| (2S,5S)-2,5-HEXANEDIOL |
|
PRODUCT
IDENTIFICATION
|
| CAS
NO. |
34338-96-0 |

|
| EINECS
NO. |
|
| FORMULA |
C6H14O2 |
| MOL
WT. |
118.18 |
|
H.S.
CODE
|
|
| TOXICITY
|
|
| SYNONYMS |
(2S,5S)-Dihydroxyhexane;
|
|
DERIVATION
|
|
|
CLASSIFICATION
|
|
|
PHYSICAL
AND CHEMICAL PROPERTIES
|
| PHYSICAL
STATE |
white to yellow crystals |
| MELTING
POINT |
50
- 53 C |
| BOILING
POINT |
212
-215 C |
| SPECIFIC
GRAVITY |
|
| SOLUBILITY
IN WATER |
|
| pH |
|
| VAPOR
DENSITY |
|
|
AUTOIGNITION
|
|
|
NFPA
RATINGS
|
|
|
REFRACTIVE
INDEX
|
|
| FLASH
POINT |
101
C
|
| STABILITY |
Stable
under ordinary conditions. |
|
GENERAL
DESCRIPTION
|
Chiral amino alcohols and their N-protected derivatives (Cbz, t-Boc, and Fmoc)
are versatile building blocks, auxiliaries, ligand or resolving
agent in asymmetric synthesis for biological research and pharmaceutical
applications such as antitumor, anesthetic, antipasmodic, hepatotoxic,
antiinflammatory or anti-HIV activities. They are used in the synthesis of
beta-blockers, HIV protease and ACE inhibitors, chiral auxiliaries and catalytic
enantioselective ligands. Their derivatives include the forms of;
- C-terminal peptibiols
- Amphiphylic antibacterial
peptides
- Oligocarbamates
- Analogs of peptides
- Aziridines, Halogen
aminoalkyls
- Enantiomerical alpha-alkyl mono and diamines
- Enantiomerical
beta-substituted amines
- Enantiomerical beta-amino acids beta-amino
sulfoxides, beta-amino sulfides and beta-amino thiols.
- The precursors of
diverse compounds such as statines, sphingolipides and peptide isosteres.
(2S,5S)-2,5-hexanediol is
an
effective diol for C2 symmetric chiral applications such
as
chiral auxiliaries, building blocks, chiral
ligands. |
| SALES
SPECIFICATION |
|
APPEARANCE
|
white to yellow crystals |
|
CHEMICAL
PURITY
|
99.0%
min |
|
OPTICAL
PUIRTY
|
99.0%
min e.e. |
| TRANSPORTATION |
| PACKING |
|
| HAZARD
CLASS |
|
| UN
NO. |
|
| OTHER
INFORMATION |
Hazard Symbols: XI, Risk Phrases: 36/37/38,
Safety Phrases: 26-37/39 Optical
Rotation: +33° ~ +37° (C=9 in Chloroform) |
|