Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
CH3C6H4CH2CH2OH
CAS Number:
Molecular Weight:
136.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
211-824-7
MDL number:
Assay:
99%
InChI key
DAVFJRVIVZOKKS-UHFFFAOYSA-N
InChI
1S/C9H12O/c1-8-2-4-9(5-3-8)6-7-10/h2-5,10H,6-7H2,1H3
SMILES string
Cc1ccc(CCO)cc1
assay
99%
refractive index
n20/D 1.526 (lit.)
bp
244-245 °C (lit.)
density
0.978 g/mL at 25 °C (lit.)
functional group
hydroxyl
Application
4-Methylphenethyl alcohol was used in the determination of adducts of 1,2- and 1,4-benzoquinone with cysteine residues of hemoglobin and albumin.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
224.6 °F - closed cup
flash_point_c
107.00 °C - closed cup
ppe
Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
T A McDonald et al.
Carcinogenesis, 14(9), 1927-1932 (1993-09-01)
Benzoquinones (BQ) are genotoxic species that stem from metabolism of phenolic compounds. We have developed a method for measuring adducts of 1,2- and 1,4-benzoquinone (1,2-BQ and 1,4-BQ) with cysteine residues of hemoglobin (Hb) and albumin (Alb). The method employs a
Kuo-Ching Wen et al.
International journal of molecular sciences, 14(12), 23420-23440 (2013-11-30)
Melanin is responsible for skin color and plays a major role in defending against harmful external factors such as ultraviolet (UV) irradiation. Tyrosinase is responsible for the critical steps of melanogenesis, including the rate-limiting step of tyrosine hydroxylation. The mechanisms
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service