Basic information
- Standard SMILES
IC(I)I- InChIKey
OKJPEAGHQZHRQV-UHFFFAOYSA-N- Molecular formula
- CHI3
- Average molar mass
- 393.732 g/mol
- Monoisotopic mass
- 393.72124403
Overview
Iodoform appears as bright yellow or yellow powder or crystals. Penetrating odor. Unctuous feel. Odor threshold 0.4 ppb. (NTP, 1992)
Names & identifiers
- Preferred name
- Iodoform
- IUPAC
- iodoform
- English name
- Iodoform
- Molecular formula
- CHI3
- Molecular weight
- 393.73
Names & synonyms
Show more names
Database identifiers
- CAS
75-47-8- PubChem CID
- 6374
- DTXSID
DTXSID4020743- ChEMBL
CHEMBL1451116- ChEBI
CHEBI:37758- UNII
- KXI2J76489
- EC Number
- 200-874-5、685-642-5
- Nikkaji
- J1.456G
Properties
Computed structural properties
- XLogP
- 2.7
- Topological polar surface area
- 0 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 0
- Rotatable bonds
- 0
- Heavy atoms
- 4
- Formal charge
- 0
- Complexity
- 8
Experimental & physicochemical properties
Density
4.008 at 68 °F (NTP, 1992) - Denser than water; will sink
Specific Gravity: 4.008 g/cu cm @ 25 °C
4.008
4.01
Color/Form
Yellow powder or crystals
YELLOW HEXAGONAL PRISMS OR NEEDLES FROM ACETONE
Solubility
less than 1 mg/mL at 75 °F (NTP, 1992)
Slightly soluble
SOL IN ACETIC ACID
13.6 g/100 ml ether @ 25 °C
7.8 g/100 ml ethanol @ 25 °C
One gram dissolves in 60 ml cold alcohol, 16 ml boiling alcohol, 10 ml chloroform, 7.5 ml ether, 80 ml glycerol, 3 ml carbon disulfide, 34 ml olive oil; freely sol in benzene, acetone, slightly sol in petr ether.
Boiling Point
424 °F at 760 mmHg (Sublimes) (NTP, 1992)
218 °C
424 °F (sublimes)
410 °F (Decomposes)
Decomposition
DECOMPOSES VIOLENTLY @ 400 °F (204 °C)
DECOMPOSES @ HIGH TEMP WITH EVOLUTION OF IODINE.
WHEN HEATED TO DECOMPOSITION ... EMITS TOXIC FUMES OF /HYDROGEN IODIDE/.
Melting Point
248 °F (NTP, 1992)
119-122
119 °C
Enthalpy of melting @ mp: 3.9 kcal/mole; enthalpy of sublimation @ 298 K: 16.7 kcal/mole; specific heat @ 400 K: 19.60 cal/K.mole, @ 600 K: 21.52 cal/K.mole, @ 800 K: 22.64 cal/K.mole, @ 1000 K: 23.38 cal/K.mole
246 °F
246 °F
Vapor Density
4.1 (NTP, 1992) - Heavier than air; will sink (Relative to Air)
13.6 (Air= 1)
4.1
Physicochemical properties
- Melting point
- 119 °C · 119 °C
- Boiling point
- 218 °C · 218°C
- Density
- 4.008 g/mL · 4.008 g/mL at 25 °C(lit.)
- refractive index
- 1.4975 · 1.4975 (estimate)
- storage temp.
- -20 °C · -20°C
- solubility
- 5 % · chloroform: soluble5%
- form
- Crystalline Powder
- color
- Bright yellow to dark yellow
- Odor
- char. pungent odor
- biological source
- mouse
- Water Solubility
- 0.1 g/100 · Insoluble. <0.1 g/100 mL at 24 ºC
- Specific Heat Capacity
- 0.19 J/ · Cp(gas): 0.19 J/(g·K), at 25℃
- Sensitive
- Light Sensitive
- Merck
- 14 · 14,5033
- BRN
- 1697010 · 1697010
- Henry's Law Constant
- 6.2 · 6.2×10-3 mol/(m3Pa) at 25℃, Fogg and Sangster (2003)
- Exposure limits
- 10 mg/m3 · PC-TWA:10 mg/m3
- Stability
- Stable. Incompatible with strong oxidizing agents, reducing agents. May explode when heated.
- Cosmetics Ingredients Functions
- ANTIMICROBIAL
- InChI
- 1S/CHI3/c2-1(3)4/h1H
- InChIKey
- OKJPEAGHQZHRQV-UHFFFAOYSA-N
- SMILES
- IC(I)I
- LogP
- 3.51 · 3.510 (est)
- Toxicology and Carcinogenesis
- Bioassay of Iodoform for Possible Carcinogenicity (CASRN 75-47-8)
- FDA 21 CFR
- 175.105 · 175.105; 177.2600
- Indirect Additives used in Food Contact Substances
- IODOFORM
- CAS DataBase Reference
- 75 · 75-47-8(CAS DataBase Reference)
- EWG's Food Scores
- 1 · 1
- FDA UNII
- 2 J76489 · KXI2J76489
- ATC code
- 9 AA13 · D09AA13
- NIST Chemistry Reference
- Methane, triiodo-(75-47-8)
- EPA Substance Registry System
- Iodoform (75-47-8)
- UNSPSC Code
- 12352203 · 12352203
- NACRES
- 41 · NA.41
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 302 · H302-H312-H315-H319-H332-H335
- Precautionary statements
- 264 · P264-P270-P280-P261-P271-P301+P312-P330-P302+P352-P312-P362+P364-P332+P313-P305+P351+P338-P337+P313-P304+P340-P403+P233-P405-P501
- target organs
- Respiratory system
- PPE
- 95 · dust mask type N95 (US), Eyeshields, Faceshields, Gloves
- Hazard Codes
- Xn
- Risk Statements
- 20 · 20/21/22-36/37/38
- Safety Statements
- 26 · 26-36/37-36/37/39-22-24/25
- RIDADR
- 1851 · UN 1851
- OEB
- B
- OEL
- 0.6 ppm · TWA: 0.6 ppm (10 mg/m3)
- WGK Germany
- 3 · 3
- RTECS
- 7000000 · PB7000000
- F
- 13 · 13
- TSCA
- TSCA listed
- HS Code
- 29033990 · 29033990
- Storage Class
- 6.1 C · 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
- Hazard Classifications
- 3 InhalationAcute · Acute Tox. 3 InhalationAcute Tox. 4 DermalAcute Tox. 4 OralAquatic Chronic 2Eye Irrit. 2Skin Irrit. 2STOT SE 3
- Hazardous Substances Data
- 75 · 75-47-8(Hazardous Substances Data)
- Toxicity
- 50 s.c · LD50 s.c. in mice: 1.6 mmoles/kg (Kutob, Plaa)
Safety & regulation
GHS classification
GHS Classification
This chemical does not meet GHS hazard criteria for < 0.1% (1 of 1363) of reports.
Warning
H302 (> 99.9%): Harmful if swallowed [Warning Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 1363 reports by companies from 15 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Warning
Hazard information
Regulatory Information
Chemical: Methane, triiodo-
Iodoform: Does not have an individual approval but may be used under an appropriate group standard
Hazards Summary
Cases of CNS depression, delirium, and hallucinations were reported when iodoform was used as a topical antiseptic and absorbed through the wound. It causes severe liver injury in animal experiments. 2021 TLV Basis: thyroid effects and fetal/neonatal damage; [ACGIH] See Iodine for the TLV of Iodides.
Special Reports
USEPA; Ambient Water Quality Criteria Doc: Halomethanes (1980) EPA 440/5-80-051
Bioassay of Iodoform for Possible Carcinogenicity (1978) Technical Rpt Series No. 110 DHEW Pub No. (NIH) 78-1365, U.S. Department of Health Education and Welfare, National Cancer Institute, Bethesda, MD 20014
Reactivity Profile
IODOFORM decomposes at high temperatures. Decomposes slowly in light at room temperature. Reacts violently with lithium. Is incompatible with mercuric oxide, calomel, silver nitrate, tannin, and balsam Peru. Is also incompatible with strong bases, strong oxidizing agents and magnesium. Vigorous reactions occur with acetone in the presence of solid potassium hydroxide or calcium hydroxide, hexamethylenetetramine at 352 °F, mercury(I) fluoride and finely divided reduced silver. (NTP, 1992)
Safety & protection
First Aid
EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.
(General first aid procedures)
Nonfire Spill Response
SMALL SPILLS AND LEAKAGE: Should a spill occur while you are handling this chemical, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with 60-70% ethanol and transfer the dampened material to a suitable container. Use absorbent paper dampened with 60-70% ethanol to pick up any remaining material. Seal the absorbent paper, and any of your clothes, which may be contaminated, in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with 60-70% ethanol followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.
Disposal Methods
SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
Preventive Measures
SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.
The worker should immediately wash the skin when it becomes contaminated.
Work clothing that becomes wet or significantly contaminated should be removed or replaced.
Workers whose clothing may have become contaminated should change into uncontaminated clothing before leaving the work premises.
Threshold Limit Values (TLV)
0.001 [ppm], as elemental iodine, inhalable fraction and vapor
8 hr Time Weighted Avg (TWA): 0.6 ppm.
Excursion Limit Recommendation: Excursions in worker exposure levels may exceed 3 times the TLV-TWA for no more than a total of 30 minutes during a work day, and under no circumstances should they exceed 5 times the TLV-TWA, provided that the TLV-TWA is not exceeded.
0.001 ppm (inhalable fraction and vapor) [2021]
Recommended Exposure Limit (REL)
0.6 ppm (10 mg/m³)
TWA 0.6 ppm (10 mg/m3)
Personal Protective Equipment (PPE)
Excerpt from NIOSH Pocket Guide for Iodoform:
Wear appropriate personal protective clothing to prevent skin contact.
Wear appropriate eye protection to prevent eye contact.
Toxicology
Ecotoxicity Values
LC50 Pimephales promelas (fathead minnows) 2.92 mg/l/96 hr, flow-through bioassay @ 25.1 °C, pH 7.7, water hardness 44.2 mg/l CaCO3 /Purity 98%/
EC50 Pimephales promelas (fathead minnows) 2.01 mg/l/96 hr, flow-through bioassay @ 25.1 °C, pH 7.7, water hardness 44.2 ml/l CaCO3 /Purity 98%/. /EC50 was based upon loss of equlibrium as manifested by the fish's inability to maintain an upright position when swimming./
Environmental Fate
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 35(SRC), determined from a structure estimation method(2), indicates that iodoform is expected to have very high mobility in soil(SRC). Volatilization of iodoform from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 3.1X10-5 atm-cu m/mole(SRC), using a fragment constant estimation method(3). Iodoform is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 0.040 mm Hg(SRC), determined from a fragment constant method(4). Data on the biodegradability of iodoform in soil is not available(SRC).
AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 35(SRC), determined from an estimation method(2), indicates that iodoform is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 3.1X10-5 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 40 hours and 25 days, respectively(SRC). According to a classification scheme(5), an estimated BCF of 43(SRC), from an estimated log Kow of 3.03(6) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low. Data on the biodegradability of iodoform in water is not available(SRC).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), iodoform, which has an estimated vapor pressure of 0.396 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase iodoform is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 56 days(SRC), from its rate constant of 0.289X10-12 cu cm/molecule-sec at 25 °C(3) determined using a structure estimation method(3). Iodoform absorbs radiation >290 nm(4) and therefore may be susceptible to direct photolysis(SRC). Photolysis rates for iodoform were not located.
Ongoing Test Status
The following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=75-47-8]
Soil Adsorption/Mobility
Using a structure estimation method based on molecular connectivity indices(1), the Koc for iodoform can be estimated to be 35(SRC). According to a classification scheme(2), this estimated Koc value suggests that iodoform is expected to have very high mobility in soil.
Human Toxicity Excerpts
SYSTEMIC INTOXICATION AND VISUAL DISTURBANCES RESULTED FROM ABSORPTION OF EXCESSIVE AMT /OF IODOFORM/ APPLIED TO WOUNDS OR ABSCESSES, OR FROM INGESTION OF LARGE QUANTITIES, BUT NOT FROM APPLICATION TO THE EYE. ... MOST CHARACTERISTICALLY VISION WAS IMPAIRED BY RETROBULBAR NEURITIS WITH ACCOMPANYING CENTRAL SCOTOMA. IN RARE INSTANCES TRANSITORY COMPLETE BLINDNESS OCCURRED. IN SOME CASES THE BULBAR PORTION OF THE OPTIC NERVE WAS INVOLVED, WITH NEURORETINITIS & OCCASIONAL RETINAL HEMORRHAGES. AS A RULE, RECOVERY WAS SLOW ... IN MOST CASES VISION WAS COMPLETELY OR PARTIALLY RECOVERED, BUT RESIDUAL PALLOR OF THE TEMPORAL PART OF THE OPTIC NERVEHEAD WAS COMMON. EXCEPTIONALLY THE WHOLE NERVEHEAD BECAME ATROPHIC AND WHITE AND LITTLE VISION WAS RECOVERED.
Both di- and tri-halogenated methane derivatives have been found to produce increased blood levels of methemoglobin; the greatest increase caused by iodo-, followed by bromo- and chloro- compounds. CNS functional disturbances are reported, including depression of rapid eyemovement sleep, as seen in carbon monoxide exposures. /Di- and tri-halogenated methane derivatives/
POISONING IS OFTEN DUE TO ABSORPTION THROUGH WOUND WHEN IODOFORM DRESSINGS ARE USED (NO MORE THAN 2 G IODOFORM SHOULD BE SO USED). MAY CAUSE DERMATITIS. SYSTEMIC EFFECTS INCL VOMITING & ALL DEGREES OF CEREBRAL DEPRESSION OR EXCITATION, INCL DELIRIUM, HALLUCINATIONS, COMA, & DEATH. VERY RAPID PULSE IS CHARACTERISTIC, WITH OR WITHOUT SLIGHT FEVER.
... Severe poisoning, which may be fatal, is characterized by headache, somnolence, delirium, and rapid feeble pulse.
Artificial Pollution Sources
Iodoform's production and use as an antiseptic and sensitizing agent in certain printing processes may result in its release to the environment through various waste streams(1,2). However its present use is rather limited. Iodoform may be formed in finished drinking water during the chlorination process(3). When iodinated trihalomethanes occur, a medicinal taste or musty odor is imparted to the water. While there are only a few reports of iodoform in treated drinking water in the literature, strong medicinal odors have long been known to occur in such water.
Carcinogen Classification
Iodoform
TR-110: Bioassay of Iodoform for Possible Carcinogenicity (CASRN 75-47-8) (1978 )
04/26/78
No Evidence
No Evidence
No Evidence
Environmental Bioconcentration
An estimated BCF of 43 was calculated for iodoform(SRC), using an estimated log Kow of 3.03(1,SRC) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low.
Regulatory information
Safety data
- F
- 13
- OEB
- B
- OEL
- TWA: 0.6 ppm (10 mg/m3)
- PPE
- dust mask type N95 (US), Eyeshields, Faceshields, Gloves
- wgk
- 3
- tsca
- TSCA listed
- rtecs
- PB7000000
- ridadr
- UN 1851
- hs_code
- 29033990
- Toxicity
- LD50 s.c. in mice: 1.6 mmoles/kg (Kutob, Plaa)
- risk_code
- 20/21/22-36/37/38
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xn
- safety_code
- 26-36/37-36/37/39-22-24/25
- Storage Class
- 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
- target organs
- Respiratory system
- Hazard statements
- H302-H312-H315-H319-H332-H335
- Hazard Classifications
- Acute Tox. 3 InhalationAcute Tox. 4 DermalAcute Tox. 4 OralAquatic Chronic 2Eye Irrit. 2Skin Irrit. 2STOT SE 3
- Precautionary statements
- P264-P270-P280-P261-P271-P301+P312-P330-P302+P352-P312-P362+P364-P332+P313-P305+P351+P338-P337+P313-P304+P340-P403+P233-P405-P501
- Hazardous Substances Data
- 75-47-8(Hazardous Substances Data)
Chemistry & industry
Pharmacology
ATC Code
D - Dermatologicals
QD - Dermatologicals
Pharmacodynamics
Iodoform exhibits antibacterial activities after topical application. In a comparative study of wound dressing agents, iodoform gauze exerted an antibacterial effect 3 hours after the start of bacterial growth of _E. coli_ and subsequently maintained the strong antibacterial effectiveness. A study demonstrated that direct and indirect exposure to high concentrations of iodoform induces a cytotoxic effect on cultures of macrophages and epithelial cells _in vitro_, while cell proliferation was enhanced at low concentrations of iodoform. This cytotoxic effect of iodoform in root canals may further lead to long-term local irritation to follicles of permanent successors and formation of cyst-like radiolucent defects.
Mechanism of Action
While the mechanism of action of iodoform remains unclear, it is proposed that iodoform releases iodine, which denatures bacterial proteins by oxidation of the free iodine. Iodoform may also play a role in chemical debridement for effective necrotic wound healing and tissue damage repair via collagen fibrinolysis; upon treatment in necrotic tissue, iodoform reduced the size of the macromolecules containing collagen I in wound surface proteins. In human gingival fibroblasts _in vitro_, high concentrations of iodoform was shown to decrease the viability of macrophages and epithelial cells and reduced the secretion of _P. gingivalis_-induced TNFα. P. gingivalis is an anaerobic bacteria present in anaerobic oral niches including periapical sites and periodontal pockets.
Metabolism/Metabolites
It is expected to be oxidized to iodine.
HALOFORMS ARE METABOLIZED TO CARBON MONOXIDE BY HEPATIC MICROSOMAL MIXED FUNCTION OXIDASES & THIS REACTION IS MARKEDLY STIMULATED BY SULFHYDRYL COMPOUNDS. /HALOFORMS/
TRIHALOMETHANES (HALOFORMS) WERE METABOLIZED TO CARBON MONOXIDE BY A RAT LIVER MICROSOMAL FRACTION REQUIRING BOTH NADPH AND MOLECULAR OXYGEN FOR MAXIMAL ACTIVITY. THE METABOLISM OF HALOFORMS TO CARBON MONOXIDE FOLLOWED THE HALIDE ORDER; IODOFORM YIELDED THE GREATEST AMOUNT OF CARBON MONOXIDE, WHEREAS CHLOROFORM YIELDED THE SMALLEST AMOUNT.
ADMINISTRATION OF HALOFORMS (TRIHALOMETHANES) TO RATS LED TO SUBSTANTIAL ELEVATIONS IN BLOOD CARBON MONOXIDE LEVELS. /TRIHALOMETHANES/
Absorption, Distribution and Excretion
Iodoform is reported to be absorbed through denuded skin, wounds or mucous membranes.
No pharmacokinetic data available.
No pharmacokinetic data available.
No pharmacokinetic data available.
Uses & manufacturing
Uses
Used as a disinfectant and veterinary antiseptic; [Merck Index, #5033]
Using Disinfectants or Biocides [Category: Clean]
Iodoform is used as a component of adhesives and as a polymerization control agent
Wound dressing and sensitizing agent in certain printing processes.
MEDICATION
MEDICATION: VET
U.S. Production
(1977) PROBABLY GREATER THAN 3.18X10+6 G
(1979) PROBABLY GREATER THAN 3.18X10+6 G
Methods of Manufacturing
Prepn from acetone, sodium hypochlorite, potassium iodide, and sodium hydroxide: Glass, Quart. J. Pharm. Pharmacol. 8, 351 (1935); from chloroform + methyl iodide: Soroos, Hinkamp, J. Am. Chem. Soc. 67, 1642 (1945); by electrolysis: Glasstone, Ind. Chem. 7, 315 (1931)
Electrolysis of an iodide solution in dilute alcohol or acetone.
Formulations/Preparations
GRADE: TECHNICAL, NF
Purified grades
BIPP gauze: sterile ribbon gauze impregnated with a sterile paste consisting of iodoform 40%, bismuth subnitrate 20%, and liquid paraffin 40%.
Bismuth subnitrate & iodoform paste: bismuth subnitrate 1, iodoform 2, sterilized liquid paraffin 1, by wt, prepared aseptically.
For more Formulations/Preparations (Complete) data for IODOFORM (8 total), please visit the HSDB record page.
Applications
DescriptionIodoform is a stable, pale yellow crystalline solid. It is volatile with a characteristic pungent, unpleasant and penetrating odour, but with a sweetish taste. It is incompatible with strong oxidising agents, reducing agents, lithium, and metallic salts such as mercuric oxide, silver nitrate, strong bases, calomel, and tannin. Reports indicate that earlier iodoform was in use as a disinfectant and as an antiseptic or dressing and healing of wounds and sores for pets. Iodoform is the active ingredient in many antiseptic or dressing powders used for dogs and cats to prevent infection.
UsesIodoform has limited use as a chemical intermediate and for medicinal purposes as disinfectant and antiseptic and has been used in veterinary medicine.
UsesTriiodomethane is a crystalline compound commonly used as a disinfectant. It can be used in the process of removing heavy metals such as mercury from fuids.
UsesIt is used as a topical anti-infective, applied to the skin.
General DescriptionBright yellow or yellow powder or crystals. Penetrating odor. Unctuous touch. Odor threshold 0.4 ppb.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers50 total
Additional notes
DefinitionA yellow crystalline compound made by warming ethanal with an alkaline solution of an iodide:CH3CHO + 3I– + 4OH– → CHI3 + HCOO– + 3H2O The reaction also occurs with all ketones of general formula CH3COR (R is an alkyl group) and with secondary alcohols CH3CH(OH)R. Iodoform is used as a test for such reactions (the iodoform reaction).
Related reactions
Linked notes
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