| Identification | More | [Name]
2-Butene-1,4-diol | [CAS]
6117-80-2 | [Synonyms]
1,4-BUTENEDIOL-[Z]
2-BUTENE-1,4-DIOL
CIS-1,4-DIHYDROXY-2-BUTENE
CIS-2-BUTENE-1,4-DIOL
(z)-2-butene-1,4-diol
(2Z)-2-Butene-1,4-diol
cis-2-Buten-1,4-diol
cis-but-2-ene-1,4-diol
cis-Butenediol
1,4-Butenediol-[2]
Butenediol,95%
cis-2-Butene-1,4-diol,97%
1,4-BUTENEDIOL (B2D)
2-Butene-1,4-diol, 97% cis
2-Butene-1,4-diol, (2Z)-
1,4-dihydroxy-cis-2-butene
2-Butene-1,4-diol
cis-2-Butene-1,4-diol, 96%, remainder trans-isomer
(Z)-1,4-Dihydroxy-2-butene
(Z)-But-2-ene-1,4-diol | [EINECS(EC#)]
228-085-1 | [Molecular Formula]
C4H8O2 | [MDL Number]
MFCD00002924 | [Molecular Weight]
88.11 | [MOL File]
6117-80-2.mol |
| Chemical Properties | Back Directory | [Appearance]
clear liquid | [Melting point ]
4-10 °C(lit.)
| [Boiling point ]
235 °C(lit.)
| [density ]
1.072 g/mL at 20 °C(lit.)
| [vapor pressure ]
0.87Pa at 25℃ | [refractive index ]
n20/D 1.479
| [Fp ]
128 °C
| [storage temp. ]
Indoors | [solubility ]
Chloroform, Methanol | [form ]
Liquid | [pka]
13.88±0.10(Predicted) | [color ]
yellow
| [Water Solubility ]
soluble | [BRN ]
1679241 | [Stability:]
Light Sensitive | [InChIKey]
ORTVZLZNOYNASJ-OWOJBTEDSA-N | [LogP]
-0.9 at 25℃ | [CAS DataBase Reference]
6117-80-2(CAS DataBase Reference) | [NIST Chemistry Reference]
2-Butene-1,4-diol, (Z)-(6117-80-2) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [RTECS ]
EM4970000 | [HS Code ]
29053980 |
| Hazard Information | Back Directory | [Chemical Properties]
clear liquid | [Uses]
cis-2-Butene-1, 4-diol is used as a probe for studying isomerization versus hydrogenation and hydrogenolysis reactions. (DPCB-OMe) efficiently catalyzes cyclodehydration of cis-2-butene-1,4-diol with active methylene compounds to give 2-vinyl-2,3-dihydrofurans in good to high yields. Grubbs's cross metathesis of eugenol with cis-2-butene-1, 4-diol to make a natural product, an organometallic experiment. | [storage]
Store at -20°C |
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