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Trimethoxymethane

Product Name
Trimethoxymethane
CAS No.
149-73-5
Chemical Name
Trimethoxymethane
Synonyms
TRIMETHYL ORTHOFORMATE;TMOF;CH(OCH3)3;METHYL ORTHOFORMATE;Trimethyl ester;Thrimethyl orthoformate;orthoformicacidmethylester;Trimethyl orthoformate,99%;TrimethylOrthoFormate(Tmof);Orthoformic acid methyl ester
CBNumber
CB4853127
Molecular Formula
C4H10O3
Formula Weight
106.12
MOL File
149-73-5.mol
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Trimethoxymethane Property

Melting point:
-53 °C
Boiling point:
101-102 °C(lit.)
Density 
0.97 g/mL at 25 °C(lit.)
vapor density 
3.67 (vs air)
vapor pressure 
23.5 mm Hg ( 20 °C)
refractive index 
n20/D 1.379(lit.)
Flash point:
60 °F
storage temp. 
Store below +30°C.
solubility 
Miscible with ether, alcohol and benzene.
form 
Liquid
color 
Clear colorless
explosive limit
1.4-44.6%(V)
Water Solubility 
10 g/L (hydrolysis)
Sensitive 
Moisture Sensitive
Merck 
14,6884
BRN 
969215
InChIKey
PYOKUURKVVELLB-UHFFFAOYSA-N
LogP
-0.03-0.09 at 20℃
CAS DataBase Reference
149-73-5(CAS DataBase Reference)
NIST Chemistry Reference
Methane, trimethoxy-(149-73-5)
EPA Substance Registry System
Trimethoxymethane (149-73-5)
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Safety

Hazard Codes 
F,Xi
Risk Statements 
11-36
Safety Statements 
9-16-26-29
RIDADR 
UN 3272 3/PG 2
WGK Germany 
1
RTECS 
RM6650000
Autoignition Temperature
255 °C
TSCA 
Yes
HazardClass 
3
PackingGroup 
II
HS Code 
29159080
Hazardous Substances Data
149-73-5(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 3130 mg/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H319Causes serious eye irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

P242Use only non-sparking tools.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.00885
Product name
Trimethyl orthoformate
Purity
for synthesis
Packaging
250ML
Price
$39
Updated
2024/03/01
Sigma-Aldrich
Product number
8.00885
Product name
Trimethyl orthoformate
Purity
for synthesis
Packaging
1L
Price
$93.8
Updated
2024/03/01
Sigma-Aldrich
Product number
108456
Product name
Trimethyl orthoformate
Purity
99%
Packaging
500ml
Price
$116
Updated
2024/03/01
Sigma-Aldrich
Product number
108456
Product name
Trimethyl orthoformate
Purity
99%
Packaging
20l
Price
$1220
Updated
2024/03/01
TCI Chemical
Product number
O0068
Product name
Trimethyl Orthoformate
Purity
>98.0%(GC)
Packaging
25mL
Price
$19
Updated
2024/03/01
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Trimethoxymethane Chemical Properties,Usage,Production

Description

Trimethyl orthoformate is an effective solvent for thallium(III) nitrate-mediated oxidations. It undergoes acid catalyzed reaction with 6-(N-D-ribitylanilino) uracils to form 8-demethyl-8-hydroxy-5-deazariboflavins.

Chemical Properties

Colorless liquid. Slightly soluble in water, miscible with alcohol and oils.
Very diffusive, ethereal, pungent or nauseating odor, pleasant in dilution, slightly wineyfruity, Brandy-like.
Sweet taste in concentrations below 100 ppm. Barely perceptible at 10 ppm.

Uses

Trimethyl Orthoformate is the most simple orthoester. Used in organic synthesis as a reagent for introducing a protecting group for aldehydes and in the creation of methoxymethylene groups and heterocyclic ring systems.

Uses

Trimethyl orthoformate is used as a protecting group for aldehydes in organic synthesis, as an additive in polyurethane coatings and as a dehydrating agent in the preparation of surface modified colloidal silica nanoparticles. It is also used as a chemical intermediate in the preparation of vitamin B1 and sulfa drugs. It acts as an effective solvent for thallium(III) nitrate-mediated oxidations. Furthermore. It is utilized for the synthesis of chromone from keto-hydroxy naphthol in the presence of trimethylamine.

Uses

Trimethyl orthoformate can be used:

  • To convert sulfonic acids to methyl esters.
  • To convert 2-acylcyclohexanones to the corresponding acetal derivatives.
  • To mediate Pinacol reaction of various 1,2-diols with tin(IV) chloride without the formation of water.
  • To synthesize 1-substituted-1H-1,2,3,4-tetrazoles via a three-component condensation with amine and sodium azide catalyzed by indium triflate under solvent-free conditions.
  • For the N-methylation of amines in the presence of sulfuric acid.

Application

Trimethyl orthoformate was used as dehydrating agent in the preparation of surface-modified colloidal silica nanoparticles.
MOM protection of Diols using Trimethyl Orthoformate
N-Formylation of Amino Acid Esters

General Description

Trimethyl orthoformate is an effective solvent for thallium(III) nitrate-mediated oxidations. It undergoes acid catalyzed reaction with 6-(N-D-ribitylanilino) uracils to form 8-demethyl-8-hydroxy-5-deazariboflavins.

Flammability and Explosibility

Highly flammable

Safety Profile

A skin and eye irritant. A very dangerous fire hazard when exposed to heat or flame; can react with oxidizing materials. Hazardous to prepare. To fight fire, use CO2, fog, haze. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS.

Synthesis

Trimethyl orthoformate is prepared on an industrial scale by the methanolysis of hydrogen cyanide:
HCN + 3 HOCH3 → HC(OCH3)3 + NH3
Trimethyl orthoformate can also be prepared from the reaction between chloroform and sodium methoxide, an example of the Williamson ether synthesis.

Precautions

Moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with acids and strong oxidizing agents.

References

Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols
P. G. M. Wuts, in Greene's Protective Groups in Organic Synthesis, 5th ed., ed. by P. G. M. Wuts, John Wiley & Sons, Inc., Hoboken, New Jersey, 2014, Chap. 2, 17.
A Facile Procedure for the Synthesis of N-Formyl Amino Acid Esters
T. Chancellor, C. Morton, Synthesis 1994, 10, 1023.

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Trimethoxymethane Suppliers

G K C H Gmbh
Tel
--
Fax
--
Email
germany@gkch.com
Country
Germany
ProdList
46
Advantage
58
Aceto FineChem Gmbh
Tel
--
Fax
--
Email
contact@de.aceto.com
Country
Germany
ProdList
49
Advantage
58
CHEMOS GmbH & Co. KG
Tel
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Email
chemos@chemos.de
Country
Germany
ProdList
6728
Advantage
58
KHBoddin GmbH
Tel
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Email
info@khboddin.com
Country
Germany
ProdList
132
Advantage
58
Evonik Industries AG.
Tel
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--
Email
@evonik.com
Country
Germany
ProdList
351
Advantage
58
Alfa Aesar, Thermo Fisher Scientific
Tel
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Fax
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Email
es@alfa.com
Country
Germany
ProdList
5126
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58
HPC Standards GmbH
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chulze@hpc-standards.com
Country
Germany
ProdList
2139
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58
Merck Millipore
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Email
ccc@merckgroup.com
Country
Germany
ProdList
2010
Advantage
58
ChemPur GmbH
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Fax
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Email
info@ChemPur.de
Country
Germany
ProdList
2738
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50
Karl H. Boddin Chemiehandel GmbH
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Country
Germany
ProdList
1037
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43
ABCR GmbH & CO. KG
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info@abcr.de
Country
Germany
ProdList
6846
Advantage
75
Service Chemical Inc.
Tel
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Email
sales@chemos-group.com
Country
Germany
ProdList
6373
Advantage
71
Degussa AG
Tel
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Email
degussa-bk@degussa.com
Country
Germany
ProdList
641
Advantage
64
Merck Schuchardt OHG
Tel
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Fax
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Email
schuchardt-vertrieb@merck.de
Country
Germany
ProdList
5831
Advantage
74
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View Lastest Price from Trimethoxymethane manufacturers

Ningxia Jinhua Chemical Co.,Ltd
Product
Trimethyl Orthoformate 149-73-5
Price
US $0.00/Kg/Drum
Min. Order
200KG
Purity
99.4
Supply Ability
1000kg
Release date
2021-05-17
Hebei Chuanghai Biotechnology Co,.LTD
Product
Trimethyl Orthoformate 149-73-5
Price
US $5.70/kg
Min. Order
10kg
Purity
99%
Supply Ability
10000kg
Release date
2024-08-21
Shandong Luning Pharmaceutical Co., Ltd.
Product
Trimethyl Orthoformate (TMOF ) 149-73-5
Price
US $606.00/T
Min. Order
1T
Purity
99%
Supply Ability
600T
Release date
2020-10-22

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