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Merck

240559

Sigma-Aldrich

1,4-丁二醇

ReagentPlus®, ≥99%

别名:

1,4-二羟基丁烷, 丁撑二醇

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About This Item

线性分子式:
HO(CH2)4OH
CAS号:
分子量:
90.12
Beilstein:
1633445
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
化驗:
≥99%
bp:
230 °C (lit.)

蒸汽密度

3.1 (vs air)

品質等級

產品線

ReagentPlus®

化驗

≥99%

自燃溫度

698 °F

折射率

n20/D 1.445 (lit.)

bp

230 °C (lit.)

mp

16 °C (lit.)

密度

1.017 g/mL at 25 °C (lit.)

官能基

hydroxyl

SMILES 字串

OCCCCO

InChI

1S/C4H10O2/c5-3-1-2-4-6/h5-6H,1-4H2

InChI 密鑰

WERYXYBDKMZEQL-UHFFFAOYSA-N

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一般說明

1,4-Butanediol is an industrial solvent that is mainly used in the preparation of important polymers such as polyurethanes and polybutylene terephthalate (PET).

應用

1,4-Butanediol may be used in the preparation of 3-buten-1-ol and tetrahydrofuran via dehydration. It may also be used as a reducing agent for carbonyl compounds to form the corresponding alcohols via transfer hydrogenation reaction.

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

Acute Tox. 4 Oral - STOT SE 3

標靶器官

Central nervous system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

273.2 °F - closed cup

閃點(°C)

134 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, 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

New diol processes: 1, 3-propanediol and 1, 4-butanediol
Haas T, et al.
Applied Catalysis A: General, 280(1), 83-88 (2005)
Kinetics and mechanism of tetrahydrofuran synthesis via 1, 4-butanediol dehydration in high-temperature water
Hunter SE, et al.
The Journal of Organic Chemistry, 71(16), 6229-6239 (2006)
Reduction of aldehydes and ketones by transfer hydrogenation with 1, 4-butanediol.
Maytum HC, et al.
Organic Letters, 9(21), 4387-4389 (2007)
Dehydration of 1,4-butanediol into 3-buten-1-ol catalyzed by ceria.
Sato S, et al.
Catalysis Communications, 5(8), 397-400 (2004)
Anders Hamberg et al.
Chemical communications (Cambridge, England), 48(80), 10013-10015 (2012-09-05)
The enzyme Candida antarctica lipase B was subjected to site directed mutagenesis suggested by molecular modelling. The selectivity for the enzyme increased towards a range of diols over their corresponding monoesters as an effect of the mutations.

实验方案

99%; Glycerol, ≥99.5%; Tetraethylene glycol, 99%

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