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4-Iodobenzoic acid

4-Iodobenzoic acid

CAS: 619-58-9

Molecular Formula: C7H5IO2

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4-Iodobenzoic acid - Names and Identifiers

Name 4-Iodobenzoic acid
Synonyms 4-iodobenzoate
4-Jodbenzoesaeure
4-iodo-benzoicaci
4-Iodobenzoic acid
P-IODOBENZOIC ACID
4-IODOBENZOIC ACID
RARECHEM AL BO 0467
Benzoylphenobarbital
BENZOIC ACID, 4-IODO-
Benzoic acid, p-iodo-
p-Iodobenzenecarboxylic acid
CAS 619-58-9
EINECS 210-603-2
InChI InChI=1/C7H5IO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)/p-1
InChIKey GHICCUXQJBDNRN-UHFFFAOYSA-N

4-Iodobenzoic acid - Physico-chemical Properties

Molecular FormulaC7H5IO2
Molar Mass248.02
Density2,184 g/cm3
Melting Point270-273°C(lit.)
Boling Point318.5±25.0 °C(Predicted)
Flash Point>110℃
Water Solubility0.04 g/L (25 ºC)
Solubility 0.04g/l
Vapor Presure0.00015mmHg at 25°C
AppearanceYellow-like crystals
ColorWhite to off-white
BRN1860232
pKa4.00(at 25℃)
Storage ConditionKeep in dark place,Sealed in dry,Room Temperature
SensitiveLight Sensitive
MDLMFCD00002533
Physical and Chemical PropertiesWhite or light yellow, shiny crystals. The melting point of 269-272 deg C, the relative density of 2.184(20/4 deg C). Soluble in hot water, alcohol and ether, difficult to dissolve in cold water. Heat to above the melting point sublimation and decomposition.
UseFor Organic synthesis

4-Iodobenzoic acid - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S37/39 - Wear suitable gloves and eye/face protection
WGK Germany3
RTECSDH2976000
TSCAYes
HS Code29163900
Hazard NoteIrritant
Hazard ClassIRRITANT, LIGHT SENS

4-Iodobenzoic acid - Introduction

Soluble in hot water, alcohol and ether, hardly soluble in cold water, solubility in water: 0.04g/L (25°C). Heat to sublimate and decompose above the melting point.
Last Update:2022-10-16 17:27:14

4-Iodobenzoic acid - Reference Information

NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
Use for organic synthesis
production method p-aminobenzoic acid is produced by diazotization and substitution. P-carbamic acid and sulfuric acid were added to the reactor, and sodium nitrite was added to diazotization below 10 °c. The potassium iodide solution was slowly added with stirring. After addition, the reaction solution was heated until the red color was removed. It was then cooled, filtered and washed with water to give a crude product. The finished product is obtained by recrystallization from acid-base and ethanol.
Last Update:2024-04-09 02:00:10
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View History
4-Iodobenzoic acid
4-溴-2-三甲基硅烷基噻唑
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