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Merck
CN

W300403

水杨醛

≥98%, FG

别名:

2-羟基苯甲醛

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线性分子式:
2-(HO)C6H4CHO
化学文摘社编号:
分子量:
122.12
FEMA Number:
3004
Council of Europe no.:
605
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
5.055
NACRES:
NA.21
Beilstein/REAXYS Number:
471388
MDL number:
Organoleptic:
medicinal; cooling; spicy
Grade:
FG, Fragrance grade, Halal, Kosher
Biological source:
synthetic
Agency:
follows IFRA guidelines, meets purity specifications of JECFA
Food allergen:
no known allergens
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SMILES string

Oc1ccccc1C=O

InChI key

SMQUZDBALVYZAC-UHFFFAOYSA-N

InChI

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

biological source

synthetic

grade

FG, Fragrance grade, Halal, Kosher

agency

follows IFRA guidelines, meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009, EU Regulation 1334/2008 & 872/2012, FDA 21 CFR 172.515

vapor density

4.2 (vs air)

vapor pressure

1 mmHg ( 33 °C)

assay

≥98%

Quality Level

bp

197 °C (lit.)

mp

1-2 °C (lit.)

density

1.146 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

salicylaldehyde

organoleptic

medicinal; cooling; spicy

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General description

水杨醛是荞麦粉的主要气味成分。它也存在于茴香和香草精中

Application

  • 亚胺化木质素的简易合成,以增强其自由基和铅离子清除能力:这项研究提出了一种使用水杨醛合成亚胺化木质素的新方法。改性木质素表现出明显改善的自由基和铅离子清除能力,突出了其在环境修复和生物化学过程中的潜在应用(Xia 等人,2024 年)。

pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2

存储类别

10 - Combustible liquids

wgk

WGK 2

flash_point_f

170.6 °F - closed cup

flash_point_c

77 °C - closed cup

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Salicylaldehyde is a characteristic aroma component of buckwheat groats.
Janes D & Kreft S.
Food Chemistry, 109(2), 293-298 (2008)
Spectrophotometric profiles of off-flavor aldehydes by using their reactions with 2-thiobarbituric acid.
Guzman-Chozas M, et al.
Journal of Agricultural and Food Chemistry, 45(7), 2452-2457 (1997)
Stephen K Murphy et al.
Organic letters, 13(23), 6216-6219 (2011-11-09)
A method has been developed for the intermolecular hydroacylation of homoallyl alcohols with salicylaldehydes to furnish homoaldol products in 50-98% yields. The method also applies to the hydroacylation of 2-hydroxystyrenes. This work highlights the use of hydroacylation as a unified
Wen-Yong Han et al.
Organic letters, 14(4), 976-979 (2012-02-02)
The catalytic enantioselective three-component Petasis reaction among salicylaldehydes, amines, and organoboronic acids with a newly designed thiourea-binol catalyst is presented. A broad range of alkylaminophenols can be obtained in good yield (up to 92%) and good to high enantioselectivity (up
Wan Yen Lee et al.
Metallomics : integrated biometal science, 4(2), 188-196 (2011-12-03)
The copper(ii) complexes of two salicylaldehyde semicarbazones, HOC(6)H(4)CH[double bond, length as m-dash]N-NHCONR(2) [H(2)Bnz(2) (R = CH(2)Ph) and H(2)Bu(2) (R = Bu)], were evaluated for their DNA binding and cleavage properties by spectrophotometric DNA titration, ethidium bromide displacement assay and electrophoretic

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