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Merck
CN

02300

D-(+)-苹果酸

unnatural form, ≥97.0% (T)

别名:

(R)-(+)-2-羟基琥珀酸, D-羟基丁二酸

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关于此项目

线性分子式:
HO2CCH2CH(OH)CO2H
化学文摘社编号:
分子量:
134.09
UNSPSC Code:
51113400
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-262-2
Beilstein/REAXYS Number:
1723540
MDL number:
Assay:
≥97.0% (T)
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Quality Level

assay

≥97.0% (T)

optical activity

[α]20/D +28.0±2°, c = 5.5% in pyridine

quality

unnatural form

mp

98-102 °C (lit.)

functional group

carboxylic acid, hydroxyl

SMILES string

O[C@H](CC(O)=O)C(O)=O

InChI

1S/C4H6O5/c5-2(4(8)9)1-3(6)7/h2,5H,1H2,(H,6,7)(H,8,9)/t2-/m1/s1

InChI key

BJEPYKJPYRNKOW-UWTATZPHSA-N

Application

D-(+)-苹果酸可用于:
  • 作为对映选择性全合成 (−)-erinapyrone B的起始材料。
  • 作为从各种醛、苯胺和亚磷酸二乙酯合成α-氨基膦酸酯的手性有机催化剂。



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pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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One pot green synthesis of α-aminophosphonates with D-Malic acid as an organocatalyst
AIP Conference Proceedings, 1860(1), 020057-020057 (2017)
Concise Total Synthesis of (-)-Erinapyrone B from D-(+)-Malic Acid
Samala R, et al.
Synthetic Communications, 44(4), 500-506 (2014)
Narendra Kumar Sharma et al.
Journal of proteomics, 79, 277-298 (2013-01-15)
Hypoxia is one of the major stressors at high altitude. Exposure to hypobaric hypoxia induces several adverse consequences to the structural and functional integrity of brain. In an attempt to understand the proteome modulation, we used 2-DE coupled with MALDI-TOF/TOF



全球贸易项目编号

货号GTIN
124281-1G04061825852881
02300-1G04061838612359
02300-25G04061833037775
02300-5G04061838612366