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100064

Sigma-Aldrich

3-Iodobenzylamine

96%

Synonym(s):

3-Iodobenzenemethanamine, m-Iodobenzylamine

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About This Item

Linear Formula:
IC6H4CH2NH2
CAS Number:
696-40-2
Molecular Weight:
233.05
MDL number:
MFCD00192227
UNSPSC Code:
12352100
PubChem Substance ID:
24846513
NACRES:
NA.22

assay

96%

form

solid

bp

132 °C/8 mmHg (lit.)

density

1.748 g/mL at 25 °C (lit.)

SMILES string

NCc1cccc(I)c1

InChI

1S/C7H8IN/c8-7-3-1-2-6(4-7)5-9/h1-4H,5,9H2

InChI key

LQLOGZQVKUNBRX-UHFFFAOYSA-N

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Repr. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

>235.4 °F - closed cup

flash_point_c

> 113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Certificates of Analysis (COA)

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S V Kharadia et al.
Experimental cell research, 201(1), 33-42 (1992-07-01)
Primary cultures of embryonic chick skeletal myogenic cells were used as an experimental model to examine the possible role of mono(ADP-ribosyl)ation reactions in myogenic differentiation. Initial studies demonstrated arginine-specific mono(ADP-ribosyl)transferase activity in the myogenic cell cultures. We then examined the
O Jónsson et al.
Biochimica et biophysica acta, 1379(1), 143-150 (1998-02-19)
Meta-iodo-benzylguanidine (MIBG), a selective inhibitor of mono-ADP-ribosylation, has been shown to inhibit histamine induced inositol-trisphosphate and prostacyclin production. The purpose of this study was to evaluate the effect of MIBG on the binding of histamine to the H1-receptor and to

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