| Identification | More | [Name]
Palmitic anhydride | [CAS]
623-65-4 | [Synonyms]
HEXADECANOIC ANHYDRIDE
PALMITIC ANHYDRIDE
hexadecanoicacid,anhydride
PALMITIC ANHYDRIDE (C16:0) GRADE II
PALMITIC ANHYDRIDE (C16:0) GRADE I
Palmitic anhydride 99+%
Bishexadecanoic anhydride
Bispalmitic anhydride
Dipalmitic anhydride | [EINECS(EC#)]
210-805-0 | [Molecular Formula]
C32H62O3 | [MDL Number]
MFCD00008992 | [Molecular Weight]
494.83 | [MOL File]
623-65-4.mol |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S25:Avoid contact with eyes . | [RIDADR ]
UN 3261 8/PG 2
| [WGK Germany ]
3
| [F ]
10-21 | [HazardClass ]
8 | [PackingGroup ]
III | [HS Code ]
29159000 |
| Hazard Information | Back Directory | [Chemical Properties]
white powder | [Uses]
Palmitic anhydride was used in the synthesis of water-soluble N-palmitoyl chitosan (PLCS) by coupling with swollen chitosan in dimethyl sulfoxide (DMSO). It was also used in the synthesis of N-acylphosphatidylserine. | [General Description]
Palmitic anhydride reacted with 20-methyl spirolide G to form a derivative with a retention time and spectrum identical with the metabolite, 17-O-palmitoyl-20-methyl spirolide G. | [Purification Methods]
It is moisture sensitive and hydrolyses in water. Purify it by refluxing with acetic anhydride for 1hour, evaporating and freeing the residue of acetic acid and anhydride by drying the residue at high vacuum and recrystallising from pet ether at low temperature. [Beilstein 2 IV 1181.] |
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