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03273

Supelco

Salicylaldehyde

analytical standard

Sinônimo(s):

2-Hydroxybenzaldehyde

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About This Item

Fórmula linear:
2-(HO)C6H4CHO
Número CAS:
90-02-8
Peso molecular:
122.12
Beilstein:
471388
Número MDL:
MFCD00003317
Código UNSPSC:
41116107
ID de substância PubChem:
329747580
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

densidade de vapor

4.2 (vs air)

pressão de vapor

1 mmHg ( 33 °C)

Ensaio

≥98.5% (GC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

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

p.e.

197 °C (lit.)

pf

1-2 °C (lit.)

densidade

1.146 g/mL at 25 °C (lit.)

aplicação(ões)

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

Formato

neat

cadeia de caracteres SMILES

Oc1ccccc1C=O

InChI

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

chave InChI

SMQUZDBALVYZAC-UHFFFAOYSA-N

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Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palavra indicadora

Warning

Frases de perigo

H302,H411

Classificações de perigo

Acute Tox. 4 Oral - Aquatic Chronic 2

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

170.6 °F - closed cup

Ponto de fulgor (°C)

77 °C - closed cup

Equipamento de proteção individual

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

Escolha uma das versões mais recentes:

Certificados de análise (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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