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  • 100-78-7 Structure
  • Basic information

    1. Product Name: Glycerin 2-acetate
    2. Synonyms: Acetic acid 1-(hydroxymethyl)-2-hydroxyethyl ester;Acetic acid 2-hydroxy-1-hydroxymethylethyl;Glycerin 2-acetate
    3. CAS NO:100-78-7
    4. Molecular Formula: C5H10O4
    5. Molecular Weight: 134.13
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100-78-7.mol
    9. Article Data: 23
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Glycerin 2-acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Glycerin 2-acetate(100-78-7)
    11. EPA Substance Registry System: Glycerin 2-acetate(100-78-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 100-78-7(Hazardous Substances Data)

100-78-7 Usage

Description

Glycerin 2-acetate, also known as 2-monoacetin, is a derivative of triacetin (T720850). It is a versatile compound that finds applications in various industries due to its unique properties.

Uses

Used in Food Industry:
Glycerin 2-acetate is used as a food additive and flavoring agent to enhance the taste and texture of food products.
Used in Pharmaceutical Industry:
Glycerin 2-acetate is used as an excipient in pharmaceutical products for various purposes. It acts as a humectant, helping to retain moisture and prevent the product from drying out. It also serves as a plasticizer, increasing the flexibility and workability of the product. Additionally, it functions as a solvent, dissolving other ingredients and facilitating their uniform distribution within the formulation.
Used in Fuel Industry:
Glycerin 2-acetate can be used as a fuel additive, specifically as an antiknock agent. This application helps to reduce engine knocking and improve the overall performance of the fuel.

Check Digit Verification of cas no

The CAS Registry Mumber 100-78-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100-78:
(5*1)+(4*0)+(3*0)+(2*7)+(1*8)=27
27 % 10 = 7
So 100-78-7 is a valid CAS Registry Number.

100-78-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name glycerine monoacetate

1.2 Other means of identification

Product number -
Other names 1,3-dihydroxypropan-2-yl acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:100-78-7 SDS

100-78-7Relevant articles and documents

A comparative study on porous solid acid oxides as catalysts in the esterification of glycerol with acetic acid

Araujo, Jesuina C. S.,Campos, Adriana F.,Filho, Josué M.,Freire, Paulo T. C.,Lang, Rossano,Neto, Antonio B. S.,Oliveira, Alcineia C.,Rodriguez-Castellón, Enrique,Sousa, Francisco F. F.

, p. 57 - 67 (2020)

Acid catalysts comprising of porous SiAl, as well as molybdophosphoric heteropolyacid, supported SiAl nanotubes were synthesized. The characterizations were through scanning electron microscopy coupled to energy-dispersive X-ray spectroscopy (SEM-EDS), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), termoprogrammed ammonia desorption (NH3-TPD) and Fourier transform infrared spectroscopy (FTIR). Esterification of glycerol into acetins reaction was evaluated over two series of SiAl-based solids. Both series displayed very good activity as well as selectivity towards the acetins within a short reaction time. However, porous SiAl deactivated due to acid sites leaching in long-term catalytic runs. The tuning of the loadings of the molybdophosphoric amount on SiAl halloysite nanotubes leads to an increase in the selectivity towards the mono, di, and triacetins. These catalysts were also recycled up to three times, and a 17 percent of conversion and 100 percent of selectivity for triacetin were obtained due to the combination of acidity, stable structure and porosity of the molybdophosphoric supported SiAl nanotubes.

Esterification of glycerol with acetic acid using double SO 3H-functionalized ionic liquids as recoverable catalysts

Liu, Xiumei,Ma, Huiyuan,Wu, Yue,Wang, Chang,Yang, Miao,Yan, Peifang,Welz-Biermann, Urs

, p. 697 - 701 (2011)

Esterification of glycerol with acetic acid was studied using a series of Bronsted acidic ionic liquids as catalysts. The results indicate that double SO3H-functionalized ionic liquids show high catalytic activity and fair reusability even at very low catalyst loadings, while the conventional non-functionalized ionic liquids show poor activity. The Bronsted acidity-catalytic activity relationships were also investigated and the results showed that the sequence of the catalytic activity observed in the transformation was in good agreement with the Bronsted acidity order determined by the Hammett method. The Royal Society of Chemistry.

A transesterification-acetalization catalytic tandem process for the functionalization of glycerol: The pivotal role of isopropenyl acetate

Calmanti, Roberto,Perosa, Alvise,Rigo, Davide,Selva, Maurizio

, p. 5487 - 5496 (2020)

At 30 °C, in the presence of Amberlyst-15 as a catalyst, a tandem sequence was implemented by which a pool of innocuous reactants (isopropenyl acetate, acetic acid and acetone) allowed upgrading of glycerol through selective acetylation and acetalization processes. The study provided evidence for the occurrence of multiple concomitant reactions. Isopropenyl acetate acted as a transesterification agent to provide glyceryl esters, and it was concurrently subjected to an acidolysis reaction promoted by AcOH. Both these transformations co-generated acetone which converted glycerol into the corresponding acetals, while acidolysis sourced also acetic anhydride that acted as an acetylation reactant. However, tuning of conditions, mostly by changing the reactant molar ratio and optimizing the reaction time, was successful to steer the set of all reactions towards the synthesis of either a 1?:?1 mixture of acetal acetates (97% of which was solketal acetate) and triacetin, or acetal acetates in up to 91% yield, at complete conversion of glycerol. To the best of our knowledge, a one-pot protocol with such a degree of control on the functionalization of glycerol via transesterification and acetalization reactions has not been previously reported. The procedure was also easily reproduced on a gram scale, thereby proving its efficiency for preparative purposes. Finally, the design of experiments with isotopically labelled reagents, particularly d4-acetic acid and d6-acetone, helped to estimate the contribution of different reaction partners (iPAc/AcOH/acetone) to the formation of final products. This journal is

Heteropolyacid-based ionic liquids as efficient homogeneous catalysts for acetylation of glycerol

Huang, Ming-Yu,Han, Xiao-Xiang,Hung, Chin-Te,Lin, Jann-Chen,Wu, Pei-Hao,Wu, Jung-Chung,Liu, Shang-Bin

, p. 42 - 51 (2014)

A series of homogeneous catalysts consisting of pyridinium propyl sulfobetaine (PPS), tungstophosphoric acid (TPA), and acetic acid (HOAc) have been synthesized and exploited for catalytic acetylation of glycerol (GL). Their acid properties were characterized by 31P NMR of trimethylphosphine oxide (TMPO) as the probe molecule, and the effects of acidic strength, PPS/TPA, TPA/GL, and HOAc/GL ratios as well as reaction temperature on catalytic performances during acetylation reaction were investigated. These water-tolerable PPS-TPA-HOAc catalysts, which tend to segregate from glycerol acetate products to form distinct biphasic liquid layers spontaneously after the reaction, were found to be highly efficient and durable for acetylation reaction under continuous operation conditions. Typically, a complete GL conversion may be achieved with a superior glycerol triacetate (GTA) selectivity of 86-99%. Moreover, the unique self-separation biphasic characteristics of the catalyst system facilitate facile separation of products and recycling of catalyst, rendering practical industrial applications in acetylation of alcohol.

The role of Nb in the formation of sulphonic species in SBA-15 and MCF functionalised with MPTMS

Trejda, Maciej,Stawicka, Katarzyna,Ziolek, Maria

, p. 130 - 135 (2012)

Mesoporous silica and niobiosilicate materials of SBA-15 and MCF types were prepared in the presence of MPTMS, i.e. (3-mercaptopropyl)trimethoxysilane and hydrogen peroxide. The samples obtained were characterised by different techniques (N2 adsorption/desorption, XRD, elemental and thermal analyses) and applied as catalysts in glycerol esterification with acetic acid. The role of niobium species on the formation of sulphonic species and stability of organosilane modifier was explored. The most important finding is that the addition of niobium to the synthesis gel improves the efficiency of -SH oxidation by hydrogen peroxide towards sulphonic species. This behaviour is not dependent on the type of structure of mesoporous materials (SBA-15 or MCF). However, the kind of mesoporous solid influences the efficiency of Nb incorporation and on the esterification process. MCF matrix improves the catalytic performance of the MPTMS modified catalyst.

Lanthanum nanocluster/ZIF-8 for boosting catalytic CO2/glycerol conversion using MgCO3as a dehydrating agent

Hu, Chechia,Chang, Chien-Wei,Yoshida, Masaaki,Wang, Ke-Hsuan

, p. 7048 - 7058 (2021)

A lanthanum-modified zeolitic imidazolate framework (La/ZIF-8) was developed to produce glycerol carbonate using CO2and glycerol as raw materials. La/ZIF-8 provides a high catalytic glycerol conversion efficiency owing to its surface-attached nanoclusters of La2O3, which can be viewed as La3+-O2?pairs that strengthen the Lewis basicity and acidity, and the large specific surface area of ZIF-8. The catalytic glycerol conversion and the yield of glycerol carbonate were 46.5% and 35.3%, respectively, using CH3CN as a dehydrating agent. With increase in the amount of CH3CN, the water molecules could react with CH3CN to reduce the selectivity. When an inorganic dehydrating agent, MgCO3, was used to physically adsorb and remove water molecules in the reaction, the selectivity of the reaction could be increased to over 95%, which is the highest ever reported. Reaction kinetics analysis also revealed that the activation energy of using MgCO3(5.4 kJ mol?1) as a dehydrating agent is lower than that using CH3CN (7.8 kJ mol?1). Moreover, the La/ZIF-8 could be recycled and reused at least three times with high catalytic performance. This study provides an effective material with dual Lewis basicity and acidity for CO2/glycerol conversion and significantly improves the catalytic performance using an inorganic dehydrating agent.

Selective formation of triacetin by glycerol acetylation using acidic ion-exchange resins as catalyst and toluene as an entrainer

Kale,Umbarkar,Dongare,Eckelt,Armbruster,Martin

, p. 10 - 16 (2015)

Esterification of glycerol with acetic acid in the presence of toluene as an entrainer was performed over acidic Amberlyst ion-exchange resins in a batch reactor. Toluene continuously removed the reaction water, thus the chemical equilibrium was effectively shifted; the selectivity for the most desired product triacetin was dramatically increased. The influence of reaction conditions such as reaction time, acetic acid: glycerol molar ratio and catalyst amount were investigated. More than 95% selectivity to triacetin at complete glycerol conversion was obtained. The ion-exchange resin catalysts were reusable in subsequent runs, but due to some deactivation the triacetin yields deteriorated.

Single-pot template-free synthesis of a glycerol-derived C-Si-Zr mesoporous composite catalyst for fuel additive production

Al-Muhtaseb, Ala'A H.,Diwakar, Jitendra,Kumar, Saurabh,Saxena, Sandeep K.,Selvamani, Arumugam,Viswanadham, Nagabhatla

, p. 8254 - 8263 (2020)

Synthesis of a highly ordered mesoporous acid- as well as metal-functionalized carbon (-SO3H/C-Si-Zr) material is achieved for the first time from a simple single-pot template-free carbonization of low-value bio-derived glycerol. Addition of TEOS to glycerol right before the carbonization was observed to facilitate molecular-level interactions between them to establish C-Si bonding, which eventually leads to the formation of a high surface area mesoporous -SO3H/C-Si composite material. Unlike this, the addition of ZrO(NO3)2·xH2O to glycerol could not have such an effect, but when Zr is used in the presence of TEOS the mixture could successfully produce the -SO3H/C-Si-Zr composite possessing mesoporosity and uniform acidity suitable for bulky tri-acetin production useful for fuel applications. Here TEOS is observed to play two roles, (1) as a surface area and porosity improver of graphitic carbon by its C-Si interaction and (2) as a mediator to involve Zr in the carbon composite structure through its Si-OH group. Thus, the combined inclusion of Zr and Si sources in the glycerol-derived carbon structure could successfully introduce the positive aspects of porosity improvement (by Si) and acidity improvement (by zirconia) in the mixed composite -SO3H/C-Si-Zr to produce the highest ever selectivity of tri-acetin (~94 wt%) from the same low-value bio-derived glycerol by an acetylation reaction. The sustainability of the process lies in the utilization of waste glycerol as a source of the carbon composite, which in turn catalyzes selective low-value glycerol conversion to industrially important fuel additives.

A highly active and stable organic-inorganic combined solid acid for the transesterification of glycerol under mild conditions

Hou, Zhaoyin,Jiang, Yuanyuan,Long, Yihua,Wang, Zhengbao,Ye, Boyong,Zhao, Huaiyuan,Zhou, Ruru

, p. 1772 - 1781 (2021/06/28)

Solid acid catalyst plays a crucial role in the petroleum refinery industry and bio-refinery technology. In this work, p-phenolsulfonic acid (PSA) was successfully grafted onto the surface of KH560-modified zirconium phosphate (K-ZrP) in a facile routine. The structure and property of this organic-inorganic combined solid acid PSA/K-ZrP-x were characterized via XRD, FTIR, 13C solid-state NMR, TG, N2 adsorption-desorption, SEM, pyridine-adsorption FTIR and XPS technologies. The characterization results showed that KH560 can bond with ZrP and promote the grafting of PSA on the surface of K-ZrP via the condensation reaction between its epoxy ring and the phenolic hydroxyl group in PSA. Consequently, PSA/K-ZrP-2 exhibited excellent performance and stability in the transesterification between glycerol and methyl acetate among the tested H3PW12O40, Amberlyst-45, HBEA, HZSM-5, ZrP, AlCl3 and FeCl3 catalysts. The calculated conversion of glycerol reached 81.3% with a 97.9% selectivity for monoacetin (MAG) and diacetin (DAG) with a 2.2% dosage of [H+] at 100 °C for 4 h. The highest specific activity of PSA/K-ZrP-2 reached 24028.2 mg-glycerol/g-cat/h in a short reaction time (at 0.17 h), and it could be recycled five times without obvious deactivation.

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