Chemical properties Uses Production Content analysis Toxicity
ChemicalBook > CAS DataBase List > Triacetin

Triacetin

Chemical properties Uses Production Content analysis Toxicity
Product Name
Triacetin
CAS No.
102-76-1
Chemical Name
Triacetin
Synonyms
GLYCEROL TRIACETATE;Triacetine;GLYCERYL TRIACETATE;triacetate;GLYCERIN TRIACETATE;Vanay;Enzactin;Fungacetin;1,2,3-TRIACETOXYPROPANE;2,3-diacetyloxypropyl acetate
CBNumber
CB7441695
Molecular Formula
C9H14O6
Formula Weight
218.2
MOL File
102-76-1.mol
More
Less

Triacetin Property

Melting point:
3 °C(lit.)
Boiling point:
258-260 °C(lit.)
Density 
1.16 g/mL at 25 °C(lit.)
vapor density 
7.52 (vs air)
vapor pressure 
0.00248 mm Hg @ 250C
FEMA 
2007 | (TRI-)ACETIN
refractive index 
n25/D 1.429-1.431(lit.)
Flash point:
300 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Soluble in water, miscible with ethanol (96 per cent) and toluene.
form 
Liquid
color 
Clear colorless
Odor
Characteristic odour
Odor Type
fruity
explosive limit
1.05%, 189°F
Water Solubility 
64.0 g/L (20 ºC)
Merck 
14,9589
JECFA Number
920
BRN 
1792353
Dielectric constant
7.2(20℃)
Stability:
Stable. Incompatible with strong oxidizing agents. Combustible.
InChIKey
URAYPUMNDPQOKB-UHFFFAOYSA-N
LogP
0.25
CAS DataBase Reference
102-76-1(CAS DataBase Reference)
NIST Chemistry Reference
1,2,3-Propanetriol, triacetate(102-76-1)
EPA Substance Registry System
Glyceryl triacetate (102-76-1)
More
Less

Safety

Safety Statements 
23-24/25
WGK Germany 
1
RTECS 
AK3675000
Autoignition Temperature
809 °F
TSCA 
Yes
HS Code 
29153930
Hazardous Substances Data
102-76-1(Hazardous Substances Data)
Toxicity
LD50 i.v. in mice: 1600 ±81 mg/kg (Wretlind)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H303May be harmfulif swallowed

Precautionary statements

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P403Store in a well-ventilated place.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W200712
Product name
Triacetin
Purity
≥99%, natural, FG
Packaging
SAMPLE-K
Price
$62.2
Updated
2024/03/01
Sigma-Aldrich
Product number
W200712
Product name
Triacetin
Purity
≥99%, natural, FG
Packaging
1KG
Price
$128
Updated
2024/03/01
Sigma-Aldrich
Product number
W200712
Product name
Triacetin
Purity
≥99%, natural, FG
Packaging
10KG
Price
$769
Updated
2024/03/01
Sigma-Aldrich
Product number
W200700
Product name
Triacetin
Purity
99%, FCC, FG
Packaging
1kg
Price
$76.5
Updated
2024/03/01
Sigma-Aldrich
Product number
W200700
Product name
Triacetin
Purity
99%, FCC, FG
Packaging
10Kg
Price
$210
Updated
2024/03/01
More
Less

Triacetin Chemical Properties,Usage,Production

Chemical properties

Colorless, odorless oily liquid. It is miscible with ethanol, ether, benzene, chloroform and other organic solvents, soluble in acetone, insoluble in mineral oil. Slightly soluble in water. 25 ° C in water solubility of 5.9g / 100ml.

Uses

  • As a plasticizer and fragrance fixative, ink solvent, also used in medicine and dye synthesis.
  • As a chromatographic fixative, solvent, toughener and fragrance fixative.
  • Humectants; carrier solvents; plasticizers; it can absorb carbon dioxide from the natural gas.
  • In the production of cosmetics, pharmaceuticals and dyes, plasticizers for cigarette filter rods, and so on.
  • Applied in cosmetics, casting, medicine, dyes and other industries. This product is non-toxic, non-irritating.
  • As the substrate for the determination of lipase, perfume fixative, solvent, gas chromatographic fixative (maximum temperature of 85 ℃, solvent: methanol, chloroform), separation of gas and aldehyde analysis.

Production

It can be derived from the esterification of glycerol and acetic acid. After preheating glycerol to 50-60 ° C, add acetic acid, benzene and sulfuric acid. Heat and stir for refluxing dehydration, and recycle the benzene. Then add acetic anhydride for heating of 4h. After cooling, the mixture was neutralized with 5% sodium carbonate to pH 7, and the crude layer was dried and the crude oil was dried with calcium chloride. Distill under reduced pressure, collect the 128-131 ° C (0.93 kPa) fraction, namely glycerol triacetate.

Content analysis

Accurately weigh about 1g of the sample, put it into a suitable pressure bottle, add 25 mL of 1mol / L. potassium hydroxide solution and 15 mL of isopropyl alcohol, add stopper, wrap with cloth and put it in a canvas bag. Put it into the water bath of 98 ℃ ± 2 ℃ for 1h, and the water level in the water bath should be slightly higher than the bottle level. Take the bottle out from the bag, cool it to room temperature in the air, unfold the cloth and stopper to release the residual pressure in the bottle, and then remove the cloth. Add 6 to 8 drops of phenolphthalein test solution (TS-167), apply 0.5mol / L sulfuric acid for titration of excess alkali until the pink could just disappeared. At the same time, perform a blank test. Each mL of 0.5mol / L sulfuric acid is equivalent to 36.37 mg of glyceryl triacetate (C9H14O6).

Toxicity

ADI is not subject to special provisions (FAO / WHO, 2001).
GR.AS (FDA, § 182.1901, 2000).
LD50 3000mg / kg (rat, oral).

Description

§ 184.1901(a) Triacetin (C8H14O6), also known as 1,2,3-propanetriol triacetate or glyceryl triacetate, is the triester of glycerin and acetic acid. Triacetin can be prepared by heating glycerin with acetic anhydride alone or in the presence of finely divided potassium hydrogen sulfate. It can also be prepared by the reaction of oxygen with a liquid-phase mixture of allyl acetate and acetic acid using a bromide salt as a catalyst.

Chemical Properties

Triacetin has a very faint, fruity odor. It has a mild, sweet taste that is bitter above 0.05%.

Chemical Properties

Colorless liquid; slight fatty odor; bitter taste. Slightly soluble in water; very soluble in alcohol, ether, and other organic solvents. Combustible.

Chemical Properties

Triacetin is a colorless, viscous liquid with a slightly fatty odor.

Originator

Enzactin,Ayerst,US,1957

Occurrence

Reported found in papaya.

Uses

Triacetin is a colorless, oily liquid of slight fatty odor and bitter taste. It is soluble with water and is miscible with alcohol and ether. It functions in foods as a humectant and solvent.

Uses

As fixative in perfumery; solvent in manufacture of celluloid, photographic films. Technical triacetin (a mixture of mono-, di-, and small quantities of triacetin) as a solvent for basic dyes, particularly indulines, and tannin in dyeing.

Uses

Triacetin, a component of cigarette filters, induced a contact dermatitis in a worker at a cigarette manufacturers.

Preparation

By direct reaction of glycerol with acetic acid in the presence of Twitchell’s reagent, or in benzene solution of glycerol and boiling acetic acid in the presence of a cationic resin (Zeo-Karb H) pretreated with dilute H2SO4.

Definition

ChEBI: A triglyceride obtained by acetylation of the three hydroxy groups of glycerol. It has fungistatic properties (based on release of acetic acid) and has been used in the topical treatment of minor dermatophyte infections.

Production Methods

Triacetin is prepared by the esterification of glycerin with acetic anhydride.

Manufacturing Process

200 grams of allyl acetate, 450 grams of glacial acetic acid and 3.71 grams of cobaltous bromide were charged to the reactor and the mixture was heated to 100°C. Pure oxygen was then introduced into the reactor below the surface of the liquid reaction mixture at the rate of 0.5 standard cubic feet per hour. Initially, all of the oxygen was consumed, but after a period of time oxygen introduced into the mixture passed through unchanged. During the course of the reaction, a small quantity of gaseous hydrogen bromide (a total of 1.9 grams) was introduced into the reaction zone, along with the oxygen. The reaction was allowed to continue for 6 hours following which the reaction mixture was distilled. Essentially complete conversion of the allyl acetate took place. A yield of 116 grams of glycerol triacetate was obtained, this being accomplished by distilling the glycerol triacetate overhead from the reaction mixture, at an absolute pressure of approximately 13 mm of mercury.

Therapeutic Function

Topical antifungal

Taste threshold values

Sweet and creamy with an oily mouthfeel.

General Description

Triacetin is a triester of glycerin and acetic acid that occurs naturally in papaya. It is mainly used as a synthetic flavoring agent in ice-creams, nonalcoholic beverages and baked goods.

Pharmaceutical Applications

Triacetin is mainly used as a hydrophilic plasticizer in both aqueous and solvent-based polymeric coating of capsules, tablets, beads, and granules; typical concentrations used are 10–35% w/w.
Triacetin is used in cosmetics, perfumery, and foods as a solvent and as a fixative in the formulation of perfumes and flavors.

Contact allergens

Triacetin is a component of cigarette filters, which induced a contact dermatitis in a worker at a cigarette manufactory.

Clinical Use

Glyceryl triacetate (Enzactin, Fungacetin) is a colorless, oilyliquid with a slight odor and a bitter taste. The compound issoluble in water and miscible with alcohol and most organicsolvents.
The activity of triacetin is a result of the acetic acid releasedby hydrolysis of the compound by esterases presentin the skin. Acid release is a self-limiting process becausethe esterases are inhibited below pH 4.

Safety Profile

Poison by ingestion. Moderately toxic by intraperitoneal, subcutaneous, and intravenous routes. An eye irritant. Combustible when exposed to heat, flame, or powerful oxidizers. To fight fire, use alcohol foam, water, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.

Safety

Triacetin is used in oral pharmaceutical formulations and is generally regarded as a relatively nontoxic and nonirritant material at the levels employed as an excipient.
LD50 (dog, IV): 1.5 g/kg
LD50 (mouse, IP): 1.4 g/kg
LD50 (mouse, IV): 1.6 g/kg
LD50 (mouse, oral): 1.1 g/kg
LD50 (mouse, SC): 2.3 g/kg
LD50 (rabbit, IV): 0.75 g/kg
LD50 (rat, IP): 2.1 g/kg
LD50 (rat, oral): 3 g/kg
LD50 (rat, SC): 2.8 g/kg

in vitro

Litton Bionetics, Inc. (1976) evaluated the mutagenic potential of Triacetin in a plate test using Salmonella typhimurium strains TA1535, TA1537, and TA1538 with and without metabolic activation. Test concentrations were 0.0013%, 0.00065%, and 0.000325% and the solvent was dimethyl sulfoxide (DMSO). A negative control (solvent) and appropriate positive controls were used and gave expected results. Triacetin was not mutagenic with or without metabolic activation.
Unichema Chemie B.V. (1994) reported that Triacetin was not mutagenic at 50 to 5000 μg/plate in an Ames test using S. typhimurium strains TA1535, TA1537, TA98, and TA100 with and without metabolic activation.

in vivo

The mutagenic potential of Triacetin was determined using adult Drosophila melanogaster (Efremova 1962). A dose of 0.2 to 0.3 mg Triacetin had a spontaneous mutation rate of approximately one mutation per 750 chromosomes.

storage

Triacetin is stable and should be stored in a well-closed, nonmetallic container, in a cool, dry place.

Incompatibilities

Triacetin is incompatible with metals and may react with oxidizing agents. Triacetin may destroy rayon fabric.

Regulatory Status

GRAS listed. Accepted in Europe as a food additive in certain applications. Included in the FDA Inactive Ingredients Database (oral capsules and tablets and gels). Included in nonparenteral medicines licensed in the UK. Included in the Canadian List of Acceptable Non-medicinal Ingredients.

Triacetin Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Triacetin Suppliers

YIXING TIANYUAN CHEMICAL CO.,LTD.
Tel
0510-87551598 13806155779
Email
yxty@tychemicals.com
Country
China
ProdList
1
Advantage
58
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9664
Advantage
60
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-6206333 18521732826;
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25015
Advantage
65
Shanghai klamar Reagent Co., LTD
Tel
4001650900 13817534909
Email
3003940895@qq.com
Country
China
ProdList
9345
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30132
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Fax
86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
ProdList
9984
Advantage
60
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696;
Email
info@hanhongsci.com
Country
China
ProdList
42982
Advantage
64
jiliang chemicals
Tel
21-62165282 15801962796;
Fax
021 61153784
Email
bidingchem@163.com
Country
China
ProdList
1165
Advantage
60
Beijing Isomersyn Technology CO;LTD
Tel
010-82954736 13391601435
Email
sales@isomersyn.com
Country
China
ProdList
3296
Advantage
57
Shandong Xiya Chemical Co., Ltd
Tel
13355009207 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18739
Advantage
57
BEST-REAGENT
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11726
Advantage
57
China Langchem Inc.
Tel
0086-21-58956006
Fax
0086-21-58956100
Country
China
ProdList
7815
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9823
Advantage
79
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11714
Advantage
57
Wuhan Fortuna Chemical Co., Ltd
Tel
027-027-59207852 13308628970
Fax
QQ3130921841
Email
buy@fortunachem.com
Country
China
ProdList
2893
Advantage
58
ShangHai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847 13636370518
Fax
021-55068248
Email
shyysw007@163.com
Country
China
ProdList
4941
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9725
Advantage
55
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9872
Advantage
52
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17779
Advantage
75
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12338
Advantage
58
Beijing innoChem Science & Technology Co.,Ltd.
Tel
400-810-7969 010-59572699
Fax
010-59572688
Email
ningzi.li@inno-chem.com.cn
Country
China
ProdList
6139
Advantage
55
Nanjing Norris-Pharm Technology Co., Ltd
Tel
13901585132
Fax
+86-25-52131256
Email
799750417@qq.com
Country
China
ProdList
8888
Advantage
55
Haoyuan Chemexpress Co., Ltd.
Tel
021-58950125
Fax
(86) 21-58955996
Email
info@chemexpress.com
Country
China
ProdList
7553
Advantage
61
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22519
Advantage
55
TargetMol Chemicals Inc.
Tel
021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7934
Advantage
58
Beijing Universal Century Technology Co., Ltd.
Tel
400-8706899
Fax
400-8706899
Email
hysj_bj.com
Country
China
ProdList
3585
Advantage
55
Shanghai JONLN Reagent Co., Ltd.
Tel
400-0066400 13621662912
Fax
021-55660885
Email
422131432@qq.com
Country
China
ProdList
9986
Advantage
55
TianJin Alta Scientific Co., Ltd.
Tel
022-65378550-8551
Fax
+86-022-2532-9655
Email
contact@altascientific.com
Country
China
ProdList
2773
Advantage
58
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41438
Advantage
60
Shanghai DiBai Chemicals Co., Ltd.
Tel
021-54359730 400-008-9730
Fax
021-54353864
Email
info@chemxyz.com
Country
China
ProdList
3993
Advantage
60
ChemStrong Scientific Co.,Ltd
Tel
0755-66853366 13670046396
Fax
0755-28363542
Email
sales@chem-strong.com
Country
China
ProdList
17982
Advantage
56
Chengdu HuaXia Chemical Reagent Co. Ltd
Tel
400-1166-196 13458535857
Fax
QQ:800101999
Email
cdhxsj@163.com
Country
China
ProdList
13358
Advantage
58
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939 15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
15878
Advantage
55
Hubei Jusheng Technology Co.,Ltd
Tel
027-59599241 18871490274
Fax
027-59599241
Email
1400878000@qq.com
Country
China
ProdList
9972
Advantage
58
Chizhou Kailong Import and Export Trade Co., Ltd.
Tel
Fax
-
Email
xg01_gj@163.com
Country
China
ProdList
9503
Advantage
50
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51471
Advantage
80
Watson Biotechnology Co.,Ltd
Tel
027-027-59207879 18140587686
Fax
QQ:1972026995
Email
kf@3600chem.com
Country
China
ProdList
4699
Advantage
55
Quzhou Rundong Chemical (Technology) Co.
Tel
0570-8789886 18892685668
Fax
0570-8789985
Email
info@rundongchemical.com
Country
China
ProdList
3991
Advantage
60
Alta Scientific Co., Ltd.
Tel
022-6537-8550 15522853686
Fax
022-2532-9655
Email
sales@altasci.com.cn
Country
China
ProdList
4515
Advantage
55
Hefei TNJ Chemical Industry Co.,Ltd.
Tel
551-65418679 15837135945
Fax
0551-65418697
Email
info@tnjchem.com
Country
China
ProdList
1889
Advantage
62
Hangzhou Dingyan Chem Co., LTD
Tel
0571-0571-87157530-8001-8003 18008611859
Fax
0571-87156470
Email
sales@dingyanchem.com
Country
China
ProdList
1997
Advantage
58
Zhengzhou Alfachem Co.,Ltd.
Tel
0371-53778726 18003825608
Fax
QQ:2885354392
Email
liuxiaoyan@alfachem.cn
Country
China
ProdList
1945
Advantage
58
VWR(Shanghai) Co., Ltd
Tel
400-821-8006
Fax
+86-21-58558801
Email
info_china@vwr.com
Country
China
ProdList
3041
Advantage
75
Shanghai Xilong Biochemical Technology Co., Ltd.
Tel
021-52907766-8042
Fax
021-52906523
Country
China
ProdList
9947
Advantage
58
Guangzhou QiYun Biotechnology Co., Ltd.
Tel
020-61288194 61288195
Fax
020-61288700
Email
505721671@qq.com
Country
China
ProdList
3868
Advantage
58
Shandong Xiya Chemical Co., Ltd.
Tel
4009903999 13395398332
Fax
0539-6365991
Email
sales@xiyashiji.com
Country
China
ProdList
20810
Advantage
60
More
Less

View Lastest Price from Triacetin manufacturers

Ouhuang Engineering Materials (Hubei) Co., Ltd
Product
Triacetin 102-76-1
Price
US $10.00/kg
Min. Order
1kg
Purity
99.8%
Supply Ability
10000ton
Release date
2024-04-25
Ouhuang Engineering Materials (Hubei) Co., Ltd
Product
Triacetin 102-76-1
Price
US $3.00/kg
Min. Order
1kg
Purity
99.92%
Supply Ability
50000tons
Release date
2024-04-19
Shaanxi TNJONE Pharmaceutical Co., Ltd
Product
Triacetin 102-76-1
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
1000kg
Release date
2024-04-02

102-76-1, TriacetinRelated Search:


  • TRIACETIN
  • TRIACETIN (C2:0)
  • Triacetyl glycerin
  • FEMA 2007
  • GLYCEROL TRIACETATE
  • GLYCERYL TRIACETATE
  • GLYCERIN TRIACETATE
  • 1,3-Diacetyloxypropan-2-yl acetate
  • propane-1,2,3-triyl triethanoate
  • triacetate
  • Glyceryl triacetate,1,2,3-Triacetoxypropane, 1,2,3-Triacetylglycerol, Glycerol triacetate, Triacetin
  • Triacetin, 99%, extra pure, Ph Eur, USP, BP
  • Triacetin, 99%, reagent grade
  • Triacetin,1,2,3-Triacetoxypropane, 1,2,3-Triacetylglycerol, Glyceryl triacetate
  • Triacetin (1 g)
  • Glyceryl Triacetate (Triacetin)
  • Triacetin, 99% 1LT
  • Triacetin, 99% 2.5LT
  • Three acetic acidglycerol ester
  • Glycerol triacetate, 99%, 99%
  • Triacetin 0.25
  • Glycerol triacetate GTC
  • GLYCERYL TRIACETATE >= 99.0% (GC)
  • 2,3-diacetyloxypropyl acetate
  • carbonic acid [4-[[2-[[(4-ethoxycarbonyloxy-3-methoxyphenyl)-oxomethyl]amino]ethylamino]-oxomethyl]-2-methoxyphenyl] ethyl ester
  • 1,2,3-propanedioltriacetate
  • 1,2,3-propanedioltriethanoate
  • 2-(Acetyloxy)-1-[(acetyloxy)methyl]ethyl acetate
  • Acetin, tri-
  • Enzactin
  • femanumber2007
  • Fungacetin
  • Glycerol triacetate tributyrin
  • Glyped
  • Kesscoflex TRA
  • kesscoflextra
  • Kodaflex triacetin
  • kodaflextriacetin
  • tri-aceti
  • Triacetine
  • Triacetyl glycerine
  • Triacetyl glycerol
  • triacetylglycerine
  • Triacetylglycerol
  • Vanay
  • GLYCEROL MONO ACETATE BULK
  • TRIACETIN (BULK)
  • TRIACETIN (TOTES)
  • TRIACETIN FCC (KOSHER)
  • TRIACETIN TOBACCO GRADE
  • TRIACETIN USP
  • TRIACETIN, 99% (EASTMAN TRIACETIN)
  • GLYCEROL TRIACETATE BIOSYNTH
  • TRIACETIN 98.5+% FCC
  • TRIACETIN, 99+%
  • Triacetin FCC, Kosher Grade
  • GlycerolTriacetateForBiochemistry(Triacetin)
  • 1,2,3-TRIACETYLGLYCEROL