3,5-Dijod-4-aminohippursaeure

3,5-Dijod-4-aminohippursaeure - Names and Identifiers

Name	4-Amino-3,5-diiodobenzoic acid
Synonyms	NSC 57118 AI3-52265 BRN 2103037 LABOTEST-BB LT00080707 4-amino-3,5-diiodobenzoate 3,5-dijod-4-aminohippursaeure 4-amino-3,5-diiodo-benzoicaci 3,5-Dijod-4-aminohippursaeure 3,5-DIIODO-4-AMINOBENZOIC ACID 4-Amino-3,5-diiodobenzoic acid 4-AMINO-3,5-DIIODOBENZOIC ACID Benzoic acid, 4-amino-3,5-diiodo- 3,5-Dijod-4-aminohippursaeure [German] 3-14-00-01161 (Beilstein Handbook Reference)
CAS	2122-61-4
EINECS	218-331-6
InChI	InChI=1/C7H5I2NO2/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2H,10H2,(H,11,12)/p-1

3,5-Dijod-4-aminohippursaeure - Physico-chemical Properties

Molecular Formula	C7H5I2NO2
Molar Mass	388.93
Density	2.3815 (estimate)
Melting Point	>300°C(lit.)
Boling Point	448.7±45.0 °C(Predicted)
Flash Point	225.2°C
Water Solubility	Soluble in water (partly miscible).
Vapor Presure	7.73E-09mmHg at 25°C
BRN	2103037
pKa	4.16±0.10(Predicted)
Storage Condition	2-8°C
Sensitive	Light Sensitive

3,5-Dijod-4-aminohippursaeure - Risk and Safety

Risk Codes	R36/37/38 - Irritating to eyes, respiratory system and skin. R22 - Harmful if swallowed
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37/39 - Wear suitable gloves and eye/face protection S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
WGK Germany	3
RTECS	DG2310000
HS Code	29224985

3,5-Dijod-4-aminohippursaeure - Introduction

4-Amino-3,5-diiodobenzoic acid is an organic compound with a chemical formula of C7H5I2NO2 and a molecular weight of 409.93. It is a white solid powder, odorless.

4-Amino-3,5-diiodobenzoic acid can be used as an important organic synthesis intermediate. It is often used in the field of medicine to synthesize biologically active compounds. It can be used as an organic semiconductor material in an organic light emitting diode device and a photoelectric conversion device.

The preparation method of 4-Amino-3,5-diiodobenzoic acid is usually obtained by alkali-catalyzed addition amination reaction at the ortho position of benzoic acid, and then 4-Amino-3 is generated by acid-base neutralization, 5-diiodobenzoic acid.

Regarding the safety information of 4-Amino-3,5-diiodobenzoic acid, no special hazardous data have been found at present. However, as an organic compound, appropriate protective measures should generally be taken to avoid contact with skin and eyes during operation, and to ensure that operation is carried out in a well-ventilated place. If necessary, please consult the relevant chemical literature and safety information for further understanding and confirmation.

Last Update：2024-04-09 21:54:55