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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:
526-37-4
Molecular Weight:
152.15
Beilstein:
1941881
MDL number:
MFCD04117961
UNSPSC Code:
85151701
PubChem Substance ID:
329767558
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

Related Categories

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

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H317,H319

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCM3229
BCCK5304
BCCH6154
BCCG6967
BCCF1460

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Formulating, Packaging, and Marketing of Natural Cosmetic Products (2011)
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)
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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