63661
(+)-薄荷呋喃
analytical standard
别名:
(6R)-4,5,6,7-四氢-3,6-二甲基苯并呋喃, (R)-3,6-二甲基-4,5,6,7-四氢苯并呋喃
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关于此项目
经验公式（希尔记法）:
C10H14O
化学文摘社编号:
分子量:
150.22
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2729
InChI
1S/C10H14O/c1-7-3-4-9-8(2)6-11-10(9)5-7/h6-7H,3-5H2,1-2H3/t7-/m1/s1
SMILES string
C[C@@H]1CCc2c(C)coc2C1
InChI key
YGWKXXYGDYYFJU-SSDOTTSWSA-N
grade
analytical standard
assay
≥99.0% (sum of enantiomers, GC)
optical activity
[α]20/D +100±2°, neat
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
refractive index
n20/D 1.484
bp
204-206 °C (lit.)
density
0.97 g/mL at 20 °C (lit.)
application(s)
food and beverages
format
neat
storage temp.
2-8°C
Quality Level
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General description
(+)-薄荷呋喃是胡薄荷酮的代谢物，存在于薄荷植物中，在某些影响因素条件下，如低光照、有限的水分和营养缺乏，基本上是由薄荷呋喃合酶从(+)-胡薄荷酮产生的。
Application
有关合适的仪器技术的更多信息，请参阅产品′的检验报告。想要获得更多支持，请联系技术服务部。
Other Notes
该化合物常见于薄荷属植物。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Council of Europe
Chemically-defined Flavouring Substances (2000)
(R)-(+)-Menthofuran is a potent, mechanism-based inactivator of human liver cytochrome P450 2A6
Khojasteh - Bakht.CS
Drug Metabolism and Disposition, 26(7), 701-704 (1998)
Rahman-U-A
Studies in Natural Products Chemistry, Volume 37, 37 (2012)
S Cyrus Khojasteh et al.
Chemical research in toxicology, 23(11), 1824-1832 (2010-10-16)
Menthofuran is a monoterpene present in mint plants that is oxidized by mammalian cytochrome P450 (CYP) to hepatotoxic metabolites. Evidence has been presented that p-cresol and other unusual oxidative products are metabolites of menthofuran in rats and that p-cresol may
Maria De Lucia et al.
The Journal of organic chemistry, 72(26), 10123-10129 (2007-11-30)
The reaction chemistry of menthofuran (1), a toxic furan terpenoid from various mint oils, with nitric acid and nitrous acid has been investigated. Treatment of 1 with nitric acid afforded a 1:1 mixture of the bisfuran derivatives 5 and 6
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