000)
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)
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)
Porphyrinogens and porphodimethenes, intermediates in the synthesis of meso-tetraphenylporphins from pyrroles and benzaldehyde.
Dolphin D.
Journal of Heterocyclic Chemistry, 7, 275-283 (1970)

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