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ChemicalBook--->CAS DataBase List--->1587-20-8

1587-20-8

1587-20-8 Structure

1587-20-8 Structure
IdentificationMore
[Name]

TRIMETHYL CITRATE
[CAS]

1587-20-8
[Synonyms]

CITRIC ACID TRIMETHYL ESTER
METHYL CITRATE
TRIMETHYL CITRATE
2,3-propanetricarboxylicacid,2-hydroxy-trimethylester
3-Hydroxy-3-methoxycarbonylpentanedioic acid, dimethyl ester
Trimethyl 2-hydroxy-1,2,3-propanetricarboxylate
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trimethyl ester
2-Hydroxy-1,2,3-propanetricarboxylic acid trimethyl ester
Citric acid trimethyl
[EINECS(EC#)]

216-449-2
[Molecular Formula]

C9H14O7
[MDL Number]

MFCD00025889
[Molecular Weight]

234.2
[MOL File]

1587-20-8.mol
Chemical PropertiesBack Directory
[Melting point ]

75-78 °C
[Boiling point ]

176 16mm
[density ]

1.3363 (rough estimate)
[vapor pressure ]

1.3hPa at 20℃
[refractive index ]

1.4455 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Sparingly), Methanol (Slightly)
[form ]

Solid
[pka]

10.43±0.29(Predicted)
[color ]

White to Off-White
[Odor]

at 100.00 %. ethereal fruity
[Odor Type]

ethereal
[Water Solubility ]

53.2g/L at 20℃
[BRN ]

1796169
[LogP]

0.7 at 20℃
[CAS DataBase Reference]

1587-20-8(CAS DataBase Reference)
[EPA Substance Registry System]

1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trimethyl ester (1587-20-8)
Safety DataBack Directory
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[HS Code ]

29181500
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methanol-->Citric acid
[Preparation Products]

Citrazinic acid
Questions And AnswerBack Directory
[Description]

Trimethyl citrate is an ester of citric acid. It is a kind of non-toxic plasticizer1. Trimethyl citrate is one of the constituents of Dioscorea opposita2. The IC50 value for monoamine oxidase-B of trimethyl citrate was studied. It has various applications3: it can do the main flame retardant candle flame color, its melting point and can fully meet the flammability requirements of candle products. It can be used for the synthesis of pharmaceutical and pesticide. It can act as the main raw material for the production of citric acid hydrochloride, citric acid hydrochloride as well as the synthetic hot melt adhesive. It can also be used as the methyl methacrylate polymer a blowing agent, a stabilizer acrylamide, polyamide adhesive initiators, PVC plasticizers. It can also be used as solvent for household and II cleaner, film-former4.
[Reference]

  1. Huang, Li, L. I. Chun-Lian, and H. U. Qing-Guo. "Study on Catalytic Synthesis of Trimethyl Citrate by Solid Acid." Liaoning Chemical Industry (2012).
  2. https://www.sigmaaldrich.com/catalog/product/aldrich/27502?lang=en&region=US
  3. www.zhonglanindustry.com/product/trimethyl-citrate
  4. https://www.lookchem.com/Trimethyl-citrate/
Hazard InformationBack Directory
[Chemical Properties]

Colorless crystals. M.P. 79℃. B.P. 287℃. (decomposes). Slightly soluble in water, soluble in alcohol and oils.
[Uses]

Trimethyl Citrate is a reagent used in the preparation of citrate-ciprofloxacin conjugates which has antibacterial activity.
[Preparation]

Trimethyl citrate is produced by direct esterification of Citric acid with Methanol using the old-fashioned method with 3% sulfuric acid and reflux to complete the esterification.
[General Description]

Trimethyl citrate is one of the constituents of Dioscorea opposita. The IC50 value for monoamine oxidase-B of trimethyl citrate was studied.
[Flammability and Explosibility]

Notclassified
[Synthesis]

Methanol

67-56-1

Citric acid

77-92-9

TRIMETHYL CITRATE

1587-20-8

(i) Synthesis of trimethyl citrate Citric acid (9.00 g, 46.8 mmol) was dissolved in anhydrous methanol and thionyl chloride (20.50 mL, 0.28 mol) was added slowly and dropwise at 0 °C and under nitrogen protection. The reaction mixture was stirred at 0 °C for 1 h, then warmed to room temperature and continued stirring overnight. Upon completion of the reaction, the volatile components were removed by distillation under reduced pressure. The resulting solid residue was recrystallized using a hexane/ethyl acetate solvent mixture to give 10.80 g of white crystalline trimethyl citrate in 98% yield. 1H NMR (acetone-d6, 200 MHz): δ 2.85 (dd, 4H, J1 = 15.4 Hz, J2 = 27.2 Hz); 3.60 (s, 6H); 3.72 (s, 3H); 4.50 (br.s, 1H). 13C NMR (acetone-d6): calculated value: M+ = 234.21.

[References]

[1] Molecules, 2006, vol. 11, # 4, p. 263 - 271
[2] Patent: WO2007/14471, 2007, A1. Location in patent: Page/Page column 30
[3] Patent: US2013/89611, 2013, A1. Location in patent: Paragraph 0133-0135
[4] Molecules, 2018, vol. 23, # 9,
[5] RSC Advances, 2014, vol. 4, # 100, p. 57297 - 57307
Spectrum DetailBack Directory
[Spectrum Detail]

TRIMETHYL CITRATE(1587-20-8)MS
TRIMETHYL CITRATE(1587-20-8)1HNMR
TRIMETHYL CITRATE(1587-20-8)13CNMR
TRIMETHYL CITRATE(1587-20-8)IR1
TRIMETHYL CITRATE(1587-20-8)IR2
TRIMETHYL CITRATE(1587-20-8)Raman
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

1587-20-8(sigmaaldrich)
[TCI AMERICA]

Trimethyl Citrate,>98.0%(GC)(1587-20-8)
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