Retatrutide dosing chart (mg to units)

PinPoint groups retatrutide under GLP-1 and describes a compound with GLP-1, GIP, and glucagon receptor activity. Its research-status field is Investigational. The chart draws on a 10 mg catalog vial and the five mg amounts present in the app's preset list.

Vial concentration

Water mL is treated as final solution mL in these columns.

Retatrutide: concentration in mg per mL
Vial contents1 mL water2 mL water3 mL water
10 mg10 mg/mL10 U-100 units per mg5 mg/mL20 U-100 units per mg3.3333 mg/mL30 U-100 units per mg

Vial source: PinPoint/Data/CompoundLibrary.swift, line 659, the Retatrutide entry. One documented amount is available.

Preset doses in PinPoint

Preset amounts are a conversion reference, not a personal dosing plan.

Retatrutide: amount to U-100 syringe units
Preset amount10 mg + 1 mL10 mg + 2 mL10 mg + 3 mL
2 mg20 units40 units60 units
4 mg40 units80 units120 unitsover one syringe
6 mg60 units120 unitsover one syringe180 unitsover one syringe
9 mg90 units180 unitsover one syringe270 unitsover one syringe
12 mg120 unitsover one syringeexceeds vial contents240 unitsover one syringeexceeds vial contents360 unitsover one syringeexceeds vial contents

Cited amounts

Retatrutide: source amounts converted using this page's vial and water columns
Amount (mg) and source contextFrequency as statedRoute as stated10 mg + 1 mL10 mg + 2 mL10 mg + 3 mLSource
1 mg2023 adult phase 2 study; assigned study amount. Once weeklySubcutaneous 10 units20 units30 units Retatrutide phase 2 study, NEJM (2023)Peer-reviewed studyRetrieved 2026-10-05
2 mg2023 adult phase 2 study; initial escalation amount in several groups. Once weeklySubcutaneous 20 units40 units60 units Retatrutide phase 2 study, NEJM (2023)Peer-reviewed studyRetrieved 2026-10-05
4 mg2023 adult phase 2 study; assigned study amount; some groups began at 2 or 4 mg. Once weeklySubcutaneous 40 units80 units120 unitsover one syringe Retatrutide phase 2 study, NEJM (2023)Peer-reviewed studyRetrieved 2026-10-05
8 mg2023 adult phase 2 study; assigned study amount; some groups began at 2 or 4 mg. Once weeklySubcutaneous 80 units160 unitsover one syringe240 unitsover one syringe Retatrutide phase 2 study, NEJM (2023)Peer-reviewed studyRetrieved 2026-10-05
12 mg2023 adult phase 2 study; assigned 12 mg study amount; this group began at 2 mg. Once weeklySubcutaneous 120 unitsover one syringeexceeds vial contents240 unitsover one syringeexceeds vial contents360 unitsover one syringeexceeds vial contents Retatrutide phase 2 study, NEJM (2023)Peer-reviewed studyRetrieved 2026-10-05

How to read this chart

Find the concentration column. Divide the amount by that concentration. Multiply the mL value by 100 for U-100 units. Match the amount units before dividing.

units = dose ÷ (vial mg ÷ water mL) × 100

Amount and volume

One mg equals 1,000 mcg; 100 U-100 units equals 1 mL. Concentration connects amount to volume. Read the full conversion guide.

A six-day decay reference

The app's retatrutide half-life input is 144 hours, which converts to six days. Its common-frequency field reads Every 7 days. A week of logged events therefore spans a little more than one elimination half-life in the base model. Looking across consecutive weeks can show how several timestamped entries contribute to the estimated timeline. That is a time-based calculation using the record's stored parameters; the vial chart instead divides a fixed amount by a fixed liquid volume and does not depend on a log date.

Investigational parameters in a tracking record

For absorption, retatrutide's entry stores 0.80 as bioavailability and 24 hours as the time-to-peak input. The library points to a peer-reviewed human clinical reference and regards exact exposure values as estimates drawn from that study context. A one-day peak parameter and a six-day half-life describe different portions of the modeled curve: the rise after an entry and the subsequent elimination timescale. The Investigational label remains part of the compound's identity even though the arithmetic tables can display precise decimal volumes.

Keeping the app amounts intact

Retatrutide is recorded in mg, with subcutaneous as its route and compounded vial as its form. The stored presets are 2, 4, 6, 9, and 12 mg. They do not form equal increments, so the chart uses those five values directly rather than filling in intermediate rows. The last amount is 120% of the documented 10 mg vial. Its contents flag is independent of the water column: adding a larger liquid volume changes concentration but leaves that 12-to-10 amount comparison unchanged.

Catalog amount, three concentrations

The vial citation is a supplier catalog specifying 10 mg per retatrutide vial. Dividing that amount into 1, 2, or 3 mL produces the three concentration columns. For the 6 mg preset, the fraction of the vial is 0.6. It occupies 0.6 mL in the first column and 1.8 mL in the third, giving 60 and 180 U-100 units respectively. The over-one-syringe marker appears in the latter case because the calculated volume exceeds the chart's one-milliliter capacity reference.

Questions about the conversion

What concentration is Retatrutide at 10 mg in 1 mL?

10 mg divided by 1 mL is 10 mg per mL. That volume spans 100 U-100 syringe units.

How does 2 mL change the concentration of this Retatrutide vial?

10 mg divided by 2 mL is 5 mg per mL, half the concentration in the 1 mL column.

What does the 3 mL column mean for Retatrutide?

10 mg divided by 3 mL is approximately 3.3333 mg per mL. The full 3 mL volume corresponds to 300 U-100 units.

How many units is 2 mg of Retatrutide from this vial in 2 mL?

2 mg divided by 5 mg per mL is 0.4 mL, or 40 U-100 units.

How many units is the 1 mg cited amount of Retatrutide from a 10 mg vial in 2 mL?

The arithmetic is 1 mg ÷ 5 mg/mL × 100 = 20 U-100 units (0.2 mL). The amount is cited in Retatrutide phase 2 study, NEJM (2023). 2023 adult phase 2 study; assigned study amount.

Track your calculations in the app

PinPoint for iOS brings vial setup, unit conversion, dose logs, site rotation, and protocol tracking together. Enter vial size and water volume for concentration and syringe units, then log injections with compound, dose, site, and pain level.

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