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Merck

207713

1,3-Di-o-tolylguanidine

99%

Synonym(s):

DTG

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About This Item

Linear Formula:
(CH3C6H4NH)2C(=NH)
CAS Number:
Molecular Weight:
239.32
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
202-577-6
MDL number:

Product Name

1,3-Di-o-tolylguanidine, 99%

InChI key

OPNUROKCUBTKLF-UHFFFAOYSA-N

InChI

1S/C15H17N3/c1-11-7-3-5-9-13(11)17-15(16)18-14-10-6-4-8-12(14)2/h3-10H,1-2H3,(H3,16,17,18)

SMILES string

Cc1ccccc1NC(=N)Nc2ccccc2C

assay

99%

form

solid

mp

176-178 °C (lit.)

solubility

water: soluble 70 mg/mL at 20 °C

functional group

amine

Quality Level

Gene Information

human ... EBP(10682)

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General description

1,3-Di-o-tolylguanidine is a selective σ-receptor agonist. 1,3-Di-o-tolylguanidine is σ site ligand and its interaction with dopamine drugs were studied in Wistar rats and Albino Swiss mice.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

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    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. What is the solubility of Product 207713, 1,3-di-o-tolylguanidine?

    1,3-Di-o-tolylguanidine is soluble in water at 70 micrograms per mL at ambient temperature.

  6. What is the nature of the biological activity of Product 207713, 1,3-di-o-tolylguanidine?

    1,3-Di-o-tolylguanidine is known to be a selective ligand for the sigma site in the mammalian central nervous system. Behavioral changes, such as hypothermia, reduced pain behavior, circling behavior, and decreased locomotor activity in mice and/or rats were observed after intraperitoneal, subcutaneous, intravenous and/or intranigral injection.

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