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Key Documents

00297

Sigma-Aldrich

异戊烯焦磷酸盐 三锂盐

≥95.0% (TLC)

同義詞:

3-甲基-3-丁烯焦磷酸盐 三锂盐, IPP

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About This Item

經驗公式(希爾表示法):
C5H9Li3O7P2
CAS號碼:
分子量::
263.89
MDL號碼:
分類程式碼代碼:
12352107
PubChem物質ID:
NACRES:
NA.25

品質等級

化驗

≥95.0% (TLC)

形狀

powder

雜質

≤10% water

儲存溫度

−20°C

SMILES 字串

[Li+].[Li+].[Li+].CC(=C)CCOP([O-])(=O)OP([O-])([O-])=O

InChI

1S/C5H12O7P2.3Li/c1-5(2)3-4-11-14(9,10)12-13(6,7)8;;;/h1,3-4H2,2H3,(H,9,10)(H2,6,7,8);;;/q;3*+1/p-3

InChI 密鑰

ZJGSIAARCDPUSN-UHFFFAOYSA-K

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相關類別

一般說明

异戊烯基焦磷酸三锂盐(3-甲基-3-丁烯基焦磷酸三锂盐,IPP)是异戊烯焦磷酸盐的锂盐。它是在聚异戊二烯化合物的生物合成过程中形成的一种中间体。它可由异戊烯醇以三步法合成。甲羟戊酸可在一种ATP依赖性的过程中转化为异戊烯焦磷酸。Melavonate和异戊烯焦磷酸盐是通过巴西橡胶胶乳而被掺入到橡胶中的。

應用

异戊烯基焦磷酸盐(IPP)可作为底物而用于研究异戊烯基-二磷酸异构酶的分布、表征和动力学。IPP可用于研究类异戊二烯/萜类化合物的生物合成。异戊烯基焦磷酸盐可用于橡胶合成。

生化/生理作用

萜烯生物合成中间体

包裝

无底玻璃瓶。内含物装在插入的融合锥内。

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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Nagendra K Sharma et al.
Biochemistry, 49(29), 6228-6233 (2010-06-22)
Isopentenyl diphosphate isomerase (IDI) catalyzes the interconversion of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), the basic five-carbon building blocks of isoprenoid molecules. Two structurally unrelated classes of IDIs are known. Type I IPP isomerase (IDI-1) utilizes a divalent metal
New aspects of rubber biosynthesis.
Archer B L and Audrey B G
Botanical Journal of the Linnean Society, 94, 181-196 (1987)
Venkatadurga Jonnalagadda et al.
Journal of the American Chemical Society, 134(15), 6568-6570 (2012-04-05)
The E. coli isopentenyl diphosphate isomerase (IDI) catalyzed reaction of isopentenyl diphosphate (IPP) in D(2)O gives a 66% yield of dimethylallyl diphosphate labeled with deuterium at the (E)-methyl group (d-DMAPP) and a 34% yield of IPP labeled with 1 mol
Nicole A Heaps et al.
Journal of the American Chemical Society, 133(47), 19017-19019 (2011-11-04)
Isopentenyl diphosphate isomerase (IDI) catalyzes the interconversion of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). These two molecules are the building blocks for construction of isoprenoid carbon skeletons in nature. Two structurally unrelated forms of IDI are known. A variety
Kazunori Okada
Bioscience, biotechnology, and biochemistry, 75(7), 1219-1225 (2011-07-09)
Plants synthesize isopentenyl diphosphate (IPP) via the mevalonate pathway and the methylerythritol phosphate (MEP) pathway. IPP is condensed to its allylic isomer, dimethylallyl diphosphate, to yield geranylgeranyl diphosphate, a common precursor for the production of cyclic diterpenoids. Studies of subcellular

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