Diazomethane

HCID 9550CAS 334-88-3

Basic information

Standard SMILES
C=[N+]=[N-]
InChIKey
YXHKONLOYHBTNS-UHFFFAOYSA-N
Molecular formula
CH2N2
Average molar mass
42.04 g/mol
Monoisotopic mass
42.02179806

Overview

Diazomethane is a yellow gas with a musty odor that is shipped as a liquid under pressure. (NIOSH, 2024) Highly toxic by inhalation.

Names & identifiers

Preferred name
Diazomethane
IUPAC
diazomethane
English name
Diazomethane
Molecular formula
CH2N2
Molecular weight
42.03998

Names & synonyms

DIAZOMETHANEAzimethyleneAcomethylene334-88-3Methane, diazo-Diazonium methylide60A625P70PDTXSID0024008CHEBI:73716azomethyleneRefChem:388924DTXCID604008
Show more names
DIAZIRINEazimethaneDIAZOMETHANE IN ETHERMethane, diazo-(8CI,9CI)Diazomethane ISO 9001:2015 REACH
206-382-7EINECS 206-382-7CCRIS 205HSDB 1628BRN 0102415UNII-60A625P70P4-01-00-03056 (Beilstein Handbook Reference)METHANE,DIAZO

Database identifiers

CAS
334-88-3
PubChem CID
9550
DTXSID
DTXSID0024008
ChEBI
CHEBI:73716
UNII
60A625P70P
EC Number
206-382-7
Nikkaji
J2.576C、J625.947B

Properties

Computed structural properties

XLogP
1.6
Topological polar surface area
2 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
1
Rotatable bonds
0
Heavy atoms
3

Experimental & physicochemical properties

Chemical Classes · 3 items

Hazardous Air Pollutants (HAPs)

Nitrogen Compounds -> Other Nitrogen Compounds

Flammable agents - 4th degree

SpringerMaterials PropertiesCoriolis coupling
PesticidesPesticide -> EPA IRIS
LogP2.00 (estimated)
OdorMusty odor
Density · 4 items

1.45

Relative density (water = 1): 1.45

1.45 @25 °C

1.45(relative gas density)

Physicochemical properties

Melting point
-145 ° · -145°
Boiling point
-23 ° · bp -23°
Density
1.45 g/cm3 · 1.45 g/cm3
refractive index
1.418 · 1.4180 (estimate)
form
Yellow gas
Odor
Musty odor (no accepted threshold value)

Safety & regulation

GHS classification

GHS Classification · 6 items

Danger

H350: May cause cancer [Danger Carcinogenicity]

P203, P280, P318, P405, and P501 (click each P-code to see the statement)

Not Classified

Danger

H350: May cause cancer [Danger Carcinogenicity]

Hazard information

Regulatory Information · 2 items

Hazard Traits - Carcinogenicity; Hepatotoxicity and Digestive System Toxicity; Ocular Toxicity; Respiratory Toxicity

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

DOT LabelPoison Gas Flammable Gas
Fire Hazards · 2 items

Excerpt from ERG Guide 119 [Gases - Toxic - Flammable]:

Extremely flammable. Many reactions may cause fire or explosion. Gives off irritating or toxic fumes (or gases) in a fire. Gas/air mixtures are explosive.

Health HazardsExcerpt from NIOSH Pocket Guide for Diazomethane:
Hazards Summary · 2 items

The major source of exposure to diazomethane is occupational. Diazomethane is a strong respiratory irritant. Acute (short-term) inhalation exposure of humans to diazomethane may cause irritation of the eyes, cough, wheezing, asthmatic symptoms, pulmonary edema, pneumonia, dizziness, weakness, headache, and chest pains. No information is available on the chronic (long-term), reproductive, developmental, or carcinogenic effects of diazomethane in humans. Increased incidences of lung tumors have been observed in rats and mice exposed to diazomethane by inhalation and in dermally exposed mice. EPA has not classified diazomethane with respect to its potential carcinogenicity.

Toxicity in experimental animals resembles that of phosgene. [ACGIH] Possible frostbite from contact with liquid; [NIOSH] A corrosive substance that can cause pulmonary edema; May cause asthma after repeated or prolonged exposures; [ICSC]

Reactive GroupAzo, Diazo, Azido, Hydrazine, and Azide Compounds

Safety & protection

Fire Fighting · 2 items

Excerpt from ERG Guide 119 [Gases - Toxic - Flammable]:

Shut off supply; if not possible and no risk to surroundings, let the fire burn itself out. In other cases extinguish with powder, carbon dioxide. Combat fire from a sheltered position.

First Aid Measures · 4 items

Fresh air, rest. Half-upright position. Artificial respiration may be needed. Refer immediately for medical attention.

ON FROSTBITE: rinse with plenty of water, do NOT remove clothes. Refer immediately for medical attention. Wear protective gloves when administering first aid.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention. Keep rinsing during transport for medical attention.

Unlikely under occupational conditions.

First Aid · 2 items

Excerpt from NIOSH Pocket Guide for Diazomethane:

(General first aid procedures)

Safe StorageSolutions of diazomethane should not be stored.
Firefighting Hazards... Vapors may travel long distances to ignition sources and flashback. Vapors in confined areas may explode when exposed to fire. Containers may explode in fire. ...
Fire Fighting Procedures · 2 items

If material /is/ on fire or involved in /a/ fire use dry chemical, dry sand, or carbon dioxide. Do not use water on material itself. If large quantities of combustibles are involved, use water in flooding quantities as spray and fog. Use water spray to knock-down vapors. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible.

Fires involving diazomethane should be fought upwind from the maximum distance possible. Diazomethane will explode in a fire. The fire area should be evacuated immediately. Keep unnecessary people away; isolate the hazard area and deny entry. Vapors may travel to a source of ignition and flash back. Vapors are an explosion and poison hazard indoors, outdoors, or in sewers.

Toxicology

InteractionsNO VANCOMYCIN WAS ADSORBED TO CELL WALLS /OF BACILLUS SUBTILIS W23/ THAT HAD BEEN ESTERIFIED BY TREATMENT WITH DIAZOMETHANE.
Target OrgansEyes, respiratory system
Environmental Fate · 3 items

TERRESTRIAL FATE: Since diazomethane is a gas and undergoes rapid hydrolysis with water, volatilization from soil is not relevant. Similarly, adsorption to soil and biodegradation are not expected due to the rapid rate of decomposition under environmental conditions. (SRC)

AQUATIC FATE: Since diazomethane is a gas and undergoes rapid hydrolysis with water, volatilization from water is not relevant. Similarly, hydrolysis, adsorption to sediments, bioconcentration, and biodegradation are not expected due to the rapid rate of decomposition under environmental conditions. (SRC)

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), diazomethane, which has an estimated vapor pressure of 3.94X10+3 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely as a gas. Gas-phase diazomethane will undergo rapid hydrolysis with atmospheric water vapor but may also be degraded by reaction with photochemically-produced hydroxyl radicals at a much slower rate(SRC); the half-life for this reaction in air is estimated to be 16 days(SRC), calculated from its rate constant of 9.34X10-13 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). The rate constant for the gas-phase reaction of diazomethane with ozone was 3.3X10-17 cu cm/molecule-sec(4). Diazomethane does not contain chromophores that absorb at wavelengths >290 nm(5), and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).

Adverse EffectsDermatotoxin - Skin burns.
Exposure Routes · 2 items

The substance can be absorbed into the body by inhalation.

inhalation, skin and/or eye contact (liquid)

Signs and Symptoms · 4 items

Sore throat. Headache. Laboured breathing. Shortness of breath. Nausea. Vomiting. Symptoms may be delayed.

Redness. Pain. Skin burns. Burning sensation. ON CONTACT WITH LIQUID: FROSTBITE.

Burning sensation. Redness. Pain. Burns. Loss of vision. ON CONTACT WITH LIQUID: FROSTBITE.

irritation eyes; cough, short breath; headache, lassitude (weakness, exhaustion); flush skin, fever; chest pain, pulmonary edema, pneumonitis; asthma; liquid: frostbite

Regulatory information

Atmospheric Standards · 1 item

Listed as a hazardous air pollutant (HAP) generally known or suspected to cause serious health problems. The Clean Air Act, as amended in 1990, directs EPA to set standards requiring major sources to sharply reduce routine emissions of toxic pollutants. EPA is required to establish and phase in specific performance based standards for all air emission sources that emit one or more of the listed pollutants. Diazomethane is included on this list.

CERCLA Reportable Quantities · 1 item

Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 100 lb or 45.4 kg. The toll free number of the NRC is (800) 424-8802. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV.D.3.b).

Safety data

OEB
C
OEL
TWA: 0.2 ppm (0.4 mg/m3)
IDLA
2 ppm
ridadr
1953
Toxicity
LCLO inhal (cat) 175 ppm (10 min)PEL (OSHA) 0.2 ppm (0.4 mg/m3)TLV-TWA (ACGIH) 0.2 ppm (0.4 mg/m3)
risk_code
45

Chemistry & industry

Uses & manufacturing

Uses · 3 items

Diazomethane is used as a methylating agent for acidic compounds such as carboxylic acids, phenols, and enols.

Diazomethane is used as a methylating agent for acidic compounds. An explosive, it is not manufactured for distribution. [ACGIH] Because of its toxicity and its explosive nature, diazomethane is freshly prepared in situ and used in solution of ether or dioxane. [ICSC]

Powerful methylating agent for acidic compounds such as carboxylic acids, phenols, enols.

Methods of Manufacturing · 3 items

REACTION OF N-NITROSOMETHYL-P-TOLUENESULFONAMIDE WITH AN ALKALI SUCH AS POTASSIUM HYDROXIDE OR POTASSIUM CARBONATE

Ether solns of diazomethane: From N-nitroso-beta-methylaminoisobutyl methyl ketone in ether and isopropanol by reaction with sodium isopropoxide or from the same ketone in ether by reaction with sodium cyclohexoxide; ... By potassium hydroxide saponification of nitrosomethylurea in ether; ... or of nitrosomethylurethan in ether. /Ether solutions of diazomethane/

Prepared from chloroform and hydrazine by reaction with potassium hydroxide; ... from potassium hydroxide and nitrosomethylurea. /Gaseous diazomethane/

General Manufacturing Information · 4 items

Diazomethane generators are generally used to produce this compound in situ for laboratory use.

Because of its toxicity and its explosive nature, diazomethane is not manufactured for distribution and sale. When used as methylating agent in the laboratory, it is produced and used in situ. Thus, there is no available information on technical products and impurities.

In the laboratory diazomethane may be prepared most simply by the action of alkali on the commercially available N-methyl-N-nitroso-N'-nitroguanidine.

One USA company offers a self-contained reaction kit for generating ether solutions of diazomethane as needed without exposing the user to the diazomethane or to the N-nitrosomethyl-p-toluenesulfonamide.

Applications · 7 items

DescriptionAt room temperature, diazomethane (CH2N2) is a toxic yellow gas which can cause significant irritation upon inhalation. Solutions that contain concentrated diazomethane are highly toxic, and they can result in explosions. When heated, Diazomethane emits toxic fumes made of nitrogen oxides; the toxic fumes are also independent of its decomposition. Diazomethane is used after its preparation in ether or in ether that contains traces of ethanol. It is rarely prepared and applied to other solvents which may include dichloromethane. Diazomethane is related to hydrogen cyanide and formaldehyde in its annotation.

UsesIt is used as a methylating agent especially for acidic compounds which may include enols, phenols, and carboxylic acids.

DescriptionDiazomethane is a flammable, yellow gas, or aliquid under pressure. Molecular weight = 42.05; Boilingpoint = 222.7℃; Freezing/Melting point = -145℃;Autoignition temperature = 100℃ (explodes). HazardIdentification (based on NFPA-704 M Rating System):Health 4, Flammability 3, Reactivity 3. Decomposes inwater; reaction.

UsesIt is used in organic synthesis as a methylating agent to methylate acidic compoundssuch as carboxylic acids and phenols. Itis used in trace environmental analysis tomethylate chlorophenoxy acid herbicides.

UsesPowerful methylating agent for acidic compounds such as carboxylic acids, phenols, enols; not manufactured for sale and distribution because of toxicity and explosivity

UsesPowerful methylating agent for acidic Compounds such as carboxylic acids, phenols, enols. For syntheses with diazomethane see the reviews by Smith, Chem. Rev. 23, 193 (1938); Eistert, Z. Angew. Chem. 54, 99, 124 (1941) translated by Spangler in Newer Methods of Preparative Organic Chemistry (New York, 1948) p 513; J. S. Pizey, Synthetic Reagents vol. 2 (John Wiley, New York, 1974) pp 65-142.

General DescriptionYellow gas with a musty odor. Highly toxic by inhalation Shipped as a liquid under pressure.

Preparation methods · 1 item

PreparationDiazomethane was generated with a diazomethane-generating glassware kit (Aldrich). A solution of N-methyl-N-nitroso-4-toluenesulfonamide (Diazald, 2.23 g, 10.4 mmol) in ether (24 mL) was added dropwise to a mixture of KOH (1.75 g, 31.2 mmol) in H2O (18 mL), ether (4 mL), and 2-(2-ethoxyethoxy)ethanol (18 mL) kept at 70 ºC. The ethereal solution of diazomethane was continuously distilled into a flask that was ready to use for the next reaction.

Suppliers9 total

Dayang Chem (Hangzhou) Co.,Ltd.+86-0571-88938639 17705817739 · [email protected]
PT CHEM GROUP LIMITED+86-85511178; +86-85511178 · [email protected]
HBCChem, Inc.+1-510-219-6317 · [email protected]
池州凯隆进出口贸易有限公司[email protected]
河南天孚化工有限公司+86-0371-55170693 +86-19937530512 · [email protected]

Additional notes

DefinitionChEBI: The simplest diazo compound, in which a diazo group is attached to a methylene group.

Related reactions

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Linked notes

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