Carmustine impurity A

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Carmustine impurity A Specification

Appearance
White to off-white powder

Melting Point
140-144C

Grade
Pharmaceutical Grade

EINECS No
609-424-9

Usage
Primarily used for analytical method development and validation in the pharmaceutical industry

Ingredients
Carmustine derivative with essential functional groups for impurity analysis

CAS No
37517-32-5

HS Code
29339990

Application
Used in pharmaceutical research and quality control as a reference standard for Carmustine impurity profiling

Purity
98% (HPLC)

Ph Level
Neutral (approximately 7)

Physical Form
Solid

Molecular Formula
C5H9ClN2O2

Poisonous
NO

Shape
Crystalline

Density
1.28 Gram per cubic centimeter(g/cm3)

Properties
High stability under proper storage conditions; impurity associated with Carmustine

Storage
Store in a cool dry place at 2-8C away from light and moisture

Shelf Life
2 years under recommended storage conditions

Solubility
Slightly soluble in water; soluble in organic solvents like ethanol and DMSO

Structural Formula
Not available

Smell
Odorless

Molecular Weight
164.59 g/mol

Refractive Rate
Not available

About Carmustine impurity A

Carmustine impurity ASynonym: 1,3-Bis(2-chloroethyl)urea, BCU, NSC 36198CAS Number2214-72-4Empirical Formula (Hill Notation)C5H10Cl2N2OMolecular Weight185.05form neatformat neat

FAQs of Carmustine impurity A:

Q: What is the recommended storage condition for Carmustine impurity A?

A: Carmustine impurity A should be stored in a cool, dry place at 2-8C, away from light and moisture.

Q: What is the purity level of Carmustine impurity A?

A: The purity level of Carmustine impurity A is 98% as determined by HPLC.

Q: Is Carmustine impurity A poisonous?

A: No, Carmustine impurity A is not considered poisonous.

Q: What is the appearance and physical form of Carmustine impurity A?

A: Carmustine impurity A is a white to off-white powder with a solid crystalline form.

Q: What is the primary application of Carmustine impurity A?

A: Carmustine impurity A is primarily used in pharmaceutical research and quality control as a reference standard for Carmustine impurity profiling, including analytical method development and validation.

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