M89617
Mucic acid
97%
동의어(들):
Galactaric acid, MTPA, Saccharolactic acid, Tetrahydroxyadipic acid, Tetrahydroxyhexanedioic acid
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모든 사진(3)
About This Item
Linear Formula:
HOOC(CHOH)4COOH
CAS Number:
Molecular Weight:
210.14
Beilstein:
1728117
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
양식
powder
mp
220-225 °C (dec.) (lit.)
SMILES string
O[C@@H]([C@@H](O)[C@H](O)C(O)=O)[C@@H](O)C(O)=O
InChI
1S/C6H10O8/c7-1(3(9)5(11)12)2(8)4(10)6(13)14/h1-4,7-10H,(H,11,12)(H,13,14)/t1-,2+,3+,4-
InChI key
DSLZVSRJTYRBFB-DUHBMQHGSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Mucic acid or galactaric acid can be used as a precursor for the synthesis of:
It can be also utilized in the surface modification of monodisperse water-soluble magnetic nanoparticles.
- 2,3,4,5-tetra-O-acetylgalactaric acid (AGA) which is used as a monomer unit along with adipic acid for the synthesis of copolyanhydrides.
- Muconic acid and adipic acid.
It can be also utilized in the surface modification of monodisperse water-soluble magnetic nanoparticles.
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
Highly Efficient Chemical Process To Convert Mucic Acid into Adipic Acid and DFT Studies of the Mechanism of the Rhenium-Catalyzed Deoxydehydration
Li X, et al.
Angewandte Chemie (International ed. in English), 53(16), 4200-4204 (2014)
Synthesis and characterization of copolyanhydrides of carbohydrate-based galactaric acid and adipic acid
Mehtio T, et al.
Carbohydrate Research, 402, 102-110 (2015)
Functionalization of monodisperse magnetic nanoparticles
Lattuada M and Hatton T A
Langmuir, 23(4), 2158-2168 (2007)
Yemin Liu et al.
Journal of the American Chemical Society, 127(9), 3004-3015 (2005-03-03)
Nucleic acid drugs have great potential to treat many devastating aliments, but their application has been hindered by the lack of efficacious and nontoxic delivery vehicles. Here, a new library of poly(glycoamidoamine)s (D1-D4, G1-G4, and M1-M4) has been synthesized by
The unusually stable crystal structure of neo-inositol.
S J Angyal et al.
Carbohydrate research, 263(1), 149-154 (1994-10-03)
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