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Home > Encyclopedia > 3-(Dimethylamino)benzoic acid

3-(Dimethylamino)benzoic acid

3-(Dimethylamino)benzoic acid structure

3-(Dimethylamino)benzoic acid 

structure
  • CAS No:

    99-64-9

  • Formula:

    C9H11NO2

  • Chemical Name:

    3-(Dimethylamino)benzoic acid

  • Synonyms:

    Benzoic acid,3-(dimethylamino)-;Benzoic acid,m-(dimethylamino)-;3-(Dimethylamino)benzoic acid;m-(Dimethylamino)benzoic acid;m-(N,N-Dimethylamino)benzoic acid;3-(N,N-Dimethylamino)benzoic acid;N,N-Dimethyl-3-carboxyaniline;N,N-Dimethyl-3-aminobenzoic acid;NSC 7197;DMAB;1884231-56-4

  • Categories:

    Biochemical Engineering  >  Amino Acids and Derivatives

Description

Light yellow to yellow-beige crystalline powder

3-(Dimethylamino)benzoic acid Basic Attributes

165.19

165.19

2208586

202-775-2

7197

DTXSID7059199

29224995

Characteristics

40.5

1.6

Light yellow to yellow-beige Crystalline Powder

1.27 g/cm3

150 °C

323.8ºC at 760mmHg

149.6±23.2 °C

1.594

soluble in methanol (50 mg/ml). Insoluble in water.

Store below +30°C.

Safety Information

NONH for all modes of transport

3

36/37/38

26-36-24/25

Xi

Stable under normal temperatures and pressures.

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 41 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

3-(dimethylamino)benzoic acid

3-(Dimethylamino)benzoic acid Use and Manufacturing

Methods of Manufacturing

In a 250 mL glass three-necked flask, 95 mL of methanol and 3 mL of tetrahydrofuran were added, 16.7 g of m-nitrobenzoic acid, 0.2 g of 5percent palladium on carbon, A constant pressure dropping funnel was charged with 15.2 mL of 37percent aqueous formaldehyde solution.The reaction system in the air pump away, and then access to atmospheric hydrogen.The temperature was raised to 64oC and the reaction was stirred until no more hydrogen was absorbed.From the dropping funnel was added formaldehyde solution, Continue to hydrogenate at this temperature until no more hydrogen is absorbed.Stop stirring, filter recovery catalyst, the filtrate was concentrated, the product is precipitated.Collect the product by filtration, wash the product with a little water, Then 100 oC dry, the productM-dimethylaminobenzoic acid 15.3 g, The yield is 93percent.After the catalyst is recovered, it is washed with the reaction solvent before being used for the next reaction.

Uses

It is an important intermediate for dyes, pigments, pesticides, medicine, photosensitive materials and organic reagents

Benzoic acid, 3-(dimethylamino)-: INACTIVE

Computed Properties

Molecular Weight:165.19
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:165.078978594
Monoisotopic Mass:165.078978594
Topological Polar Surface Area:40.5
Heavy Atom Count:12
Complexity:168
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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