ChemicalBook > CAS DataBase List > 1,2,3,6-Tetrahydrophthalic anhydride

1,2,3,6-Tetrahydrophthalic anhydride

Product Name
1,2,3,6-Tetrahydrophthalic anhydride
CAS No.
85-43-8
Chemical Name
1,2,3,6-Tetrahydrophthalic anhydride
Synonyms
TETRAHYDROPHTHALIC ANHYDRIDE;tetrahydrophthalic;thpa[qr];rikacidth[qr];Tetrahydroftalanhydrid;1,2,3,6-TetrahydrophthaL;3,6-Cyclopropylene-ΔTetrahydrophthalsureanhydrid;anhydridetetrahydrophtalique;tetrahydrophthalicanhydrides
CBNumber
CB0501956
Molecular Formula
C8H8O3
Formula Weight
152.15
MOL File
85-43-8.mol
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1,2,3,6-Tetrahydrophthalic anhydride Property

Melting point:
101-102°C
Boiling point:
195°C 5mm
Density 
1,375 g/cm3
vapor pressure 
0.021Pa at 20℃
refractive index 
1.4810 (estimate)
Flash point:
157°C
storage temp. 
Store below +30°C.
solubility 
soluble in DCM, Ethyl Acetate, Toluene
form 
Solid
pka
3.84[at 20 ℃]
color 
Off-White to Light Tan
PH
2.1 (20°C, 10g/L in H2O)
Water Solubility 
29.4g/L at 20℃
LogP
1.29 at 40℃
CAS DataBase Reference
85-43-8(CAS DataBase Reference)
EPA Substance Registry System
Tetrahydrophthalic anhydride (85-43-8)
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Safety

Risk Statements 
41-42/43-52/53
Safety Statements 
26-36/37/39
RIDADR 
2698
Autoignition Temperature
400°C
HazardClass 
8
PackingGroup 
III
Hazardous Substances Data
85-43-8(Hazardous Substances Data)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

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

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.00742
Product name
1,2,3,6-Tetrahydrophthalic anhydride
Purity
for synthesis
Packaging
100 g
Price
$36.5
Updated
2025/07/31
Sigma-Aldrich
Product number
8.00742
Product name
1,2,3,6-Tetrahydrophthalic anhydride
Purity
for synthesis
Packaging
1 kg
Price
$82.4
Updated
2025/07/31
TRC
Product number
T294176
Product name
1,2,3,6-TetrahydrophthalicAnhydride
Packaging
10g
Price
$145
Updated
2021/12/16
TRC
Product number
T294176
Product name
1,2,3,6-TetrahydrophthalicAnhydride
Packaging
100g
Price
$335
Updated
2021/12/16
TRC
Product number
T294176
Product name
1,2,3,6-TetrahydrophthalicAnhydride
Packaging
250g
Price
$590
Updated
2021/12/16
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1,2,3,6-Tetrahydrophthalic anhydride Chemical Properties,Usage,Production

Chemical Properties

white flaky solid

Uses

Chemical intermediate for light-colored alkyds, polyesters, plasticizers, and adhesives; intermediate for pesticides; hardener for resins.

Definition

ChEBI: 1,2,3,6-tetrahydrophthalic anhydride is a cyclic dicarboxylic anhydride that is 1,3,3a,4,7,7a-hexahydro-2-benzofuran carrying oxo groups at positions 1 and 3. It is a cyclic dicarboxylic anhydride and a tetrahydrofurandione.

General Description

Clear colorless to light yellow slight viscous liquid. Highly toxic and a strong irritant to skin, eyes and mucous membranes. Corrosive to skin and metal. Used in making polyester, alkyd resins, and plasticizers.

Air & Water Reactions

Reacts exothermically with water to form memtetrahydrophthalic acid.

Reactivity Profile

CIS-1,2,3,6-TETRAHYDROPHTHALIC ANHYDRIDE; >98% is combustible. Reacts with oxidizers. Reacts exothermically with water. These reactions are usually slow, but can become violent when local heating accelerates their rate. Acids accelerate the reaction with water. Incompatible with acids, strong oxidizing agents, alcohols, amines, and bases.

Hazard

Strong irritant to eyes and skin.

Health Hazard

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.

Flammability and Explosibility

Non flammable

Safety Profile

Moderately toxic by intraperitoneal route. Mildly toxic by ingestion. A corrosive irritant to skin, eyes, and mucous membranes. Combustible when exposed to heat or flame. Will react with water or steam to produce heat; can react with oxidizing materials. To fight fre, use water, foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also ANHYDRIDES.

Synthesis

95-47-6

7500-55-2

1352221-13-6

85-43-8

2.0 g of lanthanum nitrate hexahydrate was dissolved in 100 mL of deionized water, and the resulting solution was added dropwise to a suspension formed from 5.0 g of H-type Y-zeolite (Tosoh Corporation, HSZ-320H0A, Si/Al ratio = 2.8) with 200 mL of deionized water at room temperature. Subsequently, the mixture was heated at 90 °C for 3 hours. Upon completion of the reaction, the solid product was separated by centrifugation, washed five times with 45 mL of deionized water, and dried at 85 °C overnight. The dried solid was calcined in an air atmosphere at 500 °C for 2 h to obtain the alkylation catalyst (hereinafter referred to as La/HY). The content of La in the catalyst was determined to be 5.6 wt% by ICP analysis. The alkylation reaction was carried out in a SUS autoclave equipped with a 50 mL glass liner. To the glass liner were added 0.10 g of the above La/HY catalyst (100 wt% relative to the unsaturated compounds), 0.16 g of tridecane (internal standard), 0.1 g (0.53 mmol) of methyl 1-cyclohexene-4,5-dicarboxylate (hereinafter referred to as CEDA) as the unsaturated compounds, and 3.0 g (28.30 mmol) of o-xylene as the aromatic compound. The system was sealed under nitrogen atmosphere after three displacements with nitrogen. The reaction was initiated by immersing the autoclave in an oil bath preheated to 180 °C. The reaction was carried out in a water bath. After 2 hours of reaction, the reactor was cooled with water to release the internal gases. The alkylation products 3,4-dimethoxycarbonylcyclohexyl-3',4'-dimethylbenzene (hereinafter referred to as CDMB) and 1-cyclohexene-4,5-dicarboxylic anhydride, etc., in the reaction solution were quantitatively analyzed by gas chromatography with an FID detector as an internal standard method. The results showed that the yield of CDMB was 49.6% and the selectivity was 51.0%.CDMB is a new compound with the following physical properties: boiling point: 166 °C/66 Pa; 1H NMR (500 MHz, CDCl3): δ 1.44-1.48 (m, 1H), 1.69-1.76 (m, 1H), 1.95-2.04 (m, 2H), 2.13-2.16 (m, 1H), 2.22 (s, 3H), 2.24 (s, 3H), 2.33-2.38 (m, 1H), 2.48-2.56 (m, 2H), 3.37-3.96 (m, 1H), 3.71 (s, 3H*2), 6.92 (d, J=7.7 Hz, 1H), 6.96 (s, 1H), 7.06 (d, J=7.7 Hz, 1H) 7.06 (d, J=7.7 Hz, 1H); 13C NMR (500 MHz, CDCl3): δ 19.3, 19.8, 24.5, 33.2, 35.5, 39.0, 42.0, 43.3, 51.8, 123.9, 128.2, 129.7, 134.4, 136.5, 143.4, 173.8, 174.2; IR (d, J=7.7 Hz, 1H). 174.2; IR (neat, cm-1): 3450, 3000, 2950, 2860, 1734.

References

[1] Patent: US2013/41174, 2013, A1. Location in patent: Paragraph 0051; 0072

1,2,3,6-Tetrahydrophthalic anhydride Preparation Products And Raw materials

Raw materials

Preparation Products

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1,2,3,6-Tetrahydrophthalic anhydride Suppliers

Puyang Shengtong Juyuan New Materials Co.,Ltd.
Tel
0393-5331669 18567561231
Email
china_wulin@foxmail.com
Country
China
ProdList
16
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58
Puyang Huicheng Electronic Material Co. Ltd.
Tel
0393-0393-0393-8910800 15039333257
Fax
0393-8912775
Email
info@huichengchem.com
Country
China
ProdList
569
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64
Univar Solutions(China) Co., Ltd.
Tel
+86-021-61932733 +86-15902132654
Fax
021-60932700
Email
ivy.zhuang@univarsolutions.com
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China
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NANJING YIHUA BIOTECHNOLOGY Co., Ltd
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18151925475
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3105244229@qq.com
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China
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Meryer (Shanghai) Chemical Technology Co., Ltd.
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4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
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China
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40228
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ShangHai DEMO Chemical Co.,Ltd
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400-021-7337 2355568890
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0086-21-50182339
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sales@demochem.com
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China
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Beijing HwrkChemical Technology Co., Ltd
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18515581800 18501085097
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010-89508210
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sales.bj@hwrkchemical.com
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China
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Energy Chemical
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021-021-58432009 400-005-6266
Fax
021-58436166
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sales8178@energy-chemical.com
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China
ProdList
44801
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Beijing Ouhe Technology Co., Ltd
Tel
010-010-82967028 13522913783
Fax
+86-10-82967029
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2355560935@qq.com
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China
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12000
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shanghai science Bio-Pharmceutical.co,ltd.
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021-021-57872719 13761402923
Fax
02157872719
Email
245662540@qq.com
Country
China
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View Lastest Price from 1,2,3,6-Tetrahydrophthalic anhydride manufacturers

HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
Product
1,2,3,6-Tetrahydrophthalic anhydride 85-43-8
Price
US $100.00-75.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
5000
Release date
2024-08-15
Hebei Zhuanglai Chemical Trading Co Ltd
Product
1,2,3,6-Tetrahydrophthalic anhydride 85-43-8
Price
US $50.00/kg
Min. Order
1kg
Purity
99
Supply Ability
5000
Release date
2024-11-19
Henan Aochuang Chemical Co.,Ltd.
Product
1,2,3,6-Tetrahydrophthalic anhydride 85-43-8
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1ton
Release date
2022-09-27

85-43-8, 1,2,3,6-Tetrahydrophthalic anhydrideRelated Search:


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