618-51-9
3-Iodobenzoic acid
CAS: 618-51-9
Molecular Formula: C7H5IO2
618-51-9 - Names and Identifiers
| Name | 3-Iodobenzoic acid |
| Synonyms | lodbenzoicacid 3-iodobenzoate Iodobenzoic aci 3-lod-benzoic acid 3-IODOBENZOIC ACID 3-Iodobenzoic acid m-Carboxyiodobenzene 3-Carboxyiodobenzene sodium 3-iodobenzoate Acid between the iodine Pemetrexed disodium Impurity 10 |
| CAS | 618-51-9 |
| EINECS | 210-555-2 |
| InChI | InChI=1/C7H5IO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,(H,9,10)/p-1 |
618-51-9 - Physico-chemical Properties
| Molecular Formula | C7H5IO2 |
| Molar Mass | 248.02 |
| Density | 2.2170 (estimate) |
| Melting Point | 185-187°C(lit.) |
| Boling Point | 337.2±25.0 °C(Predicted) |
| Flash Point | 157.7°C |
| Water Solubility | Soluble in Chloroform and Methanol. Insoluble in water. |
| Solubility | Soluble in ethanol and ether, slightly soluble in water. |
| Vapor Presure | 4.17E-05mmHg at 25°C |
| Appearance | Crystallization |
| Color | White to beige |
| BRN | 971088 |
| pKa | 3.8(at 25℃) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Sensitive | Light Sensitive |
| MDL | MFCD00002496 |
| Physical and Chemical Properties | White to light yellow needle-like crystals. Melting Point 187-188 °c. Soluble in alcohol and ether, insoluble in water. Can sublimate. |
| Use | Used as analytical reagents, but also for organic synthesis |
618-51-9 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S37/39 - Wear suitable gloves and eye/face protection S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
| WGK Germany | 3 |
| TSCA | T |
| HS Code | 29163990 |
| Hazard Note | Irritant |
| Hazard Class | IRRITANT, LIGHT SENS |
618-51-9 - Introduction
Can sublimate. The minimum lethal dose (mouse, abdominal cavity) is 200mg/kg.
Last Update：2022-10-16 17:27:12
618-51-9 - 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) |
| purpose | used as analytical reagent, also used in organic synthesis |
| production method | is obtained by diazotization and substitution of M-aminobenzoic acid. M-aminobenzoic acid and sulfuric acid were added to the reactor and diazotized with sodium nitrite solution at 0-10 °c. After the diazotization solution was filtered, potassium iodide was added with stirring. After addition, boiling for 12min, until no bubbles, cooling, filtering, washing with thiosulfuric acid solution, and recrystallization with water to obtain the finished product. |
Last Update：2024-04-09 21:04:16
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