Quality Level
assay
99%
form
solid
mp
40-42 °C (lit.)
functional group
hydroxyl
SMILES string
COc1cc(CCO)ccc1O
InChI
1S/C9H12O3/c1-12-9-6-7(4-5-10)2-3-8(9)11/h2-3,6,10-11H,4-5H2,1H3
InChI key
XHUBSJRBOQIZNI-UHFFFAOYSA-N
General description
Homovanillyl alcohol is a key component of Queen mandibular pheromone.
Application
Homovanillyl alcohol was used in the preparation of galactosides.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
G Mårdh et al.
Biochemistry, 25(23), 7279-7282 (1986-11-18)
The class I human liver alcohol dehydrogenases (ADHs) catalyze the interconversion of the intermediary alcohols and aldehydes of dopamine metabolism in vitro, whereas those of the class II and class III do not. The individual, homogeneous class I isozymes oxidize
D J Edwards et al.
Biochemical pharmacology, 34(8), 1255-1263 (1985-04-15)
The effects in rats of intraventricular injections of 6-hydroxydopamine (6-OHDA) on the urinary excretion 1-3 weeks later of 3-methoxy-4-hydroxyphenethylene glycol (MHPG), 3,4-dihydroxyphenethanol (DHPE), 3-methoxy-4-hydroxyphenethanol (MHPE), p-hydroxyphenylglycol (pHPG), homovanillic acid (HVA) and 3,4-dihydroxyphenylacetic acid (DOPAC) were examined. The excretion of MHPG
Effects of amphetamine and amfonelic acid on the disposition of striatal newly synthesized dopamine.
H H Miller et al.
European journal of pharmacology, 78(1), 33-44 (1982-02-19)
A comparison of the in vivo biochemical actions of the psychotomimetic central stimulants, d-amphetamine (d-AMPH) and amfonelic acid (AFA), on the metabolism of rat striatal newly synthesized [3H]dopamine (DA) was made by pulse labeling with [3H]tyrosine. No evidence for the
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 148830-2.5G | 04061838738066 |
| 148830-10G | 04061832278681 |
