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Supelco

Atranol

analytical standard

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C8H8O3
Número CAS:
Peso molecular:
152.15
Beilstein:
1941881
Número MDL:
Código UNSPSC:
85151701
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

Ensaio

≥97.0% (HPLC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

Impurezas

≤8.0% water (calculated from elemental analysis)

aplicação(ões)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

formato

neat

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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

chave InChI

JASONGFGOLHLGB-UHFFFAOYSA-N

Descrição geral

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

Aplicação

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

Produtos recomendados

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.

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Declarações de precaução

Classificações de perigo

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

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Certificados de análise (COA)

Lot/Batch Number

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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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