推荐产品
生物来源
synthetic
质量水平
等级
FG
Fragrance grade
Halal
Kosher
Agency
follows IFRA guidelines
meets purity specifications of JECFA
管理合规性
EU Regulation 1223/2009
EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 172.515
蒸汽密度
4.2 (vs air)
蒸汽压
1 mmHg ( 33 °C)
检测方案
≥98%
折射率
n20/D 1.573 (lit.)
bp
197 °C (lit.)
mp
1-2 °C (lit.)
密度
1.146 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
致敏芳香化合物
salicylaldehyde
性状检查
medicinal; cooling; spicy
SMILES字符串
Oc1ccccc1C=O
InChI
1S/C7H6O2/c8-5-6-3-1-2-4-7(6)9/h1-5,9H
InChI key
SMQUZDBALVYZAC-UHFFFAOYSA-N
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一般描述
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。
应用
- Facile synthesis of iminated lignin for enhanced free radical and lead ion scavenging capabilities.: This study presents a novel method for synthesizing iminated lignin using salicylaldehyde. The modified lignin demonstrates significantly improved free radical and lead ion scavenging abilities, highlighting its potential application in environmental remediation and biochemical processes (Xia et al., 2024).
警示用语:
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Chronic 2
WGK
WGK 2
闪点(°F)
closed cup
闪点(°C)
closed cup
法规信息
危险化学品
Salicylaldehyde is a characteristic aroma component of buckwheat groats.
Food Chemistry, 109(2), 293-298 (2008)
Spectrophotometric profiles of off-flavor aldehydes by using their reactions with 2-thiobarbituric acid.
Journal of Agricultural and Food Chemistry, 45(7), 2452-2457 (1997)
Rhodium(III)-catalyzed dehydrogenative Heck reaction of salicylaldehydes.
Angewandte Chemie (International ed. in English), 51(32), 8092-8096 (2012-06-30)
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 81(1), 317-323 (2011-07-15)
Eight new lanthanide metal complexes [LnL(NO(3))(2)]NO(3) {Ln(III) = Nd, Dy, Sm, Pr, Gd, Tb, La and Er, L = bis-(salicyladehyde)-1,3-propylenediimine Schiff base ligand} were prepared. These complexes were characterized by elemental analysis, thermogravimetric analysis (TGA), molar conductivity measurements and spectral
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
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