N- Octyl Bromide

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N- Octyl Bromide Specification

Molecular Weight
193.13 g/mol

Molecular Formula
C8H17Br

Boiling point
201-203 C

Smell
Characteristic, Mild

Structural Formula
CH3(CH2)7Br

HS Code
29036910

Taste
Not Determined

Refractive Rate
n20/D 1.444

Classification
Alkyl Halide / Organic Intermediate

Grade
Analytical, Industrial

Purity
98%

Application
Pharmaceutical Intermediates, Organic Synthesis, Laboratory Reagent

Appearance
Clear Colorless to Pale Yellow Liquid

CAS No
111-83-1

EINECS No
203-911-8

Other Names
1-Bromo-octane, Octyl Bromide

Usage
Chemical Synthesis, Research, Fine Chemicals, Specialty Chemicals

Melting Point
-8 C

Density
1.077 Gram per cubic centimeter(g/cm3)

Solubility
Insoluble in Water, Soluble in Organic Solvents

Raw Material
n-Octanol, Bromine

Manufacturing Method
Bromination of n-Octanol using PBr3 or other Brominating Agent

Stability
Stable under Recommended Storage Conditions

Shelf Life
24 Months (Sealed & Proper Storage Conditions)

Precautionary Statements
Avoid Inhalation, Skin and Eye Contact; Use Personal Protective Equipment

Hazard Class
Irritant (Xi), Environmental Hazard

Storage Conditions
Store in Cool, Well-ventilated Place, Away from Sources of Ignition

UN Number
Not regulated for transport

Packing
500 ml / 1 L / 25 L Bottles or Custom Packaging

Flash Point
82 °C

About N- Octyl Bromide

Name of Product	N-Octyl Bromide
CAS No	111-83-1
Formula	C8H17Br
IUPAC Name	1-bromobutane
InChI	InChI=1S/C4H9Br/c1-2-3-4-5/h2-4H2,1H3
InChI Key	MPPPKRYCTPRNTB-UHFFFAOYSA-N
Canonical SMILES	CCCCBr
CAS	109-65-9
EC Number	203-691-9
UN Number	1126
UNII	SAV6Y78U3D
Wikipedia	1-Bromobutane
Description	Clear, colourless liquid
Water	Not more than 0.3 %
Acidity	Not more than 0.1 %
Purity by GC	Not less than 98.0%
Other name / synonyms	1-Bromooctane
	n-Octyl bromide
	Octyl bromide
	111-83-1
	1-Octylbromide
	Octane, 1-bromo-
	bromooctane
	1-Bromo octane
	1-Bromo-octane
	1-BROMO-N-OCTANE
	VMKOFRJSULQZRM-UHFFFAOYSA-N
	NSC 9821
	EINECS 203-912-9
	SBB059937
	AI3-15807
	octylbromide
	n-octylbromide
	octanyl bromide
	a-bromo octane
	n-bromooctane;
	8-bromooctane
	1-octyl bromide
	1 -octyl bromide
	CAPRYL BROMIDE
	AC1L1QCT
	AC1Q2VWM
	ACMC-1C6SS
	DSSTox_CID_1938
	UNII-Q382HPC6LC
	DSSTox_RID_76414
	Q382HPC6LC
	DSSTox_GSID_21938
	SCHEMBL33503
	WLN: E8
	KSC174K7P
	152951_ALDRICH
	AC1Q27V1
	CCRIS 8914
	CHEMBL156047
	Jsp000886
	Jsp000888
	01084_FLUKA
	CTK0H4577
	NSC9821
	MolPort-000-157-872
	LABOTEST-BB LTBB001161
	NSC-9821
	Tox21_302112
	ANW-16327
	AR-1C2044
	AKOS000119808
	AS03445
	EBD2203385
	NE10018
	RP25224
	RTR-002318
	TRA0046199
	NCGC00255306-01
	AN-43092
	CAS-111-83-1
	I860
	KB-11812
	LS-97846
	SC-19080
	DB-050360
	TR-002318
	B0626
	FT-0628359
	FT-0657190
	ST50214522
	EN300-19979
	A15118
	3B4-0648
	I14-6068

Applications and Uses

N-Octyl Bromide serves as a vital building block in pharmaceutical intermediates, specialty chemicals, and laboratory reagents. Its role as an alkyl halide makes it a preferred choice for organic synthesis, particularly for introducing the octyl group in complex molecules. Research facilities and chemical manufacturers utilize it extensively for the preparation of fine chemicals and in custom synthesis projects.

Safe Handling and Storage

Due to its irritant and environmental hazard classification, N-Octyl Bromide should be handled with care. Store in tightly sealed containers in cool, well-ventilated areas and away from ignition sources. Personal protective equipment is essential to avoid skin, eye contact, and inhalation. Stability is maintained under recommended conditions, ensuring long shelf life and consistent product quality.

Packaging and Quality Assurance

Available in 500 ml, 1 L, and 25 L bottles, as well as custom packaging, N-Octyl Bromide caters to diverse industrial and research needs. Each batch is rigorously tested for purity (98%) and physical attributes, ensuring compliance with analytical and industrial standards. Customers benefit from flexible packaging and reliable delivery methods, with product traceability for safety and regulatory transparency.

FAQs of N- Octyl Bromide:

Q: How is N-Octyl Bromide produced?

A: N-Octyl Bromide is synthesized by brominating n-Octanol using phosphorus tribromide (PBr3) or other brominating agents, resulting in a high-purity alkyl halide suited for organic synthesis and intermediary roles in fine chemical production.

Q: What are the recommended storage conditions for N-Octyl Bromide?

A: The product should be kept in a cool, well-ventilated place, away from sources of ignition. Containers should remain tightly sealed to preserve stability and maintain a shelf life of up to 24 months under proper storage.

Q: When should personal protective equipment be used with N-Octyl Bromide?

A: Personal protective equipment must be worn during all handling operations to avoid inhalation, skin, and eye contact, as the compound is classified as an irritant and poses environmental risks.

Q: Where can N-Octyl Bromide be sourced and in what packaging sizes?

A: N-Octyl Bromide is available from leading exporters, manufacturers, and suppliers in India, offered in 500 ml, 1 L, 25 L bottles, or custom packaging tailored to specific requirements.

Q: What makes N-Octyl Bromide beneficial for organic synthesis and research?

A: Its high purity (98%), chemical stability, and solubility in organic solvents make it an ideal intermediate for organic synthesis, pharmaceutical research, and laboratory-scale chemical development.

Q: What safety precautions are recommended during the usage of N-Octyl Bromide?

A: Users should avoid direct inhalation and contact with skin or eyes, keeping the product away from flames and heat. Employing suitable safety gear and working in controlled environments helps mitigate hazard risks.

Q: How is N-Octyl Bromide typically used in laboratory and industrial applications?

A: It is employed as a reagent for chemical synthesis, the preparation of specialty chemicals, and as a pharmaceutical intermediate. Its role facilitates the incorporation of octyl groups into molecular structures for various targeted reactions.

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