추천 제품
vapor density
5.2 (vs air)
Quality Level
vapor pressure
<0.01 mmHg ( 20 °C)
분석
95%
형태
flakes
mp
97-103 °C (lit.)
SMILES string
[H][C@@]12CC=CC[C@]1([H])C(=O)OC2=O
InChI
1S/C8H8O3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-2,5-6H,3-4H2/t5-,6+
InChI key
KMOUUZVZFBCRAM-OLQVQODUSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
cis-1,2,3,6-Tetrahydrophthalic anhydride (THPA) can be used as:
- A curing agent for epoxides.
- A chemical modifier in the modification of polystyrene via Friedel-Crafts acylation for enhancing the thermal stability of the polymer.
- A reactant for the synthesis of cis-tetrahydroisoindole-1,3-dione derivatives and cyclic diimides.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Resp. Sens. 1 - Skin Sens. 1
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
312.8 °F - closed cup
Flash Point (°C)
156 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
이미 열람한 고객
Polymer networks derived from curing of epoxidised linseed oil: influence of different catalysts and anhydride hardeners
Polymer, 41(24), 8603-8613 (2000)
Influence of cure schedule and stoichiometry on the dynamic mechanical behaviour of tetrafunctional epoxy resins cured with anhydrides
Polymer, 37(11), 2195-2200 (1996)
Chemical modification of polystyrene?IV. Electrophilic substitution of polystyrene with cis-1, 2, 3, 6 tetrahydrophthalic anhydride
European Polymer Journal, 19(4), 317-320 (1983)
Journal of controlled release : official journal of the Controlled Release Society, 226, 193-204 (2016-02-21)
Stepwise pH-responsive nanoparticle system containing charge reversible pullulan-based (CAPL) shell and poly(β-amino ester) (PBAE)/poly(lactic-co-glycolic acid) (PLAG) core is designed to be used as carriers of paclitaxel (PTX) and combretastatin A4 (CA4) for combining antiangiogenesis and chemotherapy to treat hepatocellular carcinoma
Montmorillonite K-10 supported one-pot synthesis of some symmetric diimides and 3a, 4, 7, 7a-tetrahydroisoindole-1, 3-dione derivatives under solvent-free conditions using microwaves
J. Serb. Chem. Soc., 70(4), 579-583 (2005)
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