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03273

Supelco

Salicylaldehyde

analytical standard

Sinonimo/i:

2-Hydroxybenzaldehyde

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About This Item

Formula condensata:
2-(HO)C6H4CHO
Numero CAS:
90-02-8
Peso molecolare:
122.12
Beilstein:
471388
Numero MDL:
MFCD00003317
Codice UNSPSC:
41116107
ID PubChem:
329747580
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Densità del vapore

4.2 (vs air)

Tensione di vapore

1 mmHg ( 33 °C)

Saggio

≥98.5% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.573 (lit.)
n20/D 1.573

P. ebollizione

197 °C (lit.)

Punto di fusione

1-2 °C (lit.)

Densità

1.146 g/mL at 25 °C (lit.)

applicazioni

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

Formato

neat

Stringa SMILE

Oc1ccccc1C=O

InChI

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

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Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H302,H411

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Chronic 2

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

170.6 °F - closed cup

Punto d’infiammabilità (°C)

77 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG3424
BCCF0565
BCCD4695
BCCC8115
BCCB9577

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Ziyad A Taha et al.
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
Junming Ho et al.
Journal of inorganic biochemistry, 119, 10-20 (2012-11-22)
A series of N,N-disubstituted salicylaldehyde semicarbazones (SSCs), HOC(6)H(4)CHN-NHCONR(2), and their rhenium(I) tricarbonyl complexes, [ReBr(CO)(3)(SSC)], have been synthesised and characterised by IR and (1)H NMR spectroscopy. Crystallographic analysis of the complex [ReBr(CO)(3)(H(2)Bu(2))] (H(2)Bu(2)=SSC where R=Bu(n)) showed that the SSC acts as
Eila Pelttari et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 66(11-12), 571-580 (2012-02-23)
Substituted salicylaldehydes are potent antibacterial and antifungal agents and may have chemotherapeutic potential. In the clinical setting, the minimal inhibitory concentration (MIC) as well as the minimal bactericidal and fungicidal concentrations (MBC and MFC, respectively) are of fundamental interest. Therefore
Vinicius Z Mota et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 99, 110-115 (2012-10-16)
The Schiff base N,N'-bis(salicylidene)-o-phenylenediamine (salophen) was prepared by the condensation of salicylaldehyde with o-phenylenediamine in ethanol solution. The compound was characterized by elemental analysis, infrared (IR), (1)H, (13)C and (1)H(15)N HMBC nuclear magnetic resonance (NMR) spectroscopic measurements, and also by
Xianglin Shi et al.
The Journal of organic chemistry, 77(2), 1154-1160 (2011-12-17)
Mild reaction conditions for Petasis reactions of substituted salicylaldehydes with various amines and arylboronic acids in the presence of molecular sieves were developed. Molecular sieves (MS) significantly accelerated the reaction rates and drove the reactions to high conversions. The conditions
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