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SRA1

Anisaldehyde solution

≥97.5% purity (GC), liquid

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About This Item

UNSPSC Code:
12171500
PubChem Substance ID:
24899867
NACRES:
NA.47
MDL number:
MFCD00003385

Key Documents

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Product Name

Anisaldehyde solution,

description

Spray reagent

Quality Level

200

assay

≥97.5% (GC)

form

liquid

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

[H]C(C1=CC=C(OC)C=C1)=O

InChI

1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3

InChI key

ZRSNZINYAWTAHE-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

Related Categories

Application

Excellent reagent for detecting a wide variety of natural products on TLC plates: steroids, prostaglandins, carbohydrates, phenols, glycosides, sapogenins, antibiotics, mycotoxins, antioxidants, etc. A range of colors is produced on heating, adding a qualitative aspect to the detection process.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2 - Met. Corr. 1 - Skin Irrit. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

flash_point_f

52.0 °F - closed cup

flash_point_c

11.1 °C - closed cup

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

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pdsc

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prtr

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fsl

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ishl_indicated

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ishl_notified

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Certificates of Analysis (COA)

Lot/Batch Number
115K9802
073K9800
073K9801
064K9811

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Synthesis of a probe for monitoring HSV1-tk
reporter gene expression using chemical exchange
saturation transfer MRI
Annon Bar
Nature (2013)
Jork, H., et al.
Thin Layer Chromatography: Reagents and Detection Methods, 195-198 (1990)
Yun-Hai Tao et al.
Bioorganic & medicinal chemistry letters, 16(3), 592-595 (2005-11-18)
4-Hydroxybenzaldehyde (HBA) derivatives were examined as inhibitors for GABA transaminase (GABA-T) and succinic semialdehyde dehydrogenase (SSADH). Investigation of structure-activity relation revealed that a carbonyl group or an amino group as well as a hydroxy group at the para position of
Li Liu et al.
Bioorganic & medicinal chemistry letters, 22(1), 154-163 (2011-12-06)
The binding between the estrogen receptor α (ER-α) and a variety of compounds in traditional Chinese formulae, Si-Wu-Tang (SWT) series decoctions, was studied using a stably-transfected human breast cancer cell line (MVLN). In 38 compounds tested from SWT series decoctions
Laura E Korhonen et al.
Journal of medicinal chemistry, 48(11), 3808-3815 (2005-05-27)
The purpose of this study was to determine the cytochrome P450 1A2 (CYP1A2) inhibition potencies of structurally diverse compounds to create a comprehensive three-dimensional quantitative structure-activity relationship (3D-QSAR) model of CYP1A2 inhibitors and to use this model to predict the
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