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77236

Supelco

Atranol

analytical standard

Synonym(s):

2,6-Dihydroxy-4-methylbenzaldehyde, 4-Methyl-γ-resorcylaldehyde, p-Orsellinaldehyde

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About This Item

Empirical Formula (Hill Notation):
C8H8O3
CAS Number:
Molecular Weight:
152.15
Beilstein:
1941881
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥97.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤8.0% water (calculated from elemental analysis)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

Cc1cc(O)c(C=O)c(O)c1

InChI

1S/C8H8O3/c1-5-2-7(10)6(4-9)8(11)3-5/h2-4,10-11H,1H3

InChI key

JASONGFGOLHLGB-UHFFFAOYSA-N

General description

Atranol is an artifact and a degradation product of atranorin, which is created during the production process of moss absolutes.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Comparison of elicitation potential of chloroatranol and atranol?2 allergens in oak moss absolute.
Johansen DJ, et al.
Contact Dermatitis, 54(4), 192-195 (2006)
Formulating, Packaging, and Marketing of Natural Cosmetic Products (2011)
Pierre Le Pogam et al.
Rapid communications in mass spectrometry : RCM, 31(23), 1993-2002 (2017-09-06)
Light-absorbing secondary metabolites from lichens were recently reported to exhibit promising Laser Desorption Ionization (LDI) properties, enabling their direct detection from crude lichen extracts. In addition, many of them display close structural homologies to commercial Matrix-Assisted Laser Desorption Ionization (MALDI)

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