2-methylbutane-1,4-diol
- CasNo:2938-98-9
Product Description
Manufacturer Sells Best Quality 2-methylbutane-1,4-diol 2938-98-9 with stock
- Molecular Formula: C5H12 O2
- Molecular Weight: 104.149
- Vapor Pressure: 0.0392mmHg at 25°C
- Melting Point: 50.86°C (estimate)
- Refractive Index: 1.45 (589.3 nm 18℃)
- Boiling Point: 126-127℃
- PKA: 14.91±0.10(Predicted)
- Flash Point: 98.9±13.0℃
- PSA： 40.46000
- Density: 1.4497 g/cm3 (20 ºC)
- LogP: -0.00280
2-methylbutane-1,4-diol(Cas 2938-98-9) Usage
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General Description |
2-methylbutane-1,4-diol is a chemical compound with the molecular formula C5H12O2. It is also known as tetramethylene glycol or 2,3-dihydroxy-2-methylbutane. 2-methylbutane-1,4-diol is a colorless, odorless liquid at room temperature and is commonly used as a solvent and as a building block in the synthesis of other chemicals. It has two hydroxyl groups, making it a diol, and the methyl group is located on the second carbon atom in the chain. 2-methylbutane-1,4-diol is used in various industries, including pharmaceuticals, cosmetics, and chemical manufacturing. It is important to handle this chemical with care, as it can be hazardous if not properly managed. |
InChI:InChI=1/C5H12O2/c1-5(4-7)2-3-6/h5-7H,2-4H2,1H3
2938-98-9 Relevant articles
Incorporation of 2-C-methyl-D-erythritol, a putative isoprenoid precursor in the mevalonate-independent pathway, into ubiquinone and menaquinone of Escherichia coli
Duvold, Tore,Cali, Patrizia,Bravo, Jean-Michel,Rohmer, Michel
, p. 6181 - 6184 (1997)
Incorporation of deuterium labelled 2-C-...
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Cinquini,M.,Cozzi,F.,Sannicolo,F.
, p. 4363 (1988)
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Absolute configuration of bongkrekic acid
Zylber,Gaudemer,Gaudemer
, p. 648 - 649 (1973)
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Hydroformylation reaction ligand, hydroformylation catalyst and diol preparation method
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Paragraph 0077-0078, (2021/06/22)
The invention discloses a hydroformylati...
MOF-derived hcp-Co nanoparticles encapsulated in ultrathin graphene for carboxylic acids hydrogenation to alcohols
Dong, Mei,Fan, Weibin,Gao, Xiaoqing,Zhu, Shanhui
, p. 201 - 211 (2021/06/03)
Highly efficient conversion of carboxyli...
SULFONIMIDAMIDE COMPOUNDS AS INHIBITORS OF INTERLEUKIN-1 ACTIVITY
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Paragraph 0561, (2020/02/14)
The present disclosure relates to novel ...
METHOD FOR PRODUCING ALCOHOL
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Paragraph 0101-0110, (2020/11/26)
PROBLEM TO BE SOLVED: To provide a metho...
2938-98-9 Process route
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124391-75-9,124506-31-6,15833-61-1
3-tetrahydrofuranmethanol
-
-
13423-15-9
3-methyltetrahydrofuran
-
-
2938-98-9
2-methyl-1,4-butandiol
| Conditions | Yield |
|---|---|
|
With
hydrogen;
In
water;
at 119.84 ℃;
for 4h;
under 60006 Torr;
|
-
-
97-65-4,25119-64-6
2-methylenesuccinic acid
-
-
13423-15-9
3-methyltetrahydrofuran
-
-
64190-48-3,65284-00-6,70470-05-2,1679-49-8
dihydro-4-methyl-2(3H)-furanone
-
-
2938-98-9
2-methyl-1,4-butandiol
-
-
79-31-2
isobutyric Acid
-
-
1679-47-6
3-methyltetrahydro-2-furanone
-
-
107-92-6
butyric acid
| Conditions | Yield |
|---|---|
|
With
hydrogen;
In
water;
at 200 ℃;
for 20h;
under 30003 Torr;
Autoclave;
|
2938-98-9 Upstream products
-
53627-41-1
(E)-2-methyl but-2-ene-1,4-diol
-
4676-51-1
Diethyl 2-methylsuccinate
-
54462-66-7
1,4-dibromo-2-methyl-butane
-
21307-96-0
methyl 2-methylsuccinate
2938-98-9 Downstream products
-
13423-15-9
3-methyltetrahydrofuran
-
54462-66-7
1,4-dibromo-2-methyl-butane
-
51814-03-0
1,4-diacetoxy-2-methyl-butane
-
2938-98-9
(R)-2-methylbutane-1,4-diol