Trimethyl phosphite Chemical Properties

Melting point:

−78 °C(lit.)

Boiling point:

111-112 °C(lit.)

Density 

1.052 g/mL at 25 °C(lit.)

vapor density 

4.3 (vs air)

vapor pressure 

17 mm Hg ( 20 °C)

refractive index 

n20/D 1.408(lit.)

Flash point:

82 °F

storage temp. 

2-8°C

solubility 

Chloroform, DMSO (Sparingly)

form 

Liquid

color 

Colorless

Specific Gravity

1.052

explosive limit

5.2-61.2%(V)

Water Solubility 

Hydrolyzes with water.

Sensitive 

Air & Moisture Sensitive

Hydrolytic Sensitivity

4: no reaction with water under neutral conditions

BRN 

956570

Exposure limits

TLV-TWA 10 mg/m³ (2 ppm) (ACGIH).

Stability:

Moisture Sensitive

CAS DataBase Reference

121-45-9(CAS DataBase Reference)

NIST Chemistry Reference

Phosphorous acid, trimethyl ester(121-45-9)

EPA Substance Registry System

Trimethyl phosphite (121-45-9)

Safety Information

Hazard Codes 

Xn,T,F,Xi

Risk Statements 

10-22-36/37/38-41-37/38-65-48/23/24/25-11-46-45-67-66-36

Safety Statements 

26-39-62-45-16-53

RIDADR 

UN 2329 3/PG 3

OEB

B

OEL

TWA: 2 ppm (10 mg/m3)

WGK Germany 

1

RTECS 

TH1400000

F 

10-13-21

Autoignition Temperature

250 °C

TSCA 

Yes

HS Code 

2920 23 00

HazardClass 

3

PackingGroup 

III

Hazardous Substances Data

121-45-9(Hazardous Substances Data)

Toxicity

LD50 orally in Rabbit: 1600 mg/kg LD50 dermal Rabbit 2600 mg/kg

MSDS

• Language:English Provider:Phosphorous acid trimethyl ester
• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

Trimethyl phosphite Usage And Synthesis

Chemical Properties

Trimethyl phosphite is a colorless liquid. Distinctive pungent, pyridine-like odor. The Odor Threshold is 0.0001 ppm.

Uses

Trimethyl phosphite has been used primarily as an intermediate in the manufacture of pesticides and the synthesis of organophosphate insecticides. It is also used as a fire retardants in the production of textiles, as an intermediate in the production of flame-retardant polymers for polyurethane foams, and as a catalyst.

Production Methods

Produced via a reaction between phosphorus trichloride and methanol in the presence of a tertiary amine catalyst such as diethylaniline.

Definition

ChEBI: Trimethyl phosphite is an organophosphorus compound that is phosphane in which the three hydrogens are replaced by methoxy groups. It is an alkylating agent used primarily in the synthesis of organophosphate compounds. It has a role as an alkylating agent.

Reactions

The reaction of trimethyl phosphite and dimethyl acetylenedicarboxylate in the presence of dimedone as the proton source/nucleophile leads to 2-(dimethoxy-phosphoryl)-3-(2-hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-succinic acid dimethyl ester in 91 % yields.
It reacts with a catalytic amount of methyl iodide in the Arbuzov reaction to give dimethyl methylphosphonate:
P(OCH3)3 → CH3P(O)(OCH3)2
It is susceptible to oxidation to trimethyl phosphate.

General Description

Trimethyl phosphite appears as a clear colorless liquid with a strong foul odor. Flash point 99°F. Denser than water and insoluble in water. Vapors heavier than air. It is used in making pesticides, flame retardants and organophosphorous additives.

Air & Water Reactions

Highly flammable. Insoluble in water and denser than water. Slowly reacts with water to form phosphoric acid and corresponding organic alcohol. Trimethyl phosphite hydrolyzes in water to form dimethyl phosphite and methanol. The hydrolysis rate of trimethyl phosphite is expected to be similar to the hydrolysis rate of triethyl phosphite(SRC).

Reactivity Profile

As soon as Trimethyl phosphite contacted a small amount of magnesium perchlorate in a flask, there was a flash and an explosion that shattered the flask (Allison 1968).

Health Hazard

Trimethyl phosphite is a skin, eye, and mucous membrane irritant with low subacute inhalation toxicity. Its irritating action on rabbits’ skin was moderate to severe. The pure liquid instilled into the eyes can cause severe irritation and swelling, which can last for a few days. Chronic exposure to 300–600 ppm concentration in air produced lung inflammation and cataracts in mice. There was no acute inhalation toxicity observed in test animals. The oral and dermal toxicities were low.
LD50 value, oral (rats): 1600 mg/kg
Teratogenic effects showing gross abnormalities were observed in newborn rats when pregnant rats were dosed with high concentrations of trimethyl phosphite.
The odor threshold for this compound was determined to be 0.0001 ppm (ACGIH 1986). The odor is irritating and pungent at high concentrations..

Fire Hazard

Special Hazards of Combustion Products: Toxic fumes of PO x

Safety Profile

Moderately toxic by ingestion and skin contact. An experimental teratogen. A severe skin and eye irritant. Flammable liquid when exposed to heat, flame, or oxidizers. To fight fire, use water, foam, fog, CO2. Violent explosive reaction on contact with magnesium perchlorate or trimethyl platinum(IV) azide tetramer. When heated to decomposition it emits toxic fumes of POx. An intermediate in the production of pesticides, fire retardants, and organic phosphorus additives. See also ESTERS.

Potential Exposure

Trimethyl phosphite is a flame retardant, and used as an intermediate in the manufacture of a number of pesticides, and organophosphorus additives.

Carcinogenicity

Trimethyl phosphite was genotoxic in mouse lymphoma assays but was not mutagenic in various bacterial assays.

Shipping

UN2329 Trimethyl phosphite, Hazard Class: 3; Labels: 3-Flammable liquid.

Purification Methods

Treat the phosphite with Na (to remove water and any dialkyl phosphonate), then decant and distil it with protection against moisture. It has also been treated with sodium wire for 24hours, then distilled in an inert atmosphere onto activated molecular sieves [Connor et al. J Chem Soc, Dalton Trans 511 1986]. It can be fractionally distilled using a spinning band column at high reflux ratio. It is a colourless liquid which is slowly hydrolysed by H2O. [Gillis et al. J Am Chem Soc 80 2999 1958, NMR: Callis et al. J Am Chem Soc 79 2719 1957, Kosolapoff Organophosphorus Compounds, Wiley p 203 1950, Beilstein 1 IV 1256.]

Incompatibilities

Vaor May form explosive mixture with air. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Violent reaction with magnesium perchlorate. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Reacts (hydrolyzes) with water. Incompatible with air, moisture.

Waste Disposal

Trimethyl phosphite may be burned in a chemical incinerator equipped with an afterburner and scrubber.

Trimethyl phosphite(121-45-9)Related Product Information

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