16-Bromohexadecanoic acid

CAS No.：2536-35-8

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This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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16-Bromohexadecanoic acid Basic information

Product Name:	16-Bromohexadecanoic acid
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
CAS:	2536-35-8
MF:	C16H31BrO2
MW:	335.32
EINECS:
Product Categories:	Organic acids;C13 to C42+;Carbonyl Compounds;Carboxylic Acids
Mol File:	2536-35-8.mol

16-Bromohexadecanoic acid Chemical 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
pka	4.78±0.10(Predicted)
CAS DataBase Reference	2536-35-8(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	38
Safety Statements	37
WGK Germany	3
Hazard Note	Irritant
HS Code	2915907098

MSDS Information

Provider	Language
SigmaAldrich	English

16-Bromohexadecanoic acid Usage And Synthesis

Uses	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.

16-Bromohexadecanoic acid Preparation Products And Raw materials

Preparation Products

16-Bromohexadecanol-->1,16-DIBROMOHEXADECANE-->16-HEXADECANOLIDE

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