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重要文件

E7500

Sigma-Aldrich

1,2,3,4-丁四醇

≥99% (GC)

同義詞:

1,2,3,4-赤丁四醇, 内消旋-1,2,3,4-四羟基丁烷, I-赤藓糖醇

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About This Item

線性公式:
HOCH2[CH(OH)]2CH2OH
CAS號碼:
分子量::
122.12
Beilstein:
1719753
EC號碼:
MDL號碼:
分類程式碼代碼:
12352201
PubChem物質ID:
NACRES:
NA.25

品質等級

化驗

≥99% (GC)

形狀

powder

甜度

0.7 × sucrose

顏色

white

bp

329-331 °C (lit.)

mp

118-120 °C (lit.)

溶解度

H2O: 50 mg/mL, clear, colorless

儲存溫度

−20°C

SMILES 字串

OC[C@@H](O)[C@@H](O)CO

InChI

1S/C4H10O4/c5-1-3(7)4(8)2-6/h3-8H,1-2H2/t3-,4+

InChI 密鑰

UNXHWFMMPAWVPI-ZXZARUISSA-N

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應用

内消旋-赤藓醇(i-赤藓糖醇)是重要的鞣剂 L-赤藓酮糖的前体,其可以由氧化葡萄糖杆菌 DSM 7145商业生成。内消旋-赤藓醇可用于支持葡糖杆菌属细菌的碳源生长要求。 它是一种脂肪族多元醇,用于化学分析各种自由基和自由基阴离子的反应性。内消旋-赤藓醇可用于封装的相变材料(PCM)中,以研究其在微电子冷却应用中的潜在用途。它可以用作开发用于测试发酵液的纯化和分析程序中的参考化合物。

生化/生理作用

Tas1r3 基因的等位变异影响对该糖醇的行为味道反应,表明它是T1R3 受体配体。

其他說明

为了全面了解我们针对客户研究提供的各种糖醇产品,建议您访问我们的碳水化合物分类页面。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析證明 (COA)

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Man-Yeon Choi et al.
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Previous studies have demonstrated various combinations of non-nutritive erythritol and sucrose having detrimental effects on Drosophila suzukii (Matsumura). Fly mortality is likely caused by 1) starvation from feeding on non-metabolizable erythritol; and 2) physiological imbalance with abnormally high osmotic pressure
H Hino et al.
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Three strains, LMG 27748(T), LMG 27749 and LMG 27882 with identical MALDI-TOF mass spectra were isolated from samples taken from the brewery environment. Analysis of the 16S rRNA gene sequence of strain LMG 27748(T) revealed that the taxon it represents
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Journal of the American Chemical Society, 135(5), 1816-1822 (2013-01-16)
The MEP pathway, which is absent in animals but present in most pathogenic bacteria, in the parasite responsible for malaria and in plant plastids, is a target for the development of antimicrobial drugs. IspH, an oxygen-sensitive [4Fe-4S] enzyme, catalyzes the
Emmanuel Jean Teinkela Mbosso et al.
Chemistry & biodiversity, 10(2), 224-232 (2013-02-19)
A chemical investigation of the Glyphaea brevis leaves and of the Monodora myristica fruits led to the identification of thirteen compounds, seven linear long-chain aliphatic compounds, 1, 2, 4, 6, and 9-11, three steroids, 3a, 3b, and 7, two triterpenes

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