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Merck
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文件

93598

Supelco

衣康酸

analytical standard

别名:

亚甲基琥珀酸

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About This Item

线性分子式:
HO2CCH2C(=CH2)CO2H
CAS号:
97-65-4
分子量:
130.10
Beilstein:
1759501
EC號碼:
202-599-6
MDL號碼:
MFCD00004260
分類程式碼代碼:
85151701
PubChem物質ID:
329770255
NACRES:
NA.24

等級

analytical standard

品質等級

100

化驗

≥96.0% (GC)

自燃溫度

1472 °F

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

雜質

≤0.5% water

mp

165-168 °C (lit.)

密度

1.573 g/mL at 25 °C (lit.)

格式

neat

SMILES 字串

OC(=O)CC(=C)C(O)=O

InChI

1S/C5H6O4/c1-3(5(8)9)2-4(6)7/h1-2H2,(H,6,7)(H,8,9)

InChI 密鑰

LVHBHZANLOWSRM-UHFFFAOYSA-N

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相关类别

一般說明

衣康酸是一种不饱和二碳酸有机酸，是衣康曲霉（ Aspergillus itaconicus）的代谢产物。
该物质被列入欧盟第10/2011号法规的阳性清单，用于与食品接触的塑料。

應用

有关合适仪器技术的更多信息，请参考产品分析证书。如需进一步支持，请联系技术服务。

象形圖

Corrosion
GHS05

訊號詞

Danger

危險聲明

H318

危險分類

Eye Dam. 1

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類（WGK）

WGK 1

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分析证书(COA)

Lot/Batch Number
BCCK5860
BCCF4378
BCBZ8506
BCBS8239V
BCBM5222V

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Sambamurthy K.
Pharmaceutical Biotechnology, 56(3-4), 289-295 (2006)
Metabolism: pathogens love the poison.
Stéphane Ménage et al.
Nature chemical biology, 10(5), 326-327 (2014-04-20)
Jahminy Sasikaran et al.
Nature chemical biology, 10(5), 371-377 (2014-03-25)
Itaconate (methylenesuccinate) was recently identified as a mammalian metabolite whose production is substantially induced during macrophage activation. This compound is a potent inhibitor of isocitrate lyase, a key enzyme of the glyoxylate cycle, which is a pathway required for the
Tobias Klement et al.
Bioresource technology, 135, 422-431 (2013-01-10)
In the last years, itaconic acid has gained increasing interest as future bio-based platform chemical. To replace petrol-based compounds such as methacrylic acid in industry, the economic efficiency of the current biotechnological production processes with the fungus Aspergillus terreus has
T Willke et al.
Applied microbiology and biotechnology, 56(3-4), 289-295 (2001-09-11)
Itaconic acid (IA) is an unsaturated dicarbonic organic acid. It can easily be incorporated into polymers and may serve as a substitute for petrochemical-based acrylic or methacrylic acid. It is used at 1-5% as a co-monomer in resins and also
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