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Merck

V403

Sigma-Aldrich

γ-戊内酯

ReagentPlus®, 99%

别名:

γ-缬草内酯, γ-甲基-γ-丁内酯, 4,5-二氢-5-甲基-2(3H)-呋喃酮, 4-羟基正戊酸内酯, γ-甲基-γ-丁内酯

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About This Item

经验公式(希尔记法):
C5H8O2
CAS号:
分子量:
100.12
Beilstein:
80420
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

蒸汽密度

3.45 (vs air)

品質等級

產品線

ReagentPlus®

化驗

99%

折射率

n20/D 1.432 (lit.)

bp

207-208 °C (lit.)
82-85 °C/10 mmHg (lit.)

mp

−31 °C (lit.)

密度

1.05 g/mL at 25 °C (lit.)

SMILES 字串

CC1CCC(=O)O1

InChI

1S/C5H8O2/c1-4-2-3-5(6)7-4/h4H,2-3H2,1H3

InChI 密鑰

GAEKPEKOJKCEMS-UHFFFAOYSA-N

基因資訊

human ... CYP1A2(1544)

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一般說明

γ-戊内酯(GVL)天然存在于水果中,经常用作燃料添加剂和食品成分。它主要用于能源和碳基产品的生产。

應用

γ-戊内酯(GVL)可用作绿色溶剂:
  • 利用固体酸催化剂氢型丝光沸石将木质纤维素转换为糠醛。
  • 合成磷脂酰丝氨酸。

法律資訊

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

204.8 °F - closed cup

閃點(°C)

96 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

γ-Valerolactone-a sustainable liquid for energy and carbon-based chemicals
Horvath I, et al.
Green Chemistry, 10(2), 238-242 (2008)
Highly efficient synthesis of phosphatidylserine in the eco-friendly solvent γ-valerolactone
Duan Z-Q and Hu Fei
Green Chemistry, 14(6), 1581-1583 (2012)
Jesse Q Bond et al.
Langmuir : the ACS journal of surfaces and colloids, 26(21), 16291-16298 (2010-06-02)
γ-Valerolactone (GVL) has been identified as a promising, sustainable platform molecule that can be produced from lignocellulosic biomass. The chemical flexibility of GVL has allowed the development of a variety of processes to prepare renewable fuels and chemicals. In the
Jean-Paul Lange et al.
Chemical communications (Cambridge, England), (33)(33), 3488-3490 (2007-08-19)
Methyl pentenoate, a promising Nylon intermediate, is produced in >95% yield via the transesterification of gamma-valerolactone, a bio-based intermediate, under catalytic distillation conditions.
Laureen J Marinetti et al.
Pharmacology, biochemistry, and behavior, 101(4), 602-608 (2012-02-22)
Gamma butyrolactone (GBL) is metabolized to gamma hydroxybutyrate (GHB) in the body. GHB is a DEA Schedule 1 compound; GBL is a DEA List 1 chemical. Gamma valerolactone (GVL) is the 4-methyl analog of GBL; GVL is metabolized to 4-methyl-GHB;

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