Skip to Content
Merck
CN

H43415

4-Hydroxy-6-methyl-2-pyrone

98%

Synonym(s):

3,5-Dihydroxysorbic acid δ-lactone

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C6H6O3
CAS Number:
Molecular Weight:
126.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-619-2
Beilstein/REAXYS Number:
113815
MDL number:
Assay:
98%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

assay

98%

mp

188-190 °C (dec.) (lit.)

SMILES string

CC1=CC(O)=CC(=O)O1

InChI

1S/C6H6O3/c1-4-2-5(7)3-6(8)9-4/h2-3,7H,1H3

InChI key

NSYSSMYQPLSPOD-UHFFFAOYSA-N

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Irreversible inactivation of chicken liver fatty acid synthetase by its substrates acetyl and malonyl CoA. Effect of temperature and NADP n fatty acid and triacetic acid lactone synthesis.
K R Srinivasan et al.
Biochemical and biophysical research communications, 99(3), 920-927 (1981-04-15)
Synthesis of acetoacetyl-CoA by bovine mammary fatty acid synthase.
S Ghayourmanesh et al.
FEBS letters, 132(2), 231-234 (1981-09-28)
J B Spencer et al.
The Biochemical journal, 288 ( Pt 3), 839-846 (1992-12-15)
6-Methylsalicylic acid synthase has been isolated in homogeneous form from Penicillium patulum grown in liquid culture from a spore inoculum. The enzyme is highly susceptible to proteolytic degradation in vivo and in vitro, but may be stabilized during purification by
Wenjuan Zha et al.
Journal of the American Chemical Society, 126(14), 4534-4535 (2004-04-09)
Metabolic pathway engineering is a powerful tool to synthesize structurally diverse and complex chemicals via genetic manipulation of multistep catalytic systems involved in cell metabolism. Here, we report the rational design of a fatty acid biosynthetic pathway, Brevibacterium ammoniagenes fatty
F Kurosaki
Archives of biochemistry and biophysics, 328(1), 213-217 (1996-04-01)
6-Hydroxymellein synthase is a polyketide biosynthetic enzyme induced in carrot cells which is organized as a homodimer composed of multifunctional subunits. The synthase liberates triacetic acid lactone, instead of 6-hydroxymellein, as a derailment product when the keto-reducing reaction at the

Global Trade Item Number

SKUGTIN
H43415-5G04061833795088
H43415-25G04061831813852

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