162353
3-Methyl-2-buten-1-ol
99%
Synonym(s):
3,3-Dimethylallyl alcohol, Prenol
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
(CH3)2C=CHCH2OH
CAS Number:
Molecular Weight:
86.13
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39020334
UNSPSC Code:
12352100
EC Number:
209-141-4
MDL number:
Beilstein/REAXYS Number:
1633479
Assay:
99%
Form:
liquid
vapor pressure
1.4 mmHg ( 20 °C)
Quality Level
assay
99%
form
liquid
expl. lim.
16.3 %
refractive index
n20/D 1.443 (lit.)
bp
140 °C (lit.)
density
0.848 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
C\C(C)=C\CO
InChI
1S/C5H10O/c1-5(2)3-4-6/h3,6H,4H2,1-2H3
InChI key
ASUAYTHWZCLXAN-UHFFFAOYSA-N
General description
3-Methyl-2-buten-1-ol reacts with nitrosocarbonyl benzene to yield 5-hydroxy-isoxazolidines. It is commonly used as fragrance ingredient.
Application
3-Methyl-2-buten-1-ol was used as starting reagent during asymmetric total syntheses of (R)-(+)- and (S)-(-)-umbelactone via Sharpless asymmetric epoxidation reaction.
Still not finding the right product?
Explore all of our products under 3-Methyl-2-buten-1-ol
signalword
Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
124.7 °F - closed cup
flash_point_c
51.5 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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.
Anastasia Zerva et al.
Molecules (Basel, Switzerland), 23(9) (2018-09-22)
Feruloyl esterases (FAEs, E.C. 3.1.1.73) are biotechnologically important enzymes with several applications in ferulic acid production from biomass, but also in synthesis of hydroxycinnamic acid derivatives. The use of such biocatalysts in commercial processes can become feasible by their immobilization
Branko Radetich et al.
Journal of the American Chemical Society, 124(11), 2430-2431 (2002-03-14)
A solution is reported to the classic unsolved problem of stereoselective synthesis of all-E oligoprenols, such as E-farnesylfarnesol, by a cationic coupling analogous to the biosynthetic pathway. The simplicity and efficacy of the method, which is outlined in Scheme 1
Lan Yang et al.
Fitoterapia, 82(6), 834-840 (2011-05-21)
The hepatoprotective effects of polyprenols from Ginkgo biloba L. leaves were evaluated against carbon tetrachloride induced hepatic damage in Sprague-Dawley rats. The elevated levels of serum ALT, AST, ALP, ALB, TP, HA, LN, TG, and CHO were restored towards normalization
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 162353-100ML | 04061838746948 |
| 162353-500ML | 04061838746955 |
| 162353-5ML | 04061838746962 |