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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
(CH3O)C6H4OH
CAS 번호:
Molecular Weight:
124.14
UNSPSC Code:
12352202
NACRES:
NA.77
PubChem Substance ID:
EC Number:
201-964-7
Beilstein/REAXYS Number:
508112
MDL number:
InChI key
LHGVFZTZFXWLCP-UHFFFAOYSA-N
InChI
1S/C7H8O2/c1-9-7-5-3-2-4-6(7)8/h2-5,8H,1H3
SMILES string
COc1ccccc1O
vapor density
4.27 (vs air)
vapor pressure
0.11 mmHg ( 25 °C)
assay
≥98.0%
form
liquid, solid
refractive index
n20/D 1.543 (lit.)
bp
205 °C (lit.)
mp
26-29 °C (lit.)
density
1.129 g/mL at 25 °C (lit.)
Quality Level
유사한 제품을 찾으십니까? 방문 제품 비교 안내
General description
Guaiacol, a phenolic compound, acts as a scavenger of superoxide radicals. It is produced from guaiacum or wood creosote. Guaiacol acts as a precursor to different favoring agents like, vanillin and roasted coffee. It is used as an antiseptic, analgesic and sedative drug for the treatment of dental pulp and periodontal tissue. Guaiacol enhances cell proliferation in vivo.
Application
Guaiacol has been used:
- as a substrate for peroxidase enzyme to determine its activity
- as a substrate to determine laccase activity
- as a reagent in peroxidase (POD) activity test
Biochem/physiol Actions
Guaiacol has an ability to inhibit prostaglandin biosynthesis, without causing damage to the gastrointestinal system, unlike classic NSAID (nonsteroidal anti-inflammatory drugs).
Guaiacol, along with 2,4,6-trichloroanisole, is responsible for cork taint in wine. A method has been developed for extraction and quantitation of the two compounds.
Disclaimer
May be liquid at room temperature.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
저장 등급
11 - Combustible Solids
wgk
WGK 1
flash_point_f
194.0 °F - closed cup
flash_point_c
90 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Constituent profiles
Essential Oil Safety-A Guide for Health Care Professionals (2014)
Encyclopedia of Food Sciences and Nutrition (Second Edition) (2003)
Effects of metoxibutropate, ibuprofen and guaiacol on the gastrointestinal system.
Fossati, et al.
International Journal of Tissue Reactions, 13(1), 45-50 (1991)
Derivatives and applications of lignin-An insight
Agrawal A, et al.
The Scitech Journal, 1(7), 30-36 (2014)
Antimicrobial Activity of Newly Prepared Endodontic Biosealer on Enterococcus Faecalis-An in vitro study
AL-Jubori SH, et al.
International journal of enhanced research in science technology and engineering. (2015)
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