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G5627

Sigma-Aldrich

Guaiacol glyceryl ether

≥98% (GC)

Sinonimo/i:

3-(o-Methoxyphenoxy)-1,2-propanediol, Glycerol guaiacolate, Guaifenesin

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About This Item

Formula empirica (notazione di Hill):
C10H14O4
Numero CAS:
93-14-1
Peso molecolare:
198.22
Numero CE:
202-222-5
Numero MDL:
MFCD00016873
Codice UNSPSC:
12352100
ID PubChem:
57654212
NACRES:
NA.22
Saggio:
≥98% (GC)

Livello qualitativo

200

Saggio

≥98% (GC)

Stringa SMILE

COc1ccccc1OCC(O)CO

InChI

1S/C10H14O4/c1-13-9-4-2-3-5-10(9)14-7-8(12)6-11/h2-5,8,11-12H,6-7H2,1H3
HSRJKNPTNIJEKV-UHFFFAOYSA-N

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Categorie correlate

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
0000361783
0000337802
0000337801
0000361783
SLCQ9237

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Sigma-Aldrich

105120

2-Bromo-2′-acetonaphthone

(±)-Chlorpheniramine maleate salt ≥99% (perchloric acid titration)

Sigma-Aldrich

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(±)-Chlorpheniramine maleate salt

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Sigma-Aldrich

17803

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Guaiacolo Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1136

Guaiacolo

Natividad Isabel Navarro Pacheco et al.
Nanomaterials (Basel, Switzerland), 11(1) (2021-01-23)
Titanium dioxide nanoparticles (TiO2 NPs) are manufactured worldwide. Once they arrive in the soil environment, they can endanger living organisms. Hence, monitoring and assessing the effects of these nanoparticles is required. We focus on the Eisenia andrei earthworm immune cells
Robert J Brosnan et al.
American journal of veterinary research, 72(12), 1569-1575 (2011-12-01)
To evaluate whether guaifenesin can prevent adverse anesthetic induction events caused by propofol and whether a guaifenesin-propofol induction combination has brief cardiovascular effects commensurate with rapid drug washout. 8 healthy adult horses. Guaifenesin was administered IV for 3 minutes followed
Mehdi Hatami et al.
Journal of separation science, 34(21), 2933-2939 (2011-10-06)
A simple, rapid, and efficient method, dispersive liquid-liquid microextraction (DLLME) coupled with high-performance liquid chromatography-fluorescence detector, has been developed for the determination of guaifenesin (GUA) enantiomers in human urine samples after an oral dose administration of its syrup formulation. Urine
Mallinath B Hadimani et al.
Journal of medicinal chemistry, 56(12), 5071-5078 (2013-06-14)
In diabetic patients, an early index of peripheral neuropathy is the slowing of conduction velocity in large myelinated neurons and a lack of understanding of the basic pathogenic mechanisms hindered therapeutics development. Racemic (R/S)-guaifenesin (1) was identified as a potent
Monzure-Khoda Kazi et al.
Journal of chromatography. A, 1231, 22-30 (2012-03-01)
This work addresses optimization of an improved single-column chromatographic (ISCC) process for the separation of guaifenesin enantiomers. Conventional feed injection and fraction collection systems have been replaced with customized components facilitating simultaneous separation and online monitoring with the ultimate objective
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