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V900789

Sigma-Aldrich

3-Hydroxybenzoic acid

Vetec™, reagent grade, 98%

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About This Item

Formula condensata:
HOC6H4CO2H
Numero CAS:
99-06-9
Peso molecolare:
138.12
Beilstein:
508160
Numero CE:
202-726-5
Numero MDL:
MFCD00002506
Codice UNSPSC:
12352100
ID PubChem:
329830157

Grado

reagent grade

Nome Commerciale

Vetec™

Saggio

98%

Punto di fusione

200-203 °C (lit.)

Stringa SMILE

OC(=O)c1cccc(O)c1

InChI

1S/C7H6O3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H,(H,9,10)
IJFXRHURBJZNAO-UHFFFAOYSA-N

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Note legali

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302,H315,H319,H335

Consigli di prudenza

P261 - P305 + P351 + P338

Classi di pericolo

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

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Yi-Li Lin et al.
Journal of hazardous materials, 137(1), 324-331 (2006-04-11)
This research is dedicated to determine the rejection ratios of disinfection by-products (DBPs) precursors including resorcinol, phloroglucinol, 3-hydroxybenzoic acid, and tannic acid solution in the presence of calcium by nanofiltration with NF70 membrane. The rejections of these model compounds also
N Laman et al.
Applied spectroscopy, 62(3), 319-326 (2008-03-15)
Low frequency vibrational modes of pharmaceutical molecules are dependent on the molecule as a whole and can be used for identification purposes. However, conventional Fourier transform far-infrared spectroscopy (FT-IR) and terahertz time-domain spectroscopy (THz-TDS) often result in broad, overlapping features
Ya-Wen He et al.
Molecular plant-microbe interactions : MPMI, 24(8), 948-957 (2011-05-05)
Xanthomonas campestris pv. campestris produces a membrane-bound yellow pigment called xanthomonadin. A diffusible factor (DF) has been reported to regulate xanthomonadin biosynthesis. In this study, DF was purified from bacterial culture supernatants using a combination of solvent extraction, flash chromatography
Fredrik L Nordström et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 28(5), 377-384 (2006-06-20)
Solution and solid-state properties of m-hydroxybenzoic acid have been investigated. Two polymorphs were found where the monoclinic modification exhibits a higher stability than the orthorhombic form. The solubility of the monoclinic polymorph was determined between 10 and 50 degrees C
Yi-Li Lin et al.
Journal of hazardous materials, 146(1-2), 20-29 (2007-01-11)
The removal of small trihalomethane precursors (THMPs) from aqueous solution by two commercial nanofiltration membranes (NF70 and NF270) was investigated. Resorcinol, phloroglucinol, and 3-hydroxybenzoic acid were selected as model compounds of small THMPs, while tannic acid was chosen as a
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