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Safety Information

P49503

Sigma-Aldrich

Piperonylamine

97%

Synonym(s):

1,3-Benzodioxole-5-methylamine, 3,4-(Methylenedioxy)benzylamine

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25 G
CN¥698.44

CN¥698.44

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25 G
CN¥698.44

About This Item

Empirical Formula (Hill Notation):
C8H9NO2
CAS Number:
2620-50-0
Molecular Weight:
151.16
Beilstein:
136996
EC Number:
220-056-1
MDL number:
MFCD00005840
UNSPSC Code:
12352100
PubChem Substance ID:
24898573
NACRES:
NA.22

CN¥698.44

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Request a Bulk Order

Assay

97%

refractive index

n20/D 1.564 (lit.)

bp

138-139 °C/13 mmHg (lit.)

density

1.214 g/mL at 25 °C (lit.)

SMILES string

NCc1ccc2OCOc2c1

InChI

1S/C8H9NO2/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-3H,4-5,9H2

InChI key

ZILSBZLQGRBMOR-UHFFFAOYSA-N

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Show Differences

1 of 4

This Item
P49104P49406678848
Piperonylamine 97%

P49503

Piperonylamine

Piperonal 99%

P49104

Piperonal

Piperonyl alcohol 98%

P49406

Piperonyl alcohol

2-Aminomethyl-1,4-benzodioxane 97%

678848

2-Aminomethyl-1,4-benzodioxane

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

density

1.214 g/mL at 25 °C (lit.)

density

-

density

-

density

1.1679 g/mL at 25 °C

refractive index

n20/D 1.564 (lit.)

refractive index

-

refractive index

-

refractive index

n20/D 1.5594

bp

138-139 °C/13 mmHg (lit.)

bp

264 °C (lit.)

bp

-

bp

105-110 °C/3 mmHg

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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    Certificates of Analysis (COA)

    Lot/Batch Number
    STBK6813
    STBK3655
    STBJ8152
    STBJ1763
    STBH0639

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    Mariana C F C B Damião et al.
    Archiv der Pharmazie, 347(12), 885-895 (2014-10-07)
    A novel class of benzo[d][1,3]dioxol-5-ylmethyl alkyl/aryl amide and ester analogues of capsaicin were designed, synthesized, and evaluated for their cytotoxic activity against human and murine cancer cell lines (B16F10, SK-MEL-28, NCI-H1299, NCI-H460, SK-BR-3, and MDA-MB-231) and human lung fibroblasts (MRC-5).

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