Propan-2-amine-d₇ hydrochloride

Name: Propan-2-amine-d 7 hydrochloride
Brand: MedChemExpress
SKU: HY-W101563S1
Rating: 4.5 (0 reviews)

Cat. No.: HY-W101563S1 Purity: 98.0%: Data Sheet
COA

SDS
Handling Instructions
FAQs
Technical Support

Propan-2-amine-d₇ (hydrochloride) is the deuterium labeled Propan-2-amine hydrochloride.

For research use only. We do not sell to patients.

Propan-2-amine-d<sub>7</sub> hydrochloride

Propan-2-amine-d₇ hydrochloride Chemical Structure

CAS No. : 106658-10-0

Size	Stock	Quantity
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO ready for reconstitution	Get quote 2-4 weeks 2-4 weeks 2-4 weeks 2-4 weeks	Estimated Time of Arrival: December 31
Solution
10 mM * 1 mL in DMSO	Get quote 2-4 weeks 2-4 weeks 2-4 weeks 2-4 weeks	Estimated Time of Arrival: December 31
Solid
25 mg	Get quote 2-4 weeks 2-4 weeks 2-4 weeks 2-4 weeks	Estimated Time of Arrival: December 31
50 mg	Get quote 2-4 weeks 2-4 weeks 2-4 weeks 2-4 weeks	Estimated Time of Arrival: December 31
100 mg	Get quote 2-4 weeks 2-4 weeks 2-4 weeks 2-4 weeks	Estimated Time of Arrival: December 31
200 mg	Get quote
500 mg	Get quote

Synthetic products have potential research and development risk.

or Bulk Inquiry

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Customer Review

Based on 1 Customer Validation

Featured Recommendations

•Related Small Molecules:

•Related Proteins:

Biological Activity
Purity & Documentation
References
Customer Review

Description

Propan-2-amine-d₇ (hydrochloride) is the deuterium labeled Propan-2-amine hydrochloride^[1].

Application

1. This compound can be used as a tracer.
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.

In Vitro

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

102.61

Formula

C₃H₃D₇ClN

CAS No.

106658-10-0

Unlabeled CAS

15572-56-2

Appearance

Solid

Color

White to off-white

SMILES

[2H]C([2H])([2H])C(N)([2H])C([2H])([2H])[2H].Cl

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Store at room temperature, keep dry and cool

In solvent	-80°C	1 year
	-20°C	6 months

Solvent & Solubility

In Vitro:

DMSO : 100 mg/mL (974.56 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions

Concentration Solvent Mass	1 mg	5 mg	10 mg

1 mM	9.7456 mL	48.7282 mL	97.4564 mL
5 mM	1.9491 mL	9.7456 mL	19.4913 mL
10 mM	0.9746 mL	4.8728 mL	9.7456 mL

View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

Molarity Calculator
Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

Concentration _(start)

Volume _(start)

Concentration _(final)

Volume _(final)

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Calculation results:

Working solution concentration: mg/mL

Purity & Documentation

Purity: 98.0%

Select Batch:

Data Sheet (277 KB) SDS (393 KB)

COA (257 KB) HNMR (197 KB)

Handling Instructions (2659 KB)

References

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief]

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg

DMSO	1 mM	9.7456 mL	48.7282 mL	97.4564 mL	243.6410 mL
	5 mM	1.9491 mL	9.7456 mL	19.4913 mL	48.7282 mL
	10 mM	0.9746 mL	4.8728 mL	9.7456 mL	24.3641 mL
	15 mM	0.6497 mL	3.2485 mL	6.4971 mL	16.2427 mL
	20 mM	0.4873 mL	2.4364 mL	4.8728 mL	12.1820 mL
	25 mM	0.3898 mL	1.9491 mL	3.8983 mL	9.7456 mL
	30 mM	0.3249 mL	1.6243 mL	3.2485 mL	8.1214 mL
	40 mM	0.2436 mL	1.2182 mL	2.4364 mL	6.0910 mL
	50 mM	0.1949 mL	0.9746 mL	1.9491 mL	4.8728 mL
	60 mM	0.1624 mL	0.8121 mL	1.6243 mL	4.0607 mL
	80 mM	0.1218 mL	0.6091 mL	1.2182 mL	3.0455 mL
	100 mM	0.0975 mL	0.4873 mL	0.9746 mL	2.4364 mL