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(S)-1,2,4-Butanetriol

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CAS:42890-76-6
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Related articles

  • What is (S)-1,2,4-Butanetriol?
  • (S)-(-)-1,2,4-Butanetriol may be used as a starting material in the enantioselective total syntheses of (+)-azimine and (+)-ca....
  • Feb 11,2020
(S)-1,2,4-Butanetriol Basic information
Description
Product Name:(S)-1,2,4-Butanetriol
Synonyms:(S)-Butane-1,2,4-triol;(S)-1,2,4-Butanetriol,95%,99% ee;(2S)-(-)-1,2,4-Trihydroxybutane;ASTM D6584 1,2,4-Butanetriol Solution ;(2S)-BUTANE-1,2,4-TRIOL;1,2,4-BUTANETRIOL, (S);BUTANETRIOL(CAS#: 42890-76-6),INT STD#1&;(S)-()-1,2,4-Butanetriol 98%
CAS:42890-76-6
MF:C4H10O3
MW:106.12
EINECS:610-080-4
Product Categories:Chiral Building Blocks;Organic Building Blocks;Polyols;Chiral Building Blocks;Simple Alcohols (Chiral);Synthetic Organic Chemistry
Mol File:42890-76-6.mol
(S)-1,2,4-Butanetriol Structure
(S)-1,2,4-Butanetriol Chemical Properties
alpha -30 º (c=1, MeOH)
Boiling point 150 °C0.04 mm Hg(lit.)
density 1.19 g/mL at 25 °C(lit.)
refractive index n20/D 1.475(lit.)
Fp >110°C
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform (Slightly), Methanol (Sparingly), Water (Slightly)
pka14.02±0.20(Predicted)
form Oil
color Colourless
Specific Gravity1.190
AppearanceSolid Powder
Optical Rotation[α]19/D 28±2, c = 1 in methanol
Water Solubility soluble
Sensitive Hygroscopic
BRN 1719408
Stability:Hygroscopic
Major Applicationpetroleum
InChI1S/C4H10O3/c5-2-1-4(7)3-6/h4-7H,1-3H2/t4-/m0/s1
InChIKeyARXKVVRQIIOZGF-BYPYZUCNSA-N
SMILESO[C@H](CO)CCO
CAS DataBase Reference42890-76-6(CAS DataBase Reference)
Safety Information
Hazard Codes F,Xn
Risk Statements 36/37/38-41-20/21/22-11
Safety Statements 23-24/25-39-26-16-36/37-28-33-29-9
RIDADR UN 3316 9/PG 2
WGK Germany 3
3-10-21
HS Code 2905490090
Storage Class3 - Flammable liquids
Hazard ClassificationsAcute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Flam. Liq. 2
Skin Irrit. 2
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
(S)-1,2,4-Butanetriol Usage And Synthesis
Description

(S)-(-)-1,2,4-Butanetriol can be prepared via reduction of (S)-malic acid in the presence of borane-dimethyl sulfide. (S)-(-)-1,2,4-Butanetriol may be used as a starting material in the enantioselective total syntheses of (+)-azimine and (+)-carpaine. It can also be used to prepare the organic building blocks (+)-3,4-epoxy-1-butanol, (2S,4S)-4-(hydroxymethyl)-2-ferrocenyl-1,3-dioxan, (S)-1,2,4-triacetoxybutane via acetylation with acetic anhydride, and (S)-1,2,4-tris-(3,5-dinitrobenzoy1oxy)butane via esterification with 3,5-dinitrobenzoyl chloride, and so on.

Description

β-Py-C10-HPC is a violet-fluorescent analog of phosphocholine with the fluorophore on the lipophilic sn-2 acyl chain and a phosphocholine headgroup, and it is used to study the mechanism of spontaneous phospholipid transfer between single-walled phospholi

Chemical Propertiesclear colorless viscous liquid
UsesGlycerophospholipids act as regulators of various enzyme activities, and can be used as biological markers to indicate pathological states.
DefinitionChEBI: 2-deoxyerythritol is a secondary alcohol.
Biological ActivityThe DC-Chol/DOPE blend is widely useful in liposome preparation as it influences the process of encapsulation. 1:2 or 3:2 is a preferred molar ratio for DC-Chol/DOPE liposomes.
Excitation / Emission Maximum342 nm/376 nm
(S)-1,2,4-Butanetriol Preparation Products And Raw materials
Raw materials2-Butanol, 1,4-bis(phenylmethoxy)-, (2S)--->Dimethyl malate
Tag:(S)-1,2,4-Butanetriol(42890-76-6) Related Product Information
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