16-Bromohexadecanoic acid
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- ₹35278.68
- Product name: 16-Bromohexadecanoic acid
- CAS: 2536-35-8
- MF: C16H31BrO2
- MW: 335.32
- EINECS:
- MDL Number:MFCD00040779
- Synonyms:16-BROMO-HEXADECANECARBOXYLIC ACID;16-BROMOHEXADECANOIC ACID;16-BROMOHEXADECANOIC ACID, TECHNICAL GRADE, 85%;16-BROMOHEXADECANOIC ACID, 99+%;16-Brom-hexadecanoicacid;16-Bromohexadecanoic acid (work in progress);16-Brom-hexadecaneSre;16-Bromopalmitic acid
1 prices
Selected condition：
Brand
- Sigma-Aldrich(India)
Package
- 5G
- ManufacturerSigma-Aldrich(India)
- Product number568708
- Product description16-Bromohexadecanoic acid ≥99%
- Packaging5G
- Price₹35278.68
- Updated2022-06-14
- Buy
| Manufacturer | Product number | Product description | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|
| Sigma-Aldrich(India) | 568708 | 16-Bromohexadecanoic acid ≥99% | 5G | ₹35278.68 | 2022-06-14 | Buy |
Properties
Melting point :68-71 °C (lit.)
70-73 °C (lit.)
Boiling point :214-217 °C/1 mmHg (lit.)
Density :1.116±0.06 g/cm3(Predicted)
storage temp. :Keep in dark place,Inert atmosphere,Room temperature
form :solid
pka :4.78±0.10(Predicted)
color :White
InChI :InChI=1S/C16H31BrO2/c17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16(18)19/h1-15H2,(H,18,19)
InChIKey :PFNCOYVEMJYEED-UHFFFAOYSA-N
SMILES :C(O)(=O)CCCCCCCCCCCCCCCBr
CAS DataBase Reference :2536-35-8(CAS DataBase Reference)
Boiling point :214-217 °C/1 mmHg (lit.)
Density :1.116±0.06 g/cm3(Predicted)
storage temp. :Keep in dark place,Inert atmosphere,Room temperature
form :solid
pka :4.78±0.10(Predicted)
color :White
InChI :InChI=1S/C16H31BrO2/c17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16(18)19/h1-15H2,(H,18,19)
InChIKey :PFNCOYVEMJYEED-UHFFFAOYSA-N
SMILES :C(O)(=O)CCCCCCCCCCCCCCCBr
CAS DataBase Reference :2536-35-8(CAS DataBase Reference)
Safety Information
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| Signal word: | Warning | ||||||||||||||
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Description
16-Bromohexadecanoic acid can be used:- As a starting material in the synthesis of ceramides with ultralong chains.
- In the synthesis of 6-(nitrooxy)hexadecanoic acid intermediate, which on reacting with (L)-carnitine ethyl ester iodide gave carnitine nitro-derivatives.
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