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A86406

α-Angelica lactone

98%

Synonym(s):

alpha-Angelica lactone, 4-Hydroxy-3-pentenoic acid γ-lactone, 5-Methyl-2(3H)-furanone

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$242.00

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About This Item

Empirical Formula (Hill Notation):
C5H6O2
CAS Number:
591-12-8
Molecular Weight:
98.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24891351
EC Number:
209-701-8
Beilstein/REAXYS Number:
108394
MDL number:
MFCD00005375
Assay:
98%
Form:
liquid

Key Documents

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InChI

1S/C5H6O2/c1-4-2-3-5(6)7-4/h2H,3H2,1H3

InChI key

QOTQFLOTGBBMEX-UHFFFAOYSA-N

SMILES string

CC1=CCC(=O)O1

assay

98%

form

liquid

refractive index

n20/D 1.448 (lit.)

bp

55-56 °C/12 mmHg (lit.)

mp

13-17 °C (lit.)

density

1.092 g/mL at 25 °C (lit.)

Quality Level

100

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1 of 4

This Item
D80472777W329355
α-Angelica lactone 98%

Sigma-Aldrich

A86406

α-Angelica lactone

γ-Decanolactone 98%

Sigma-Aldrich

D804

γ-Decanolactone

trans-Quercus lactone analytical standard

Supelco

72777

trans-Quercus lactone

α-Angelica lactone natural (US), ≥90%, sum of isomers

Sigma-Aldrich

W329355

α-Angelica lactone

assay

98%

assay

98%

assay

≥94.0% (GC)

assay

≥90%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

400

bp

55-56 °C/12 mmHg (lit.)

bp

-

bp

-

bp

55-56 °C/12 mmHg (lit.)

refractive index

n20/D 1.448 (lit.)

refractive index

n20/D 1.449 (lit.)

refractive index

-

refractive index

n20/D 1.448 (lit.)

mp

13-17 °C (lit.)

mp

-

mp

-

mp

13-17 °C (lit.)

form

liquid

form

liquid

form

-

form

-

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317

Hazard Classifications

Skin Sens. 1

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificates of Analysis (COA)

Lot/Batch Number
SHBT5016
MKBH6614V
STBB9922V
STBB2448
S47014

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W A Nijhoff et al.
Carcinogenesis, 16(3), 607-612 (1995-03-01)
The naturally occurring anticarcinogens flavone and alpha-angelicalactone incorporated separately and simultaneously in the diet at 0.5, 0.1, 0.05 and 0.01% w/w, were studied with respect to their effects on oesophageal, gastric, intestinal, colonic and hepatic (i) glutathione S-transferase (GST) enzyme
Lin Zhou et al.
Organic letters, 13(12), 3056-3059 (2011-05-21)
A direct highly diastereo- and enantioselective asymmetric vinylogous Mannich-type (AVM) reaction of aldimines with nonactivated natural α-angelica lactone has been successfully developed. It was demonstrated that the nonactivated natural α-angelica lactone is a useful vinylogous nucleophile to give the chiral
Y M Ioannou et al.
Cancer research, 42(4), 1199-1204 (1982-04-01)
The effects of alpha-angelica lactone (alpha-AL), butylated hydroxyanisole (BHA), and beta-naphthoflavone (beta-NF) on the amount of benzo(alpha)pyrene (BP) metabolite:DNA adducts formed in the forestomach, lung, and liver of ICR/Ha mice were investigated 48 hr after p.o. administration of BP. BP
Xin Huang et al.
Chemical communications (Cambridge, England), 48(18), 2439-2441 (2012-01-24)
The first organocatalytic asymmetric assembly of Morita-Baylis-Hillman carbonates of isatins and α-angelica lactone has been studied, affording multifunctional products containing two valuable pharmacophores and vicinal quaternary chiral centers in high stereoselectivity (up to 92% ee, dr >95:5).
Hagai Tavori et al.
Bioorganic & medicinal chemistry, 16(15), 7504-7509 (2008-06-24)
Paraoxonase1 (PON1) is a HDL bound enzyme and many of the anti-atherogenic properties of HDL are attributed to PON1. The enzyme precise mechanism of protective action and its endogenous substrate remain elusive. PON1 hydrolyzes organophosphates, arylesters and lactones, whereas the

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