Carmustine impurity A

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Carmustine impurity A Specification

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

Structural Formula
Not available

Density
1.28 Gram per cubic centimeter(g/cm3)

Molecular Weight
164.59 g/mol

CAS No
37517-32-5

Ph Level
Neutral (approximately 7)

Physical Form
Solid

Smell
Odorless

Molecular Formula
C5H9ClN2O2

Poisonous
NO

HS Code
29339990

Grade
Pharmaceutical Grade

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

Melting Point
140-144C

Appearance
White to off-white powder

Shape
Crystalline

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

EINECS No
609-424-9

Purity
98% (HPLC)

Shelf Life
2 years under recommended storage conditions

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

Ingredients
Carmustine derivative with essential functional groups for impurity analysis

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

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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